NCBI Taxonomy: 32436

Cianidanol

C15H14O6 (290.079)

Catechin, also known as cyanidanol or catechuic acid, belongs to the class of organic compounds known as catechins. Catechins are compounds containing a catechin moiety, which is a 3,4-dihydro-2-chromene-3,5.7-tiol. Catechin also belongs to the group of compounds known as flavan-3-ols (or simply flavanols), part of the chemical family of flavonoids. Catechin is one of the 4 catechin known diastereoisomers. Two of the isomers are in trans configuration and are called catechin and the other two are in cis configuration and are called epicatechin. The most common catechin isomer is the (+)-catechin. The other stereoisomer is (-)-catechin or ent-catechin. The most common epicatechin isomer is (-)-epicatechin. Catechin is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Catechin is a bitter tasting compound and is associated with the bitterness in tea. Catechin is a plant secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Catechin is an antioxidant flavonoid, occurring especially in woody plants as both Catechin and (-)-Catechin (cis) forms. Outside of the human body, Catechin is found, on average, in the highest concentration in foods, such as blackcurrants (Ribes nigrum), evergreen blackberries (Rubus laciniatus), and blackberries (Rubus) and in a lower concentration in dills (Anethum graveolens), hot chocolates, and medlars (Mespilus germanica). Catechin has also been detected, but not quantified in, several different foods, such as rice (Oryza sativa), apple ciders, peanuts (Arachis hypogaea), fruit juices, and red teas. This could make catechin a potential biomarker for the consumption of these foods. Based on a literature review a significant number of articles have been published on Catechin. (+)-catechin is the (+)-enantiomer of catechin and a polyphenolic antioxidant plant metabolite. It has a role as an antioxidant and a plant metabolite. It is an enantiomer of a (-)-catechin. An antioxidant flavonoid, occurring especially in woody plants as both (+)-catechin and (-)-epicatechin (cis) forms. Cianidanol is a natural product found in Visnea mocanera, Salacia chinensis, and other organisms with data available. Catechin is a metabolite found in or produced by Saccharomyces cerevisiae. An antioxidant flavonoid, occurring especially in woody plants as both (+)-catechin and (-)-epicatechin (cis) forms. See also: Gallocatechin (related); Crofelemer (monomer of); Bilberry (part of) ... View More ... Present in red wine. Widespread in plants; found in a variety of foodstuffs especies apricots, broad beans, cherries, chocolate, grapes, nectarines, red wine, rhubarb, strawberries and tea The (+)-enantiomer of catechin and a polyphenolic antioxidant plant metabolite. Catechin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=154-23-4 (retrieved 2024-07-12) (CAS RN: 154-23-4). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). (±)-Catechin (rel-Cianidanol) is the racemate of Catechin. (±)-Catechin has two steric forms of (+)-Catechin and its enantiomer (-)-Catechin. (+)-Catechin inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM. Anticancer, anti-obesity, antidiabetic, anticardiovascular, anti-infectious, hepatoprotective, and neuroprotective effects[1]. (±)-Catechin (rel-Cianidanol) is the racemate of Catechin. (±)-Catechin has two steric forms of (+)-Catechin and its enantiomer (-)-Catechin. (+)-Catechin inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM. Anticancer, anti-obesity, antidiabetic, anticardiovascular, anti-infectious, hepatoprotective, and neuroprotective effects[1]. Catechin ((+)-Catechin) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM. Catechin ((+)-Catechin) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM.

Fucoxanthin

C42H58O6 (658.4233)

Fucoxanthin is an epoxycarotenol that is found in brown seaweed and which exhibits anti-cancer, anti-diabetic, anti-oxidative and neuroprotective properties. It has a role as an algal metabolite, a CFTR potentiator, a food antioxidant, a neuroprotective agent, a hypoglycemic agent, an apoptosis inhibitor, a hepatoprotective agent, a marine metabolite and a plant metabolite. It is an epoxycarotenol, an acetate ester, a secondary alcohol, a tertiary alcohol and a member of allenes. Fucoxanthin is a natural product found in Aequipecten opercularis, Ascidia zara, and other organisms with data available. Fucoxanthin is a carotenoid, with formula C40H60O6. It is found as an accessory pigment in the chloroplasts of brown algae and most other heterokonts, giving them a brown or olive-green color. Fucoxanthin absorbs light primarily in the blue-green to yellow-green part of the visible spectrum, peaking at around 510-525 nm by various estimates and absorbing significantly in the range of 450 to 540 nm. -- Wikipedia [HMDB] Fucoxanthin is a carotenoid, with formula C40H60O6. It is found as an accessory pigment in the chloroplasts of brown algae and most other heterokonts, giving them a brown or olive-green color. Fucoxanthin absorbs light primarily in the blue-green to yellow-green part of the visible spectrum, peaking at around 510-525 nm by various estimates and absorbing significantly in the range of 450 to 540 nm. -- Wikipedia. D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids Fucoxanthin (all-trans-Fucoxanthin) is a marine carotenoid and shows anti-obesity, anti-diabetic, anti-oxidant, anti-inflammatory and anticancer activities[1][2][3][4][5][6][7][8][9]. Fucoxanthin is a marine carotenoid and shows anti-obesity, anti-diabetic, anti-oxidant, anti-inflammatory and anticancer activities. Fucoxanthin (all-trans-Fucoxanthin) is a marine carotenoid and shows anti-obesity, anti-diabetic, anti-oxidant, anti-inflammatory and anticancer activities[1][2][3][4][5][6][7][8][9]. Fucoxanthin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=3351-86-8 (retrieved 2024-11-06) (CAS RN: 3351-86-8). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Thymidine

C10H14N2O5 (242.0903)

Deoxythymidine, also known as 2-deoxy-5-methyluridine or 5-methyl-2-deoxyuridine, is a member of the class of compounds known as pyrimidine 2-deoxyribonucleosides. Pyrimidine 2-deoxyribonucleosides are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 2. Deoxythymidine is soluble (in water) and a very weakly acidic compound (based on its pKa). Deoxythymidine can be synthesized from thymine. Deoxythymidine is also a parent compound for other transformation products, including but not limited to, tritiated thymidine, alpha-tritiated thymidine, and 5,6-dihydrothymidine. Deoxythymidine can be found in a number of food items such as butternut squash, mammee apple, catjang pea, and climbing bean, which makes deoxythymidine a potential biomarker for the consumption of these food products. Deoxythymidine can be found primarily in most biofluids, including blood, amniotic fluid, cerebrospinal fluid (CSF), and urine, as well as throughout most human tissues. Deoxythymidine exists in all living species, ranging from bacteria to humans. In humans, deoxythymidine is involved in the pyrimidine metabolism. Deoxythymidine is also involved in few metabolic disorders, which include beta ureidopropionase deficiency, dihydropyrimidinase deficiency, MNGIE (mitochondrial neurogastrointestinal encephalopathy), and UMP synthase deficiency (orotic aciduria). Moreover, deoxythymidine is found to be associated with canavan disease and degenerative disc disease. Thymidine (deoxythymidine; other names deoxyribosylthymine, thymine deoxyriboside) is a pyrimidine deoxynucleoside. Deoxythymidine is the DNA nucleoside T, which pairs with deoxyadenosine (A) in double-stranded DNA. In cell biology it is used to synchronize the cells in G1/early S phase . Thymidine, also known as deoxythymidine or deoxyribosylthymine or thymine deoxyriboside, is a pyrimidine deoxynucleoside. It consists of the nucleobase thymine attached to deoxyribose through a beta N- glycosidic bond. Thymidine also belongs to the class of organic compounds known as pyrimidine 2-deoxyribonucleosides. Pyrimidine 2-deoxyribonucleosides are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 2. Deoxythymidine (or thymidine) is the DNA nucleoside T, which pairs with deoxyadenosine (A) in double-stranded DNA. Therefore, thymidine is essential to all life. Indeed, thymidine exists in all living species, ranging from bacteria to plants to humans. Within humans, thymidine participates in a number of enzymatic reactions. In particular, thymidine can be biosynthesized from 5-thymidylic acid through its interaction with the enzyme cytosolic purine 5-nucleotidase. In addition, thymidine can be converted into 5-thymidylic acid; which is catalyzed by the enzyme thymidine kinase. Deoxythymidine can be phosphorylated with one, two or three phosphoric acid groups, creating dTMP (deoxythymidine monophosphate), dTDP, or dTTP (for the di- and tri- phosphates, respectively). dTMP can be incorporated into DNA via DNA polymerases. In cell biology, thymidine can be used to synchronize the cells in S phase. Derivatives of thymidine are used in a number of drugs, including Azidothymidine (AZT), which is used in the treatment of HIV infection. AZT inhibits the process of reverse transcription in the human immunodeficiency virus. Thymidine is a pyrimidine 2-deoxyribonucleoside having thymine as the nucleobase. It has a role as a metabolite, a human metabolite, an Escherichia coli metabolite and a mouse metabolite. It is functionally related to a thymine. It is an enantiomer of a telbivudine. Thymidine is a pyrimidine deoxynucleoside. Thymidine is the DNA nucleoside T, which pairs with deoxyadenosine (A) in double-stranded DNA. In cell biology it is used to synchronize the cells in S phase. Thymidine is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Thymidine is a natural product found in Fritillaria thunbergii, Saussurea medusa, and other organisms with data available. Thymidine is a pyrimidine nucleoside that is composed of the pyrimidine base thymine attached to the sugar deoxyribose. As a constituent of DNA, thymidine pairs with adenine in the DNA double helix. (NCI04) Thymidine is a metabolite found in or produced by Saccharomyces cerevisiae. A nucleoside in which THYMINE is linked to DEOXYRIBOSE. A pyrimidine 2-deoxyribonucleoside having thymine as the nucleobase. KEIO_ID T014; [MS2] KO009272 KEIO_ID T014 Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication[1][2][3]. Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication[1][2][3].

