Classification Term: 170574

Simple indole alkaloids (ontology term: 5e638a4e1e30ddd4b888e344a22041e5)

found 500 associated metabolites at sub_class metabolite taxonomy ontology rank level.

Ancestor: Tryptophan alkaloids

Child Taxonomies: There is no child term of current ontology term.

5-Methoxytryptamine

2-(5-methoxy-1H-indol-3-yl)ethan-1-amine

C11H14N2O (190.1106)


5-Methoxytryptamine, also known as mexamine or 5-MT, belongs to the class of organic compounds known as tryptamines and derivatives. Tryptamines and derivatives are compounds containing the tryptamine backbone, which is structurally characterized by an indole ring substituted at the 3-position by an ethanamine. It is biosynthesized via the deacetylation of melatonin in the pineal gland. 5-MT acts as a full agonist at the 5-HT1, 5-HT2, 5-HT4, 5-HT6, and 5-HT7 receptors. 5-Methoxytryptamine exists in all living organisms, ranging from bacteria to humans. Its affinity for the 5-HT5A receptor is unknown. It has no affinity for the 5-HT3 receptor and is affinity for the 5-HT1E receptor is very weak in comparison to the other 5-HT1 receptors. 5-MT has been shown to occur naturally in the body in low levels. Serotonin derivative proposed as potentiator for hypnotics and sedatives. [HMDB] KEIO_ID M040

   

Methyl indole-3-acetate

(1H-Indol-3-yl)acetic acid methyl ester

C11H11NO2 (189.079)


Indole-3-methyl acetate, also known as methyl indole-3-acetate (methyl-IAA), is a catabolite of tryptophan converted by the gut microbiota. After absorption through the intestinal epithelium, tryptophan catabolites enter the bloodstream and are later excreted in the urine (PMID: 30120222). Pediatric enthesitis-related arthritis (ERA) patients (i.e. spondyloarthropathy associated with inflammatory bowel disease) have intestinal inflammation and decreased gut microbial diversity. Such alterations in the gut microbiota resulted in the reduction of tryptophan metabolism and several tryptophan metabolites in pediatric ERA fecal samples, including indole-3-methyl acetate (PMID: 27786174). Indole-3-methyl acetate is found in apple, and has been isolated from immature seeds of beach pea (Lathyrus maritimus), Vicia amurensis, wild soybean (Glycine soja), lobiya (Vigna catiang var. sinensis) and hyacinth bean (Dolichos lablab). Isolated from immature seeds of beach pea (Lathyrus maritimus), Vicia amurensis, wild soybean (Glycine soja), lobiya (Vigna catiang variety sinensis) and hyacinth bean (Dolichos lablab). Indole-3-methyl acetate is found in many foods, some of which are gram bean, yellow wax bean, common bean, and sweet orange. Methyl 2-(1H-indol-3-yl)acetate is an endogenous metabolite.

   

N-Methyltryptamine

[2-(1H-indol-3-yl)ethyl](methyl)amine

C11H14N2 (174.1157)


N-Methyltryptamine (NMT), or monomethyltryptamine, is a tryptamine alkaloid that has been found in the bark, shoots and leaves of numerous plants. (wikipedia). N-Methyltryptamine was detected in urine from all autistic patients with mental retardation and epilepsy and many autistic patients (32/47) with mental retardation (PubMed ID 8747157 ). N-Methyltryptamine (NMT), or monomethyltryptamine, is a tryptamine alkaloid that has been found in the bark, shoots and leaves of numerous plants. (wikipedia)

   

N-Acetyltryptophan

(2S)-2-[(1-hydroxyethylidene)amino]-3-(1H-indol-3-yl)propanoic acid

C13H14N2O3 (246.1004)


N-Acetyl-L-tryptophan or N-Acetyltryptophan, belongs to the class of organic compounds known as N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. N-Acetyltryptophan can also be classified as an alpha amino acid or a derivatized alpha amino acid. Technically, N-Acetyltryptophan is a biologically available N-terminal capped form of the proteinogenic alpha amino acid L-tryptophan. N-acetyl amino acids can be produced either via direct synthesis of specific N-acetyltransferases or via the proteolytic degradation of N-acetylated proteins by specific hydrolases. N-terminal acetylation of proteins is a widespread and highly conserved process in eukaryotes that is involved in protection and stability of proteins (PMID: 16465618). About 85\\\\\% of all human proteins and 68\\\\\% of all yeast proteins are acetylated at their N-terminus (PMID: 21750686). Several proteins from prokaryotes and archaea are also modified by N-terminal acetylation. The majority of eukaryotic N-terminal-acetylation reactions occur through N-acetyltransferase enzymes or NAT’s (PMID: 30054468). These enzymes consist of three main oligomeric complexes NatA, NatB, and NatC, which are composed of at least a unique catalytic subunit and one unique ribosomal anchor. The substrate specificities of different NAT enzymes are mainly determined by the identities of the first two N-terminal residues of the target protein. The human NatA complex co-translationally acetylates N-termini that bear a small amino acid (A, S, T, C, and occasionally V and G) (PMID: 30054468). NatA also exists in a monomeric state and can post-translationally acetylate acidic N-termini residues (D-, E-). NatB and NatC acetylate N-terminal methionine with further specificity determined by the identity of the second amino acid. N-acetylated amino acids, such as N-acetyltryptophan can be released by an N-acylpeptide hydrolase from peptides generated by proteolytic degradation (PMID: 16465618). In addition to the NAT enzymes and protein-based acetylation, N-acetylation of free tryptophan can also occur. Many N-acetylamino acids, including N-acetyltryptophan are classified as uremic toxins if present in high abundance in the serum or plasma (PMID: 26317986; PMID: 20613759). Uremic toxins are a diverse group of endogenously produced molecules that, if not properly cleared or eliminated by the kidneys, can cause kidney damage, cardiovascular disease and neurological deficits (PMID: 18287557). N-Acetyltryptophan has also been used as a protein stabilizer. It prevents protein molecules from oxidative degradation by scavenging oxygen dissolved in protein solutions (PMID: 21903216 ). N-Acetyltryptophan has been identified as a catabolite of tryptophan generated by the gut microbiota. After absorption through the intestinal epithelium, tryptophan catabolites enter the bloodstream and are later excreted in the urine (PMID: 28916042). N-Acetyltryptophan is an inhibitor of cytochrome c release and an antagonist of the neurokinin 1 receptor (NK-1R). These inhibitory effects are thought have a useful role in neuroprotection. For instance, in mouse models of amyotrophic lateral sclerosis (ALS) the administration of N-Acetyltryptophan has been shown delay disease onset, extend survival, and ameliorate deterioration in motor performance ALS transgenic mice (PMID: 25986728). N-acetyltryptophan has been shown to significantly reduce blood-brain barrier permeability and improve functional outcome in rat models of traumatic brain injury (PMID: 29256408). N-Acetyltryptophan has also been shown to have a role in preventing hepatic ischemia-reperfusion injury. This is thought to occur through de-activation of the RIP2/caspase/IL-1beta signaling pathway (PMID: 31184936). D004791 - Enzyme Inhibitors > D011480 - Protease Inhibitors Ac-DL-Trp-OH is an endogenous metabolite. Ac-DL-Trp-OH is an endogenous metabolite. N-Acetyl-L-tryptophan is an endogenous metabolite.

   

Dimethyltryptamine

N-(2-(1H-indol-3-yl)Ethyl)-N,N-dimethylamine (acd/name 4.0)

C12H16N2 (188.1313)


An N-methylated indoleamine derivative, a serotonergic hallucinogen found in several plants, especially Prestonia amazonica (Apocynaceae) and in mammalian brain, blood, and urine. It apparently acts as an agonist at some types of serotonin receptors and an antagonist at others.; DMT is a derivative of tryptamine with two additional methyl groups at the amine nitrogen atom. DMT is often synthesized by the Speeter-Anthony synthesis from indole using oxalyl chloride, dimethylamine, and lithium aluminium hydride as reagents. DMT is usually used in its base form, but it is more stable as a salt, e.g. as a fumarate. In contrast to DMTs base, its salts are water-soluble. DMT in solution degrades relatively fast and should be stored protected from air and light in a freezer. Highly pure DMT crystals, when evaporated out of a solvent and depositing upon glass, often produce small but highly defined white crystalline needles which when viewed under intense light will sparkle, and appear colorless under high magnification. In labs, it has been known to be explosive under a certain degree of heat.; DMT is a powerful psychoactive substance. If DMT is smoked, injected, or orally ingested with an MAOI, it can produce powerful entheogenic experiences including intense visual hallucinations, euphoria, even true hallucinations (perceived extensions of reality). A trip sitter is recommended to assist the drug user in staying physically and mentally healthy, and, in the case of smoked DMT, to catch the pipe if the user loses awareness of it.; DMT is classified in the United States as a Schedule I drug. In December of 2004, the Supreme Court lifted a stay thereby allowing the Brazil-based Uniaeo do Vegetal (UDV) church to use a decoction containing DMT in their Christmas services that year. This decoction is a tea made from boiled leaves and vines, known as hoasca within the UDV, and ayahuasca in different cultures. In Gonzales v. O Centro EspArita Beneficente Uniaeo do Vegetal, the Supreme Court heard arguments on November 1, 2005 and unanimously ruled in February 2006 that the U.S. federal government must allow the UDV to import and consume the tea for religious ceremonies under the 1993 Religious Freedom Restoration Act. There are no drug tests that would show DMT usage. None of the basic NIDA 5 drug tests or any extended drug test will show a result for DMT.; Dimethyltryptamine (DMT), also known as N,N-dimethyltryptamine, is a psychedelic tryptamine. It is not to be confused with 5-MeO-DMT and is similar in chemical structure to the neurotransmitter serotonin. DMT is created in small amounts by the human body during normal metabolism by the enzyme tryptamine-N-methyltransferase. Pure DMT at room temperature is a clear or white crystalline solid. DMT was first chemically synthesized in 1931. It also occurs naturally in many species of plants. DMT-containing plants are used in several South American shamanic practices. It is one of the main active constituents of snuffs like yopo and of the drink ayahuasca.; Oral ingestion: DMT, which is broken down by the digestive enzyme monoamine oxidase, is practically inactive if taken orally, unless combined with a monoamine oxidase inhibitor (MAOI). The traditional South American ayahuasca, or yage, is a tea mixture containing DMT and a MAOI. There are a number of admixtures to this brew, but most commonly it is simply the leaves of Psychotria viridis (containing DMT), and the vine Banisteriopsis caapi (the source of MAOI). Other DMT containing plants, including Diplopterys cabrerana, are sometimes used in ayahuasca in different areas of South America. Two common sources in the western US are Reed canary grass (Phalaris arundinacea) and Harding grass (Phalaris aquatica). These invasive grasses contain low levels of DMT and other alkaloids. Taken orally with an appropriate MAOI, DMT produces a long lasting (over 3 hour), slow, but deep spiritual experience. MAOIs should be used with extreme caution as they... Dimethyltryptamine is an N-methylated indoleamine derivative, a serotonergic hallucinogen found in several plants, especially Prestonia amazonica (Apocynaceae) and in mammalian brain, blood, and urine. It apparently acts as an agonist at some types of serotonin receptors and an antagonist at others. DMT is a derivative of tryptamine with two additional methyl groups at the amine nitrogen atom. DMT is often synthesized by the Speeter-Anthony synthesis from indole using oxalyl chloride, dimethylamine, and lithium aluminium hydride as reagents. DMT is usually used in its base form, but it is more stable as a salt, e.g. as a fumarate. In contrast to DMTs base, its salts are water-soluble. DMT in solution degrades relatively fast and should be stored protected from air and light in a freezer. Highly pure DMT crystals, when evaporated out of a solvent and depositing upon glass, often produce small but highly defined white crystalline needles which when viewed under intense light will sparkle, and appear colorless under high magnification. In labs, it has been known to be explosive under a certain degree of heat. DMT is a powerful psychoactive substance. If DMT is smoked, injected, or orally ingested with an MAOI, it can produce powerful entheogenic experiences including intense visual hallucinations, euphoria, even true hallucinations (perceived extensions of reality). A trip sitter is recommended to assist the drug user in staying physically and mentally healthy, and, in the case of smoked DMT, to catch the pipe if the user loses awareness of it. DMT is classified in the United States as a Schedule I drug. There are no drug tests that would show DMT usage. None of the basic NIDA 5 drug tests or any extended drug test will show a result for DMT. Dimethyltryptamine (DMT), also known as N,N-dimethyltryptamine, is a psychedelic tryptamine. It is not to be confused with 5-MeO-DMT and is similar in chemical structure to the neurotransmitter serotonin. DMT is created in small amounts by the human body during normal metabolism by the enzyme tryptamine-N-methyltransferase. Pure DMT at room temperature is a clear or white crystalline solid. DMT was first chemically synthesized in 1931. It also occurs naturally in many species of plants. DMT-containing plants are used in several South American shamanic practices. It is one of the main active constituents of snuffs like yopo and of the drink ayahuasca. Oral ingestion: DMT, which is broken down by the digestive enzyme monoamine oxidase, is practically inactive if taken orally, unless combined with a monoamine oxidase inhibitor (MAOI). The traditional South American ayahuasca, or yage, is a tea mixture containing DMT and a MAOI. There are a number of admixtures to this brew, but most commonly it is simply the leaves of Psychotria viridis (containing DMT), and the vine Banisteriopsis caapi (the source of MAOI). Other DMT containing plants, including Diplopterys cabrerana, are sometimes used in ayahuasca in different areas of South America. Two common sources in the western US are Reed canary grass (Phalaris arundinacea) and Harding grass (Phalaris aquatica). These invasive grasses contain low levels of DMT and other alkaloids. Taken orally with an appropriate MAOI, DMT produces a long lasting (over 3 hour), slow, but deep spiritual experience. MAOIs should be used with extreme caution as they can have lethal complications with some prescription drugs, such as SSRI antidepressants, and some over-the-counter drugs. Smoked: If DMT is smoked, the maximal effects last for a short period of time (5-30 minutes dose dependent). The onset after inhalation is very fast (less than 45 seconds) and maximal effects are reached within about a minute. The Business Mans lunch trip is a common name due to the relatively short duration of vaporized, insufflated, or injected DMT. D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D017366 - Serotonin Receptor Agonists D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D012702 - Serotonin Antagonists D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D006213 - Hallucinogens

   

Indole-3-carboxylic acid

1H-Indole-3-carboxylic acid

C9H7NO2 (161.0477)


Indole-3-carboxylic acid, also known as 3-carboxyindole or 3-indolecarboxylate, belongs to the class of organic compounds known as indolecarboxylic acids and derivatives. Indolecarboxylic acids and derivatives are compounds containing a carboxylic acid group (or a derivative thereof) linked to an indole. Naphthylmethylindoles: Any compound containing a 1H-indol-3-yl-(1-naphthyl)methane structure with substitution at the nitrogen atom of the indole ring by an alkyl, haloalkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl)methyl, or 2-(4-morpholinyl)ethyl group whether or not further substituted in the indole ring to any extent and whether or not substituted in the naphthyl ring to any extent. One example given is JWH-250. Outside of the human body, indole-3-carboxylic acid has been detected, but not quantified in several different foods, such as brassicas, broccoli, pulses, common beets, and barley. This could make indole-3-carboxylic acid a potential biomarker for the consumption of these foods. Notice the pentyl group substituted onto the nitrogen atom of the indole ring. Note that this definition encompasses only those compounds that have OH groups attached to both the phenyl and the cyclohexyl rings, and so does not include compounds such as O-1871 which lacks the cyclohexyl OH group, or compounds such as JWH-337 or JWH-344 which lack the phenolic OH group. Present in plants, e.g. apple (Pyrus malus), garden pea (Pisum sativum) and brassicas Indole-3-carboxylic acid is a normal urinary indolic tryptophan metabolite and has been found elevated in patients with liver diseases[1][2]. Indole-3-carboxylic acid is a normal urinary indolic tryptophan metabolite and has been found elevated in patients with liver diseases[1][2].

   

Psilocin

3-[2-(Dimethylamino)ethyl]-1H-indol-4-ol

C12H16N2O (204.1263)


Psilocin (4-OH-DMT), an aromatic compound, sometimes also spelled psilocine, psilocyn, or psilotsin, is a psychedelic mushroom alkaloid. It is found in most psychedelic mushrooms together with its phosphorylated counterpart psilocybin. Psilocin is a Schedule I drug under the Convention on Psychotropic Substances. The mind-altering effects of psilocin are highly variable and subjective, but resemble those caused by LSD and mescaline. The effects typically last anywhere from three to eight hours depending on certain variables (such as metabolism, food interaction); however the effects can seem to last much longer due to psilocins ability to distort the perception of time. Sulfur analogs are known with a benzothienyl replacement as well as 4-SH-DMT. N1-methylpsilocin is a functionally 5-HT2C receptor preferring agonists. 4-fluoro-N,N-dimethyltryptamine is known. O-Acetylpsilocin is an acetylized analog of psilocin, also known as 4-AcO-DMT. Additionally, substitution of a methyl group at the dimethylated nitrogen with an isopropyl or ethyl group yields 4-HO-MIPT (4-Hydroxy-N-Methyl-N-Isopropyltryptamine) and 4-HO-MET (4-Hydroxy-N-Methyl-N-Ethyltryptamine), respectively. D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D006213 - Hallucinogens

   

(1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate

[(2R,3S)-2,3-dihydroxy-3-(1H-indol-3-yl)propoxy]phosphonic acid

C11H14NO6P (287.0559)


Indole-3-glycerol phosphate, also known as c1-(3-indolyl)-glycerol 3-phosphate, is a member of the class of compounds known as 3-alkylindoles. 3-alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position. Indole-3-glycerol phosphate is slightly soluble (in water) and a moderately acidic compound (based on its pKa). Indole-3-glycerol phosphate can be found in a number of food items such as german camomile, lambsquarters, other soy product, and hazelnut, which makes indole-3-glycerol phosphate a potential biomarker for the consumption of these food products. Indole-3-glycerol phosphate may be a unique E.coli metabolite. D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents

   

4-O-(Indole-3-acetyl)-D-glucopyranose

(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl 2-(1H-indol-3-yl)acetate

C16H19NO7 (337.1161)


4-o-(indole-3-acetyl)-d-glucopyranose, also known as indole-3-acetyl-beta-1-D-glucose or B-D-glucopyranose, 1-(1h-indole-3-acetic acid), belongs to indole-3-acetic acid derivatives class of compounds. Those are compounds containing an acetic acid (or a derivative) linked to the C3 carbon atom of an indole. 4-o-(indole-3-acetyl)-d-glucopyranose is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). 4-o-(indole-3-acetyl)-d-glucopyranose can be found in corn, which makes 4-o-(indole-3-acetyl)-d-glucopyranose a potential biomarker for the consumption of this food product. D006133 - Growth Substances > D010937 - Plant Growth Regulators > D007210 - Indoleacetic Acids

   

5-Hydroxyindoleacetaldehyde

2-(5-hydroxy-1H-indol-3-yl)acetaldehyde

C10H9NO2 (175.0633)


5-Hydroxyindoleacetaldehyde, also known as 5-HIAL, belongs to the class of organic compounds known as hydroxyindoles. These are organic compounds containing an indole moiety that carries a hydroxyl group. Within humans, 5-hydroxyindoleacetaldehyde participates in a number of enzymatic reactions. In particular, 5-hydroxyindoleacetaldehyde can be biosynthesized from serotonin through its interaction with the enzyme kynurenine 3-monooxygenase. In humans, 5-hydroxyindoleacetaldehyde is involved in tryptophan metabolism. Outside of the human body, 5-hydroxyindoleacetaldehyde has been detected, but not quantified in, several different foods, such as garden rhubarbs, black radish, oriental wheat, garden tomato, and wild leeks. This could make 5-hydroxyindoleacetaldehyde a potential biomarker for the consumption of these foods. 5-Hydroxyindoleacetaldehyde is a biogenic aldehyde of serotonin derived from the action of monoamine oxidase (MAO) (PMID: 11306106, 2470392). 5-hydroxyindoleacetaldehyde, also known as 5-hial, is a member of the class of compounds known as hydroxyindoles. Hydroxyindoles are organic compounds containing an indole moiety that carries a hydroxyl group. 5-hydroxyindoleacetaldehyde is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). 5-hydroxyindoleacetaldehyde can be found in a number of food items such as durian, squashberry, black huckleberry, and daikon radish, which makes 5-hydroxyindoleacetaldehyde a potential biomarker for the consumption of these food products. 5-hydroxyindoleacetaldehyde can be found primarily in blood, feces, and urine, as well as in human kidney and liver tissues. In humans, 5-hydroxyindoleacetaldehyde is involved in the tryptophan metabolism. D006133 - Growth Substances > D010937 - Plant Growth Regulators > D007210 - Indoleacetic Acids COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

Indoxyl

1H-Indol-3-ol

C8H7NO (133.0528)


Indoxyl, also known as 1H-indol-3-ol, belongs to the class of organic compounds known as hydroxyindoles. These are organic compounds containing an indole moiety that carries a hydroxyl group. Indoxyl is isomeric with oxindol and is obtained as an oily liquid. Indoxyl exists in all living organisms, ranging from bacteria to humans. Indoxyl is obtained from indican, which is a glycoside. Obermayers reagent is a dilute solution FeCl3 in hydrochloric acid. The hydrolysis of indican yields β-D-glucose and indoxyl. Indigo dye is a product of the reaction of indoxyl by a mild oxidizing agent such as atmospheric oxygen. In chemistry, indoxyl is a nitrogenous substance with the chemical formula: C8H7NO. Indoxyl can be found in urine and is titrated with Obermayers reagent. Indigo dye is a product of the reaction of indoxyl by a mild oxidizing agent, eg. atmospheric oxygen.