Inosine

C10H12N4O5 (268.0808)

Inosine, also known as hypoxanthosine or inotin, belongs to the class of organic compounds known as purine nucleosides. Purine nucleosides are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety. Inosine is formed when hypoxanthine is attached to a ribose ring a beta-N9-glycosidic bond. Inosine is an intermediate in the degradation of purines and purine nucleosides to uric acid. Inosine is also an intermediate in the purine salvage pathway. Inosine occurs in the anticodon of certain transfer RNA molecules and is essential for proper translation of the genetic code in wobble base pairs. Inosine exists in all living species, ranging from bacteria to plants to humans. Inosine participates in a number of enzymatic reactions. In particular, inosine can be biosynthesized from inosinic acid through its interaction with the enzyme known as cytosolic purine 5-nucleotidase. In addition, inosine can be converted into hypoxanthine and ribose 1-phosphate through its interaction with the enzyme known as purine nucleoside phosphorylase. Altered levels of inosine have also been associated with purine nucleoside phosphorylase deficiency and xanthinuria type I, both of which are inborn errors of metabolism. Animal studies have suggested that inosine has neuroprotective properties. It has been proposed as a potential treatment for spinal cord injury (PMID: 16317421) and for administration after stroke, as inosine appears to induce axonal rewiring (PMID: 12084941). After ingestion, inosine is metabolized into uric acid, which has been found to be a natural antioxidant and peroxynitrite scavenger. As such, inosine may have potential benefits to patients with multiple sclerosis and Parkinson’s disease (PMID: 19425822). Inosine can also be produced by gut bacteria and appears to have a number of beneficial effects. Inosine, has been shown to activate peroxisome proliferator-activated receptor (PPAR)-gamma signaling in human colon epithelial cells. Furthermore, exogenous treatment of inosine has been found to protect against DSS-induced colitis in rodents by improving adenosine 2A receptor (A2AR)/PPAR-gamma-dependent mucosal barrier functions (PMID: 33820558). Microbiome-derived inosine has also been shown to modulate the response to checkpoint inhibitor immunotherapy in cancer models. In particular, decreased gut barrier function induced by immunotherapy increases systemic translocation of bacterially derived inosine and activates antitumor T cells. The effect of inosine is dependent on T cell expression of the adenosine A2A receptor and requires co-stimulation. Inosine appears to have other roles in non-mammalian system. For instance, it has been found to be an important feed stimulant by itself or in combination with certain amino acids in some species of farmed fish. For example, inosine and inosine-5-monophosphate have been reported as specific feeding stimulants for turbot fry, (Scophthalmus maximus) and Japanese amberjack. Inosine is a purine nucleoside in which hypoxanthine is attached to ribofuranose via a beta-N(9)-glycosidic bond. It has a role as a human metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite. It is a purines D-ribonucleoside and a member of inosines. It is functionally related to a hypoxanthine and a ribofuranose. A purine nucleoside that has hypoxanthine linked by the N9 nitrogen to the C1 carbon of ribose. It is an intermediate in the degradation of purines and purine nucleosides to uric acid and in pathways of purine salvage. It also occurs in the anticodon of certain transfer RNA molecules. (Dorland, 28th ed) Inosine is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Inosine is a natural product found in Fritillaria thunbergii, Cichorium endivia, and other organisms with data available. Inosine is a metabolite found in or produced by Saccharomyces cerevisiae. A purine nucleoside that has hypoxanthine linked by the N9 nitrogen to the C1 carbon of ribose. It is an intermediate in the degradation of purines and purine nucleosides to uric acid and in pathways of purine salvage. It also occurs in the anticodon of certain transfer RNA molecules. (Dorland, 28th ed) G - Genito urinary system and sex hormones > G01 - Gynecological antiinfectives and antiseptics > G01A - Antiinfectives and antiseptics, excl. combinations with corticosteroids D - Dermatologicals > D06 - Antibiotics and chemotherapeutics for dermatological use > D06B - Chemotherapeutics for topical use > D06BB - Antivirals A purine nucleoside in which hypoxanthine is attached to ribofuranose via a beta-N(9)-glycosidic bond. COVID info from COVID-19 Disease Map, clinicaltrial, clinicaltrials, clinical trial, clinical trials S - Sensory organs > S01 - Ophthalmologicals Present in meat extracts and sugar beet Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS [Spectral] Inosine (exact mass = 268.08077) and L-Methionine (exact mass = 149.05105) and Adenosine (exact mass = 267.09675) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. [Spectral] Inosine (exact mass = 268.08077) and L-Tyrosine (exact mass = 181.07389) and Guanosine (exact mass = 283.09167) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. [Spectral] Inosine (exact mass = 268.08077) and S-Adenosyl-L-homocysteine (exact mass = 384.12159) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. [Spectral] Inosine (exact mass = 268.08077) and Guanosine (exact mass = 283.09167) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. Acquisition and generation of the data is financially supported in part by CREST/JST. CONFIDENCE standard compound; INTERNAL_ID 110 KEIO_ID I003 Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors[1][2][3]. Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors[1][2][3]. Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors[1][2][3]. Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors[1][2][3].

Uridine

C9H12N2O6 (244.0695)

Uridine, also known as beta-uridine or 1-beta-D-ribofuranosylpyrimidine-2,4(1H,3H)-dione, is a member of the class of compounds known as pyrimidine nucleosides. Pyrimidine nucleosides are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety. More specifically, uridine is a nucleoside consisting of uracil and D-ribose and a component of RNA. Uridine is soluble (in water) and a very weakly acidic compound (based on its pKa). Uridine can be synthesized from uracil. It is one of the five standard nucleosides which make up nucleic acids, the others being adenosine, thymidine, cytidine and guanosine. The five nucleosides are commonly abbreviated to their one-letter codes U, A, T, C and G respectively. Uridine is also a parent compound for other transformation products, including but not limited to, nikkomycin Z, 3-(enolpyruvyl)uridine 5-monophosphate, and 5-aminomethyl-2-thiouridine. Uridine can be found in most biofluids, including urine, breast milk, cerebrospinal fluid (CSF), and blood. Within the cell, uridine is primarily located in the mitochondria, in the nucleus and the lysosome. It can also be found in the extracellular space. As an essential nucleoside, uridine exists in all living species, ranging from bacteria to humans. In humans, uridine is involved in several metabolic disorders, some of which include dhydropyrimidinase deficiency, MNGIE (mitochondrial neurogastrointestinal encephalopathy), and beta-ureidopropionase deficiency. Moreover, uridine is found to be associated with Lesch-Nyhan syndrome, which is an inborn error of metabolism. Uridine is a nucleoside consisting of uracil and D-ribose and a component of RNA. Uridine plays a role in the glycolysis pathway of galactose. In humans there is no catabolic process to metabolize galactose. Therefore, galactose is converted to glucose and metabolized via the normal glucose metabolism pathways. More specifically, consumed galactose is converted into galactose 1-phosphate (Gal-1-P). This molecule is a substrate for the enzyme galactose-1-phosphate uridyl transferase which transfers a UDP molecule to the galactose molecule. The end result is UDP-galactose and glucose-1-phosphate. This process is continued to allow the proper glycolysis of galactose. Uridine is found in many foods (anything containing RNA) but is destroyed in the liver and gastrointestinal tract, and so no food, when consumed, has ever been reliably shown to elevate blood uridine levels. On the other hand, consumption of RNA-rich foods may lead to high levels of purines (adenine and guanosine) in blood. High levels of purines are known to increase uric acid production and may aggravate or lead to conditions such as gout. Uridine is a ribonucleoside composed of a molecule of uracil attached to a ribofuranose moiety via a beta-N(1)-glycosidic bond. It has a role as a human metabolite, a fundamental metabolite and a drug metabolite. It is functionally related to a uracil. Uridine is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Uridine is a Pyrimidine Analog. The chemical classification of uridine is Pyrimidines, and Analogs/Derivatives. Uridine is a natural product found in Ulva australis, Synechocystis, and other organisms with data available. Uridine is a nucleoside consisting of uracil and D-ribose and a component of RNA. Uridine has been studied as a rescue agent to reduce the toxicities associated with 5-fluorouracil (5-FU), thereby allowing the administration of higher doses of 5-FU in chemotherapy regimens. (NCI04) Uridine is a metabolite found in or produced by Saccharomyces cerevisiae. A ribonucleoside in which RIBOSE is linked to URACIL. Uridine is a molecule (known as a nucleoside) that is formed when uracil is attached to a ribose ring (also known as a ribofuranose) via a b-N1-glycosidic bond. ; Uridine is a molecule (known as a nucleoside) that is formed when uracil is attached to a ribose ring (also known as a ribofuranose) via a ?-N1-glycosidic bond. Uridine is found in many foods, some of which are celery leaves, canola, common hazelnut, and hickory nut. A ribonucleoside composed of a molecule of uracil attached to a ribofuranose moiety via a beta-N(1)-glycosidic bond. [Spectral] Uridine (exact mass = 244.06954) and Adenosine (exact mass = 267.09675) and Glutathione (exact mass = 307.08381) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. [Spectral] Uridine (exact mass = 244.06954) and Glutathione (exact mass = 307.08381) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. Uridine. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=58-96-8 (retrieved 2024-06-29) (CAS RN: 58-96-8). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond. Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond. Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond.

Salicin

C13H18O7 (286.1052)

Salicin, also known as salicoside or delta-salicin, is an aryl beta-D-glucoside that is salicyl alcohol in which the phenolic hydrogen has been replaced by a beta-D-glucosyl residue. It has a role as a prodrug, an antipyretic, a non-narcotic analgesic, a non-steroidal anti-inflammatory drug, an EC 1.14.99.1 (prostaglandin-endoperoxide synthase) inhibitor and a metabolite. It is an aryl beta-D-glucoside, an aromatic primary alcohol and a member of benzyl alcohols. It derives from a salicyl alcohol. Salicin belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. Salicin exists in all living organisms, ranging from bacteria to humans. Salicin is a bitter tasting compound. Salicin is an aryl beta-D-glucoside that is salicyl alcohol in which the phenolic hydrogen has been replaced by a beta-D-glucosyl residue. It has a role as a prodrug, an antipyretic, a non-narcotic analgesic, a non-steroidal anti-inflammatory drug, an EC 1.14.99.1 (prostaglandin-endoperoxide synthase) inhibitor and a metabolite. It is an aryl beta-D-glucoside, an aromatic primary alcohol and a member of benzyl alcohols. It is functionally related to a salicyl alcohol. Salicin is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Salicin is a natural product found in Salix candida, Populus tremula, and other organisms with data available. Salicin is an alcoholic β-glycoside that contains D-glucose. Salicin is an anti-inflammatory agent that is produced from willow bark. Salicin is closely related in chemical make-up to aspirin and has a very similar action in the human body. When consumed by humans, Salicin is metabolized into salicylic acid. [HMDB] An aryl beta-D-glucoside that is salicyl alcohol in which the phenolic hydrogen has been replaced by a beta-D-glucosyl residue. D018501 - Antirheumatic Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D016861 - Cyclooxygenase Inhibitors D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent D002491 - Central Nervous System Agents > D000700 - Analgesics D000893 - Anti-Inflammatory Agents D004791 - Enzyme Inhibitors Salicin is a natural COX inhibitor. Salicin is a natural COX inhibitor.