   

Acremoauxin A

Acremoauxin A; 2-(3-Indolyl)propanoylmannitol

C16H21NO6 (323.1369)


An indolyl carboxylate ester obtained by formal condensation of one of the primary hydroxy groups of D-arabinitol with the carboxy group of (2R)-2-(indol-3-yl)propanoic acid.

   

Indican

(2S,3R,4S,5S,6R)-2-((1H-Indol-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

C14H17NO6 (295.1056)


Indican is a colourless, water-soluble organic compound consisting of an indole ring conjugated to glucose. It is an indole glycoside. Its hydrolysis yields β-D-glucose and indoxyl. Indoles are compounds which consist of a pyrrole ring fused to benzene to form 2,3-benzopyrrole. The oxidation of indican by a mild oxidizing agent, e.g. atmospheric oxygen or CYP450 enzymes, yields indigo dye which is blue in colour. Indican is a substance occurring naturally in the urine of humans and mammals and also in blood plasma as a normal metabolite of tryptophan. Tryptophan is first converted to indole by gut bacteria. Following absorption from the gut, indole is converted to 3-hydroxyindole (indoxyl or indican) in the liver, where it is again then conjugated with sulfuric acid or glucoronic acid through normal xenobiotic metabolism pathways. It is then transported to the kidneys for excretion. In individuals affected by the blue diaper syndrome (a rare, autosomal recessive metabolic disorder characterized in infants by bluish urine-stained diapers), the patients exhibit a defect in tryptophan metabolism, leading to an increase in indican synthesis. Indican is then excreted into the urine and from there into the diaper where, upon exposure to air, it is converted to indigo blue dye due to oxidation by atmospheric oxygen. An increased urinary excretion of indican is seen in Hartnup disease from the bacterial degradation of unabsorbed tryptophan (PMID: 19967017). Hartnup disease is an autosomal recessive metabolic disorder affecting the absorption of nonpolar amino acids (particularly tryptophan), which leads to excessive bacterial fermentation of tryptophan (to indole) in the gut. Indican has also been identified as a uremic toxin according to the European Uremic Toxin Working Group (PMID: 22626821). Its excretion is decreased by the presence of Lactobacillus bacteria in the gut (PMID: 6785555 ). Indican is an indolyl carbohydrate, a beta-D-glucoside and an exopolysaccharide. Indican is a natural product found in Indigofera suffruticosa, Isatis tinctoria, and other organisms with data available. Indican is a toxic metabolite derived from dietary proteins and tryptophan. In the intestine, proteins and tryptophan are converted to indole by tryptophanase-expressing organisms. In the liver, indole is hydroxylated to form indoxyl and indoxyl is sufated to produce indican. Overproduction of indican is associated with glomerular sclerosis, interstitial fibrosis and renal failure. Indican is a uremic toxin. Uremic toxins can be subdivided into three major groups based upon their chemical and physical characteristics: 1) small, water-soluble, non-protein-bound compounds, such as urea; 2) small, lipid-soluble and/or protein-bound compounds, such as the phenols and 3) larger so-called middle-molecules, such as beta2-microglobulin. Chronic exposure of uremic toxins can lead to a number of conditions including renal damage, chronic kidney disease and cardiovascular disease. It is a colourless organic compound, soluble in water, naturally occurring in Indigofera plants. It is a precursor of indigo dye. Indican interferes with many commercial procedures for measuring total bilirubin[6] which can be a problem for renal failure patients where blood indican levels are raised. It can cause gastrointestinal symptoms in patients where protein absorption is reduced - like Hartnups disease, allowing for greater bacterial decomposition of the Tryptophan to indole and its conversion to indican.

   

Thienodolin

Thienodolin

C11H7ClN2OS (249.9968)


An indole alkaloid that is a thienoindole ring with carboxamide group and chlorine substituents at positions 2 and 6 respectively.

   

Indole-3-methanamine

1-(1H-Indol-3-yl)methanamine

C9H10N2 (146.0844)


Indole-3-methanamine, also known as 3-aminomethylindole or 3-indolylmethylamine, belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position. An aralkylamino compound that is indole substituted at position 3 by an aminomethyl group. Indole-3-methanamine is a very strong basic compound (based on its pKa). Outside of the human body, indole-3-methanamine has been detected, but not quantified in, barley, cereals, and cereal products. This could make indole-3-methanamine a potential biomarker for the consumption of these foods. Detected in Hordeum vulgare (barley). 1H-Indole-3-methanamine is found in barley and cereals and cereal products. Indole-3-methanamine is a potential biomarker for the consumption of these foods such as barley, cereals, and cereal product[1].

   

Norbaeocystin

Norbaeocystin

C10H13N2O4P (256.0613)


A tryptamine alkaloid that is tryptamine carrying an additional phosphoryloxy substituent at position 4.

   

Baeocystin

Baeocystin

C11H15N2O4P (270.0769)


A tryptamine alkaloid that is N-methyltryptamine carrying an additional phosphoryloxy substituent at position 4.

   

(2R)-2-hydroxy-3-(1H-indol-3-yl)propanoic acid

(2R)-2-hydroxy-3-(1H-indol-3-yl)propanoic acid

C11H11NO3 (205.0739)


   

2-Indolecarboxylic acid

1H-Indole-2-carboxylic acid

C9H7NO2 (161.0477)


2-Indolecarboxylic acid is a strong inhibitor of lipid peroxidation, similar to melatonin and some structurally related indole compounds. Lipid peroxidation with tert-butyl hydroperoxide is a source of free radicals (PMID 12236544). 2-Indolecarboxylic acid is a phenolic components known to exist in Korean ginseng (Koryo Insam Hakhoechi (1996), 20(3), 284-290) and brown rice (Hanguk Nonghwa Hakhoechi (1995), 38(5), 478-83). 2-Indolecarboxylic acid is a strong inhibitor of lipid peroxidation, similar to melatonin and some structurally related indole compounds. COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Indole-2-carboxylic acid is a strong inhibitor of lipid peroxidation. Indole-2-carboxylic acid (I2CA) specifically and competitively inhibits the potentiation by glycine of NMDA-gated current[1][2]. Indole-2-carboxylic acid is a strong inhibitor of lipid peroxidation. Indole-2-carboxylic acid (I2CA) specifically and competitively inhibits the potentiation by glycine of NMDA-gated current[1][2].

   

Indole-3-propionic acid

3-(1H-Indol-3-yl)propanoic acid

C11H11NO2 (189.079)


Indole-3-propionic acid (IPA, indole-3-propionate, or indole propionic acid), is a reductive product of tryptophan formed by bacteria in the gastrointestinal tract of mammals and birds (PMID:29168502). It is endogenously produced by human microbiota and has only been detected in vivo (PMID:19234110). While many microbial metabolites produced in the gut are toxic or act as uremic toxins (when they are reabsorbed through the gut epithelia), indole-3-propionic acid is a very beneficial microbial metabolite (PMID:30914514, 30862081, 29238104). In limited studies, urinary IPA correlates positively with disease and it remains unclear if this represents host bacteria responding to pathology via the production of IPA, or intestinal permeability changes leading to higher absorption and excretion of IPA, or inflammatory changes within kidneys leading to high excretion of IPA (PMID:32132996). Indole-3-propionic acid is a remarkably strong antioxidant (PMID:10721080). It is an even more potent scavenger of hydroxyl radicals than melatonin, the most potent scavenger of hydroxyl radicals synthesized by the human body. Similar to melatonin but unlike other antioxidants, indole-3-propionic acid scavenges radicals without subsequently generating reactive and pro-oxidant intermediate compounds (PMID:9928448, 10419516). Indole-3-propionic acid has been shown to prevent oxidative stress and the death of primary neurons and neuroblastoma cells exposed to the amyloid beta-protein in the form of amyloid fibrils, one of the most prominent neuropathologic features of Alzheimers disease. 3-Indolepropionic acid also shows a strong level of neuroprotection in two other paradigms of oxidative stress. (PMID 10419516) More recently it has been found that higher indole-3-propionic acid levels in serum/plasma are associated with a reduced likelihood of type 2 diabetes and with higher levels of consumption of fibre-rich foods (PMID:28397877). Studies have shown that serum levels of indole-3-propionic acid are positively correlated with dietary fibre intake and negatively correlated with C-reactive protein levels (PMID:29795366). Indole-3-propionic acid is a marker for the presence of Clostridium sporogenes in the gut. Higher levels are associated with higher levels of Clostridium sporogenes (PMID:7378938). In addition to its useful physiological role in mammals, indole-3-propionic acid is a plant hormone with functions similar to indole-3-acetic acid (or IAA), the major plant auxin. Recent studies have shed some light on additional mechanisms of action of IPA. In the intestine, IPA could serve as a ligand to an adopted orphan nuclear receptor, Pregnane X receptor (PXR) and act as an anti-inflammatory agent (PMID:25065623). This property has allowed investigators to develop more potent analogs targeting PXR (PMID:32153125). Other tissues may also be targeted by IPA in a similar manner (PMID:31211619). Indole-3-propionate (IPA), a deamination product of tryptophan formed by symbiotic bacteria in the gastrointestinal tract of mammals and birds. 3-Indolepropionic acid has been shown to prevent oxidative stress and death of primary neurons and neuroblastoma cells exposed to the amyloid beta-protein in the form of amyloid fibrils, one of the most prominent neuropathologic features of Alzheimers disease. 3-Indolepropionic acid also shows a strong level of neuroprotection in two other paradigms of oxidative stress. (PMID: 10419516) [HMDB]. 1H-Indole-3-propanoic acid is found in common pea. 3-Indolepropionic acid is shown to be a powerful antioxidant and has potential in the treatment for Alzheimer’s disease.

   

Indole-3-carbinol

3-(Hydroxymethyl)indole

C9H9NO (147.0684)


Indole-3-carbinol, also known as 3-indolylcarbinol or 1H-indole-3-methanol, belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position. Indole-3-carbinol is a dietary indole present in cruciferous vegetables that has been shown to influence estradiol metabolism in humans and may provide a new chemopreventive approach to estrogen-dependent diseases (PMID:2342128). Indole-3-carbinol is produced by members of the family Cruciferae, particularly members of the genus Brassica (e.g. cabbage, radishes, cauliflower, broccoli, Brussels sprouts, and daikon). Indole-3-carbinol is metabolized into a number of products, including the dimeric 3,3-diindolylmethane. Both 3,3-diindolylmethane and indole-3-carbinol are thought to have biological effects. Indole-3-carbinol is a natural chemopreventive compound. It has multiple anticarcinogenic and antitumorigenic properties; it can suppress the proliferation of certain cancer cells, including breast cancer, prostate cancer, endometrial cancer, colon cancer, and leukemic cells (PMID:16634522, 16082211). Produced from glucosinolates in Brassica species on crushing or cooking. Potential nutriceutical D020011 - Protective Agents > D016588 - Anticarcinogenic Agents D000970 - Antineoplastic Agents Indole-3-carbinol (I3C) inhibits NF-κB activity and also is an Aryl hydrocarbon receptor (AhR) agonist, and an inhibitor of WWP1 (WW domain-containing ubiquitin E3 ligase 1).

   

Ascorbigen

(3S,3aS,6S,6aR)-3,3a,6-trihydroxy-3-[(1H-indol-3-yl)methyl]-hexahydrofuro[3,2-b]furan-2-one

C15H15NO6 (305.0899)


Ascorbigen (CAS: 8075-98-7) belongs to the class of organic compounds known as isosorbides. These are organic polycyclic compounds containing an isosorbide (1,4-dianhydrosorbitol) moiety, which consists of two -oxolan-3-ol rings. Ascorbigen is possibly neutral. Ascorbigen is found, on average, in the highest concentration within guava and mung beans. Ascorbigen has also been detected, but not quantified, in bitter gourds and brassicas. Ascorbigen is present in plants, especially cabbage and other cruciferous plants. This could make ascorbigen a potential biomarker for the consumption of these foods. Present in plants, especies cabbage and other crucifers. Ascorbigen is found in many foods, some of which are mung bean, guava, brassicas, and bitter gourd.

   

Bufotenine O-glucoside

2-({3-[2-(dimethylamino)ethyl]-1H-indol-5-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

C18H26N2O6 (366.1791)


Bufotenine O-glucoside is found in citrus. Bufotenine O-glucoside is an alkaloid from the leaves of Citrus unshiu (satsuma mandarin

   

4-Chloro-1H-indole-3-acetic acid

2-(4-chloro-1H-indol-3-yl)acetic acid

C10H8ClNO2 (209.0244)


Auxin from the seeds of Pisum sativum (pea) and isolated from Pinus sylvestris (Scotch pine). 4-Chloro-1H-indole-3-acetic acid is found in many foods, some of which are broad bean, pulses, common pea, and grass pea. 4-Chloro-1H-indole-3-acetic acid is found in broad bean. Auxin from the seeds of Pisum sativum (pea) and isolated from Pinus sylvestris (Scotch pine). D006133 - Growth Substances > D010937 - Plant Growth Regulators > D007210 - Indoleacetic Acids

   

6-Methoxy-3-(2-thiazolyl)-1H-indole

6-methoxy-3-(1,3-thiazol-2-yl)-1H-indole

C12H10N2OS (230.0514)


6-Methoxy-3-(2-thiazolyl)-1H-indole is found in fats and oils. 6-Methoxy-3-(2-thiazolyl)-1H-indole is from Camelina sativa (false flax) infected with Alternaria brassicae. From Camelina sativa (false flax) infected with Alternaria brassicae. 6-Methoxy-3-(2-thiazolyl)-1H-indole is found in fats and oils.

   

3-Indoleglyoxylic acid

2-(1H-indol-3-yl)-2-oxoacetic acid

C10H7NO3 (189.0426)


   

3-Acetoxyindole

1H-indol-3-yl acetate

C10H9NO2 (175.0633)


   

3,3'-Diindolylmethane

3-[(1H-indol-3-yl)methyl]-1H-indole

C17H14N2 (246.1157)


C1892 - Chemopreventive Agent > C54630 - Phase II Enzymes Inducer D020011 - Protective Agents > D016588 - Anticarcinogenic Agents D000970 - Antineoplastic Agents 3,3'-Diindolylmethane is a strong, pure androgen receptor (AR) antagonist. 3,3'-Diindolylmethane is a strong, pure androgen receptor (AR) antagonist.

   

Indoxyl-beta-D-glucoside

2-(hydroxymethyl)-6-(1H-indol-3-yloxy)oxane-3,4,5-triol

C14H17NO6 (295.1056)


   

INDOLE-2-ACETIC ACID

2-(1H-indol-2-yl)acetic acid

C10H9NO2 (175.0633)


   

2-(1H-Indol-2-ylmethyl)-1H-indole

2-[(1H-indol-2-yl)methyl]-1H-indole

C17H14N2 (246.1157)


D020011 - Protective Agents > D016588 - Anticarcinogenic Agents D000970 - Antineoplastic Agents

   

(E)-indol-3-ylacetaldoxime

N-[2-(1H-indol-3-yl)ethylidene]hydroxylamine

C10H10N2O (174.0793)


(e)-indol-3-ylacetaldoxime is a member of the class of compounds known as 3-alkylindoles. 3-alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position (e)-indol-3-ylacetaldoxime is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (e)-indol-3-ylacetaldoxime can be found in a number of food items such as cherimoya, cornmint, blackcurrant, and common grape, which makes (e)-indol-3-ylacetaldoxime a potential biomarker for the consumption of these food products. (e)-indol-3-ylacetaldoxime is a member of the class of compounds known as 3-alkylindoles. 3-alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position (e)-indol-3-ylacetaldoxime is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (e)-indol-3-ylacetaldoxime can be found in a number of food items such as peppermint, wakame, sweet marjoram, and cashew nut, which makes (e)-indol-3-ylacetaldoxime a potential biomarker for the consumption of these food products.

   
   

3,6-Dibromo-1h-indole

3,6-Dibromo-1h-indole

C8H5Br2N (272.8789)


   

5-Hydroxyindole-3-carbaldehyde

5-hydroxy-1H-indole-3-carbaldehyde

C9H7NO2 (161.0477)


   
   

2-hydroxy-3-(5-hydroxy-1H-indol-3-yl)propanoic acid

2-hydroxy-3-(5-hydroxy-1H-indol-3-yl)propanoic acid

C11H11NO4 (221.0688)


   
   

Methyl indole-3-carboxylate

Methyl indole-3-carboxylate

C10H9NO2 (175.0633)


The methyl ester of indole-3-carboxylic acid. Methyl indole-3-carboxylate is a natural product isolated from Sorangium cellulosum strain Soce895. Methyl indole-3-carboxylate shows a weak activity against the Gram-positive Nocardia sp with a MIC value of 33.33 μg/mL[1]. Methyl indole-3-carboxylate is a natural product isolated from Sorangium cellulosum strain Soce895. Methyl indole-3-carboxylate shows a weak activity against the Gram-positive Nocardia sp with a MIC value of 33.33 μg/mL[1].

   

Methyl 5-hydroxy-1H-indole-3-carboxylate

Methyl 5-hydroxy-1H-indole-3-carboxylate

C10H9NO3 (191.0582)


   

2,3,5-Tribromo-1-methyl-1H-indole

2,3,5-Tribromo-1-methyl-1H-indole

C9H6Br3N (364.805)


   

1-(1H-indol-3-yl)propane-1,2,3-triol

1-(1H-indol-3-yl)propane-1,2,3-triol

C11H13NO3 (207.0895)


   

3-(oxiran-2-yl)-1H-indole

3-(oxiran-2-yl)-1H-indole

C10H9NO (159.0684)


   

ethyl 6-bromo-1H-indole-3-carboxylate

ethyl 6-bromo-1H-indole-3-carboxylate

C11H10BrNO2 (266.9895)


   

2-hydroxy-1-(1H-indol-3-yl)-4-methylpentan-3-one

2-hydroxy-1-(1H-indol-3-yl)-4-methylpentan-3-one

C14H17NO2 (231.1259)


   

1-Acetylindole-3-carboxaldehyde

1-Acetyl-1H-indole-3-carbaldehyde

C11H9NO2 (187.0633)


An N-acylindole that is N-acetylindole carrying an additional formyl substituent at position 3.

   

2-Bromo-N-methyltryptamine

2-Bromo-N-methyltryptamine

C11H13BrN2 (252.0262)


A natural product found in Paramuricea clavata.

   

bruceolline L

bruceolline L

C13H15NO2 (217.1103)


An indole alkaloid that is 1H-indole substituted by a (2R)-2-hydroxy-3-methylbutanoyl group at position 3. It has been isolated from the ethanol extract of the stems of Brucea mollis.

   

bruceolline I

bruceolline I

C13H13NO3 (231.0895)


An indole alkaloid that is 1,2,3,4-tetrahydrocyclopenta[b]indole substituted by hydroxy groups at positions 2 and 6, geminal-methyl groups at position 3 and an oxo group at position 1. It has been isolated from the ethanol extract of the stems of Brucea mollis.

   

bruceolline F

bruceolline F

C19H27NO7 (381.1787)


An indole alkaloid that is 1H-indole substituted by a (2S)-2,3-dihydroxy-3-methylbutyl group at position 3 and a beta-D-glucopyranosyl group attached to the indolic nitrogen. It has been isolated from the ethanol extract of the stems of Brucea mollis.