Salidroside

C14H20O7 (300.1209)

Salidroside is a glycoside. Salidroside is a natural product found in Plantago australis, Plantago coronopus, and other organisms with data available. See also: Sedum roseum root (part of); Rhodiola crenulata root (part of). Salidroside is a prolyl endopeptidase inhibitor. Salidroside alleviates cachexia symptoms in mouse models of cancer cachexia via activating mTOR signalling. Salidroside protects dopaminergic neurons by enhancing PINK1/Parkin-mediated mitophagy. Salidroside is a prolyl endopeptidase inhibitor. Salidroside alleviates cachexia symptoms in mouse models of cancer cachexia via activating mTOR signalling. Salidroside protects dopaminergic neurons by enhancing PINK1/Parkin-mediated mitophagy.

beta-Carotene

C40H56 (536.4382)

Beta-carotene is a cyclic carotene obtained by dimerisation of all-trans-retinol. A strongly-coloured red-orange pigment abundant in plants and fruit and the most active and important provitamin A carotenoid. It has a role as a biological pigment, a provitamin A, a plant metabolite, a human metabolite, a mouse metabolite, a cofactor, a ferroptosis inhibitor and an antioxidant. It is a cyclic carotene and a carotenoid beta-end derivative. Beta-carotene, with the molecular formula C40H56, belongs to the group of carotenoids consisting of isoprene units. The presence of long chains of conjugated double bonds donates beta-carotene with specific colors. It is the most abundant form of carotenoid and it is a precursor of the vitamin A. Beta-carotene is composed of two retinyl groups. It is an antioxidant that can be found in yellow, orange and green leafy vegetables and fruits. Under the FDA, beta-carotene is considered as a generally recognized as safe substance (GRAS). Beta-Carotene is a natural product found in Epicoccum nigrum, Lonicera japonica, and other organisms with data available. Beta-Carotene is a naturally-occurring retinol (vitamin A) precursor obtained from certain fruits and vegetables with potential antineoplastic and chemopreventive activities. As an anti-oxidant, beta carotene inhibits free-radical damage to DNA. This agent also induces cell differentiation and apoptosis of some tumor cell types, particularly in early stages of tumorigenesis, and enhances immune system activity by stimulating the release of natural killer cells, lymphocytes, and monocytes. (NCI04) beta-Carotene is a metabolite found in or produced by Saccharomyces cerevisiae. A carotenoid that is a precursor of VITAMIN A. Beta carotene is administered to reduce the severity of photosensitivity reactions in patients with erythropoietic protoporphyria (PORPHYRIA, ERYTHROPOIETIC). See also: Lycopene (part of); Broccoli (part of); Lycium barbarum fruit (part of). Beta-Carotene belongs to the class of organic compounds known as carotenes. These are a type of polyunsaturated hydrocarbon molecules containing eight consecutive isoprene units. Carotenes are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Beta-carotene is therefore considered to be an isoprenoid lipid molecule. Beta-carotene is a strongly coloured red-orange pigment abundant in fungi, plants, and fruits. It is synthesized biochemically from eight isoprene units and therefore has 40 carbons. Among the carotenes, beta-carotene is distinguished by having beta-rings at both ends of the molecule. Beta-Carotene is biosynthesized from geranylgeranyl pyrophosphate. It is the most common form of carotene in plants. In nature, Beta-carotene is a precursor (inactive form) to vitamin A. Vitamin A is produed via the action of beta-carotene 15,15-monooxygenase on carotenes. In mammals, carotenoid absorption is restricted to the duodenum of the small intestine and dependent on a class B scavenger receptor (SR-B1) membrane protein, which is also responsible for the absorption of vitamin E. One molecule of beta-carotene can be cleaved by the intestinal enzyme Beta-Beta-carotene 15,15-monooxygenase into two molecules of vitamin A. Beta-Carotene contributes to the orange color of many different fruits and vegetables. Vietnamese gac and crude palm oil are particularly rich sources, as are yellow and orange fruits, such as cantaloupe, mangoes, pumpkin, and papayas, and orange root vegetables such as carrots and sweet potatoes. Excess beta-carotene is predominantly stored in the fat tissues of the body. The most common side effect of excessive beta-carotene consumption is carotenodermia, a physically harmless condition that presents as a conspicuous orange skin tint arising from deposition of the carotenoid in the outermost layer of the epidermis. Yellow food colour, dietary supplement, nutrient, Vitamin A precursor. Nutriceutical with antioxidation props. beta-Carotene is found in many foods, some of which are summer savory, gram bean, sunburst squash (pattypan squash), and other bread product. A cyclic carotene obtained by dimerisation of all-trans-retinol. A strongly-coloured red-orange pigment abundant in plants and fruit and the most active and important provitamin A carotenoid. D - Dermatologicals > D02 - Emollients and protectives > D02B - Protectives against uv-radiation > D02BB - Protectives against uv-radiation for systemic use A - Alimentary tract and metabolism > A11 - Vitamins > A11C - Vitamin a and d, incl. combinations of the two > A11CA - Vitamin a, plain D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids D018977 - Micronutrients > D014815 - Vitamins > D000072664 - Provitamins

Zeaxanthin

C40H56O2 (568.428)

Zeaxanthin is a carotenoid xanthophyll and is one of the most common carotenoid found in nature. It is the pigment that gives corn, saffron, and many other plants their characteristic color. Zeaxanthin breaks down to form picrocrocin and safranal, which are responsible for the taste and aroma of saffron Carotenoids are among the most common pigments in nature and are natural lipid soluble antioxidants. Zeaxanthin is one of the two carotenoids (the other is lutein) that accumulate in the eye lens and macular region of the retina with concentrations in the macula greater than those found in plasma and other tissues. Lutein and zeaxanthin have identical chemical formulas and are isomers, but they are not stereoisomers. The main difference between them is in the location of a double bond in one of the end rings. This difference gives lutein three chiral centers whereas zeaxanthin has two. A relationship between macular pigment optical density, a marker of lutein and zeaxanthin concentration in the macula, and lens optical density, an antecedent of cataractous changes, has been suggested. The xanthophylls may act to protect the eye from ultraviolet phototoxicity via quenching reactive oxygen species and/or other mechanisms. Some observational studies have shown that generous intakes of lutein and zeaxanthin, particularly from certain xanthophyll-rich foods like spinach, broccoli and eggs, are associated with a significant reduction in the risk for cataract (up to 20\\%) and for age-related macular degeneration (up to 40\\%). While the pathophysiology of cataract and age-related macular degeneration is complex and contains both environmental and genetic components, research studies suggest dietary factors including antioxidant vitamins and xanthophylls may contribute to a reduction in the risk of these degenerative eye diseases. Further research is necessary to confirm these observations. (PMID: 11023002). Zeaxanthin has been found to be a microbial metabolite, it can be produced by Algibacter, Aquibacter, Escherichia, Flavobacterium, Formosa, Gramella, Hyunsoonleella, Kordia, Mesoflavibacter, Muricauda, Nubsella, Paracoccus, Siansivirga, Sphingomonas, Zeaxanthinibacter and yeast (https://reader.elsevier.com/reader/sd/pii/S0924224417302571?token=DE6BC6CC7DCDEA6150497AA3E375097A00F8E0C12AE03A8E420D85D1AC8855E62103143B5AE0B57E9C5828671F226801). It is a marker for the activity of Bacillus subtilis and/or Pseudomonas aeruginosa in the intestine. Higher levels are associated with higher levels of Bacillus or Pseudomonas. (PMID: 17555270; PMID: 12147474) Zeaxanthin is a carotenol. It has a role as a bacterial metabolite, a cofactor and an antioxidant. It derives from a hydride of a beta-carotene. Zeaxanthin is a most common carotenoid alcohols found in nature that is involved in the xanthophyll cycle. As a coexistent isomer of lutein, zeaxanthin is synthesized in plants and some micro-organisms. It gives the distinct yellow color to many vegetables and other plants including paprika, corn, saffron and wolfberries. Zeaxanthin is one of the two primary xanthophyll carotenoids contained within the retina of the eye and plays a predominant component in the central macula. It is available as a dietary supplement for eye health benefits and potential prevention of age-related macular degeneration. Zeaxanthin is also added as a food dye. Zeaxanthin is a natural product found in Bangia fuscopurpurea, Erythrobacter longus, and other organisms with data available. Carotenoids found in fruits and vegetables. Zeaxanthin accumulates in the MACULA LUTEA. See also: Saffron (part of); Corn (part of); Lycium barbarum fruit (part of). D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids

Xanthurenic acid

C10H7NO4 (205.0375)

Xanthurenic acid, also known as xanthurenate or 8-hydroxykynurenic acid, is a member of the class of compounds known as quinoline carboxylic acids. Quinoline carboxylic acids are quinolines in which the quinoline ring system is substituted by a carboxyl group at one or more positions. Xanthurenic acid is slightly soluble (in water). Xanthurenic acid can be found primarily in blood, feces, and urine, as well as in human epidermis tissue. Within the cell, xanthurenic acid is primarily located in the membrane. Xanthurenic acid exists in all eukaryotes, ranging from yeast to humans. In humans, xanthurenic acid is involved in the tryptophan metabolism. Moreover, xanthurenic acid is found to be associated with citrullinemia type I, which is an inborn error of metabolism. Xanthurenic acid is a metabolite from tryptophan catabolism. It is a substrate of the enzyme methyltransferases (EC 2.1.1.-) in pathway tryptophan metabolism (KEGG). Xanthurenic acid is a metabolite from tryptophan catabolism. It is a substrate of the enzyme methyltransferases [EC 2.1.1.-] in pathway tryptophan metabolism (KEGG). [HMDB] D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents [Raw Data] CBA13_Xanthurenic-aci_neg_40eV_1-5_01_737.txt [Raw Data] CBA13_Xanthurenic-aci_neg_50eV_1-5_01_738.txt [Raw Data] CBA13_Xanthurenic-aci_neg_10eV_1-5_01_734.txt [Raw Data] CBA13_Xanthurenic-aci_neg_30eV_1-5_01_736.txt [Raw Data] CBA13_Xanthurenic-aci_pos_40eV_1-5_01_684.txt [Raw Data] CBA13_Xanthurenic-aci_pos_50eV_1-5_01_685.txt [Raw Data] CBA13_Xanthurenic-aci_pos_30eV_1-5_01_683.txt [Raw Data] CBA13_Xanthurenic-aci_pos_10eV_1-5_01_681.txt [Raw Data] CBA13_Xanthurenic-aci_pos_20eV_1-5_01_682.txt [Raw Data] CBA13_Xanthurenic-aci_neg_20eV_1-5_01_735.txt Xanthurenic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=59-00-7 (retrieved 2024-07-01) (CAS RN: 59-00-7). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Xanthurenic acid is a putative endogenous Group II metabotropic glutamate receptor agonist, on sensory transmission in the thalamus. Xanthurenic acid is a putative endogenous Group II metabotropic glutamate receptor agonist, on sensory transmission in the thalamus.

Dimethylglycine

C4H9NO2 (103.0633)

Dimethylglycine (DMG) is an amino acid derivative found in the cells of all plants and animals and can be obtained in the diet in small amounts from grains and meat. The human body produces DMG when metabolizing choline into glycine. Dimethylglycine that is not metabolized in the liver is transported by the circulatory system to body tissue. Dimethylglycine was popular with Russian athletes and cosmonauts owing to its reputed ability to increase endurance and reduce fatigue. DMG is also a byproduct of homocysteine metabolism. Homocysteine and betaine are converted to methionine and N,N-dimethylglycine by betaine-homocysteine methyltransferase. DMG in the urine is a biomarker for the consumption of legumes. It is also a microbial metabolite (PMID: 25901889). Dimethylglycine (DMG) is an amino acid derivative found in the cells of all plants and animals and can be obtained in the diet in small amounts from grains and meat. The human body produces DMG when metabolizing choline into Glycine. Dimethylglycine that is not metabolized in the liver is transported by the circulatory system to body tissue. Dimethylglycine was popular with Russian athletes and cosmonauts owing to its reputed ability to increase endurance and reduce fatigue. DMG is also a byproduct of homocysteine metabolism. Homocysteine and betaine are converted to methionine and N, N-dimethylglycine by betaine-homocysteine methyltransferase. [HMDB]. Dimethylglycine in the urine is a biomarker for the consumption of legumes. N,N-Dimethylglycine. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=1118-68-9 (retrieved 2024-07-16) (CAS RN: 1118-68-9). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). N-Methylsarcosine is an amino acid building block for protein, found in a small amount in the body.

Picein

C14H18O7 (298.1052)

Picein is a glycoside. Picein is a natural product found in Salix candida, Halocarpus biformis, and other organisms with data available. Picein, isolated from Picrorhiza kurroa, is a naturally occurring antioxidant[1]. Picein, isolated from Picrorhiza kurroa, is a naturally occurring antioxidant[1].

Cyanidin

[C15H11O6]+ (287.0556)

Cyanidin, also known as cyanidin chloride (CAS: 528-58-5), belongs to the class of organic compounds known as 7-hydroxyflavonoids. These are flavonoids that bear one hydroxyl group at the C-7 position of the flavonoid skeleton. Thus, cyanidin is considered to be a flavonoid lipid molecule. Cyanidin is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Cyanidin (and its glycosides) is the most commonly occurring of the anthocyanins, a widespread group of pigments responsible for the red-blue colour of many fruits and vegetables (PMID: 14711454). BioTransformer predicts that cyanidin is a product of cyanidin 3-​glucoside metabolism via a glycoside-hydrolysis reaction occurring in human gut microbiota and catalyzed by the EC.3.2.1.X enzyme (PMID: 30612223). Widely distributed anthocyanidin, found especies in Vaccinium subspecies (blueberries, bilberries, whortleberries), cherries, raspberries, red onions, red wine and black tea. Cyanidin is found in many foods, some of which are papaya, hyacinth bean, sweet basil, and abalone. Cyanidin cation is an anthocyanidin cation that is flavylium substituted at positions 3, 3', 4', 5 and 7 by hydroxy groups. It has a role as a metabolite, a neuroprotective agent and an antioxidant. It is a conjugate acid of a cyanidin(1-).

Okadaic acid

C44H68O13 (804.466)

Okadaic acid is found in mollusks. Okadaic acid is found in the marine sponges Halichondria okadai and Halichondria melanodocia and shellfish. It is a metabolite of Prorocentrum lima. It is a diarrhetic shellfish toxin. Okadaic acid is a toxin that accumulates in bivalves and causes diarrhetic shellfish poisoning. The molecular formula of okadaic acid, which is a derivative of a C38 fatty acid, is C44H68O13. The IUPAC name of okadaic acid is (2R)-2-hydroxy-3-{(2S,5R,6R,8S)-5-hydroxy-[(1R,2E)-3-((2R,5R,6S,8R,8aS)-8-hydroxy-6-{(1S,3S)-1-hydroxy-3-[(3R,6S)-3-methyl-1,7-dioxaspiro[5.5]undec-2-yl]butyl}-7-methyleneoctahydro-3H,3H-spiro[furan-2,2-pyrano[3,2-b]pyran]-5-yl)-1-methylprop-2-en-1-yl]-10-methyl-1,7-dioxaspiro[5.5]undec-10-en-2-yl}-2-methylpropanoic acid. Okadaic acid was named from the marine sponge Halichondria okadai, from which okadaic acid was isolated for the first time. It has also been isolated from another marine sponge, H. malanodocia, as a cytotoxin. The real producer of okadaic acid is a marine dinoflagellate D009676 - Noxae > D011042 - Poisons > D008387 - Marine Toxins D009676 - Noxae > D002273 - Carcinogens D049990 - Membrane Transport Modulators D004791 - Enzyme Inhibitors D007476 - Ionophores

Geranylbenzoquinone

C16H20O2 (244.1463)

Grandidentatin

C21H28O9 (424.1733)

geranylhydroquinone

C16H22O2 (246.162)

Eudistomin G

C15H12BrN3 (313.0215)

eudistomin C

C14H16BrN3O2S (369.0147)

An organic heterotetracyclic compound that has formula C14H16BrN3O2S. It is a natural product isolated from the Caribbean tunicate Eudistoma olivaceum and exhibits potent anti-tumor and antiviral activities.

Eudistomin H

C15H12BrN3 (313.0215)

Eudistomin N

C11H7BrN2 (245.9793)

2-Polyprenyl-6-methoxy-1,4-benzoquinone

C17H22O3 (274.1569)

This compound belongs to the family of Prenylquinones. These are quinones whose structure is charaterized by the quinone ring substitued by an prenyl side-chain.

Methyl Arachidonate

C21H34O2 (318.2559)

Methyl Arachidonate, also known as Arachidonate methyl ester or (5Z,8Z,11Z,14Z)-Icosatetraenoate methyl ester, is classified as a member of the Fatty acid methyl esters. Fatty acid methyl esters are compounds containing a fatty acid that is esterified with a methyl group. They have the general structure RC(=O)OR, where R=fatty aliphatic tail or organyl group and R=methyl group. Methyl Arachidonate is considered to be practically insoluble (in water) and basic. Methyl Arachidonate can be synthesized from arachidonic acid. Methyl Arachidonate can be synthesized into 12(R)-HPETE methyl ester and 12(S)-HPETE methyl ester

2-Piperidinone

C5H9NO (99.0684)

2-Piperidinone is a derivative of piperidine which is an organic compound. Piperidine is a colorless fuming liquid with an odor described as ammoniacal, pepper-like, the name comes from the genus name Piper, which is the Latin word for pepper. Piperidine is a widely used building block and chemical reagent in the synthesis of organic compounds, including pharmaceuticals.The piperidine structural motif is present in numerous natural alkaloids. These include piperine, which gives black pepper the hot taste. This gave the compound its name. [HMDB] 2-Piperidinone is a derivative of piperidine which is an organic compound. Piperidine is a colorless fuming liquid with an odor described as ammoniacal, pepper-like, the name comes from the genus name Piper, which is the Latin word for pepper. Piperidine is a widely used building block and chemical reagent in the synthesis of organic compounds, including pharmaceuticals.The piperidine structural motif is present in numerous natural alkaloids. These include piperine, which gives black pepper the hot taste. This gave the compound its name. 2-Piperidone is an endogenous metabolite.

Alloxanthin

C40H52O2 (564.3967)

Alloxanthin is found in channel catfish. Alloxanthin is a constituent of many shellfish including the giant scallop (Pecten maximus) and edible mussel (Mytilus edulis). Constituent of many shellfish including the giant scallop (Pecten maximus) and edible mussel (Mytilus edulis). Alloxanthin is found in channel catfish and mollusks.

Mytiloxanthin

C40H54O4 (598.4022)

Mytiloxanthin is found in blue mussel. Mytiloxanthin is isolated from the mussels Mytilus edulis. Isolated from the mussels Mytilus edulis. Mytiloxanthin is found in blue mussel and mollusks.

C-glycosyltryptophan

C17H22N2O7 (366.1427)

Tryptophan 2-C-mannoside, also known as 2-alpha-D-mannopyranosyl-L-tryptophan or C-mannosyltryptophan, belongs to the class of organic compounds known as indolyl carboxylic acids and derivatives. Indolyl carboxylic acids and derivatives are compounds containing a carboxylic acid chain (of at least 2 carbon atoms) linked to an indole ring. It is an L-tryptophan derivative and a C-glycosyl compound in which the hydrogen at position 2 on the indole portion has been replaced by an alpha-mannosyl residue. Tryptophan 2-C-mannoside is a very strong basic compound (based on its pKa). Tryptophan 2-C-mannoside has been identified in blood and urine and is a marker of kidney function (PMID: 29234020).