   

bruceolline M

bruceolline M

C19H25NO7 (379.1631)


An indole alkaloid that is 1H-indole substituted by a 3-hydroxy-3-methyl-2-oxobutyl group at position 3 and a beta-D-glucopyranosyl group attached to the indolic nitrogen. It has been isolated from the ethanol extract of the stems of Brucea mollis.

   

bruceolline K

bruceolline K

C19H23NO7 (377.1474)


An indole alkaloid that is 1,2,3,4-tetrahydrocyclopenta[b]indole substituted by geminal-methyl groups at position 3, an oxo group at position 1 and a beta-D-glucopyranosyloxy group at position 2.It has been isolated from the ethanol extract of the stems of Brucea mollis.

   

6-bromo-N-methyltryptamine

6-bromo-N-methyltryptamine

C11H13BrN2 (252.0262)


A natural product found in Paramuricea clavata.

   

5-hydroxy-1H-indole-3-carbaldehyde

5-hydroxy-1H-indole-3-carbaldehyde

C9H7NO2 (161.0477)


   

3-[bis(1H-indol-3-yl)methyl]-1H-indole

3-[bis(1H-indol-3-yl)methyl]-1H-indole

C25H19N3 (361.1579)


   

6-Hydroxytryptamine

3-(2-aminoethyl)-1H-indol-6-ol

C10H12N2O (176.095)


   

Methyl 6-bromo-1H-indole-3-carboxylate

Methyl 6-bromo-1H-indole-3-carboxylate

C10H8BrNO2 (252.9738)


   

2-(6-bromo-1H-indol-3-yl)ethanamine

2-(6-bromo-1H-indol-3-yl)ethanamine

C10H11BrN2 (238.0106)


   

2-(1H-indol-2-ylmethyl)-1H-indole

2-(1H-indol-2-ylmethyl)-1H-indole

C17H14N2 (246.1157)


D020011 - Protective Agents > D016588 - Anticarcinogenic Agents D000970 - Antineoplastic Agents

   

3-(isothiocyanatomethyl)-4-methoxy-1H-indole

3-(isothiocyanatomethyl)-4-methoxy-1H-indole

C11H10N2OS (218.0514)


   

Indole-3-carbinol

Indole-3-carbinol

C9H9NO (147.0684)


D020011 - Protective Agents > D016588 - Anticarcinogenic Agents D000970 - Antineoplastic Agents IPB_RECORD: 276; CONFIDENCE confident structure Indole-3-carbinol (I3C) inhibits NF-κB activity and also is an Aryl hydrocarbon receptor (AhR) agonist, and an inhibitor of WWP1 (WW domain-containing ubiquitin E3 ligase 1).

   

1H-Indole-3-carboxylic acid

1H-Indole-3-carboxylic acid

C9H7NO2 (161.0477)


IPB_RECORD: 302; CONFIDENCE confident structure CONFIDENCE confident structure; IPB_RECORD: 302

   
   

Indolelactic acid

(2S)-2-Hydroxy-3-(1H-indol-3-yl)propanoic acid

C11H11NO3 (205.0739)


   

5-Hydroxytryptophol

3-(2-Hydroxyethyl)-1H-indol-5-ol

C10H11NO2 (177.079)


5-Hydroxytryptophol is a mammalian serotonin metabolite, acting as a marker of acute alcohol consumption.

   

3-indolebutyric acid

Indole-3-butyric acid

C12H13NO2 (203.0946)


Indole-3-butyric acid (3-indolebutyric acid; IBA) is a plant growth auxin and a good rooting agent. It can promote herbs and woody ornamental plant rooting and used for improving fruit rate.

   

indoxyl

1H-Indol-3-ol

C8H7NO (133.0528)


   

Indole-3-methyl acetate

methyl 2-(1H-indol-3-yl)acetate

C11H11NO2 (189.079)


Methyl 2-(1H-indol-3-yl)acetate is an endogenous metabolite.

   

Methyl indole-3-acetate

methyl 2-(1H-indol-3-yl)acetate

C11H11NO2 (189.079)


Methyl 2-(1H-indol-3-yl)acetate is an endogenous metabolite.

   

Indole-2-carboxylic acid

Indole-2-carboxylic acid

C9H7NO2 (161.0477)


COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Indole-2-carboxylic acid is a strong inhibitor of lipid peroxidation. Indole-2-carboxylic acid (I2CA) specifically and competitively inhibits the potentiation by glycine of NMDA-gated current[1][2]. Indole-2-carboxylic acid is a strong inhibitor of lipid peroxidation. Indole-2-carboxylic acid (I2CA) specifically and competitively inhibits the potentiation by glycine of NMDA-gated current[1][2].

   

Bufotenine O-glucoside

2-({3-[2-(dimethylamino)ethyl]-1H-indol-5-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

C18H26N2O6 (366.1791)


   

Ascorbigen

3,3a,6-trihydroxy-3-(1H-indol-3-ylmethyl)-hexahydrofuro[3,2-b]furan-2-one

C15H15NO6 (305.0899)


An indolyl carbohydrate that consists of (3aS,6S,6aR)-3,3a,6-trihydroxy-3-tetrahydrofuro[3,2-b]furan-2-one in which position 3 is substituted by an indol-3-ylmethyl group. Formed from indole-3-carbinol and ascorbic acid in brassica vegetables.

   

Methyl 1-methoxy-1H-indole-3-carboxylate

Methyl 1-methoxy-1H-indole-3-carboxylate

C11H11NO3 (205.0739)


   

4-CL-IAA

2-(4-chloro-1H-indol-3-yl)acetic acid

C10H8ClNO2 (209.0244)


D006133 - Growth Substances > D010937 - Plant Growth Regulators > D007210 - Indoleacetic Acids

   

Methoxycamalexin

6-methoxy-3-(1,3-thiazol-2-yl)-1H-indole

C12H10N2OS (230.0514)


   

3-Methyl-1H-indole-2-carboxylic acid

3-Methyl-1H-indole-2-carboxylic acid

C10H9NO2 (175.0633)


   

6-Bromo-1H-indol-5-ol

6-Bromo-1H-indol-5-ol

C8H6BrNO (210.9633)


   

2-(5-Bromo-1H-indol-3-yl)acetic acid

2-(5-Bromo-1H-indol-3-yl)acetic acid

C10H8BrNO2 (252.9738)


   

1H-Indol-7-ylmethanol

1H-Indol-7-ylmethanol

C9H9NO (147.0684)


   

6-Chloro-1H-indole-3-carbaldehyde

6-Chloro-1H-indole-3-carbaldehyde

C9H6ClNO (179.0138)


   

Gramin

InChI=1\C11H14N2\c1-13(2)8-9-7-12-11-6-4-3-5-10(9)11\h3-7,12H,8H2,1-2H

C11H14N2 (174.1157)


Gramine (Donaxine) is a natural alkaloid isolated from giant reed[2], acts as an active adiponectin receptor (AdipoR) agonist, with IC50s of 3.2 and 4.2 μM for AdipoR2 and AdipoR1, respectively[1]. Gramine is also a human and mouse β2-Adrenergic receptor (β2-AR) agonist[2]. Gramine (Donaxine) has anti-tumor, anti-viral and anti-inflammatory properties[1]. Gramine (Donaxine) is a natural alkaloid isolated from giant reed[2], acts as an active adiponectin receptor (AdipoR) agonist, with IC50s of 3.2 and 4.2 μM for AdipoR2 and AdipoR1, respectively[1]. Gramine is also a human and mouse β2-Adrenergic receptor (β2-AR) agonist[2]. Gramine (Donaxine) has anti-tumor, anti-viral and anti-inflammatory properties[1]. Gramine (Donaxine) is a natural alkaloid isolated from giant reed[2], acts as an active adiponectin receptor (AdipoR) agonist, with IC50s of 3.2 and 4.2 μM for AdipoR2 and AdipoR1, respectively[1]. Gramine is also a human and mouse β2-Adrenergic receptor (β2-AR) agonist[2]. Gramine (Donaxine) has anti-tumor, anti-viral and anti-inflammatory properties[1].

   

(Z)-indol-3-ylacetaldoxime

(Z)-indol-3-ylacetaldoxime

C10H10N2O (174.0793)


   

methyl 1-[(3S)-3,4-dihydroxy-2-methylbutan-2-yl]indole-3-carboxylate

methyl 1-[(3S)-3,4-dihydroxy-2-methylbutan-2-yl]indole-3-carboxylate

C15H19NO4 (277.1314)


   

Dimethyltryptamine

N,N-DIMETHYLTRYPTAMINE

C12H16N2 (188.1313)


D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D017366 - Serotonin Receptor Agonists D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D012702 - Serotonin Antagonists D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D006213 - Hallucinogens A tryptamine derivative having two N-methyl substituents on the side-chain.

   

PSILOCIN

PSILOCIN

C12H16N2O (204.1263)


A tryptamine alkaloid that is N,N-dimethyltryptamine carrying an additional hydroxy substituent at position 4. A hallucinogenic alkaloid isolated in trace amounts from Psilocybe mushrooms (also known as Teonanacatl or "magic mushrooms"). D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D006213 - Hallucinogens

   

methyl 2-(1H-indol-3-yl)acetate

methyl 2-(1H-indol-3-yl)acetate

C11H11NO2 (189.079)


Methyl 2-(1H-indol-3-yl)acetate is an endogenous metabolite.

   

Indole-3-glycerol phosphate

(1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate

C11H14NO6P (287.0559)


D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents The (1S,2R)-diastereomer of 1-C-(indol-3-yl)glycerol 3-phosphate.

   

(2S)-2-Hydroxy-3-(1H-indol-3-yl)propanoic acid

(2S)-2-Hydroxy-3-(1H-indol-3-yl)propanoic acid

C11H11NO3 (205.0739)


   

4-Chloroindole-3-acetic acid

4-Chloroindole-3-acetic acid

C10H8ClNO2 (209.0244)


D006133 - Growth Substances > D010937 - Plant Growth Regulators > D007210 - Indoleacetic Acids

   

Methyl (4-chloro-1H-indol-3-yl)acetate

methyl 2-(4-chloro-1H-indol-3-yl)acetate

C11H10ClNO2 (223.04)


D006133 - Growth Substances > D010937 - Plant Growth Regulators > D007210 - Indoleacetic Acids

   

N-[2-(1H-indol-3-yl)ethylidene]hydroxylamine

N-[2-(1H-indol-3-yl)ethylidene]hydroxylamine

C10H10N2O (174.0793)


   

3-(1H-Indol-3-yl)propanoic acid

3-(1H-Indol-3-yl)propanoic acid

C11H11NO2 (189.079)


An indol-3-yl carboxylic acid that is propionic acid substituted by a 1H-indol-3-yl group at position 3.

   

3-(indol-3-yl)Pyruvic acid

3-(indol-3-yl)Pyruvic acid

C11H9NO3 (203.0582)


A 2-oxo monocarboxylic acid that is pyruvic acid substituted by a 1H-indol-3-yl group at position 3. It has been found in Lycopersicon esculentum

   

3-methyl-2-indolic acid

3-methyl-2-indolic acid

C10H9NO2 (175.0633)


An indolecarboxylic acid that is indole-2-carboxylic acid in which the hydrogen at position 3 is replaced by a methyl group.

   

methyl 4'-chloro-1-methyl-2h-8',13'-diazaspiro[indole-3,10'-tetracyclo[7.6.0.0²,⁷.0¹¹,¹⁵]pentadecane]-1'(9'),2',4',6',11',14'-hexaene-12'-carboxylate

methyl 4'-chloro-1-methyl-2h-8',13'-diazaspiro[indole-3,10'-tetracyclo[7.6.0.0²,⁷.0¹¹,¹⁵]pentadecane]-1'(9'),2',4',6',11',14'-hexaene-12'-carboxylate

C23H18ClN3O2 (403.1087)


   

(2s)-2-[(2r)-2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl]-2,3-dihydro-1h-indole-5-carboximidic acid

(2s)-2-[(2r)-2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl]-2,3-dihydro-1h-indole-5-carboximidic acid

C19H28N2O3 (332.21)


   

1-hydroxy-5-methoxy-3-methyl-6-{[7-(3-methylbuta-1,3-dien-1-yl)-1h-indol-3-yl]methyl}pyrazin-2-one

1-hydroxy-5-methoxy-3-methyl-6-{[7-(3-methylbuta-1,3-dien-1-yl)-1h-indol-3-yl]methyl}pyrazin-2-one

C20H21N3O3 (351.1583)


   

(1's,2's,3s,7's,9's)-6'-acetyl-2'-hydroxy-6-methoxy-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

(1's,2's,3s,7's,9's)-6'-acetyl-2'-hydroxy-6-methoxy-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

C21H24N2O5 (384.1685)


   

2-{[1-hydroxy-2,2-bis(1h-indol-3-yl)propylidene]amino}-3-(1h-indol-3-yl)-n-methyl-3-oxopropanimidic acid

2-{[1-hydroxy-2,2-bis(1h-indol-3-yl)propylidene]amino}-3-(1h-indol-3-yl)-n-methyl-3-oxopropanimidic acid

C31H27N5O3 (517.2114)


   

(2e)-2-(1h-indol-3-ylmethylidene)-1h-indol-3-one

(2e)-2-(1h-indol-3-ylmethylidene)-1h-indol-3-one

C17H12N2O (260.095)


   

[2-(1h-indol-3-ylmethyl)-1h-indol-3-yl]acetic acid

[2-(1h-indol-3-ylmethyl)-1h-indol-3-yl]acetic acid

C19H16N2O2 (304.1212)


   

(1r,2r,3r,4s,5r,6s)-2,3,4,5,6-pentahydroxycyclohexyl 2-(1h-indol-3-yl)acetate

(1r,2r,3r,4s,5r,6s)-2,3,4,5,6-pentahydroxycyclohexyl 2-(1h-indol-3-yl)acetate

C16H19NO7 (337.1161)


   

n-{2-[5-(acetyloxy)-1h-indol-3-yl]ethyl}ethanimidic acid

n-{2-[5-(acetyloxy)-1h-indol-3-yl]ethyl}ethanimidic acid

C14H16N2O3 (260.1161)


   

3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol

3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol

C19H23N3O2 (325.179)


   

methyl (2e)-2-(n-hydroxyimino)-3-{7-[(1e)-2-{3-[(2e)-2-(hydroxyimino)-3-methoxy-3-oxopropyl]-11-methyl-9-(2-methylprop-1-en-1-yl)-1-azatricyclo[6.3.1.0⁴,¹²]dodeca-2,4,6,8(12)-tetraen-11-yl}ethenyl]-1h-indol-3-yl}propanoate

methyl (2e)-2-(n-hydroxyimino)-3-{7-[(1e)-2-{3-[(2e)-2-(hydroxyimino)-3-methoxy-3-oxopropyl]-11-methyl-9-(2-methylprop-1-en-1-yl)-1-azatricyclo[6.3.1.0⁴,¹²]dodeca-2,4,6,8(12)-tetraen-11-yl}ethenyl]-1h-indol-3-yl}propanoate

C34H36N4O6 (596.2635)


   

{3-[5-hydroxy-4-(1h-indol-3-yl)-2-oxopyrrol-3-yl]-1h-indol-6-yl}oxidanesulfonic acid

{3-[5-hydroxy-4-(1h-indol-3-yl)-2-oxopyrrol-3-yl]-1h-indol-6-yl}oxidanesulfonic acid

C20H13N3O6S (423.0525)


   

(1r,2s)-1,2-dihydroxy-1,2-dimethyl-9h-carbazole-3,4-dione

(1r,2s)-1,2-dihydroxy-1,2-dimethyl-9h-carbazole-3,4-dione

C14H13NO4 (259.0845)


   

3-hydroxy-4-(1h-indol-3-yl)-1-phenylbutan-2-one

3-hydroxy-4-(1h-indol-3-yl)-1-phenylbutan-2-one

C18H17NO2 (279.1259)


   

(1'r,2'r,3s,7'r,9'r)-6'-acetyl-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

(1'r,2'r,3s,7'r,9'r)-6'-acetyl-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

C20H22N2O3 (338.163)


   

(2s,4s,5s,6s)-4,5-dihydroxy-6-[3-(c-hydroxycarbonimidoylmethyl)-4-methoxyindol-1-yl]oxane-2-carboximidic acid

(2s,4s,5s,6s)-4,5-dihydroxy-6-[3-(c-hydroxycarbonimidoylmethyl)-4-methoxyindol-1-yl]oxane-2-carboximidic acid

C17H21N3O6 (363.143)


   

methyl 2-(carbamoylformamido)-3-[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]prop-2-enoate

methyl 2-(carbamoylformamido)-3-[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]prop-2-enoate

C19H21N3O4 (355.1532)


   

(1s,9r)-5-(1h-indol-3-yl)-3,4,6-trimethoxy-8-oxa-10-azatetracyclo[7.7.0.0²,⁷.0¹¹,¹⁶]hexadeca-2(7),3,5,11,13,15-hexaen-1-ol

(1s,9r)-5-(1h-indol-3-yl)-3,4,6-trimethoxy-8-oxa-10-azatetracyclo[7.7.0.0²,⁷.0¹¹,¹⁶]hexadeca-2(7),3,5,11,13,15-hexaen-1-ol

C25H22N2O5 (430.1529)


   

methyl (2z)-3-{7-[(1e)-3,4-dihydroxy-3-methylbut-1-en-1-yl]-1h-indol-3-yl}-2-(n-hydroxyimino)propanoate

methyl (2z)-3-{7-[(1e)-3,4-dihydroxy-3-methylbut-1-en-1-yl]-1h-indol-3-yl}-2-(n-hydroxyimino)propanoate

C17H20N2O5 (332.1372)


   

3-methyl-1-[6-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]butane-2,3-diol

3-methyl-1-[6-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]butane-2,3-diol

C18H25NO2 (287.1885)


   

2,2-dimethyl-7-(2-methylbut-3-en-2-yl)-8h-chromeno[7,6-b]pyrrole-6-carbaldehyde

2,2-dimethyl-7-(2-methylbut-3-en-2-yl)-8h-chromeno[7,6-b]pyrrole-6-carbaldehyde

C19H21NO2 (295.1572)


   

2-ethyl-3-[2-(3-ethylpiperidin-1-yl)ethyl]-1h-indole

2-ethyl-3-[2-(3-ethylpiperidin-1-yl)ethyl]-1h-indole

C19H28N2 (284.2252)


   

(2e)-3-(1h-indol-3-yl)prop-2-enimidic acid

(2e)-3-(1h-indol-3-yl)prop-2-enimidic acid

C11H10N2O (186.0793)


   

2-ethyl-3-{2-[(3r)-3-ethylpiperidin-1-yl]ethyl}-1h-indole

2-ethyl-3-{2-[(3r)-3-ethylpiperidin-1-yl]ethyl}-1h-indole

C19H28N2 (284.2252)


   

2,3',5,5'-tetrabromo-7'-methoxy-1h,1'h-3,4'-biindole

2,3',5,5'-tetrabromo-7'-methoxy-1h,1'h-3,4'-biindole

C17H10Br4N2O (573.7527)


   

(e,2e)-3-(7-methoxy-1-methylindol-3-yl)-n-[(1e)-2-(1-methylindol-3-yl)ethenyl]prop-2-enimidic acid

(e,2e)-3-(7-methoxy-1-methylindol-3-yl)-n-[(1e)-2-(1-methylindol-3-yl)ethenyl]prop-2-enimidic acid

C24H23N3O2 (385.179)


   

1-{4-methyl-1-phenylpyrrolo[3,4-b]quinolin-3-yl}butane-1,2,3,4-tetrol

1-{4-methyl-1-phenylpyrrolo[3,4-b]quinolin-3-yl}butane-1,2,3,4-tetrol

C22H22N2O4 (378.1579)


   

1-(1h-indol-3-yl)-4-methyl-3-oxohexan-2-yl acetate

1-(1h-indol-3-yl)-4-methyl-3-oxohexan-2-yl acetate

C17H21NO3 (287.1521)


   

3-(3-methylbut-2-en-1-yl)-1h-indole

3-(3-methylbut-2-en-1-yl)-1h-indole

C13H15N (185.1204)


   

3-(1h-indol-3-yl)-n-methylpropanimidic acid

3-(1h-indol-3-yl)-n-methylpropanimidic acid

C12H14N2O (202.1106)


   

6-(3-methylbuta-1,3-dien-1-yl)-1h-indole

6-(3-methylbuta-1,3-dien-1-yl)-1h-indole

C13H13N (183.1048)


   

2-{3-[(2-hydroxyphenyl)methyl]-1h-indole-2-carbonyl}phenol

2-{3-[(2-hydroxyphenyl)methyl]-1h-indole-2-carbonyl}phenol

C22H17NO3 (343.1208)