1-[(2R,3S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione

C9H12N2O6 (244.0695)

1-beta-D-Arabinofuranosyluracil (Uracil 1-β-D-arabinofuranoside) isolated from the Caribbean sponge Tectitethya crypta, is a methoxyadenosine derivative. 1-beta-D-Arabinofuranosyluracil has demonstrated a diverse bioactivity profile including anti-inflammatory activity, analgesic and vasodilation properties[1]. 1-beta-D-Arabinofuranosyluracil reduces a proliferation of mouse lymphoma cells[2]. 1-beta-D-Arabinofuranosyluracil (Uracil 1-β-D-arabinofuranoside) isolated from the Caribbean sponge Tectitethya crypta, is a methoxyadenosine derivative. 1-beta-D-Arabinofuranosyluracil has demonstrated a diverse bioactivity profile including anti-inflammatory activity, analgesic and vasodilation properties[1]. 1-beta-D-Arabinofuranosyluracil reduces a proliferation of mouse lymphoma cells[2]. 1-beta-D-Arabinofuranosyluracil (Uracil 1-β-D-arabinofuranoside) isolated from the Caribbean sponge Tectitethya crypta, is a methoxyadenosine derivative. 1-beta-D-Arabinofuranosyluracil has demonstrated a diverse bioactivity profile including anti-inflammatory activity, analgesic and vasodilation properties[1]. 1-beta-D-Arabinofuranosyluracil reduces a proliferation of mouse lymphoma cells[2].

Ara-HX

C10H12N4O5 (268.0808)

L-Thymidine

C10H14N2O5 (242.0903)

Isolated from seedlings of Phaseolus vulgaris (kidney bean)

Salidroside

C14H20O7 (300.1209)

Salidroside is a member of the class of compounds known as O-glycosyl compounds. O-glycosyl compounds are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. Salidroside is soluble (in water) and a very weakly acidic compound (based on its pKa). Salidroside can be found in olive, which makes salidroside a potential biomarker for the consumption of this food product. Salidroside (Rhodioloside) is a glucoside of tyrosol found in the plant Rhodiola rosea. It is thought to be one of the compounds responsible for the antidepressant and anxiolytic actions of this plant, along with rosavin. Salidroside may be more active than rosavin, even though many commercially marketed Rhodiola rosea extracts are standardised for rosavin content rather than salidroside . Salidroside is a prolyl endopeptidase inhibitor. Salidroside alleviates cachexia symptoms in mouse models of cancer cachexia via activating mTOR signalling. Salidroside protects dopaminergic neurons by enhancing PINK1/Parkin-mediated mitophagy. Salidroside is a prolyl endopeptidase inhibitor. Salidroside alleviates cachexia symptoms in mouse models of cancer cachexia via activating mTOR signalling. Salidroside protects dopaminergic neurons by enhancing PINK1/Parkin-mediated mitophagy.

2-(beta-D-Mannopyranosyl)-L-tryptophan

C17H22N2O7 (366.1427)

Sulfolane

C4H8O2S (120.0245)

Xestoaminol C

C14H31NO (229.2406)

Inosine

C10H12N4O5 (268.0808)

G - Genito urinary system and sex hormones > G01 - Gynecological antiinfectives and antiseptics > G01A - Antiinfectives and antiseptics, excl. combinations with corticosteroids D - Dermatologicals > D06 - Antibiotics and chemotherapeutics for dermatological use > D06B - Chemotherapeutics for topical use > D06BB - Antivirals COVID info from COVID-19 Disease Map, clinicaltrial, clinicaltrials, clinical trial, clinical trials S - Sensory organs > S01 - Ophthalmologicals Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors[1][2][3]. Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors[1][2][3]. Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors[1][2][3]. Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors[1][2][3].

Uridine

C9H12N2O6 (244.0695)

C26170 - Protective Agent > C2459 - Chemoprotective Agent > C2080 - Cytoprotective Agent COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond. Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond. Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond.

Halocynthiaxanthin

C40H54O4 (598.4022)

D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids CONE_VOLTAGE is 20 V.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 19HP8024 to the Mass Spectrometry Society of Japan. This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 19HP8024 to the Mass Spectrometry Society of Japan.

Pibocin B

C17H21BrN2O (348.0837)

Vimalin

C16H22O7 (326.1365)

3,6-Dibromo-1h-indole

C8H5Br2N (272.8789)

Dimethylglycine

C4H9NO2 (103.0633)

MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; FFDGPVCHZBVARC_STSL_0036_Dimethylglycine_0500fmol_180430_S2_LC02_MS02_57; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. N-Methylsarcosine is an amino acid building block for protein, found in a small amount in the body.

Methyl arachidonate

C21H34O2 (318.2559)

A fatty acid methyl ester resulting from the formal condensation of the carboxy group of arachidonic acid with methanol.

cyanidin

C15H11O6+ (287.0556)

2-Polyprenyl-6-methoxy-1,4-benzoquinone

C17H22O3 (274.1569)

This compound belongs to the family of Prenylquinones. These are quinones whose structure is charaterized by the quinone ring substitued by an prenyl side-chain.

ascidiathiazone A

C12H8N2O6S (308.0103)

An organic heterotricyclic compound, that is 3,4-dihydro-2H-[1,4]thiazino[2,3-g]quinoline-5,10 dione S,S-dioxide substituted at position 7 by a carboxyl group. It is an anti-inflmmatory alkaloid obtained from Aplidium.

lissoclibadin 1

C39H57N3O6S7 (887.2292)

An organosulfur heterocyclic compound isolated from the ascidian Lissoclinum badium. It has been shown to exhibit cytotoxicity against human cancer cell lines.

Salicortin

C20H24O10 (424.1369)

SULFOLANE

C4H8O2S (120.0245)

D002491 - Central Nervous System Agents > D000697 - Central Nervous System Stimulants > D003292 - Convulsants D020011 - Protective Agents > D011837 - Radiation-Protective Agents

Lamellarin D

C28H21NO8 (499.1267)

3-(4-hydroxyphenyl)-2-methoxyprop-2-enamide

C10H11NO3 (193.0739)

lissoclibadin 2

C26H38N2O4S5 (602.1435)

An organosulfur heterocyclic compound isolated from the ascidian Lissoclinum badium. It has been shown to exhibit cytotoxicity against human cancer cell lines.

Ascididemin

C18H9N3O (283.0746)

okadaic acid

C44H68O13 (804.466)

D009676 - Noxae > D011042 - Poisons > D008387 - Marine Toxins D009676 - Noxae > D002273 - Carcinogens D049990 - Membrane Transport Modulators D004791 - Enzyme Inhibitors D007476 - Ionophores A polycyclic ether that is produced by several species of dinoflagellates, and is known to accumulate in both marine sponges and shellfish. A polyketide, polyether derivative of a C38 fatty acid, it is one of the primary causes of diarrhetic shellfish poisoning (DSP). It is a potent inhibitor of specific protein phosphatases and is known to have a variety of negative effects on cells.

2-Chlorophyscion

C16H11ClO5 (318.0295)

4-(2-Aminoethyl)-2-iodophenol

C8H10INO (262.9807)

VARACIN

C10H13NO2S5 (338.955)

Didemnidine A

C17H24N4O2 (316.1899)

A natural product found in Didemnum species.

Didemnidine B

C17H23BrN4O2 (394.1004)

A natural product found in Didemnum species.

methyl icosa-5,8,11,14,17-pentaenoate

C21H32O2 (316.2402)

Salireposide

C20H22O9 (406.1264)

1,3,7-trimethylisoguanine

C8H11N5O (193.0964)

A natural product found in Paramuricea clavata and Pseudodistoma cereum.

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

C10H11BrN2 (238.0106)

lissoclibadin 3

C26H38N2O4S4 (570.1714)

A member of the class of thianthrenes that is thianthrene substituted by methoxy groups at positions 3, 4, 8 and 9, methylsulfanyl groups at positions 2 and 7 and 2-(dimethylamino)ethyl groups at positions 1 and 6. Isolated from the ascidian Lissoclinum badium, it exhibits cytotoxicity against human cancer cells.

3,5-dibromo-2-(3,5-dibromo-2-methoxyphenoxy)phenol

C13H8Br4O3 (527.7207)

Norharmane

C11H8N2 (168.0687)

D009676 - Noxae > D009498 - Neurotoxins D009676 - Noxae > D009153 - Mutagens IPB_RECORD: 2981; CONFIDENCE confident structure Norharmane (Norharman), a β-carboline alkaloid, is a potent and reversible monoamine oxidase inhibitor, with IC50 values of 6.5 and 4.7 μM for MAO-A and MAO-B, respectively. Norharmane causes antidepressant responses. Norharmane is also a prospective anti-cancer photosensitizer. Norharmane alters polar auxin transport (PAT) by inhibiting PIN2, PIN3 and PIN7 transport proteins, thus causing a significant inhibitory effect on the growth of Arabidopsis thaliana seedlings[1][2][3][4][5][6]. Norharmane (Norharman), a β-carboline alkaloid, is a potent and reversible monoamine oxidase inhibitor, with IC50 values of 6.5 and 4.7 μM for MAO-A and MAO-B, respectively. Norharmane causes antidepressant responses. Norharmane is also a prospective anti-cancer photosensitizer. Norharmane alters polar auxin transport (PAT) by inhibiting PIN2, PIN3 and PIN7 transport proteins, thus causing a significant inhibitory effect on the growth of Arabidopsis thaliana seedlings[1][2][3][4][5][6].

Thymidine

C10H14N2O5 (242.0903)

relative retention time with respect to 9-anthracene Carboxylic Acid is 0.220 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.211 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.213 Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication[1][2][3]. Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication[1][2][3].

Salicin

C13H18O7 (286.1052)

D018501 - Antirheumatic Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D016861 - Cyclooxygenase Inhibitors D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent D002491 - Central Nervous System Agents > D000700 - Analgesics D000893 - Anti-Inflammatory Agents D004791 - Enzyme Inhibitors relative retention time with respect to 9-anthracene Carboxylic Acid is 0.253 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.247 Salicin is a natural COX inhibitor. Salicin is a natural COX inhibitor.

Inosine

C10H12N4O5 (268.0808)

G - Genito urinary system and sex hormones > G01 - Gynecological antiinfectives and antiseptics > G01A - Antiinfectives and antiseptics, excl. combinations with corticosteroids D - Dermatologicals > D06 - Antibiotics and chemotherapeutics for dermatological use > D06B - Chemotherapeutics for topical use > D06BB - Antivirals Formula(Parent): C10H12N4O5; Bottle Name:Inosine; PRIME Parent Name:Inosine; PRIME in-house No.:0256, Purines COVID info from COVID-19 Disease Map, clinicaltrial, clinicaltrials, clinical trial, clinical trials S - Sensory organs > S01 - Ophthalmologicals Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; UGQMRVRMYYASKQ_STSL_0164_Inosine_2000fmol_180430_S2_LC02_MS02_125; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. relative retention time with respect to 9-anthracene Carboxylic Acid is 0.054 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.053 Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors[1][2][3]. Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors[1][2][3]. Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors[1][2][3]. Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors[1][2][3].