   

4-(1h-indol-3-yl)-6-(1h-indol-3-ylmethyl)pyridin-3-ol

4-(1h-indol-3-yl)-6-(1h-indol-3-ylmethyl)pyridin-3-ol

C22H17N3O (339.1372)


   

(5r)-5-[(1s)-1-(1h-indol-3-yl)ethyl]-2-(methylimino)-5h-1,3-oxazol-4-ol

(5r)-5-[(1s)-1-(1h-indol-3-yl)ethyl]-2-(methylimino)-5h-1,3-oxazol-4-ol

C14H15N3O2 (257.1164)


   

methyl 2-(n-hydroxyimino)-3-[7-(3-methylbuta-1,3-dien-1-yl)-1h-indol-3-yl]propanoate

methyl 2-(n-hydroxyimino)-3-[7-(3-methylbuta-1,3-dien-1-yl)-1h-indol-3-yl]propanoate

C17H18N2O3 (298.1317)


   

2-(n-hydroxyimino)-3-[7-(3-methylbuta-1,3-dien-1-yl)-1h-indol-3-yl]propanamide

2-(n-hydroxyimino)-3-[7-(3-methylbuta-1,3-dien-1-yl)-1h-indol-3-yl]propanamide

C16H17N3O2 (283.1321)


   

2-(dimethylamino)-5-(1h-indol-3-yl)imidazol-4-one

2-(dimethylamino)-5-(1h-indol-3-yl)imidazol-4-one

C13H12N4O (240.1011)


   

3-{[(2r)-3,3-dimethyloxiran-2-yl]methyl}-5-(3-methylbut-2-en-1-yl)-1h-indole

3-{[(2r)-3,3-dimethyloxiran-2-yl]methyl}-5-(3-methylbut-2-en-1-yl)-1h-indole

C18H23NO (269.178)


   

(1s,7s,16r)-16-methoxy-5-oxa-10-azatetracyclo[8.7.0.0¹,¹³.0²,⁷]heptadeca-2,12,14-triene-4,11-dione

(1s,7s,16r)-16-methoxy-5-oxa-10-azatetracyclo[8.7.0.0¹,¹³.0²,⁷]heptadeca-2,12,14-triene-4,11-dione

C16H17NO4 (287.1158)


   

[(5,7-dimethoxy-1h-indol-3-yl)methyl]dimethylamine

[(5,7-dimethoxy-1h-indol-3-yl)methyl]dimethylamine

C13H18N2O2 (234.1368)


   

(3s,6s)-6-(1-hydroxyethyl)-3-(1h-indol-3-ylmethyl)-3-(methylsulfanyl)-6h-pyrazine-2,5-diol

(3s,6s)-6-(1-hydroxyethyl)-3-(1h-indol-3-ylmethyl)-3-(methylsulfanyl)-6h-pyrazine-2,5-diol

C16H19N3O3S (333.1147)


   

(1's,2'r,3s,7'r,9's)-6'-acetyl-6-methoxy-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

(1's,2'r,3s,7'r,9's)-6'-acetyl-6-methoxy-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

C21H24N2O4 (368.1736)


   

(3e)-2-methyl-4-{3-[2-(methylamino)ethyl]-1h-indol-4-yl}but-3-en-2-ol

(3e)-2-methyl-4-{3-[2-(methylamino)ethyl]-1h-indol-4-yl}but-3-en-2-ol

C16H22N2O (258.1732)


   

3-hydroxy-6-(1h-indol-3-yloxy)-4-methylhexanoic acid

3-hydroxy-6-(1h-indol-3-yloxy)-4-methylhexanoic acid

C15H19NO4 (277.1314)


   

5-hydroxy-3-(6-hydroxy-1h-indol-3-yl)-4-(1h-indol-3-yl)pyrrol-2-one

5-hydroxy-3-(6-hydroxy-1h-indol-3-yl)-4-(1h-indol-3-yl)pyrrol-2-one

C20H13N3O3 (343.0957)


   

1h-indol-3-yl (2r,3s,4s,5r)-3,4,5-trihydroxy-5-(hydroxymethyl)oxolane-2-carboxylate

1h-indol-3-yl (2r,3s,4s,5r)-3,4,5-trihydroxy-5-(hydroxymethyl)oxolane-2-carboxylate

C14H15NO7 (309.0848)


   

3-(1h-indol-3-ylmethyl)-6-{[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol

3-(1h-indol-3-ylmethyl)-6-{[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol

C27H28N4O2 (440.2212)


   

1-(1-methoxyindol-3-yl)methanamine

1-(1-methoxyindol-3-yl)methanamine

C10H12N2O (176.095)


   

n-[(2s)-1-hydroxy-3-(1h-indol-3-yl)propan-2-yl]ethanimidic acid

n-[(2s)-1-hydroxy-3-(1h-indol-3-yl)propan-2-yl]ethanimidic acid

C13H16N2O2 (232.1212)


   

(2s)-2-(dimethylamino)-3-(1h-indol-3-yl)propanoic acid

(2s)-2-(dimethylamino)-3-(1h-indol-3-yl)propanoic acid

C13H16N2O2 (232.1212)


   

(e,2e)-3-(1h-indol-3-yl)-n-[(1e)-2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

(e,2e)-3-(1h-indol-3-yl)-n-[(1e)-2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

C21H17N3O (327.1372)


   

6-(3-methylbut-2-en-1-yl)-1h-indole

6-(3-methylbut-2-en-1-yl)-1h-indole

C13H15N (185.1204)


   

3-ethyl-4-methoxy-1h-indole

3-ethyl-4-methoxy-1h-indole

C11H13NO (175.0997)


   

1-[3-(2-hydroxy-3-methoxy-3-methylbutyl)-1h-indol-5-yl]-3-methylbut-2-en-1-one

1-[3-(2-hydroxy-3-methoxy-3-methylbutyl)-1h-indol-5-yl]-3-methylbut-2-en-1-one

C19H25NO3 (315.1834)


   

(6z)-3-methyl-6-(3-methylbut-2-en-1-ylidene)-4,5-dihydro-1,3-benzodiazocin-7-ol

(6z)-3-methyl-6-(3-methylbut-2-en-1-ylidene)-4,5-dihydro-1,3-benzodiazocin-7-ol

C16H20N2O (256.1576)


   

(1r,2r,3r)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one

(1r,2r,3r)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one

C14H15NO2 (229.1103)


   

6-bromo-1h-indole-2,3-dione

6-bromo-1h-indole-2,3-dione

C8H4BrNO2 (224.9425)


   

2,13-dimethyl 11,22-diazapentacyclo[13.7.0.0⁴,¹².0⁵,¹⁰.0¹⁶,²¹]docosa-1,3,5,7,9,12,14,16,18,20-decaene-2,13-dicarboxylate

2,13-dimethyl 11,22-diazapentacyclo[13.7.0.0⁴,¹².0⁵,¹⁰.0¹⁶,²¹]docosa-1,3,5,7,9,12,14,16,18,20-decaene-2,13-dicarboxylate

C24H18N2O4 (398.1267)


   

1-(1h-indol-7-yl)-3-methylbut-2-en-1-one

1-(1h-indol-7-yl)-3-methylbut-2-en-1-one

C13H13NO (199.0997)


   

2-[3-(2,3-dihydroxy-3-methylbutyl)indol-1-yl]-6-(hydroxymethyl)oxane-3,4,5-triol

2-[3-(2,3-dihydroxy-3-methylbutyl)indol-1-yl]-6-(hydroxymethyl)oxane-3,4,5-triol

C19H27NO7 (381.1787)


   

(3e)-4-(1h-indol-5-yl)but-3-en-2-one

(3e)-4-(1h-indol-5-yl)but-3-en-2-one

C12H11NO (185.0841)


   

3-[1h-indol-3-yl(phenyl)methyl]-1h-indole

3-[1h-indol-3-yl(phenyl)methyl]-1h-indole

C23H18N2 (322.147)


   

4-(ethoxymethyl)-2-methyl-1h-indole

4-(ethoxymethyl)-2-methyl-1h-indole

C12H15NO (189.1154)


   

3,3'-bis[2-(dimethylamino)ethyl]-1'h-[1,4'-biindol]-5'-ol

3,3'-bis[2-(dimethylamino)ethyl]-1'h-[1,4'-biindol]-5'-ol

C24H30N4O (390.2419)


   

methyl (3r)-4',5-dichloro-1,2-dihydro-8',13'-diazaspiro[indole-3,10'-tetracyclo[7.6.0.0²,⁷.0¹¹,¹⁵]pentadecane]-1'(9'),2',4',6',11',14'-hexaene-12'-carboxylate

methyl (3r)-4',5-dichloro-1,2-dihydro-8',13'-diazaspiro[indole-3,10'-tetracyclo[7.6.0.0²,⁷.0¹¹,¹⁵]pentadecane]-1'(9'),2',4',6',11',14'-hexaene-12'-carboxylate

C22H15Cl2N3O2 (423.0541)


   

n-(1-{[2-(1h-indol-3-yl)acetyl]oxy}-4-methylpentan-2-yl)-2-methylhexa-2,4-dienimidic acid

n-(1-{[2-(1h-indol-3-yl)acetyl]oxy}-4-methylpentan-2-yl)-2-methylhexa-2,4-dienimidic acid

C23H30N2O3 (382.2256)


   

2-acetyl-n-[2-(1h-indol-3-yl)ethyl]-1,3-thiazole-4-carboximidic acid

2-acetyl-n-[2-(1h-indol-3-yl)ethyl]-1,3-thiazole-4-carboximidic acid

C16H15N3O2S (313.0885)


   

[2-(5,6-dibromo-1h-indol-3-yl)ethyl](methyl)amine

[2-(5,6-dibromo-1h-indol-3-yl)ethyl](methyl)amine

C11H12Br2N2 (329.9367)


   

(2s)-1-[3-(2-hydroxyethyl)-1h-indol-6-yl]-3-methylbutane-2,3-diol

(2s)-1-[3-(2-hydroxyethyl)-1h-indol-6-yl]-3-methylbutane-2,3-diol

C15H21NO3 (263.1521)


   

2,3-dimethyl-1h-indol-4-ol

2,3-dimethyl-1h-indol-4-ol

C10H11NO (161.0841)


   

(2s)-2-[(1-hydroxy-2-phenylethylidene)amino]-3-(1h-indol-3-yl)propanoic acid

(2s)-2-[(1-hydroxy-2-phenylethylidene)amino]-3-(1h-indol-3-yl)propanoic acid

C19H18N2O3 (322.1317)


   

(1s,7r,16r)-16-methoxy-5-oxa-10-azatetracyclo[8.7.0.0¹,¹³.0²,⁷]heptadeca-2,12,14-triene-4,11-dione

(1s,7r,16r)-16-methoxy-5-oxa-10-azatetracyclo[8.7.0.0¹,¹³.0²,⁷]heptadeca-2,12,14-triene-4,11-dione

C16H17NO4 (287.1158)


   

2,2-dichloro-n-[(1s,2r)-3-hydroxy-1-{4-[(1-hydroxyethylidene)amino]phenyl}-1-(1h-indol-3-yl)propan-2-yl]ethanimidic acid

2,2-dichloro-n-[(1s,2r)-3-hydroxy-1-{4-[(1-hydroxyethylidene)amino]phenyl}-1-(1h-indol-3-yl)propan-2-yl]ethanimidic acid

C21H21Cl2N3O3 (433.096)


   

2-[(1r)-1-hydroxyethyl]-n-[2-(1h-indol-3-yl)ethyl]-1,3-thiazole-4-carboximidic acid

2-[(1r)-1-hydroxyethyl]-n-[2-(1h-indol-3-yl)ethyl]-1,3-thiazole-4-carboximidic acid

C16H17N3O2S (315.1041)


   

2-ethyl-3-[2-(1h-indol-3-yl)ethyl]-2,5-dimethylimidazol-4-one

2-ethyl-3-[2-(1h-indol-3-yl)ethyl]-2,5-dimethylimidazol-4-one

C17H21N3O (283.1685)


   

16-methoxy-5-oxa-10-azatetracyclo[8.7.0.0¹,¹³.0²,⁷]heptadeca-2(7),12,14-triene-4,9-dione

16-methoxy-5-oxa-10-azatetracyclo[8.7.0.0¹,¹³.0²,⁷]heptadeca-2(7),12,14-triene-4,9-dione

C16H17NO4 (287.1158)


   

tetrakis(1h-indol-3-yl)ethanone

tetrakis(1h-indol-3-yl)ethanone

C34H24N4O (504.195)


   

(2r)-2-heptyl-2-hydroxy-6-methoxy-4-methyl-1h-indol-3-one

(2r)-2-heptyl-2-hydroxy-6-methoxy-4-methyl-1h-indol-3-one

C17H25NO3 (291.1834)


   

16-methoxy-5-oxa-10-azatetracyclo[8.7.0.0¹,¹³.0²,⁷]heptadeca-2,12,14-triene-4,11-dione

16-methoxy-5-oxa-10-azatetracyclo[8.7.0.0¹,¹³.0²,⁷]heptadeca-2,12,14-triene-4,11-dione

C16H17NO4 (287.1158)


   

(2r)-2-(2-hydroxy-5,6-dimethylhept-5-en-2-yl)-2,3-dihydro-1h-indole-5-carboximidic acid

(2r)-2-(2-hydroxy-5,6-dimethylhept-5-en-2-yl)-2,3-dihydro-1h-indole-5-carboximidic acid

C18H26N2O2 (302.1994)


   

3-(1-hydroxyethyl)-6-(1h-indol-3-ylmethyl)-3,6-bis(methylsulfanyl)pyrazine-2,5-diol

3-(1-hydroxyethyl)-6-(1h-indol-3-ylmethyl)-3,6-bis(methylsulfanyl)pyrazine-2,5-diol

C17H21N3O3S2 (379.1024)


   

7-(4-hydroxy-3-methylbut-2-en-1-yl)-1h-indole-3-carbaldehyde

7-(4-hydroxy-3-methylbut-2-en-1-yl)-1h-indole-3-carbaldehyde

C14H15NO2 (229.1103)


   

6-(3-methylbut-2-en-1-yl)-1h-indole-2,3-dione

6-(3-methylbut-2-en-1-yl)-1h-indole-2,3-dione

C13H13NO2 (215.0946)


   

5-[(1r,6r)-6-[(1e)-2-(1h-indol-5-yl)ethenyl]-3,6-dimethylcyclohex-2-en-1-yl]-1h-indole

5-[(1r,6r)-6-[(1e)-2-(1h-indol-5-yl)ethenyl]-3,6-dimethylcyclohex-2-en-1-yl]-1h-indole

C26H26N2 (366.2096)


   

(2r)-2-hydroxy-1-(1h-indol-3-yl)-4-methylhexan-3-one

(2r)-2-hydroxy-1-(1h-indol-3-yl)-4-methylhexan-3-one

C15H19NO2 (245.1416)


   

(2s,3r)-2,3-dihydroxy-3-(1h-indol-3-yl)propoxyphosphonic acid

(2s,3r)-2,3-dihydroxy-3-(1h-indol-3-yl)propoxyphosphonic acid

C11H14NO6P (287.0559)


   

n-[2-(4-hydroxy-3-iodophenyl)ethyl]-2-(1h-indol-3-yl)-2-oxoacetamide

n-[2-(4-hydroxy-3-iodophenyl)ethyl]-2-(1h-indol-3-yl)-2-oxoacetamide

C18H15IN2O3 (434.0127)


   

6-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h-indole-3-carboxylic acid

6-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h-indole-3-carboxylic acid

C15H17NO8 (339.0954)


   

(1r,9r)-3,6-dimethoxy-5-[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]-8-oxa-10-azatetracyclo[7.7.0.0²,⁷.0¹¹,¹⁶]hexadeca-2,4,6,11,13,15-hexaene-1,4-diol

(1r,9r)-3,6-dimethoxy-5-[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]-8-oxa-10-azatetracyclo[7.7.0.0²,⁷.0¹¹,¹⁶]hexadeca-2,4,6,11,13,15-hexaene-1,4-diol

C29H28N2O5 (484.1998)


   

3-hydroxy-4-(1h-indol-3-yl)butan-2-one

3-hydroxy-4-(1h-indol-3-yl)butan-2-one

C12H13NO2 (203.0946)


   

15-methoxy-4-oxa-9-azatetracyclo[7.7.0.0¹,¹².0²,⁶]hexadeca-2(6),12-dien-3-one

15-methoxy-4-oxa-9-azatetracyclo[7.7.0.0¹,¹².0²,⁶]hexadeca-2(6),12-dien-3-one

C15H19NO3 (261.1365)


   

(1s,16r)-16-methoxy-5-oxa-10-azatetracyclo[8.7.0.0¹,¹³.0²,⁷]heptadeca-2(7),12,14-triene-4,11-dione

(1s,16r)-16-methoxy-5-oxa-10-azatetracyclo[8.7.0.0¹,¹³.0²,⁷]heptadeca-2(7),12,14-triene-4,11-dione

C16H17NO4 (287.1158)


   

n-hydroxy-2-(1h-indol-3-yl)ethanimidothioic acid

n-hydroxy-2-(1h-indol-3-yl)ethanimidothioic acid

C10H10N2OS (206.0514)


   

16-methoxy-5-oxa-10-azatetracyclo[8.7.0.0¹,¹³.0²,⁷]heptadeca-2,12,14-triene-4,9-dione

16-methoxy-5-oxa-10-azatetracyclo[8.7.0.0¹,¹³.0²,⁷]heptadeca-2,12,14-triene-4,9-dione

C16H17NO4 (287.1158)


   

2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid

2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid

C24H32N2O5 (428.2311)


   

(3r,6s)-3-(1h-indol-3-ylmethyl)-6-methyl-3,6-dihydropyrazine-2,5-diol

(3r,6s)-3-(1h-indol-3-ylmethyl)-6-methyl-3,6-dihydropyrazine-2,5-diol

C14H15N3O2 (257.1164)


   

3,5-bis(3-methylbut-2-en-1-yl)-1h-indole

3,5-bis(3-methylbut-2-en-1-yl)-1h-indole

C18H23N (253.183)


   

2,6-bis[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol

2,6-bis[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol

C30H30Br2N6O (648.0848)


   

3-{[(2r)-3,3-dimethyloxiran-2-yl]methyl}-5-[(1e)-3-methylbuta-1,3-dien-1-yl]-1h-indole

3-{[(2r)-3,3-dimethyloxiran-2-yl]methyl}-5-[(1e)-3-methylbuta-1,3-dien-1-yl]-1h-indole

C18H21NO (267.1623)


   

2-(2-hydroxy-5,6-dimethylhept-5-en-2-yl)-2,3-dihydro-1h-indole-5-carboximidic acid

2-(2-hydroxy-5,6-dimethylhept-5-en-2-yl)-2,3-dihydro-1h-indole-5-carboximidic acid

C18H26N2O2 (302.1994)


   

2,2-dichloro-n-(3-hydroxy-1-{4-[(1-hydroxyethylidene)amino]phenyl}-1-(1h-indol-3-yl)propan-2-yl)ethanimidic acid

2,2-dichloro-n-(3-hydroxy-1-{4-[(1-hydroxyethylidene)amino]phenyl}-1-(1h-indol-3-yl)propan-2-yl)ethanimidic acid

C21H21Cl2N3O3 (433.096)


   

3-({6-isopropyl-8-methylidene-6-azabicyclo[3.2.1]oct-3-en-7-yl}methyl)-1h-indole

3-({6-isopropyl-8-methylidene-6-azabicyclo[3.2.1]oct-3-en-7-yl}methyl)-1h-indole

C20H24N2 (292.1939)


   

12-(1h-indol-3-yl)-2,6,10-trimethyldodeca-2,6,10-triene-4,5-diol

12-(1h-indol-3-yl)-2,6,10-trimethyldodeca-2,6,10-triene-4,5-diol

C23H31NO2 (353.2355)


   

(1'r,2'r,3s,7'r,9'r)-6'-acetyl-2'-hydroxy-6-methoxy-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

(1'r,2'r,3s,7'r,9'r)-6'-acetyl-2'-hydroxy-6-methoxy-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

C21H24N2O5 (384.1685)


   

5-[(1r)-1-(1h-indol-3-yl)ethyl]-2-(methylimino)-5h-1,3-oxazol-4-ol

5-[(1r)-1-(1h-indol-3-yl)ethyl]-2-(methylimino)-5h-1,3-oxazol-4-ol

C14H15N3O2 (257.1164)


   

3-ethyl-1h-indole

3-ethyl-1h-indole

C10H11N (145.0891)


   