Uridine

C9H12N2O6 (244.0695)

C26170 - Protective Agent > C2459 - Chemoprotective Agent > C2080 - Cytoprotective Agent COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; DRTQHJPVMGBUCF_STSL_0179_Uridine_8000fmol_180506_S2_LC02_MS02_83; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. relative retention time with respect to 9-anthracene Carboxylic Acid is 0.088 Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond. Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond. Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond.

XANTHURENIC ACID

C10H7NO4 (205.0375)

β-Carotene

C40H56 (536.4382)

The novel carbohydrate-derived b-carboline, 1-pentahydroxypentyl-1,2,3,4-tetrahydro-b-carboline-3-carboxylic acid, was identified in fruit- and vegetable-derived products such as juices, jams, and tomato sauces. This compound occurred as two diastereoisomers, a cis isomer (the major compound) and a trans isomer, ranging from undetectable amounts to 6.5 ug/g. Grape, tomato, pineapple, and tropical juices exhibited the highest amount of this alkaloid (up to 3.8 mg/L), whereas apple, banana, and peach juices showed very low or nondetectable levels. This tetrahydro-b-carboline was also found in jams (up to 0.45 ug/g), and a relative high amount was present in tomato concentrate (6.5 ug/g) and sauce (up to 1.8 ug/g). This b-carboline occurred in fruit-derived products as a glycoconjugate from a chemical condensation of d-glucose and l-tryptophan that is highly favored at low pH values and high temperature. Production, processing treatments, and storage of fruit juices and jams can then release this b-carboline. Fruit-derived products and other foods containing this compound might be an exogenous dietary source of this glucose-derived tetrahydro-b-carboline.(PMID: 12137498) [HMDB] Window width to select the precursor ion was 3 Da.; CONE_VOLTAGE is 20 V.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 19HP8024 to the Mass Spectrometry Society of Japan. D - Dermatologicals > D02 - Emollients and protectives > D02B - Protectives against uv-radiation > D02BB - Protectives against uv-radiation for systemic use A - Alimentary tract and metabolism > A11 - Vitamins > A11C - Vitamin a and d, incl. combinations of the two > A11CA - Vitamin a, plain D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids D018977 - Micronutrients > D014815 - Vitamins > D000072664 - Provitamins Window width to select the precursor ion was 3 Da.; CONE_VOLTAGE is 10 V.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 19HP8024 to the Mass Spectrometry Society of Japan.

Xanthurenic acid

C10H7NO4 (205.0375)

A quinolinemonocarboxylic acid that is quinoline-2-carboxylic acid substituted by hydroxy groups at C-4 and C-8. D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents D009676 - Noxae > D000963 - Antimetabolites Xanthurenic acid is a putative endogenous Group II metabotropic glutamate receptor agonist, on sensory transmission in the thalamus. Xanthurenic acid is a putative endogenous Group II metabotropic glutamate receptor agonist, on sensory transmission in the thalamus.

Zeaxanthin

C40H56O2 (568.428)

Meso-zeaxanthin (3R,3´S-zeaxanthin) is a xanthophyll carotenoid, as it contains oxygen and hydrocarbons, and is one of the three stereoisomers of zeaxanthin. Of the three stereoisomers, meso-zeaxanthin is the second most abundant in nature after 3R,3´R-zeaxanthin, which is produced by plants and algae. To date, meso-zeaxanthin has been identified in specific tissues of marine organisms and in the macula lutea, also known as the "yellow spot", of the human retina . Meso-zeaxanthin is a member of the class of compounds known as xanthophylls. Xanthophylls are carotenoids containing an oxygenated carotene backbone. Carotenes are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Carotenes belonging form a subgroup of the carotenoids family. Xanthophylls arise by oxygenation of the carotene backbone. Meso-zeaxanthin is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Meso-zeaxanthin can be found in channel catfish, crustaceans, and fishes, which makes meso-zeaxanthin a potential biomarker for the consumption of these food products. D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids Window width for selecting the precursor ion was 3 Da.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 16HP2005 to the Mass Spectrometry Society of Japan.

2-Deoxyuridine

C9H12N2O5 (228.0746)

Fucoxanthin

C42H58O6 (658.4233)

Fucoxanthin is an epoxycarotenol that is found in brown seaweed and which exhibits anti-cancer, anti-diabetic, anti-oxidative and neuroprotective properties. It has a role as an algal metabolite, a CFTR potentiator, a food antioxidant, a neuroprotective agent, a hypoglycemic agent, an apoptosis inhibitor, a hepatoprotective agent, a marine metabolite and a plant metabolite. It is an epoxycarotenol, an acetate ester, a secondary alcohol, a tertiary alcohol and a member of allenes. Fucoxanthin is a natural product found in Aequipecten opercularis, Ascidia zara, and other organisms with data available. An epoxycarotenol that is found in brown seaweed and which exhibits anti-cancer, anti-diabetic, anti-oxidative and neuroprotective properties. D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids Window width to select the precursor ion was 3 Da.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 19HP8024 to the Mass Spectrometry Society of Japan. Window width for selecting the precursor ion was 3 Da.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 16HP2005 to the Mass Spectrometry Society of Japan. Fucoxanthin (all-trans-Fucoxanthin) is a marine carotenoid and shows anti-obesity, anti-diabetic, anti-oxidant, anti-inflammatory and anticancer activities[1][2][3][4][5][6][7][8][9]. Fucoxanthin is a marine carotenoid and shows anti-obesity, anti-diabetic, anti-oxidant, anti-inflammatory and anticancer activities. Fucoxanthin (all-trans-Fucoxanthin) is a marine carotenoid and shows anti-obesity, anti-diabetic, anti-oxidant, anti-inflammatory and anticancer activities[1][2][3][4][5][6][7][8][9]. Fucoxanthin is a marine carotenoid and shows anti-obesity, anti-diabetic, anti-oxidant, anti-inflammatory and anticancer activities.

2-deoxyuridine

C9H12N2O5 (228.0746)

A pyrimidine 2-deoxyribonucleoside having uracil as the nucleobase. D009676 - Noxae > D000963 - Antimetabolites COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine.

cyanidin

[C15H11O6]+ (287.0556)

cyanidin

C15H11O6 (287.0556)

Alloxanthin

C40H52O2 (564.3967)

D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids Window width for selecting the precursor ion was 3 Da.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 16HP2005 to the Mass Spectrometry Society of Japan.

cyanidin

C15H10O6 (286.0477)

Mytiloxanthin

C40H54O4 (598.4022)

Amarouciaxanthin B/ Sidnyaxanthin

C40H52O4 (596.3865)

Xestoaminol C

C14H31NO (229.2406)

Obscuraminol A

C18H31NO (277.2406)

Clavepictine B

C20H35NO (305.2719)

5-hydroxypipecolic acid

C6H11NO3 (145.0739)

A piperidinemonocarboxylic acid that is pipecolic acid with a hydroxy substituent at position 5.

2-aminoethanesulfonic acid

C2H7NO3S (125.0147)

9H-Purine-2,6-diol

C5H4N4O2 (152.0334)

piperidine-2-carboxylic acid

C6H11NO2 (129.079)

Tremuloidin

C20H22O8 (390.1315)

An aryl beta-D-glucoside that is salicin in which the hydrogen of the 2-hydroxy group is replaced by a benzoyl group. It is found in the leaves and bark of willows and poplars.

Sachaliside

C15H20O7 (312.1209)

2-Phenylethylamine

C8H11N (121.0891)

A phenylethylamine having the phenyl substituent at the 2-position.

(1s,4e,8z)-1,5,9-trimethyl-17-oxatricyclo[9.5.3.0¹⁴,¹⁸]nonadeca-4,8,11,13,15,18-hexaen-12-ol

C21H26O2 (310.1933)

(3r,5s,7ar,11as)-3-(chloromethyl)-5-hexyl-1h,2h,3h,5h,6h,7h,7ah,11h-pyrrolo[2,1-j]quinolin-10-one

C19H30ClNO (323.2016)

4-(5-bromo-1h-indol-3-yl)-1,3-diazinan-2-imine

C12H13BrN4 (292.0324)

2-methyl-5-(octa-1,3-dien-1-yl)-decahydroquinolin-3-ol

C18H31NO (277.2406)

2-methyl-2-(4-methylpenta-1,3-dien-1-yl)chromen-6-ol

C16H18O2 (242.1307)

(2s)-n-[(2e,4e)-5-[(2s,3s,4e,6e,8s,11z,13e,16s,17e,19e,21r,22e)-8,16-dimethoxy-3,12,18,21,23-pentamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,17,19,22-heptaen-2-yl]-2-methylhexa-2,4-dien-1-yl]-2-[(hydroxymethylidene)amino]-3-(sulfooxy)propanimidic acid

C41H60N2O10S (772.3968)

(2s,3r,4as,5s,8ar)-5-[(5r)-5-hydroxyoctyl]-2-methyl-decahydroquinolin-3-yl (2e,4e)-octa-2,4-dienoate

C26H45NO3 (419.3399)

(2s)-5-carbamimidamido-2-[2-(6-hydroxy-1h-indol-3-yl)-2-oxoacetamido]pentanoic acid

C16H19N5O5 (361.1386)

4,4a,6-trihydroxy-2-[2-(2-hydroxyethyl)-2-methyl-3-(6-methylheptan-2-yl)cyclopentyl]-8a-methyl-5,6,7,8-tetrahydro-4h-naphthalen-1-one

C27H46O5 (450.3345)

n-{2-[(11r)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),2,4,6,8,10(14)-hexaen-11-yl]ethyl}guanidine

C16H14N4O4 (326.1015)

(16s,20s,23s)-17-hydroxy-13-methoxy-20,23-dimethyl-1,11,18-triazahexacyclo[10.8.2.1¹⁶,²⁰.0²,⁷.0⁸,²².0¹⁵,²¹]tricosa-2,4,6,8(22),9,11,13,15(21),17-nonaen-19-one

C23H19N3O3 (385.1426)

5-(5-hydroxyoctyl)-2-methyl-decahydroquinolin-3-yl oct-2-enoate

C26H47NO3 (421.3556)