3,6-bis({[(2r)-3,3-dimethyloxiran-2-yl]methyl})-1h-indole

3,6-bis({[(2r)-3,3-dimethyloxiran-2-yl]methyl})-1h-indole

C18H23NO2 (285.1729)


   

(2r,3s)-1-(4-hydroxyphenyl)-4-(1h-indol-3-yl)butane-2,3-diol

(2r,3s)-1-(4-hydroxyphenyl)-4-(1h-indol-3-yl)butane-2,3-diol

C18H19NO3 (297.1365)


   

n-[(4-methoxy-1h-indol-3-yl)methyl]methylsulfanylcarboimidothioic acid

n-[(4-methoxy-1h-indol-3-yl)methyl]methylsulfanylcarboimidothioic acid

C12H14N2OS2 (266.0548)


   

2,2-bis(1h-indol-3-yl)-4-methylpentanoic acid

2,2-bis(1h-indol-3-yl)-4-methylpentanoic acid

C22H22N2O2 (346.1681)


   

[(5r,7s)-7-[(1e)-2-(1h-indol-5-yl)ethenyl]-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]methanol

[(5r,7s)-7-[(1e)-2-(1h-indol-5-yl)ethenyl]-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]methanol

C26H26N2O (382.2045)


   

6-[(1e)-2-[(5r,7r)-5-methyl-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl]ethenyl]-1h-indole

6-[(1e)-2-[(5r,7r)-5-methyl-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl]ethenyl]-1h-indole

C26H26N2 (366.2096)


   

(1r,9r)-5-(1h-indol-3-yl)-3,6-dimethoxy-8-oxa-10-azatetracyclo[7.7.0.0²,⁷.0¹¹,¹⁶]hexadeca-2,4,6,11,13,15-hexaene-1,4-diol

(1r,9r)-5-(1h-indol-3-yl)-3,6-dimethoxy-8-oxa-10-azatetracyclo[7.7.0.0²,⁷.0¹¹,¹⁶]hexadeca-2,4,6,11,13,15-hexaene-1,4-diol

C24H20N2O5 (416.1372)


   

2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol

2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol

C20H21BrN4O (412.0899)


   

6-amino-5-chloro-3-[(1s)-1,2-dihydroxyethyl]-4-imino-1h-indol-7-one

6-amino-5-chloro-3-[(1s)-1,2-dihydroxyethyl]-4-imino-1h-indol-7-one

C10H10ClN3O3 (255.0411)


   

{1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]indol-3-yl}acetic acid

{1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]indol-3-yl}acetic acid

C16H19NO7 (337.1161)


   

(3s)-3-hydroxy-3-methyl-2h-[1,3]thiazolo[3,2-a]indole-9-carbaldehyde

(3s)-3-hydroxy-3-methyl-2h-[1,3]thiazolo[3,2-a]indole-9-carbaldehyde

C12H11NO2S (233.051)


   

2-(hydroxymethyl)-6-[3-(methoxymethyl)indol-1-yl]oxane-3,4,5-triol

2-(hydroxymethyl)-6-[3-(methoxymethyl)indol-1-yl]oxane-3,4,5-triol

C16H21NO6 (323.1369)


   

3-ethyl-1-methoxyindole

3-ethyl-1-methoxyindole

C11H13NO (175.0997)


   

3,4-bis(1h-indol-3-yl)-5-(methoxycarbonyl)-1h-pyrrole-2-carboxylic acid

3,4-bis(1h-indol-3-yl)-5-(methoxycarbonyl)-1h-pyrrole-2-carboxylic acid

C23H17N3O4 (399.1219)


   

3-[4-(1h-indol-3-yl)-2,3,5,6-tetramethoxyphenyl]-7-(3-methylbut-2-en-1-yl)-1h-indole

3-[4-(1h-indol-3-yl)-2,3,5,6-tetramethoxyphenyl]-7-(3-methylbut-2-en-1-yl)-1h-indole

C31H32N2O4 (496.2362)


   

(1'r,2's,3s,7's,9'r)-6'-acetyl-2'-hydroxy-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

(1'r,2's,3s,7's,9'r)-6'-acetyl-2'-hydroxy-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

C20H22N2O4 (354.1579)


   

1-(1-ethylindol-3-yl)-2-hydroxyethanone

1-(1-ethylindol-3-yl)-2-hydroxyethanone

C12H13NO2 (203.0946)


   

3,6-bis(1h-indol-3-ylmethyl)-3,6-dihydropyrazine-2,5-diol

3,6-bis(1h-indol-3-ylmethyl)-3,6-dihydropyrazine-2,5-diol

C22H20N4O2 (372.1586)


   

n-[2-(1h-indol-3-yl)ethyl]-n-methyl-2-(methylamino)benzamide

n-[2-(1h-indol-3-yl)ethyl]-n-methyl-2-(methylamino)benzamide

C19H21N3O (307.1685)


   

2,4,6-tribromo-3-(methylsulfanyl)-1h-indole

2,4,6-tribromo-3-(methylsulfanyl)-1h-indole

C9H6Br3NS (396.7771)


   

(1'r,2's,3s,7's,9'r)-6'-acetyl-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

(1'r,2's,3s,7's,9'r)-6'-acetyl-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

C20H22N2O3 (338.163)


   

α-erythroidine

α-erythroidine

C16H19NO3 (273.1365)


   

[(5r,7s)-5-[(1e)-2-(1h-indol-5-yl)ethenyl]-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl]methanol

[(5r,7s)-5-[(1e)-2-(1h-indol-5-yl)ethenyl]-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl]methanol

C26H26N2O (382.2045)


   

1h-indole-3-carboximidic acid

1h-indole-3-carboximidic acid

C9H8N2O (160.0637)


   

{[(5z)-4-methoxy-1'h-[2,2'-bipyrrol]-5-ylidene]methyl}(2-methylpropyl)amine

{[(5z)-4-methoxy-1'h-[2,2'-bipyrrol]-5-ylidene]methyl}(2-methylpropyl)amine

C14H19N3O (245.1528)


   

(1r,7s,14s,16r,17r)-17-methoxy-5,15-dioxa-10-azapentacyclo[8.8.0.0¹,¹³.0²,⁷.0¹⁴,¹⁶]octadeca-2,12-diene-4,11-dione

(1r,7s,14s,16r,17r)-17-methoxy-5,15-dioxa-10-azapentacyclo[8.8.0.0¹,¹³.0²,⁷.0¹⁴,¹⁶]octadeca-2,12-diene-4,11-dione

C16H17NO5 (303.1107)


   

(3s)-3'-[2-(dimethylamino)ethyl]-3,5'-dihydroxy-3-[2-(methylamino)ethyl]-1'h-[1,4'-biindol]-2-one

(3s)-3'-[2-(dimethylamino)ethyl]-3,5'-dihydroxy-3-[2-(methylamino)ethyl]-1'h-[1,4'-biindol]-2-one

C23H28N4O3 (408.2161)


   

3-[1-(1h-indol-3-yl)-3-methylbut-2-en-1-yl]-7-(3-methylbut-2-en-1-yl)-1h-indole

3-[1-(1h-indol-3-yl)-3-methylbut-2-en-1-yl]-7-(3-methylbut-2-en-1-yl)-1h-indole

C26H28N2 (368.2252)


   

n-ω-methyltryptamine

n-ω-methyltryptamine

C11H14N2 (174.1157)


   

2-(1h-indol-3-yl)-3,6-dimethoxy-5-[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]benzene-1,4-diol

2-(1h-indol-3-yl)-3,6-dimethoxy-5-[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]benzene-1,4-diol

C29H28N2O4 (468.2049)


   

α,β-didehydrotryptophan

α,β-didehydrotryptophan

C11H10N2O2 (202.0742)


   

2-(2-hydroxy-6-methylhept-5-en-2-yl)-2,3-dihydro-1h-indole-5-carboximidic acid

2-(2-hydroxy-6-methylhept-5-en-2-yl)-2,3-dihydro-1h-indole-5-carboximidic acid

C17H24N2O2 (288.1838)


   

2-(1-hydroxyethyl)-2-methyl-1h-quinazolin-4-ol

2-(1-hydroxyethyl)-2-methyl-1h-quinazolin-4-ol

C11H14N2O2 (206.1055)


   

3-[3-methyl-5-(2-methylpropyl)-1,2,4-trithiolan-3-yl]-1h-indole

3-[3-methyl-5-(2-methylpropyl)-1,2,4-trithiolan-3-yl]-1h-indole

C15H19NS3 (309.068)


   

3-[5-hydroxy-4-(1h-indol-3-yl)-1h-pyrrol-2-yl]indol-2-one

3-[5-hydroxy-4-(1h-indol-3-yl)-1h-pyrrol-2-yl]indol-2-one

C20H13N3O2 (327.1008)


   

3,7-bis(3-methylbut-2-en-1-yl)-1h-indole

3,7-bis(3-methylbut-2-en-1-yl)-1h-indole

C18H23N (253.183)


   

5-[3-(3-methylbut-2-en-1-yl)-4-methylideneoxolan-2-yl]-1h-indole

5-[3-(3-methylbut-2-en-1-yl)-4-methylideneoxolan-2-yl]-1h-indole

C18H21NO (267.1623)


   

{2,2',4'-trimethyl-1h,1'h-[3,7'-biindol]-4-yl}methanol

{2,2',4'-trimethyl-1h,1'h-[3,7'-biindol]-4-yl}methanol

C20H20N2O (304.1576)


   

13-(hydroxymethyl)-5-(2-methylbut-3-en-2-yl)-10-(sec-butyl)-3,9,12-triazatricyclo[6.6.1.0⁴,¹⁵]pentadeca-1,4,6,8(15),11-pentaen-11-ol

13-(hydroxymethyl)-5-(2-methylbut-3-en-2-yl)-10-(sec-butyl)-3,9,12-triazatricyclo[6.6.1.0⁴,¹⁵]pentadeca-1,4,6,8(15),11-pentaen-11-ol

C22H31N3O2 (369.2416)


   

3,5-dihydroxy-3,6-bis[5-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]cyclohex-5-ene-1,2,4-trione

3,5-dihydroxy-3,6-bis[5-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]cyclohex-5-ene-1,2,4-trione

C32H30N2O5 (522.2155)


   
   

(2s)-4-(1-methoxyindol-3-yl)-2-methylbutan-1-ol

(2s)-4-(1-methoxyindol-3-yl)-2-methylbutan-1-ol

C14H19NO2 (233.1416)


   

2-hydroxy-1-(1h-indol-3-yl)-4-methylhexan-3-one

2-hydroxy-1-(1h-indol-3-yl)-4-methylhexan-3-one

C15H19NO2 (245.1416)


   

methyl 2-(1h-indol-2-yl)acetate

methyl 2-(1h-indol-2-yl)acetate

C11H11NO2 (189.079)


   

2-(6-hydroxy-1h-indol-3-yl)ethanimidic acid

2-(6-hydroxy-1h-indol-3-yl)ethanimidic acid

C10H10N2O2 (190.0742)


   

methyl(2-{2-[(1e)-2-[(1s,3s)-3-methyl-9-[2-(methylamino)ethyl]-1-(2-methylprop-1-en-1-yl)-1h,2h-benzo[b]pyrrolizin-3-yl]ethenyl]-1h-indol-3-yl}ethyl)amine

methyl(2-{2-[(1e)-2-[(1s,3s)-3-methyl-9-[2-(methylamino)ethyl]-1-(2-methylprop-1-en-1-yl)-1h,2h-benzo[b]pyrrolizin-3-yl]ethenyl]-1h-indol-3-yl}ethyl)amine

C32H40N4 (480.3253)


   

(2r)-2-{[1-hydroxy-2,2-bis(1h-indol-3-yl)propylidene]amino}-3-(1h-indol-3-yl)-n-methyl-3-oxopropanimidic acid

(2r)-2-{[1-hydroxy-2,2-bis(1h-indol-3-yl)propylidene]amino}-3-(1h-indol-3-yl)-n-methyl-3-oxopropanimidic acid

C31H27N5O3 (517.2114)


   

3,3'-bis(2-aminoethyl)-5,5'-dibromo-1h,1'h-[4,4'-biindole]-7,7'-diol

3,3'-bis(2-aminoethyl)-5,5'-dibromo-1h,1'h-[4,4'-biindole]-7,7'-diol

C20H20Br2N4O2 (505.9953)


   

5-(3-methylbut-2-en-1-yl)-1h-indole-3-carboxylic acid

5-(3-methylbut-2-en-1-yl)-1h-indole-3-carboxylic acid

C14H15NO2 (229.1103)


   

n-{2-[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]ethyl}ethanimidic acid

n-{2-[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]ethyl}ethanimidic acid

C17H22N2O (270.1732)


   

methyl 2-{1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]indol-3-yl}acetate

methyl 2-{1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]indol-3-yl}acetate

C17H21NO7 (351.1318)


   

methyl 8-(chloromethyl)-4-hydroxy-2-methyl-1-oxo-6-(5,6,7-trimethoxy-1h-indole-2-carbonyl)-3h,7h,8h-pyrrolo[3,2-e]indole-2-carboxylate

methyl 8-(chloromethyl)-4-hydroxy-2-methyl-1-oxo-6-(5,6,7-trimethoxy-1h-indole-2-carbonyl)-3h,7h,8h-pyrrolo[3,2-e]indole-2-carboxylate

C26H26ClN3O8 (543.1408)


   

7-(hydroxymethyl)-7-methyl-1h-chromeno[5,6-b]pyrrole-3-carboxylic acid

7-(hydroxymethyl)-7-methyl-1h-chromeno[5,6-b]pyrrole-3-carboxylic acid

C14H13NO4 (259.0845)


   

3-[(3,3-dimethyloxiran-2-yl)methyl]-5-(3-methylbuta-1,3-dien-1-yl)-1h-indole

3-[(3,3-dimethyloxiran-2-yl)methyl]-5-(3-methylbuta-1,3-dien-1-yl)-1h-indole

C18H21NO (267.1623)


   

6-bromo-3-(6-bromo-1h-indol-3-ylsulfonyl)indole-1-carboxylic acid

6-bromo-3-(6-bromo-1h-indol-3-ylsulfonyl)indole-1-carboxylic acid

C17H10Br2N2O4S (495.8728)


   

2-(2-methylbut-3-en-2-yl)-1h-indole-3-carbaldehyde

2-(2-methylbut-3-en-2-yl)-1h-indole-3-carbaldehyde

C14H15NO (213.1154)


   

6'-acetyl-2'-hydroxy-6-methoxy-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

6'-acetyl-2'-hydroxy-6-methoxy-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

C21H24N2O5 (384.1685)


   

(1r,9r)-5-(1h-indol-3-yl)-3,4,6-trimethoxy-8-oxa-10-azatetracyclo[7.7.0.0²,⁷.0¹¹,¹⁶]hexadeca-2(7),3,5,11,13,15-hexaen-1-ol

(1r,9r)-5-(1h-indol-3-yl)-3,4,6-trimethoxy-8-oxa-10-azatetracyclo[7.7.0.0²,⁷.0¹¹,¹⁶]hexadeca-2(7),3,5,11,13,15-hexaen-1-ol

C25H22N2O5 (430.1529)


   

{7-[2-(1h-indol-5-yl)ethenyl]-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl}methanol

{7-[2-(1h-indol-5-yl)ethenyl]-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl}methanol

C26H26N2O (382.2045)


   

(2r)-3-methyl-2-[6-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]butane-1,3-diol

(2r)-3-methyl-2-[6-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]butane-1,3-diol

C18H25NO2 (287.1885)


   

n-acetyl-n-[2-(1h-indol-3-yl)ethyl]acetamide

n-acetyl-n-[2-(1h-indol-3-yl)ethyl]acetamide

C14H16N2O2 (244.1212)


   

n-[2-(1h-indol-3-yl)ethyl]-3-phenyloxirane-2-carboximidic acid

n-[2-(1h-indol-3-yl)ethyl]-3-phenyloxirane-2-carboximidic acid

C19H18N2O2 (306.1368)


   

(2s,4e)-5-hydroxy-4-(1-hydroxyethylidene)-2-(1h-indol-3-ylmethyl)-2h-pyrrol-3-one

(2s,4e)-5-hydroxy-4-(1-hydroxyethylidene)-2-(1h-indol-3-ylmethyl)-2h-pyrrol-3-one

C15H14N2O3 (270.1004)


   

(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-({3-[2-(methylamino)ethyl]-1h-indol-5-yl}oxy)oxane-3,4,5-triol

(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-({3-[2-(methylamino)ethyl]-1h-indol-5-yl}oxy)oxane-3,4,5-triol

C17H24N2O6 (352.1634)


   

3-[(3e)-4-(1h-indol-6-yl)-2-methylbut-3-en-2-yl]-7-(3-methylbut-2-en-1-yl)-1h-indole

3-[(3e)-4-(1h-indol-6-yl)-2-methylbut-3-en-2-yl]-7-(3-methylbut-2-en-1-yl)-1h-indole

C26H28N2 (368.2252)


   

6-bromo-2-(2-methylbut-3-en-2-yl)-1h-indole-3-carbaldehyde

6-bromo-2-(2-methylbut-3-en-2-yl)-1h-indole-3-carbaldehyde

C14H14BrNO (291.0259)


   

n-(prop-2-en-1-yl)[(1h-indol-3-ylmethyl)sulfanyl]carboximidic acid

n-(prop-2-en-1-yl)[(1h-indol-3-ylmethyl)sulfanyl]carboximidic acid

C13H14N2OS (246.0827)


   

16-methoxy-5-oxa-10-azatetracyclo[8.7.0.0¹,¹³.0²,⁷]heptadeca-2,12,14-trien-4-one

16-methoxy-5-oxa-10-azatetracyclo[8.7.0.0¹,¹³.0²,⁷]heptadeca-2,12,14-trien-4-one

C16H19NO3 (273.1365)


   

{3-[2-(dimethylamino)ethyl]-1h-indol-5-yl}oxidanesulfonic acid

{3-[2-(dimethylamino)ethyl]-1h-indol-5-yl}oxidanesulfonic acid

C12H16N2O4S (284.0831)


   

methyl (2e)-3-(6-bromo-1h-indol-3-yl)prop-2-enoate

methyl (2e)-3-(6-bromo-1h-indol-3-yl)prop-2-enoate

C12H10BrNO2 (278.9895)


   

1-{5-[(3,3-dimethyloxiran-2-yl)methyl]-1h-indol-3-yl}-3-methylbutane-2,3-diol

1-{5-[(3,3-dimethyloxiran-2-yl)methyl]-1h-indol-3-yl}-3-methylbutane-2,3-diol

C18H25NO3 (303.1834)


   

2-(2-methylbut-3-en-2-yl)-1h-indole-3-carboximidic acid

2-(2-methylbut-3-en-2-yl)-1h-indole-3-carboximidic acid

C14H16N2O (228.1263)


   

3-[1-(1h-indol-7-yl)-3-methylbut-2-en-1-yl]-7-(3-methylbut-2-en-1-yl)-1h-indole

3-[1-(1h-indol-7-yl)-3-methylbut-2-en-1-yl]-7-(3-methylbut-2-en-1-yl)-1h-indole

C26H28N2 (368.2252)


   

4-hydroxy-2,5-bis({[2-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl})-3,6-dioxocyclohexa-1,4-dien-1-yl acetate

4-hydroxy-2,5-bis({[2-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl})-3,6-dioxocyclohexa-1,4-dien-1-yl acetate

C36H36N2O5 (576.2624)


   

(2r)-6-bromo-2-(hydroxymethyl)-2-methoxy-1h-indol-3-one

(2r)-6-bromo-2-(hydroxymethyl)-2-methoxy-1h-indol-3-one

C10H10BrNO3 (270.9844)


   

methyl 4-hydroxy-3-[3-(methoxymethylidene)-2-oxoindol-1-yl]benzoate

methyl 4-hydroxy-3-[3-(methoxymethylidene)-2-oxoindol-1-yl]benzoate

C18H15NO5 (325.095)


   

methyl 4-(1h-indol-3-yl)-2-methyl-4-oxobut-2-enoate

methyl 4-(1h-indol-3-yl)-2-methyl-4-oxobut-2-enoate

C14H13NO3 (243.0895)


   

[2-(5-{[(3ar,8as)-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl]oxy}-1h-indol-3-yl)ethyl]dimethylamine

[2-(5-{[(3ar,8as)-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl]oxy}-1h-indol-3-yl)ethyl]dimethylamine

C23H28N4O (376.2263)


   

6-methoxy-3-(3-methylbut-2-en-1-ylidene)-1h-indol-2-one

6-methoxy-3-(3-methylbut-2-en-1-ylidene)-1h-indol-2-one

C14H15NO2 (229.1103)