3-{[(4z)-2-(5-bromo-1h-indole-3-carbonyl)-5-hydroxyimidazol-4-ylidene]methyl}-1h-indol-6-ol

C21H13BrN4O3 (448.0171)

3-{[(4z)-5-hydroxy-2-(1h-indole-3-carbonyl)imidazol-4-ylidene]methyl}-1h-indol-6-ol

C21H14N4O3 (370.1066)

(2s,3z,3ar)-2-hydroxy-6a-(hydroxymethyl)-3-(prop-2-en-1-ylidene)-2h,3ah-cyclopenta[b]furan-4-one

C11H12O4 (208.0736)

4-hydroxy-1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one

C9H12N2O5 (228.0746)

2-{1-[1-(2-hydroxypropanoyl)pyrrolidin-2-yl]-n-methylformamido}-4-methyl-n-{1,8,11,18-tetrahydroxy-3-[(4-hydroxyphenyl)methyl]-15-isopropyl-6,17-dimethyl-20-(2-methylpropyl)-4,13,16,21-tetraoxo-10-(sec-butyl)-3h,6h,7h,10h,11h,12h,15h,17h,20h,23h,24h,25h,25ah-pyrrolo[2,1-f]1,15-dioxa-4,7,10,20-tetraazacyclotricosan-7-yl}pentanimidic acid

C55H85N7O15 (1083.6103)

(2r,4r,5s)-5-amino-2-[(6e,8e)-trideca-6,8-dien-1-yl]piperidin-4-ol

C18H34N2O (294.2671)

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

C16H11BrN4O2 (370.0065)

n-{5-[11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl}-3-methylbut-2-enimidic acid

C33H48N2O7 (584.3461)

(1r,3ar,7s,8r,9ar,9bs,11ar)-7,8-dihydroxy-1-[(2r)-6-hydroxy-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-5-one

C27H42O4 (430.3083)

(2s,3r)-3-hydroxy-4-({1-hydroxy-2-[(2s,3s,6r)-3-methyl-6-[(3e)-2-oxopent-3-en-1-yl]oxan-2-yl]ethylidene}amino)-n-{3-[(2r,3s,6s,8r)-8-[(3s,4e,6s)-6-hydroxy-3,5-dimethylhept-4-en-1-yl]-3-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]propyl}-2-methylbutanimidic acid

C40H68N2O8 (704.4975)

7,8-dihydroxy-1-(6-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-5-one

C27H42O4 (430.3083)

(2s)-5-carbamimidamido-2-[(4-hydroxyphenyl)formamido]pentanoic acid

C13H18N4O4 (294.1328)

(2s,3s,4as,5s,8ar)-2-methyl-5-[(1z,3e)-octa-1,3-dien-1-yl]-decahydroquinolin-3-yl 2-hydroxyacetate

C20H33NO3 (335.246)

(5e)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1z)-3-hydroxyprop-1-en-1-yl]furan-2-one

C11H12O4 (208.0736)

3-hydroxy-4-[(1-hydroxy-2-{3-methyl-6-[(3z)-2-oxopent-3-en-1-yl]oxan-2-yl}ethylidene)amino]-n-(3-{8-[(4e)-6-hydroxy-3,5-dimethylhept-4-en-1-yl]-3-methyl-1,7-dioxaspiro[5.5]undecan-2-yl}propyl)-2-methylbutanimidic acid

C40H68N2O8 (704.4975)

(2s,3r)-3-hydroxy-4-({1-hydroxy-2-[(2s,3s,6r)-3-methyl-6-[(3e)-2-oxopent-3-en-1-yl]oxan-2-yl]ethylidene}amino)-n-{4-[(2r,6s,8s)-8-[(3s,4e,6s)-6-hydroxy-3,5-dimethylhept-4-en-1-yl]-1,7-dioxaspiro[5.5]undecan-2-yl]butyl}-2-methylbutanimidic acid

C40H68N2O8 (704.4975)

1-(1h-pyrrol-2-yl)-9h-pyrido[3,4-b]indol-6-yl acetate

C17H13N3O2 (291.1008)

12-(3,4-dimethoxyphenyl)-7-hydroxy-8,16,17-trimethoxy-4-oxa-1-azapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-2(11),5(10),6,8,12,14,16,18-octaen-3-one

C30H27NO8 (529.1737)

(2s)-2-{[(2s)-2-[bis(3-methylbut-2-en-1-yl)amino]-1-hydroxy-3-phenylpropylidene]amino}-3-methyl-n-[(1s)-2-methyl-1-(1,3-thiazol-2-yl)propyl]butanimidic acid

C31H46N4O2S (538.3341)

(3z,7e,11e,13r)-13-methoxy-3,7,11-trimethylbicyclo[12.2.2]octadeca-1(16),3,7,11,14,17-hexaene-15,17-diol

C22H30O3 (342.2195)

2-[(2z)-3,7-dimethylocta-2,6-dien-1-yl]-6-methoxycyclohexa-2,5-diene-1,4-dione

C17H22O3 (274.1569)

n-{15-bromo-14-hydroxy-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-yl}methoxycarboximidic acid

C16H18BrN3O4S (427.0201)

4-{2-[(1as,4ar,5s,6r,8as)-1a,5,6-trimethyl-octahydrocyclopropa[e]naphthalen-5-yl]ethyl}-5-hydroxy-5h-furan-2-one

C20H30O3 (318.2195)

(5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one

C11H12O4 (208.0736)

(4s,11s,18s)-4,11,18-triisopropyl-7-methyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),7,9,12(23),14,16,19(22)-nonaene-2,9,16-triol

C25H32N6O4S2 (544.1926)

2,12,15-triazapentacyclo[11.7.1.0³,⁸.0⁹,²¹.0¹⁴,¹⁹]henicosa-1,3(8),4,6,9(21),10,12,14(19)-octaene-18,20-dione

C18H11N3O2 (301.0851)

8-benzyl-10,17,24-trihydroxy-15-isopropyl-26-methyl-22-(sec-butyl)-27-oxa-13,20-dithia-6,9,16,23,28,29,30-heptaazapentacyclo[23.2.1.1¹¹,¹⁴.1¹⁸,²¹.0²,⁶]triaconta-1(28),9,11,14(30),16,21(29),23-heptaen-7-one

C35H45N7O5S2 (707.2923)

(3r,5s,7r,7ar,11ar)-5-butyl-3-(isothiocyanatomethyl)-decahydro-1h-pyrrolo[2,1-j]quinolin-7-yl acetate

C20H32N2O2S (364.2184)

1-{6-bromo-9h-pyrido[3,4-b]indol-1-yl}-2-phenylethanone

C19H13BrN2O (364.0211)

6-(2,6-dimethylhepta-1,5-dien-1-yl)-8-(3,7-dimethylocta-2,6-dien-1-yl)-10-hydroxy-1,2,3,6-tetrahydro-7-oxa-4λ⁶-thia-1-azatetraphene-4,4,5,12-tetrone

C34H41NO6S (591.2654)

(2s)-2-[(5e,7e)-dodeca-5,7-dien-3-yn-1-yl]-1-ethylpyrrolidine

C18H29N (259.23)

(1as,4as,7s,8ar)-7-hydroxy-3-[(1r,2r,3r)-2-(2-hydroxyethyl)-2-methyl-3-[(2r)-6-methylheptan-2-yl]cyclopentyl]-4a-methyl-1ah,5h,6h,7h,8h-naphtho[1,8a-b]oxiren-4-one

C27H44O4 (432.3239)

4-(3,5-dibromo-4-hydroxyphenyl)-5-[(4-hydroxyphenyl)methylidene]furan-2-one

C17H10Br2O4 (435.8946)

(2s,8r,15r,18r,22s,25s,26r)-8-benzyl-10,17,24-trihydroxy-15-isopropyl-26-methyl-22-(sec-butyl)-27-oxa-13,20-dithia-6,9,16,23,28,29,30-heptaazapentacyclo[23.2.1.1¹¹,¹⁴.1¹⁸,²¹.0²,⁶]triaconta-1(28),9,11,14(30),16,21(29),23-heptaen-7-one

C35H45N7O5S2 (707.2923)

12-(3,4-dihydroxyphenyl)-7,8,16,17-tetrahydroxy-4-oxa-1-azapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-5,7,9,12,14,16,18,20-octaen-3-one

C25H17NO8 (459.0954)

(3r)-3-[(2s,3as,5as,8s,9ar,9br)-8-chloro-3a,6,6,9a-tetramethyl-5-oxo-octahydronaphtho[2,1-b]furan-2-yl]-5-hydroxy-3,4-dihydropyrrol-2-one

C20H28ClNO4 (381.1707)

(6s,7ar)-2-[(2e,4e,6e,8e,10e,12e,14e)-17-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-6,11,15-trimethylheptadeca-2,4,6,8,10,12,14-heptaen-16-yn-2-yl]-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-6-ol

C40H54O3 (582.4073)

(2s)-n-[(1z)-2-(5-bromo-1h-indol-3-yl)ethenyl]-4-[(2r)-butan-2-yl]-2-isopropyl-5-oxo-1h-imidazole-2-carboximidic acid

C21H25BrN4O2 (444.1161)

4-(4-hydroxyphenyl)-5-[(4-hydroxyphenyl)methylidene]furan-2-one

C17H12O4 (280.0736)

n-[(2s,3r)-3-(acetyloxy)hexadec-15-en-2-yl]ethanimidic acid

C20H37NO3 (339.2773)

7,15-bis[2-(dimethylamino)ethyl]-5,13-dimethoxy-2,9,10-trithiatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-4,12-diol

C22H30N2O4S3 (482.1368)

(1r,4r,5s,8r,15r,18s,21r)-21-benzyl-8-[(2r)-butan-2-yl]-18-[(1r)-1-hydroxyethyl]-4-methyl-3-oxa-10,23,29,30-tetrathia-7,14,17,20,27,32,33,34-octaazapentacyclo[13.12.4.1²,⁵.1⁹,¹².1²²,²⁵]tetratriaconta-2(34),6,9(33),11,13,16,19,22(32),24,26-decaene-6,13,16,19,26-pentol

C35H42N8O7S4 (814.2059)

(5z)-3-chloro-5-[(3,5-dibromo-4-hydroxyphenyl)methylidene]-4-(4-hydroxyphenyl)furan-2-one

C17H9Br2ClO4 (469.8556)