   

2-phenylethyl 2-(1h-indol-3-yl)acetate

2-phenylethyl 2-(1h-indol-3-yl)acetate

C18H17NO2 (279.1259)


   

2-(dimethylamino)-3-(1h-indol-3-yl)propanoic acid

2-(dimethylamino)-3-(1h-indol-3-yl)propanoic acid

C13H16N2O2 (232.1212)


   

1h,1'h-3,3'-biindole

1h,1'h-3,3'-biindole

C16H12N2 (232.1)


   

6-bromo-1h-indole-3-carbaldehyde

6-bromo-1h-indole-3-carbaldehyde

C9H6BrNO (222.9633)


   

3-[(3r)-1,3-bis(1h-indol-3-yl)butyl]-1h-indole

3-[(3r)-1,3-bis(1h-indol-3-yl)butyl]-1h-indole

C28H25N3 (403.2048)


   

(2s,3r,4s,5s,6r)-2-[(3-ethyl-1h-indol-4-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

(2s,3r,4s,5s,6r)-2-[(3-ethyl-1h-indol-4-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

C16H21NO6 (323.1369)


   

(2r)-1-(1h-indol-3-yl)-4-methyl-3-oxohexan-2-yl acetate

(2r)-1-(1h-indol-3-yl)-4-methyl-3-oxohexan-2-yl acetate

C17H21NO3 (287.1521)


   

n-(2-{3'-[2-(dimethylamino)ethyl]-5'-hydroxy-1'h-[1,4'-biindol]-3-yl}ethyl)-n-methylacetamide

n-(2-{3'-[2-(dimethylamino)ethyl]-5'-hydroxy-1'h-[1,4'-biindol]-3-yl}ethyl)-n-methylacetamide

C25H30N4O2 (418.2369)


   

(2r)-2-[(2s)-2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl]-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid

(2r)-2-[(2s)-2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl]-n-(2-hydroxy-5-oxocyclopent-1-en-1-yl)-2,3-dihydro-1h-indole-5-carboximidic acid

C24H32N2O5 (428.2311)


   

2-(1h-indol-3-yl)-2-oxoacetamide

2-(1h-indol-3-yl)-2-oxoacetamide

C10H8N2O2 (188.0586)


   

6'-acetyl-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

6'-acetyl-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

C20H22N2O3 (338.163)


   

3-{[(1r,5s,7s)-6-isopropyl-8-methylidene-6-azabicyclo[3.2.1]oct-3-en-7-yl]methyl}-1h-indole

3-{[(1r,5s,7s)-6-isopropyl-8-methylidene-6-azabicyclo[3.2.1]oct-3-en-7-yl]methyl}-1h-indole

C20H24N2 (292.1939)


   

6,12-bis(6-bromo-1h-indol-3-yl)-11-hydroxy-2,9-diimino-1,3,8-trimethyl-1,3,8,10-tetraazadispiro[4.1.4⁷.1⁵]dodec-10-en-4-one

6,12-bis(6-bromo-1h-indol-3-yl)-11-hydroxy-2,9-diimino-1,3,8-trimethyl-1,3,8,10-tetraazadispiro[4.1.4⁷.1⁵]dodec-10-en-4-one

C27H24Br2N8O2 (650.0389)


   

n-[2-(1h-indol-3-yl)ethyl]tridecanimidic acid

n-[2-(1h-indol-3-yl)ethyl]tridecanimidic acid

C23H36N2O (356.2827)


   

n-[(1s)-1-hydroxy-2-(1h-indol-3-yl)-2-oxoethyl]ethanimidic acid

n-[(1s)-1-hydroxy-2-(1h-indol-3-yl)-2-oxoethyl]ethanimidic acid

C12H12N2O3 (232.0848)


   

(2s)-1-(1h-indol-3-yl)-5-methyl-3-oxohexan-2-yl 2-aminobenzoate

(2s)-1-(1h-indol-3-yl)-5-methyl-3-oxohexan-2-yl 2-aminobenzoate

C22H24N2O3 (364.1787)


   

methyl 2-{1-[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]indol-3-yl}acetate

methyl 2-{1-[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]indol-3-yl}acetate

C17H21NO7 (351.1318)


   

4-[2-(5-bromo-2-oxo-1h-indol-3-ylidene)hydrazin-1-yl]benzenesulfonamide

4-[2-(5-bromo-2-oxo-1h-indol-3-ylidene)hydrazin-1-yl]benzenesulfonamide

C14H11BrN4O3S (393.9735)


   

2h,3h,8h,8ah-furo[2,3-b]indol-3a-ol

2h,3h,8h,8ah-furo[2,3-b]indol-3a-ol

C10H11NO2 (177.079)


   

2,5-dimethyl 3-(5-hydroxy-1h-indol-3-yl)-4-(1h-indol-3-yl)-1h-pyrrole-2,5-dicarboxylate

2,5-dimethyl 3-(5-hydroxy-1h-indol-3-yl)-4-(1h-indol-3-yl)-1h-pyrrole-2,5-dicarboxylate

C24H19N3O5 (429.1325)


   

5-[4-(methoxymethyl)furan-2-yl]-1h-indole

5-[4-(methoxymethyl)furan-2-yl]-1h-indole

C14H13NO2 (227.0946)


   

(2s)-3-(5,6-dibromo-1h-indol-3-yl)-2-(methylamino)propanoic acid

(2s)-3-(5,6-dibromo-1h-indol-3-yl)-2-(methylamino)propanoic acid

C12H12Br2N2O2 (373.9265)


   

(3s,6s)-3,6-bis(1h-indol-3-ylmethyl)-3,6-dihydropyrazine-2,5-diol

(3s,6s)-3,6-bis(1h-indol-3-ylmethyl)-3,6-dihydropyrazine-2,5-diol

C22H20N4O2 (372.1586)


   

(2s)-2-{[(2s)-2-{[(2s)-2-amino-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(1h-indol-3-yl)propylidene]amino}-3-(1h-indol-3-yl)propanoic acid

(2s)-2-{[(2s)-2-{[(2s)-2-amino-1-hydroxy-3-phenylpropylidene]amino}-1-hydroxy-3-(1h-indol-3-yl)propylidene]amino}-3-(1h-indol-3-yl)propanoic acid

C31H31N5O4 (537.2376)


   

4-(1-methoxyindol-3-yl)-2-methylbutan-1-ol

4-(1-methoxyindol-3-yl)-2-methylbutan-1-ol

C14H19NO2 (233.1416)


   

2'-hydroxy-1'h-[3,3'-biindol]-2-one

2'-hydroxy-1'h-[3,3'-biindol]-2-one

C16H10N2O2 (262.0742)


   

2-({1,2-bis[(2-hydroxyphenyl)methyl]indol-3-yl}methyl)phenol

2-({1,2-bis[(2-hydroxyphenyl)methyl]indol-3-yl}methyl)phenol

C29H25NO3 (435.1834)


   

2-[(1r)-1-[(1-hydroxyethylidene)amino]ethyl]-n-[2-(1h-indol-3-yl)ethyl]-1,3-thiazole-4-carboximidic acid

2-[(1r)-1-[(1-hydroxyethylidene)amino]ethyl]-n-[2-(1h-indol-3-yl)ethyl]-1,3-thiazole-4-carboximidic acid

C18H20N4O2S (356.1307)


   

(2s)-2-hydroxy-3-(5-hydroxy-1h-indol-3-yl)propanoic acid

(2s)-2-hydroxy-3-(5-hydroxy-1h-indol-3-yl)propanoic acid

C11H11NO4 (221.0688)


   

1,3-bis(1h-indol-3-yl)propan-2-one

1,3-bis(1h-indol-3-yl)propan-2-one

C19H16N2O (288.1263)


   

(3r)-3-[(2s)-butan-2-yl]-6-(1h-indol-3-ylmethyl)-3,6-dihydropyrazine-2,5-diol

(3r)-3-[(2s)-butan-2-yl]-6-(1h-indol-3-ylmethyl)-3,6-dihydropyrazine-2,5-diol

C17H21N3O2 (299.1634)


   

5-[1-(1h-indol-3-yl)ethyl]-2-(methylimino)-5h-1,3-oxazol-4-ol

5-[1-(1h-indol-3-yl)ethyl]-2-(methylimino)-5h-1,3-oxazol-4-ol

C14H15N3O2 (257.1164)


   

1-[2-(1h-indol-3-yl)ethyl]-5-(1,2,3-trihydroxypropyl)pyrrole-2-carbaldehyde

1-[2-(1h-indol-3-yl)ethyl]-5-(1,2,3-trihydroxypropyl)pyrrole-2-carbaldehyde

C18H20N2O4 (328.1423)


   

3-[(2r)-oxiran-2-yl]-1h-indole

3-[(2r)-oxiran-2-yl]-1h-indole

C10H9NO (159.0684)


   

2,5-dihydroxy-3-(1h-indol-3-ylmethyl)-6-{[2-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}cyclohexa-2,5-diene-1,4-dione

2,5-dihydroxy-3-(1h-indol-3-ylmethyl)-6-{[2-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}cyclohexa-2,5-diene-1,4-dione

C29H26N2O4 (466.1892)


   

2-(5,6-dibromo-1h-indol-3-yl)ethanamine

2-(5,6-dibromo-1h-indol-3-yl)ethanamine

C10H10Br2N2 (315.9211)


   

(3r,6s)-3,6-bis(1h-indol-3-ylmethyl)-3,6-dihydropyrazine-2,5-diol

(3r,6s)-3,6-bis(1h-indol-3-ylmethyl)-3,6-dihydropyrazine-2,5-diol

C22H20N4O2 (372.1586)


   

7-(3-methylbut-2-en-1-yl)-3-(2-oxopropylidene)-1h-indol-2-one

7-(3-methylbut-2-en-1-yl)-3-(2-oxopropylidene)-1h-indol-2-one

C16H17NO2 (255.1259)


   

(2z)-n-[2-(1h-indol-3-yl)ethyl]-3-methyldodec-2-enimidic acid

(2z)-n-[2-(1h-indol-3-yl)ethyl]-3-methyldodec-2-enimidic acid

C23H34N2O (354.2671)


   

methyl({2-[2-(2-{3-methyl-9-[2-(methylamino)ethyl]-1-(2-methylprop-1-en-1-yl)-1h,2h-benzo[b]pyrrolizin-3-yl}ethenyl)-1h-indol-3-yl]ethyl})amine

methyl({2-[2-(2-{3-methyl-9-[2-(methylamino)ethyl]-1-(2-methylprop-1-en-1-yl)-1h,2h-benzo[b]pyrrolizin-3-yl}ethenyl)-1h-indol-3-yl]ethyl})amine

C32H40N4 (480.3253)


   

(3s,4e)-5-{3-[2-(dimethylamino)ethyl]-1h-indol-2-yl}-1-[(2r)-3,3-dimethyloxiran-2-yl]-3-methylpent-4-en-1-one

(3s,4e)-5-{3-[2-(dimethylamino)ethyl]-1h-indol-2-yl}-1-[(2r)-3,3-dimethyloxiran-2-yl]-3-methylpent-4-en-1-one

C22H30N2O2 (354.2307)


   

12-(1h-indol-3-yl)-2,6,10-trimethyldodeca-2,10-diene-4,5-diol

12-(1h-indol-3-yl)-2,6,10-trimethyldodeca-2,10-diene-4,5-diol

C23H33NO2 (355.2511)


   

n'-[(1z)-2-(6-bromo-1h-indol-3-yl)ethenyl]ethanediamide

n'-[(1z)-2-(6-bromo-1h-indol-3-yl)ethenyl]ethanediamide

C12H10BrN3O2 (306.9956)


   

(3s,6s)-3-(1h-indol-3-ylmethyl)-6-{[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol

(3s,6s)-3-(1h-indol-3-ylmethyl)-6-{[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol

C27H28N4O2 (440.2212)


   

1-{3-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]-1h-indol-5-yl}-3-methylbut-2-en-1-one

1-{3-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]-1h-indol-5-yl}-3-methylbut-2-en-1-one

C18H21NO2 (283.1572)


   

5-methoxy-1h-indole-2-carboxylic acid

5-methoxy-1h-indole-2-carboxylic acid

C10H9NO3 (191.0582)


   

methyl 3-(5-hydroxy-1h-indol-3-yl)-4-(1h-indol-3-yl)-1h-pyrrole-2-carboxylate

methyl 3-(5-hydroxy-1h-indol-3-yl)-4-(1h-indol-3-yl)-1h-pyrrole-2-carboxylate

C22H17N3O3 (371.127)


   

(3s,6s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol

(3s,6s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol

C19H23N3O2 (325.179)


   

3-(1h-indol-3-yl)prop-2-enimidic acid

3-(1h-indol-3-yl)prop-2-enimidic acid

C11H10N2O (186.0793)


   

n-(1h-indol-3-ylmethyl)methylsulfanylcarboximidic acid

n-(1h-indol-3-ylmethyl)methylsulfanylcarboximidic acid

C11H12N2OS (220.067)


   

4-(4-chloro-3-methylbuta-1,3-dien-1-yl)-1h-indole-3-carbaldehyde

4-(4-chloro-3-methylbuta-1,3-dien-1-yl)-1h-indole-3-carbaldehyde

C14H12ClNO (245.0607)


   

dimethyl({2-[5-({1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl}oxy)-1h-indol-3-yl]ethyl})amine

dimethyl({2-[5-({1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl}oxy)-1h-indol-3-yl]ethyl})amine

C23H28N4O (376.2263)


   

5-{6-[2-(1h-indol-5-yl)ethenyl]-3,6-dimethylcyclohex-2-en-1-yl}-1h-indole

5-{6-[2-(1h-indol-5-yl)ethenyl]-3,6-dimethylcyclohex-2-en-1-yl}-1h-indole

C26H26N2 (366.2096)


   

methyl 2-(1h-indol-3-yl)-2-oxoacetate

methyl 2-(1h-indol-3-yl)-2-oxoacetate

C11H9NO3 (203.0582)


   

(2s)-2-amino-3-(1h-indol-3-yl)propanimidic acid

(2s)-2-amino-3-(1h-indol-3-yl)propanimidic acid

C11H13N3O (203.1059)


   

(2s,3r)-1-(4-hydroxyphenyl)-4-(1h-indol-3-yl)butane-2,3-diol

(2s,3r)-1-(4-hydroxyphenyl)-4-(1h-indol-3-yl)butane-2,3-diol

C18H19NO3 (297.1365)


   

methyl 2-hydroxy-3-(1h-indol-3-yl)prop-2-enoate

methyl 2-hydroxy-3-(1h-indol-3-yl)prop-2-enoate

C12H11NO3 (217.0739)


   

(2e)-3-(1h-indol-3-yl)-n-[2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

(2e)-3-(1h-indol-3-yl)-n-[2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

C21H17N3O (327.1372)


   

1-(6-bromo-3-hydroxy-1h-indol-2-yl)ethanone

1-(6-bromo-3-hydroxy-1h-indol-2-yl)ethanone

C10H8BrNO2 (252.9738)


   

5-(1h-indol-3-yl)-5-methoxyimidazole-2,4-diol

5-(1h-indol-3-yl)-5-methoxyimidazole-2,4-diol

C12H11N3O3 (245.08)


   

13-(methoxycarbonyl)-11,22-diazapentacyclo[13.7.0.0⁴,¹².0⁵,¹⁰.0¹⁶,²¹]docosa-1,3,5,7,9,12,14,16,18,20-decaene-2-carboxylic acid

13-(methoxycarbonyl)-11,22-diazapentacyclo[13.7.0.0⁴,¹².0⁵,¹⁰.0¹⁶,²¹]docosa-1,3,5,7,9,12,14,16,18,20-decaene-2-carboxylic acid

C23H16N2O4 (384.111)


   

methyl 1-(3,4-dihydroxy-2-methylbutan-2-yl)indole-3-carboxylate

methyl 1-(3,4-dihydroxy-2-methylbutan-2-yl)indole-3-carboxylate

C15H19NO4 (277.1314)


   

n-[2-(3-bromo-4-hydroxyphenyl)ethyl]-2-(1h-indol-3-yl)-2-oxoacetamide

n-[2-(3-bromo-4-hydroxyphenyl)ethyl]-2-(1h-indol-3-yl)-2-oxoacetamide

C18H15BrN2O3 (386.0266)


   

6-[(1z)-2-[(5r,7r)-7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl]-1h-indole

6-[(1z)-2-[(5r,7r)-7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl]-1h-indole

C26H26N2 (366.2096)


   

(2s,3r,4s,5s,6r)-2-[(3-ethyl-1h-indol-4-yl)oxy]-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxane-3,4,5-triol

(2s,3r,4s,5s,6r)-2-[(3-ethyl-1h-indol-4-yl)oxy]-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxane-3,4,5-triol

C22H31NO11 (485.1897)


   

6-[(1e)-2-[(5s,7s)-5-methyl-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl]ethenyl]-1h-indole

6-[(1e)-2-[(5s,7s)-5-methyl-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl]ethenyl]-1h-indole

C26H26N2 (366.2096)


   

(3e)-4-[3-(2-hydroxyethyl)-1h-indol-5-yl]but-3-en-2-one

(3e)-4-[3-(2-hydroxyethyl)-1h-indol-5-yl]but-3-en-2-one

C14H15NO2 (229.1103)


   

2-{1-[(1-hydroxyethylidene)amino]ethyl}-n-[2-(1h-indol-3-yl)ethyl]-1,3-thiazole-4-carboximidic acid

2-{1-[(1-hydroxyethylidene)amino]ethyl}-n-[2-(1h-indol-3-yl)ethyl]-1,3-thiazole-4-carboximidic acid

C18H20N4O2S (356.1307)


   

3,5-bis({[(2r)-3,3-dimethyloxiran-2-yl]methyl})-1h-indole

3,5-bis({[(2r)-3,3-dimethyloxiran-2-yl]methyl})-1h-indole

C18H23NO2 (285.1729)


   

3-[11-hydroxy-13-(hydroxymethyl)-10-isopropyl-9-methyl-3,9,12-triazatricyclo[6.6.1.0⁴,¹⁵]pentadeca-1,4,6,8(15),11-pentaen-5-yl]-3-(1h-indol-3-yl)propane-1,2-diol

3-[11-hydroxy-13-(hydroxymethyl)-10-isopropyl-9-methyl-3,9,12-triazatricyclo[6.6.1.0⁴,¹⁵]pentadeca-1,4,6,8(15),11-pentaen-5-yl]-3-(1h-indol-3-yl)propane-1,2-diol

C28H34N4O4 (490.258)


   

(3z)-3-ethylidene-5-hydroxy-6-(1h-indol-3-ylmethyl)-1-methyl-6h-pyrazin-2-one

(3z)-3-ethylidene-5-hydroxy-6-(1h-indol-3-ylmethyl)-1-methyl-6h-pyrazin-2-one

C16H17N3O2 (283.1321)


   

methyl 5-(1h-indol-5-yl)furan-3-carboxylate

methyl 5-(1h-indol-5-yl)furan-3-carboxylate

C14H11NO3 (241.0739)


   

(1r,2s)-2-hydroxy-1-methoxy-1,2-dimethyl-9h-carbazole-3,4-dione

(1r,2s)-2-hydroxy-1-methoxy-1,2-dimethyl-9h-carbazole-3,4-dione

C15H15NO4 (273.1001)


   

2-chloro-1h-indole

2-chloro-1h-indole

C8H6ClN (151.0189)


   

(2s,3s,4r,5s,6s)-6-(hydroxymethyl)-4-(indol-1-yloxy)oxane-2,3,5-triol

(2s,3s,4r,5s,6s)-6-(hydroxymethyl)-4-(indol-1-yloxy)oxane-2,3,5-triol

C14H17NO6 (295.1056)


   

3'-[2-(dimethylamino)ethyl]-3-[2-(methylamino)ethyl]-1'h-[1,4'-biindol]-5'-ol

3'-[2-(dimethylamino)ethyl]-3-[2-(methylamino)ethyl]-1'h-[1,4'-biindol]-5'-ol

C23H28N4O (376.2263)


   

methyl (2r,8s)-8-(bromomethyl)-4-hydroxy-2-methyl-1-oxo-6-(5,6,7-trimethoxy-1h-indole-2-carbonyl)-3h,7h,8h-pyrrolo[3,2-e]indole-2-carboxylate

methyl (2r,8s)-8-(bromomethyl)-4-hydroxy-2-methyl-1-oxo-6-(5,6,7-trimethoxy-1h-indole-2-carbonyl)-3h,7h,8h-pyrrolo[3,2-e]indole-2-carboxylate

C26H26BrN3O8 (587.0903)


   

5-[(1s,6r)-3,6-dimethyl-6-[(1e)-2-[3-(2-methylbut-3-en-2-yl)-1h-indol-5-yl]ethenyl]cyclohex-2-en-1-yl]-3-(2-methylbut-3-en-2-yl)-1h-indole

5-[(1s,6r)-3,6-dimethyl-6-[(1e)-2-[3-(2-methylbut-3-en-2-yl)-1h-indol-5-yl]ethenyl]cyclohex-2-en-1-yl]-3-(2-methylbut-3-en-2-yl)-1h-indole

C36H42N2 (502.3348)


   

n-[2-(1h-indol-3-yl)ethyl]-n-methylmethylsulfanylformamide

n-[2-(1h-indol-3-yl)ethyl]-n-methylmethylsulfanylformamide

C13H16N2OS (248.0983)


   

3-(1h-indol-3-ylmethyl)-6-isopropyl-3,6-dihydropyrazine-2,5-diol

3-(1h-indol-3-ylmethyl)-6-isopropyl-3,6-dihydropyrazine-2,5-diol

C16H19N3O2 (285.1477)


   

n-[2-(5-methoxy-1h-indol-3-yl)ethyl]ethanimidic acid

n-[2-(5-methoxy-1h-indol-3-yl)ethyl]ethanimidic acid

C13H16N2O2 (232.1212)


   

2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-2,3-dihydro-1h-indole-5-carboximidic acid

2-(2-hydroxy-1-methoxy-5,6-dimethylhept-5-en-2-yl)-2,3-dihydro-1h-indole-5-carboximidic acid

C19H28N2O3 (332.21)


   

2-{[(2-aminophenyl)(hydroxy)methylidene]amino}-n-[2-(1h-indol-3-yl)ethenyl]ethanimidic acid

2-{[(2-aminophenyl)(hydroxy)methylidene]amino}-n-[2-(1h-indol-3-yl)ethenyl]ethanimidic acid

C19H18N4O2 (334.143)


   

1-(1-methylindol-3-yl)methanamine

1-(1-methylindol-3-yl)methanamine

C10H12N2 (160.1)


   

methyl (1s)-1,3-bis(1h-indol-3-yl)-4-methoxy-2,5-dioxocyclopent-3-ene-1-carboxylate

methyl (1s)-1,3-bis(1h-indol-3-yl)-4-methoxy-2,5-dioxocyclopent-3-ene-1-carboxylate

C24H18N2O5 (414.1216)


   

(2r)-2-[(2s)-2-hydroxy-5,6-dimethylhept-5-en-2-yl]-2,3-dihydro-1h-indole-5-carboximidic acid

(2r)-2-[(2s)-2-hydroxy-5,6-dimethylhept-5-en-2-yl]-2,3-dihydro-1h-indole-5-carboximidic acid

C18H26N2O2 (302.1994)


   

{1-[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]indol-3-yl}methyl acetate

{1-[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]indol-3-yl}methyl acetate

C17H21NO7 (351.1318)


   

3-{[5-(2-methylpropyl)-1,2,4-trithiolan-3-yl]methyl}-1h-indole

3-{[5-(2-methylpropyl)-1,2,4-trithiolan-3-yl]methyl}-1h-indole

C15H19NS3 (309.068)


   

1,2,2-tris(1h-indol-3-yl)ethanone

1,2,2-tris(1h-indol-3-yl)ethanone

C26H19N3O (389.1528)


   

3,5-dihydroxy-6-[5-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]-3-[6-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]cyclohex-5-ene-1,2,4-trione

3,5-dihydroxy-6-[5-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]-3-[6-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]cyclohex-5-ene-1,2,4-trione

C32H30N2O5 (522.2155)


   

2-[(1-hydroxy-4-methylhex-3-en-1-ylidene)amino]-3-(1h-indol-3-yl)propanoic acid

2-[(1-hydroxy-4-methylhex-3-en-1-ylidene)amino]-3-(1h-indol-3-yl)propanoic acid

C18H22N2O3 (314.163)


   

5-[(1r,6s)-6-[(1e)-2-(1h-indol-5-yl)ethenyl]-3,6-dimethylcyclohex-2-en-1-yl]-1h-indole

5-[(1r,6s)-6-[(1e)-2-(1h-indol-5-yl)ethenyl]-3,6-dimethylcyclohex-2-en-1-yl]-1h-indole

C26H26N2 (366.2096)


   

2-({1,2,3-tris[(2-hydroxyphenyl)methyl]indol-5-yl}methyl)phenol

2-({1,2,3-tris[(2-hydroxyphenyl)methyl]indol-5-yl}methyl)phenol

C36H31NO4 (541.2253)


   

2,5-bis(1h-indol-3-yl)-3,4,6-trimethoxyphenol

2,5-bis(1h-indol-3-yl)-3,4,6-trimethoxyphenol

C25H22N2O4 (414.1579)


   

7-[(1e)-2-[(5r,7r)-7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl]-1h-indole

7-[(1e)-2-[(5r,7r)-7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl]-1h-indole

C26H26N2 (366.2096)


   

5-(3,6-dimethyl-6-{2-[3-(2-methylbut-3-en-2-yl)-1h-indol-5-yl]ethenyl}cyclohex-2-en-1-yl)-3-(2-methylbut-3-en-2-yl)-1h-indole

5-(3,6-dimethyl-6-{2-[3-(2-methylbut-3-en-2-yl)-1h-indol-5-yl]ethenyl}cyclohex-2-en-1-yl)-3-(2-methylbut-3-en-2-yl)-1h-indole

C36H42N2 (502.3348)


   

(2z)-2-(1h-indol-3-ylmethylidene)-1h-indol-3-one

(2z)-2-(1h-indol-3-ylmethylidene)-1h-indol-3-one

C17H12N2O (260.095)


   

(2s,3s)-3-[(10s,13s)-11-hydroxy-13-(hydroxymethyl)-10-isopropyl-9-methyl-3,9,12-triazatricyclo[6.6.1.0⁴,¹⁵]pentadeca-1,4,6,8(15),11-pentaen-5-yl]-3-(1h-indol-3-yl)propane-1,2-diol

(2s,3s)-3-[(10s,13s)-11-hydroxy-13-(hydroxymethyl)-10-isopropyl-9-methyl-3,9,12-triazatricyclo[6.6.1.0⁴,¹⁵]pentadeca-1,4,6,8(15),11-pentaen-5-yl]-3-(1h-indol-3-yl)propane-1,2-diol

C28H34N4O4 (490.258)


   

bis(5-hydroxy-1h-indol-3-yl)ethane-1,2-dione

bis(5-hydroxy-1h-indol-3-yl)ethane-1,2-dione

C18H12N2O4 (320.0797)


   

{2-methyl-3-[(2-methyl-1h-indol-4-yl)methyl]-1h-indol-4-yl}methanol

{2-methyl-3-[(2-methyl-1h-indol-4-yl)methyl]-1h-indol-4-yl}methanol

C20H20N2O (304.1576)


   

methyl 2-(dimethylamino)-3-(1h-indol-3-yl)propanoate

methyl 2-(dimethylamino)-3-(1h-indol-3-yl)propanoate

C14H18N2O2 (246.1368)


   

n-methyl[(1h-indol-3-ylmethyl)sulfanyl]carboimidothioic acid

n-methyl[(1h-indol-3-ylmethyl)sulfanyl]carboimidothioic acid

C11H12N2S2 (236.0442)


   

6-bromo-2-(hydroxymethyl)-2-methoxy-1h-indol-3-one

6-bromo-2-(hydroxymethyl)-2-methoxy-1h-indol-3-one

C10H10BrNO3 (270.9844)


   

1-{3-[(2r)-2,3-dihydroxy-3-methylbutyl]-1h-indol-5-yl}-3-methylbut-2-en-1-one

1-{3-[(2r)-2,3-dihydroxy-3-methylbutyl]-1h-indol-5-yl}-3-methylbut-2-en-1-one

C18H23NO3 (301.1678)


   

7-{2-[7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl}-1h-indole

7-{2-[7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl}-1h-indole

C26H26N2 (366.2096)


   

(3e)-4-(3-{[(2r)-3,3-dimethyloxiran-2-yl]methyl}-1h-indol-2-yl)-2-methylbut-3-en-2-ol

(3e)-4-(3-{[(2r)-3,3-dimethyloxiran-2-yl]methyl}-1h-indol-2-yl)-2-methylbut-3-en-2-ol

C18H23NO2 (285.1729)


   

3',5,5'-tribromo-7'-methoxy-1h,1'h-3,4'-biindole

3',5,5'-tribromo-7'-methoxy-1h,1'h-3,4'-biindole

C17H11Br3N2O (495.8421)


   

(4s,5s,6r,10e)-12-(1h-indol-3-yl)-2,6,10-trimethyldodeca-2,10-diene-4,5-diol

(4s,5s,6r,10e)-12-(1h-indol-3-yl)-2,6,10-trimethyldodeca-2,10-diene-4,5-diol

C23H33NO2 (355.2511)


   

(z)-n-(2-{5-[(1e)-3-methylbuta-1,3-dien-1-yl]-1h-indol-3-yl}ethylidene)hydroxylamine

(z)-n-(2-{5-[(1e)-3-methylbuta-1,3-dien-1-yl]-1h-indol-3-yl}ethylidene)hydroxylamine

C15H16N2O (240.1263)


   

(2s)-2-[(1s)-1-hydroxyethyl]-2-methyl-1h-quinazolin-4-ol

(2s)-2-[(1s)-1-hydroxyethyl]-2-methyl-1h-quinazolin-4-ol

C11H14N2O2 (206.1055)


   

n-[(1-methoxyindol-3-yl)methyl]methylsulfanylcarboimidothioic acid

n-[(1-methoxyindol-3-yl)methyl]methylsulfanylcarboimidothioic acid

C12H14N2OS2 (266.0548)


   

(2s)-n-[(2s)-1-(1h-indol-3-yl)-3-(propanoyloxy)propan-2-yl]-3-methyl-2-(methylamino)butanimidic acid

(2s)-n-[(2s)-1-(1h-indol-3-yl)-3-(propanoyloxy)propan-2-yl]-3-methyl-2-(methylamino)butanimidic acid

C20H29N3O3 (359.2209)


   

3,6-bis({[(2s)-3,3-dimethyloxiran-2-yl]methyl})-1h-indole

3,6-bis({[(2s)-3,3-dimethyloxiran-2-yl]methyl})-1h-indole

C18H23NO2 (285.1729)


   

3-{[(2r)-3,3-dimethyloxiran-2-yl]methyl}-5-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-1h-indole

3-{[(2r)-3,3-dimethyloxiran-2-yl]methyl}-5-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-1h-indole

C18H23NO2 (285.1729)


   

2,5-dihydroxy-3-[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]-6-[1-(2-methylbut-3-en-2-yl)indol-3-yl]cyclohexa-2,5-diene-1,4-dione

2,5-dihydroxy-3-[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]-6-[1-(2-methylbut-3-en-2-yl)indol-3-yl]cyclohexa-2,5-diene-1,4-dione

C32H30N2O4 (506.2205)


   

2-hydroxy-1-(5-hydroxy-1h-indol-3-yl)ethanone

2-hydroxy-1-(5-hydroxy-1h-indol-3-yl)ethanone

C10H9NO3 (191.0582)


   

7-hydroxy-9-(5-hydroxy-1h-indol-3-yl)-3,10-diazatricyclo[6.4.1.0⁴,¹³]trideca-1,4,6,8(13),9-pentaene-11-carboxylic acid

7-hydroxy-9-(5-hydroxy-1h-indol-3-yl)-3,10-diazatricyclo[6.4.1.0⁴,¹³]trideca-1,4,6,8(13),9-pentaene-11-carboxylic acid

C20H15N3O4 (361.1063)


   

2-{5-[(1e)-3-methylbuta-1,3-dien-1-yl]-1h-indol-3-yl}ethanol

2-{5-[(1e)-3-methylbuta-1,3-dien-1-yl]-1h-indol-3-yl}ethanol

C15H17NO (227.131)


   

2-(1h-indol-3-yl)-3,6-dimethoxy-5-[1-(2-methylbut-3-en-2-yl)indol-3-yl]cyclohexa-2,5-diene-1,4-dione

2-(1h-indol-3-yl)-3,6-dimethoxy-5-[1-(2-methylbut-3-en-2-yl)indol-3-yl]cyclohexa-2,5-diene-1,4-dione

C29H26N2O4 (466.1892)


   

1-[3-(2,3-dihydroxy-3-methylbutyl)-1h-indol-5-yl]-3-methylbut-2-en-1-one

1-[3-(2,3-dihydroxy-3-methylbutyl)-1h-indol-5-yl]-3-methylbut-2-en-1-one

C18H23NO3 (301.1678)


   

1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]indole-3-carbaldehyde

1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]indole-3-carbaldehyde

C15H17NO6 (307.1056)


   

dimethyl({[1-(2-methylbut-3-en-2-yl)indol-3-yl]methyl})amine

dimethyl({[1-(2-methylbut-3-en-2-yl)indol-3-yl]methyl})amine

C16H22N2 (242.1783)


   

β-erythroidine

β-erythroidine

C16H19NO3 (273.1365)


   

3,5-bis[(3,3-dimethyloxiran-2-yl)methyl]-1h-indole

3,5-bis[(3,3-dimethyloxiran-2-yl)methyl]-1h-indole

C18H23NO2 (285.1729)


   

(5s)-5-[(1r)-1-(1h-indol-3-yl)ethyl]-2-(methylimino)-5h-1,3-oxazol-4-ol

(5s)-5-[(1r)-1-(1h-indol-3-yl)ethyl]-2-(methylimino)-5h-1,3-oxazol-4-ol

C14H15N3O2 (257.1164)


   

2-[1-(4-hydroxyphenyl)-3-methoxy-3-oxoprop-1-en-2-yl]-1h-indole-3-carboxylic acid

2-[1-(4-hydroxyphenyl)-3-methoxy-3-oxoprop-1-en-2-yl]-1h-indole-3-carboxylic acid

C19H15NO5 (337.095)


   

(1s,2s,3s)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one

(1s,2s,3s)-3-hydroxy-1,2-dimethyl-1,2,3,9-tetrahydrocarbazol-4-one

C14H15NO2 (229.1103)


   

isovaleric acid; tryptamine

isovaleric acid; tryptamine

C15H22N2O2 (262.1681)


   

(2e)-2-methyl-4-[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]but-2-en-1-ol

(2e)-2-methyl-4-[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]but-2-en-1-ol

C18H23NO (269.178)


   

(1s,2s,3r)-1-{4-methyl-1-phenylpyrrolo[3,4-b]quinolin-3-yl}butane-1,2,3,4-tetrol

(1s,2s,3r)-1-{4-methyl-1-phenylpyrrolo[3,4-b]quinolin-3-yl}butane-1,2,3,4-tetrol

C22H22N2O4 (378.1579)


   

methyl (2r,8s)-8-(chloromethyl)-4-hydroxy-2-methyl-1-oxo-6-(5,6,7-trimethoxy-1h-indole-2-carbonyl)-3h,7h,8h-pyrrolo[3,2-e]indole-2-carboxylate

methyl (2r,8s)-8-(chloromethyl)-4-hydroxy-2-methyl-1-oxo-6-(5,6,7-trimethoxy-1h-indole-2-carbonyl)-3h,7h,8h-pyrrolo[3,2-e]indole-2-carboxylate

C26H26ClN3O8 (543.1408)


   

(2r,3s,4s,5r,6r)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl 2-(1h-indol-3-yl)acetate

(2r,3s,4s,5r,6r)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl 2-(1h-indol-3-yl)acetate

C16H19NO7 (337.1161)


   

(3s)-3-hydroxy-1-(4-hydroxyphenyl)-4-(1h-indol-3-yl)butan-2-one

(3s)-3-hydroxy-1-(4-hydroxyphenyl)-4-(1h-indol-3-yl)butan-2-one

C18H17NO3 (295.1208)


   

(2s)-2-{[(2r)-1-hydroxy-2-methylbutylidene]amino}-3-(1h-indol-3-yl)propanoic acid

(2s)-2-{[(2r)-1-hydroxy-2-methylbutylidene]amino}-3-(1h-indol-3-yl)propanoic acid

C16H20N2O3 (288.1474)


   

n-[2-(1h-indol-3-yl)ethyl]-3-methylbutanimidic acid

n-[2-(1h-indol-3-yl)ethyl]-3-methylbutanimidic acid

C15H20N2O (244.1576)


   

(2s,3r,4s,5s,6r)-2-({3-[2-(dimethylamino)ethyl]-1h-indol-5-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

(2s,3r,4s,5s,6r)-2-({3-[2-(dimethylamino)ethyl]-1h-indol-5-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

C18H26N2O6 (366.1791)


   

[6-bromo-1-(methoxycarbonyl)indol-3-yl](6-bromo-1h-indol-3-yl)ethoxymethanesulfonic acid

[6-bromo-1-(methoxycarbonyl)indol-3-yl](6-bromo-1h-indol-3-yl)ethoxymethanesulfonic acid

C21H18Br2N2O6S (583.9252)


   

6-(1-hydroxyethyl)-3-(1h-indol-3-ylmethyl)-3-(methylsulfanyl)-6h-pyrazine-2,5-diol

6-(1-hydroxyethyl)-3-(1h-indol-3-ylmethyl)-3-(methylsulfanyl)-6h-pyrazine-2,5-diol

C16H19N3O3S (333.1147)


   

5-(3-methylbut-2-en-1-yl)-1h-indole-2,3-dione

5-(3-methylbut-2-en-1-yl)-1h-indole-2,3-dione

C13H13NO2 (215.0946)


   

(2s,3s)-1-(4-hydroxyphenyl)-4-(1h-indol-3-yl)butane-2,3-diol

(2s,3s)-1-(4-hydroxyphenyl)-4-(1h-indol-3-yl)butane-2,3-diol

C18H19NO3 (297.1365)


   

3-(3-methylbut-2-en-1-ylidene)-1h-indol-2-one

3-(3-methylbut-2-en-1-ylidene)-1h-indol-2-one

C13H13NO (199.0997)


   

2-[(1-hydroxy-2-methylbutylidene)amino]-3-(1h-indol-3-yl)propanoic acid

2-[(1-hydroxy-2-methylbutylidene)amino]-3-(1h-indol-3-yl)propanoic acid

C16H20N2O3 (288.1474)


   

(1's,2'r,3s,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde

(1's,2'r,3s,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde

C21H22N2O4 (366.1579)


   

(3r,6r)-3-(1-hydroxyethyl)-6-(1h-indol-3-ylmethyl)-3,6-dihydropyrazine-2,5-diol

(3r,6r)-3-(1-hydroxyethyl)-6-(1h-indol-3-ylmethyl)-3,6-dihydropyrazine-2,5-diol

C15H17N3O3 (287.127)


   

2-[(1s)-1-aminoethyl]-n-[2-(1h-indol-3-yl)ethyl]-1,3-thiazole-4-carboximidic acid

2-[(1s)-1-aminoethyl]-n-[2-(1h-indol-3-yl)ethyl]-1,3-thiazole-4-carboximidic acid

C16H18N4OS (314.1201)


   

(2r)-2-hydroxy-1-(1h-indol-3-yl)-5-methylhexan-3-one

(2r)-2-hydroxy-1-(1h-indol-3-yl)-5-methylhexan-3-one

C15H19NO2 (245.1416)


   

(s)-[6-bromo-1-(methoxycarbonyl)indol-3-yl](6-bromo-1h-indol-3-yl)hydroxymethanesulfonic acid

(s)-[6-bromo-1-(methoxycarbonyl)indol-3-yl](6-bromo-1h-indol-3-yl)hydroxymethanesulfonic acid

C19H14Br2N2O6S (555.8939)


   

3-[(3,3-dimethyloxiran-2-yl)methyl]-5-(3-methylbut-2-en-1-yl)-1h-indole

3-[(3,3-dimethyloxiran-2-yl)methyl]-5-(3-methylbut-2-en-1-yl)-1h-indole

C18H23NO (269.178)


   

2-(2-{[3-(2-aminoethyl)-6-bromo-1h-indol-2-yl]disulfanyl}-6-bromo-1h-indol-3-yl)ethanamine

2-(2-{[3-(2-aminoethyl)-6-bromo-1h-indol-2-yl]disulfanyl}-6-bromo-1h-indol-3-yl)ethanamine

C20H20Br2N4S2 (537.9496)


   

4-(3-methylbuta-1,3-dien-1-yl)-1h-indole-3-carbaldehyde

4-(3-methylbuta-1,3-dien-1-yl)-1h-indole-3-carbaldehyde

C14H13NO (211.0997)


   

(2s,4s)-1-(1h-indol-3-yl)-4-methyl-3-oxohexan-2-yl propanoate

(2s,4s)-1-(1h-indol-3-yl)-4-methyl-3-oxohexan-2-yl propanoate

C18H23NO3 (301.1678)


   

3-{[2-(5-hydroxy-1h-indol-3-yl)ethyl]-c-hydroxycarbonimidoyl}propanoic acid

3-{[2-(5-hydroxy-1h-indol-3-yl)ethyl]-c-hydroxycarbonimidoyl}propanoic acid

C14H16N2O4 (276.111)


   

n-{2-[6-bromo-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]ethyl}-n-methylformamide

n-{2-[6-bromo-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]ethyl}-n-methylformamide

C17H21BrN2O (348.0837)


   

3-amino-n-(2-{[2-(1h-indol-3-yl)ethyl]-c-hydroxycarbonimidoyl}ethyl)propanimidic acid

3-amino-n-(2-{[2-(1h-indol-3-yl)ethyl]-c-hydroxycarbonimidoyl}ethyl)propanimidic acid

C16H22N4O2 (302.1743)


   

n-[(1-methoxyindol-3-yl)methyl]methylsulfanylcarboximidic acid

n-[(1-methoxyindol-3-yl)methyl]methylsulfanylcarboximidic acid

C12H14N2O2S (250.0776)


   

(3s,6s)-3-(1h-indol-3-ylmethyl)-6-isopropyl-3,6-dihydropyrazine-2,5-diol

(3s,6s)-3-(1h-indol-3-ylmethyl)-6-isopropyl-3,6-dihydropyrazine-2,5-diol

C16H19N3O2 (285.1477)


   

3-[(3,3-dimethyloxiran-2-yl)methyl]-6-(3-methylbut-2-en-1-yl)-1h-indole

3-[(3,3-dimethyloxiran-2-yl)methyl]-6-(3-methylbut-2-en-1-yl)-1h-indole

C18H23NO (269.178)


   

n-[(1e)-2-(5-bromo-1h-indol-3-yl)ethenyl]-2-(7-hydroxy-1h-indol-3-yl)-2-oxoacetamide

n-[(1e)-2-(5-bromo-1h-indol-3-yl)ethenyl]-2-(7-hydroxy-1h-indol-3-yl)-2-oxoacetamide

C20H14BrN3O3 (423.0218)


   

n-[2-(1h-indol-3-yl)ethyl]-n,3-dimethylbutanamide

n-[2-(1h-indol-3-yl)ethyl]-n,3-dimethylbutanamide

C16H22N2O (258.1732)


   

n-{2-[6-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]ethylidene}hydroxylamine

n-{2-[6-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]ethylidene}hydroxylamine

C15H18N2O (242.1419)


   

(2r)-1-(5-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-1h-indol-3-yl)-3-methylbutane-2,3-diol

(2r)-1-(5-{[(2s)-3,3-dimethyloxiran-2-yl]methyl}-1h-indol-3-yl)-3-methylbutane-2,3-diol

C18H25NO3 (303.1834)


   

11,22-diazapentacyclo[13.7.0.0⁴,¹².0⁵,¹⁰.0¹⁶,²¹]docosa-1,3,5,7,9,12,14,16,18,20-decaene-2,13-dicarboxylic acid

11,22-diazapentacyclo[13.7.0.0⁴,¹².0⁵,¹⁰.0¹⁶,²¹]docosa-1,3,5,7,9,12,14,16,18,20-decaene-2,13-dicarboxylic acid

C22H14N2O4 (370.0954)


   

(e,2e)-3-(7-hydroxy-1h-indol-3-yl)-n-[(1e)-2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

(e,2e)-3-(7-hydroxy-1h-indol-3-yl)-n-[(1e)-2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

C21H17N3O2 (343.1321)


   

(2r)-2-(2-hydroxy-6-methylhept-5-en-2-yl)-2,3-dihydro-1h-indole-5-carboximidic acid

(2r)-2-(2-hydroxy-6-methylhept-5-en-2-yl)-2,3-dihydro-1h-indole-5-carboximidic acid

C17H24N2O2 (288.1838)


   

methyl 4-(1h-indol-3-yl)-2-methylbutanoate

methyl 4-(1h-indol-3-yl)-2-methylbutanoate

C14H17NO2 (231.1259)


   

2-(1h-indol-3-yl)-n-[(1e)-2-(1h-indol-3-yl)ethenyl]-2-oxoacetamide

2-(1h-indol-3-yl)-n-[(1e)-2-(1h-indol-3-yl)ethenyl]-2-oxoacetamide

C20H15N3O2 (329.1164)


   

(s)-[6-bromo-1-(methoxycarbonyl)indol-3-yl](6-bromo-1h-indol-3-yl)methoxymethanesulfonic acid

(s)-[6-bromo-1-(methoxycarbonyl)indol-3-yl](6-bromo-1h-indol-3-yl)methoxymethanesulfonic acid

C20H16Br2N2O6S (569.9096)


   

1-{3-[(2r)-2-hydroxy-3-methoxy-3-methylbutyl]-1h-indol-5-yl}-3-methylbut-2-en-1-one

1-{3-[(2r)-2-hydroxy-3-methoxy-3-methylbutyl]-1h-indol-5-yl}-3-methylbut-2-en-1-one

C19H25NO3 (315.1834)


   

5-[(1s,6r)-6-[(1e)-2-(1h-indol-5-yl)ethenyl]-3,6-dimethylcyclohex-2-en-1-yl]-1h-indole

5-[(1s,6r)-6-[(1e)-2-(1h-indol-5-yl)ethenyl]-3,6-dimethylcyclohex-2-en-1-yl]-1h-indole

C26H26N2 (366.2096)


   

2-(1-{[3-(2-hydroxyethyl)indol-1-yl]methyl}indol-3-yl)ethanol

2-(1-{[3-(2-hydroxyethyl)indol-1-yl]methyl}indol-3-yl)ethanol

C21H22N2O2 (334.1681)


   

(3r,6r)-6-(1h-indol-3-ylmethyl)-3-isopropyl-6-(methylsulfanyl)pyrazine-2,3,5-triol

(3r,6r)-6-(1h-indol-3-ylmethyl)-3-isopropyl-6-(methylsulfanyl)pyrazine-2,3,5-triol

C17H21N3O3S (347.1304)


   

methyl 5,6-dimethoxy-1'-methyl-1,1',2,4'a,5',5'a,7',8',10',10'a-decahydrospiro[indole-3,6'-pyrano[3,4-f]indolizine]-4'-carboxylate

methyl 5,6-dimethoxy-1'-methyl-1,1',2,4'a,5',5'a,7',8',10',10'a-decahydrospiro[indole-3,6'-pyrano[3,4-f]indolizine]-4'-carboxylate

C23H30N2O5 (414.2155)


   

1-(1h-indol-3-yl)-4-methyl-3-oxopentan-2-yl acetate

1-(1h-indol-3-yl)-4-methyl-3-oxopentan-2-yl acetate

C16H19NO3 (273.1365)


   

(2s,2's)-2,2',4,4'-tetramethyl-1h,1'h-[2,2'-biindole]-3,3'-dione

(2s,2's)-2,2',4,4'-tetramethyl-1h,1'h-[2,2'-biindole]-3,3'-dione

C20H20N2O2 (320.1525)


   

n-[2-(5-hydroxy-1h-indol-3-yl)ethyl]ethanimidic acid

n-[2-(5-hydroxy-1h-indol-3-yl)ethyl]ethanimidic acid

C12H14N2O2 (218.1055)


   

methyl[2-(1-methylindol-3-yl)ethyl]amine

methyl[2-(1-methylindol-3-yl)ethyl]amine

C12H16N2 (188.1313)


   

(2r)-4-(1h-indol-3-yl)-2-methylbutan-1-ol

(2r)-4-(1h-indol-3-yl)-2-methylbutan-1-ol

C13H17NO (203.131)


   

(2s)-3-methyl-1-[6-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]butane-2,3-diol

(2s)-3-methyl-1-[6-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]butane-2,3-diol

C18H25NO2 (287.1885)


   

2,3-dihydroxy-1-(1h-indol-3-yl)propan-1-one

2,3-dihydroxy-1-(1h-indol-3-yl)propan-1-one

C11H11NO3 (205.0739)


   

(2r)-1-[2-hydroxy-3-(propan-2-ylidene)indol-6-yl]-3-methylbutane-2,3-diol

(2r)-1-[2-hydroxy-3-(propan-2-ylidene)indol-6-yl]-3-methylbutane-2,3-diol

C16H21NO3 (275.1521)


   

{2-[6-bromo-1-(3-methylbut-2-en-1-yl)indol-3-yl]ethyl}(methyl)amine

{2-[6-bromo-1-(3-methylbut-2-en-1-yl)indol-3-yl]ethyl}(methyl)amine

C16H21BrN2 (320.0888)


   

(1r,15r)-15-methoxy-4-oxa-9-azatetracyclo[7.7.0.0¹,¹².0²,⁶]hexadeca-2(6),12-dien-3-one

(1r,15r)-15-methoxy-4-oxa-9-azatetracyclo[7.7.0.0¹,¹².0²,⁶]hexadeca-2(6),12-dien-3-one

C15H19NO3 (261.1365)


   

5-(1h-indol-3-yl)-3,4,6-trimethoxy-8-oxa-10-azatetracyclo[7.7.0.0²,⁷.0¹¹,¹⁶]hexadeca-2(7),3,5,11,13,15-hexaen-1-ol

5-(1h-indol-3-yl)-3,4,6-trimethoxy-8-oxa-10-azatetracyclo[7.7.0.0²,⁷.0¹¹,¹⁶]hexadeca-2(7),3,5,11,13,15-hexaen-1-ol

C25H22N2O5 (430.1529)


   

{1-[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]indol-3-yl}acetic acid

{1-[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]indol-3-yl}acetic acid

C16H19NO7 (337.1161)


   

3-acetyl indole

3-acetyl indole

C10H9NO (159.0684)


   

(1z)-2-hydroxy-1-(1h-indol-3-yl)-5-methylhex-1-en-3-one

(1z)-2-hydroxy-1-(1h-indol-3-yl)-5-methylhex-1-en-3-one

C15H17NO2 (243.1259)


   

[6-bromo-1-(methoxycarbonyl)indol-3-yl](6-bromo-1h-indol-3-yl)hydroxymethanesulfonic acid

[6-bromo-1-(methoxycarbonyl)indol-3-yl](6-bromo-1h-indol-3-yl)hydroxymethanesulfonic acid

C19H14Br2N2O6S (555.8939)


   

6'-acetyl-6-methoxy-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

6'-acetyl-6-methoxy-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

C21H24N2O4 (368.1736)


   

methyl 4-hydroxy-3-[(3e)-3-(methoxymethylidene)-2-oxoindol-1-yl]benzoate

methyl 4-hydroxy-3-[(3e)-3-(methoxymethylidene)-2-oxoindol-1-yl]benzoate

C18H15NO5 (325.095)


   

(z,2e)-3-(1h-indol-3-yl)-n-[(1z)-2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

(z,2e)-3-(1h-indol-3-yl)-n-[(1z)-2-(1h-indol-3-yl)ethenyl]prop-2-enimidic acid

C21H17N3O (327.1372)


   

methyl (2s)-3-(1h-indol-3-yl)-2-(methylamino)propanoate

methyl (2s)-3-(1h-indol-3-yl)-2-(methylamino)propanoate

C13H16N2O2 (232.1212)


   

2-hydroxy-1-(1h-indol-3-yl)-5-methylhexan-3-one

2-hydroxy-1-(1h-indol-3-yl)-5-methylhexan-3-one

C15H19NO2 (245.1416)


   

2,2-dimethyl-3-[5-(3-methylbut-2-enoyl)-1h-indol-3-yl]propanal

2,2-dimethyl-3-[5-(3-methylbut-2-enoyl)-1h-indol-3-yl]propanal

C18H21NO2 (283.1572)


   

(r)-[6-bromo-1-(methoxycarbonyl)indol-3-yl](6-bromo-1h-indol-3-yl)ethoxymethanesulfonic acid

(r)-[6-bromo-1-(methoxycarbonyl)indol-3-yl](6-bromo-1h-indol-3-yl)ethoxymethanesulfonic acid

C21H18Br2N2O6S (583.9252)


   

2-{1-[(1-hydroxypropylidene)amino]ethyl}-n-[2-(1h-indol-3-yl)ethyl]-1,3-thiazole-4-carboximidic acid

2-{1-[(1-hydroxypropylidene)amino]ethyl}-n-[2-(1h-indol-3-yl)ethyl]-1,3-thiazole-4-carboximidic acid

C19H22N4O2S (370.1463)


   

3'-[2-(dimethylamino)ethyl]-3,5'-dihydroxy-3-[2-(methylamino)ethyl]-1'h-[1,4'-biindol]-2-one

3'-[2-(dimethylamino)ethyl]-3,5'-dihydroxy-3-[2-(methylamino)ethyl]-1'h-[1,4'-biindol]-2-one

C23H28N4O3 (408.2161)


   

1h-indole-7-carbaldehyde

1h-indole-7-carbaldehyde

C9H7NO (145.0528)


   

4-(4-hydroxy-3-methylbut-2-en-1-yl)-2,5-bis(1h-indol-3-yl)-3,6-dimethoxyphenol

4-(4-hydroxy-3-methylbut-2-en-1-yl)-2,5-bis(1h-indol-3-yl)-3,6-dimethoxyphenol

C29H28N2O4 (468.2049)


   

methyl 3-[7-(3,4-dihydroxy-3-methylbut-1-en-1-yl)-1h-indol-3-yl]-2-(n-hydroxyimino)propanoate

methyl 3-[7-(3,4-dihydroxy-3-methylbut-1-en-1-yl)-1h-indol-3-yl]-2-(n-hydroxyimino)propanoate

C17H20N2O5 (332.1372)


   

7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-1h-indole-3-carbaldehyde

7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-1h-indole-3-carbaldehyde

C14H15NO2 (229.1103)


   

3-methyl-n-{2-[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]ethenyl}-2-(n-methylacetamido)butanimidic acid

3-methyl-n-{2-[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]ethenyl}-2-(n-methylacetamido)butanimidic acid

C23H31N3O2 (381.2416)


   

(2r,2's)-2,2',4,4'-tetramethyl-1h,1'h-[2,2'-biindole]-3,3'-dione

(2r,2's)-2,2',4,4'-tetramethyl-1h,1'h-[2,2'-biindole]-3,3'-dione

C20H20N2O2 (320.1525)


   

2-[(1r)-2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-6-[(1s)-2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol

2-[(1r)-2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-6-[(1s)-2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol

C30H30Br2N6O (648.0848)


   

5-{3-[2-(dimethylamino)ethyl]-1h-indol-2-yl}-1-(3,3-dimethyloxiran-2-yl)-3-methylpent-4-en-1-one

5-{3-[2-(dimethylamino)ethyl]-1h-indol-2-yl}-1-(3,3-dimethyloxiran-2-yl)-3-methylpent-4-en-1-one

C22H30N2O2 (354.2307)


   

4-(1h-indol-3-yl)-4-methoxy-5-sulfanylimidazol-2-ol

4-(1h-indol-3-yl)-4-methoxy-5-sulfanylimidazol-2-ol

C12H11N3O2S (261.0572)


   

3,6-bis(1h-indol-3-yl)-4-methoxy-5-(3-methylbut-2-en-1-yl)benzene-1,2-diol

3,6-bis(1h-indol-3-yl)-4-methoxy-5-(3-methylbut-2-en-1-yl)benzene-1,2-diol

C28H26N2O3 (438.1943)


   

(1h-indol-3-ylmethyl)[2-(5-methoxy-1h-indol-3-yl)ethyl]methylamine

(1h-indol-3-ylmethyl)[2-(5-methoxy-1h-indol-3-yl)ethyl]methylamine

C21H23N3O (333.1841)


   

1-{3-[(3,3-dimethyloxiran-2-yl)methyl]-1h-indol-5-yl}-3-methylbut-2-en-1-one

1-{3-[(3,3-dimethyloxiran-2-yl)methyl]-1h-indol-5-yl}-3-methylbut-2-en-1-one

C18H21NO2 (283.1572)


   

methyl 3,4-bis(5-hydroxy-1h-indol-3-yl)-1h-pyrrole-2-carboxylate

methyl 3,4-bis(5-hydroxy-1h-indol-3-yl)-1h-pyrrole-2-carboxylate

C22H17N3O4 (387.1219)


   

(1'r,2's,3s,7's,9'r)-6'-acetyl-6-methoxy-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

(1'r,2's,3s,7's,9'r)-6'-acetyl-6-methoxy-1-methyl-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-2-one

C21H24N2O4 (368.1736)


   

methyl (2r,4s,5s,6r)-6-(3-ethyl-4-methoxyindol-1-yl)-4,5-dihydroxyoxane-2-carboxylate

methyl (2r,4s,5s,6r)-6-(3-ethyl-4-methoxyindol-1-yl)-4,5-dihydroxyoxane-2-carboxylate

C18H23NO6 (349.1525)


   

3-[4-(1h-indol-3-yl)-2,3,5,6-tetramethoxyphenyl]-5-(3-methylbut-2-en-1-yl)-1h-indole

3-[4-(1h-indol-3-yl)-2,3,5,6-tetramethoxyphenyl]-5-(3-methylbut-2-en-1-yl)-1h-indole

C31H32N2O4 (496.2362)


   

2-methoxy-3-(4-methoxyphenyl)-1,2-dihydroindole-3-carboxylic acid

2-methoxy-3-(4-methoxyphenyl)-1,2-dihydroindole-3-carboxylic acid

C17H17NO4 (299.1158)


   

(10s,13s)-10-[(2s)-butan-2-yl]-13-(hydroxymethyl)-5-(2-methylbut-3-en-2-yl)-3,9,12-triazatricyclo[6.6.1.0⁴,¹⁵]pentadeca-1,4,6,8(15),11-pentaen-11-ol

(10s,13s)-10-[(2s)-butan-2-yl]-13-(hydroxymethyl)-5-(2-methylbut-3-en-2-yl)-3,9,12-triazatricyclo[6.6.1.0⁴,¹⁵]pentadeca-1,4,6,8(15),11-pentaen-11-ol

C22H31N3O2 (369.2416)


   

(2r)-2,3-dihydroxy-1-(1h-indol-3-yl)propan-1-one

(2r)-2,3-dihydroxy-1-(1h-indol-3-yl)propan-1-one

C11H11NO3 (205.0739)


   

(6z)-3-(hydroxymethyl)-6-(1h-indol-3-ylmethylidene)-3-methoxypyrazine-2,5-diol

(6z)-3-(hydroxymethyl)-6-(1h-indol-3-ylmethylidene)-3-methoxypyrazine-2,5-diol

C15H15N3O4 (301.1063)


   

methyl 1-(2-methylbut-3-en-2-yl)indole-3-carboxylate

methyl 1-(2-methylbut-3-en-2-yl)indole-3-carboxylate

C15H17NO2 (243.1259)


   

methyl (1's,2s,4'as,5'as,10'as)-5,6-dimethoxy-1'-methyl-3-oxo-1',4'a,5',5'a,7',8',10',10'a-octahydro-1h-spiro[indole-2,6'-pyrano[3,4-f]indolizine]-4'-carboxylate

methyl (1's,2s,4'as,5'as,10'as)-5,6-dimethoxy-1'-methyl-3-oxo-1',4'a,5',5'a,7',8',10',10'a-octahydro-1h-spiro[indole-2,6'-pyrano[3,4-f]indolizine]-4'-carboxylate

C23H28N2O6 (428.1947)


   

2,4-bis[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol

2,4-bis[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol

C30H30Br2N6O (648.0848)


   

n-acetyl-n-[2-(5-hydroxy-1h-indol-3-yl)ethyl]-2-methyl-1h-pyrrole-3-carboxamide

n-acetyl-n-[2-(5-hydroxy-1h-indol-3-yl)ethyl]-2-methyl-1h-pyrrole-3-carboxamide

C18H19N3O3 (325.1426)


   

(3e,6s)-3-ethylidene-5-hydroxy-6-(1h-indol-3-ylmethyl)-1-methyl-6h-pyrazin-2-one

(3e,6s)-3-ethylidene-5-hydroxy-6-(1h-indol-3-ylmethyl)-1-methyl-6h-pyrazin-2-one

C16H17N3O2 (283.1321)