(5z)-5-[(3-bromo-4-hydroxyphenyl)methylidene]-3-chloro-4-(3,5-dibromo-4-hydroxyphenyl)furan-2-one

C17H8Br3ClO4 (547.7661)

n-[3-(acetyloxy)hexadeca-11,15-dien-2-yl]ethanimidic acid

C20H35NO3 (337.2617)

(5z)-4-(3-bromo-4-hydroxyphenyl)-3-chloro-5-[(3,5-dibromo-4-hydroxyphenyl)methylidene]furan-2-one

C17H8Br3ClO4 (547.7661)

(21r)-12-(3,4-dihydroxyphenyl)-7,21-dihydroxy-8,16,17,18-tetramethoxy-4-oxa-1-azapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-2(11),5(10),6,8,12,14(19),15,17-octaen-3-one

C29H25NO10 (547.1478)

n-(2-{8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),2,4,6,8,10(14)-hexaen-11-yl}ethyl)guanidine

C16H14N4O4 (326.1015)

9-{3h-pyrrolo[2,3-c]quinolin-4-ylmethyl}purin-6-amine

C17H13N7 (315.1232)

(12bs)-10-bromo-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine

C15H17BrN2 (304.0575)

5-(2-aminoethyl)-2-methoxy-3,4-bis(methylsulfanyl)phenol

C11H17NO2S2 (259.0701)

2-phenyl-1-{9h-pyrido[3,4-b]indol-1-yl}ethanone

C19H14N2O (286.1106)

(2s,3s)-2-benzoyl-1,3,8-trihydroxy-9-(4-methoxy-6-oxopyran-2-yl)-5-oxatricyclo[4.3.1.0³,⁸]decan-4-one

C22H20O9 (428.1107)

6-{[(3,5-dibromo-4-hydroxyphenyl)methyl]amino}-9h-purin-8-ol

C12H9Br2N5O2 (412.9123)

(z,2z,4e)-n-[(1e)-3-[(8e)-10,17-dihydroxy-7,11-dimethyl-1,5-dioxo-4,7,10,13-tetrahydro-3h-2,6-benzodioxacyclopentadecin-3-yl]prop-1-en-1-yl]-4-(methoxyimino)but-2-enimidic acid

C27H32N2O8 (512.2159)

(10s,13s,20s,21r)-13-amino-17-bromo-3,35-dichloro-10-isopropyl-8,37,40-trioxa-4,11,22,34,39-pentaazadecacyclo[27.6.1.1²,⁵.1⁶,⁹.1¹⁵,¹⁹.1¹⁸,²¹.0⁷,²⁰.0²⁰,²⁴.0²³,²⁸.0³³,³⁶]tetraconta-1(35),2,4,6,9(39),11,15,17,19(38),23(28),24,26,29(36),30,32-pentadecaen-12-ol

C35H25BrCl2N6O4 (742.0498)

(1r,3as,7s,8r,9ar,9br,11ar)-3a,7,8-trihydroxy-1-[(2r)-6-hydroxy-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-5-one

C27H42O5 (446.3032)

(2s,3s,4s,5s,6s)-4,5-dihydroxy-6-{[(2r,3r,4r,5r)-4-hydroxy-5-(hydroxymethyl)-2-(6-hydroxypurin-9-yl)oxolan-3-yl]oxy}-2-methyloxan-3-yl (2e,4e,7z,9s)-9-[(2z,4z)-octa-2,4-dienoyloxy]deca-2,4,7-trienoate

C34H44N4O12 (700.2956)

2-(3,7-dimethylocta-2,6-dien-1-yl)benzene-1,4-diol

C16H22O2 (246.162)

3-[(3r,21s,22s)-16-ethenyl-11-ethyl-3-(methoxycarbonyl)-12,17,21,26-tetramethyl-4-oxo-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaen-22-yl]propanoic acid

C35H36N4O5 (592.2686)

n-[2-(3-bromo-4-hydroxyphenyl)ethenyl]-3-(4-hydroxyphenyl)-2-methoxyprop-2-enamide

C18H16BrNO4 (389.0263)

15-benzyl-10,17,24-trihydroxy-8,22-diisopropyl-12-methyl-13-oxa-20,27-dithia-6,9,16,23,28,29,30-heptaazapentacyclo[23.2.1.1¹¹,¹⁴.1¹⁸,²¹.0²,⁶]triaconta-1(28),9,14(30),16,18,21(29),23-heptaen-7-one

C34H43N7O5S2 (693.2767)

2-({1-hydroxy-2-[(2-methylbut-3-en-2-yl)amino]-3-phenylpropylidene}amino)-n-[2-methyl-1-(1,3-thiazol-2-yl)propyl]-3-phenylpropanimidic acid

C30H38N4O2S (518.2715)

(4s,7r,8s,11r,18r,21s,24r)-11-benzyl-4,18-bis[(2s)-butan-2-yl]-21-[(1r)-1-hydroxyethyl]-7,24-dimethyl-6-oxa-13,26-dithia-3,10,17,20,23,28,29,30-octaazatetracyclo[23.2.1.1⁵,⁸.1¹²,¹⁵]triaconta-1(27),2,5(30),9,12(29),14,16,19,22,25(28)-decaene-2,9,16,19,22-pentol

C38H50N8O7S2 (794.3244)

(1s,3ar,7r,8s,9as,9bs,11as)-3a,7,8-trihydroxy-1-[(2s)-6-hydroxy-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-5-one

C27H42O5 (446.3032)

(4s,5s)-4-hydroxy-4-(hydroxymethyl)-5-[(2e)-1-hydroxypenta-2,4-dien-2-yl]cyclopent-2-en-1-one

C11H14O4 (210.0892)

2-{9h-pyrido[3,4-b]indol-1-yl}-4,5-dihydro-3h-pyrrole

C15H13N3 (235.1109)

(2s,3s,4s,5s,6s)-4,5-dihydroxy-6-{[(2r,3r,4r,5r)-4-hydroxy-5-(hydroxymethyl)-2-(6-hydroxypurin-9-yl)oxolan-3-yl]oxy}-2-methyloxan-3-yl (2e,4e,7z,9s)-9-[(2e,4z)-octa-2,4-dienoyloxy]deca-2,4,7-trienoate

C34H44N4O12 (700.2956)

(2s)-n-[(10s,13s,20s,21r)-3,35-dichloro-12-hydroxy-10-isopropyl-8,37,40-trioxa-4,11,22,34,39-pentaazadecacyclo[27.6.1.1²,⁵.1⁶,⁹.1¹⁵,¹⁹.1¹⁸,²¹.0⁷,²⁰.0²⁰,²⁴.0²³,²⁸.0³³,³⁶]tetraconta-1(35),2,4,6,9(39),11,15,17,19(38),23(28),24,26,29(36),30,32-pentadecaen-13-yl]-2-hydroxy-3-methylbutanimidic acid

C40H34Cl2N6O6 (764.1917)

12-[4-(acetyloxy)-3-methoxyphenyl]-8,16,17,18-tetramethoxy-3-oxo-4-oxa-1-azapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-2(11),5(10),6,8,12,14(19),15,17-octaen-7-yl acetate

C34H31NO11 (629.1897)

3-amino-13-bromo-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-14-ol

C14H16BrN3O2S (369.0147)

13-methoxy-3,7,11-trimethylbicyclo[12.2.2]octadeca-1(16),3,7,11,14,17-hexaene-15,17-diol

C22H30O3 (342.2195)

(2r,3s,8z)-2-aminododec-8-en-3-ol

C12H25NO (199.1936)

n-[(4r)-4-(5-bromo-1-methoxyindol-3-yl)-3,4,5,6-tetrahydropyrimidin-2-yl]ethanimidic acid

C15H17BrN4O2 (364.0535)

2-{[6-(3,7-dimethylocta-2,6-dien-1-yl)-1,1,5,8-tetraoxo-3,4-dihydro-2h-1λ⁶,4-benzothiazin-7-yl]amino}ethanesulfonic acid

C20H28N2O7S2 (472.1338)

(2r,4s,5r)-5-amino-2-[(1e,3e,8e,10e)-pentadeca-1,3,8,10-tetraen-1-yl]piperidin-4-ol

C20H34N2O (318.2671)

(6as,10ar)-6,6,9-trimethyl-6ah,7h,8h,10ah-benzo[c]isochromen-2-ol

C16H20O2 (244.1463)

8,15-dibenzyl-10,17,24-trihydroxy-22-isopropyl-26-methyl-27-oxa-13,20-dithia-6,9,16,23,28,29,30-heptaazapentacyclo[23.2.1.1¹¹,¹⁴.1¹⁸,²¹.0²,⁶]triaconta-1(28),9,14(30),16,21(29),23-hexaen-7-one

C38H45N7O5S2 (743.2923)

2-[(1e,3r)-3-methoxy-3,7-dimethylocta-1,6-dien-1-yl]benzene-1,4-diol

C17H24O3 (276.1725)

(2s)-2-amino-5-[({[(2z)-1-hydroxy-3-(4-hydroxyphenyl)-2-methoxyprop-2-en-1-ylidene]amino}methanimidoyl)amino]pentanoic acid

C16H22N4O5 (350.159)

(4s,7r,8s,11s,18s)-4,11,18-triisopropyl-7-methyl-6,13-dioxa-20-thia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),14,16,19(22)-octaene-2,9,16-triol

C25H34N6O5S (530.2311)

n,n'-bis[2-(3,5-diiodo-4-methoxyphenyl)ethyl]ethanediamide

C20H20I4N2O4 (859.7602)

(3r,5s,7ar,11ar)-5-hexyl-3-(methoxymethyl)-decahydropyrrolo[2,1-j]quinolin-7-one

C20H35NO2 (321.2668)

n-{4-[(1s)-7-bromo-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]butyl}guanidine

C16H22BrN5 (363.1058)

(2-{9-[2-(dimethylamino)ethyl]-3,4,6,7-tetramethoxy-2,8-bis(methylsulfanyl)thianthren-1-yl}ethyl)dimethylamine

C26H38N2O4S4 (570.1714)

(1r,3r,9r,10r,13r,15r,21s,23r)-23-{[(2r,3r,4r,5r,6s)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-13-hydroxy-15-(hydroxymethyl)-3,10-dimethyl-16,25,26-trioxatricyclo[19.3.1.1⁹,¹²]hexacosa-4,6,18-trien-17-one

C33H52O11 (624.3509)

[17-hydroxy-12-(3-hydroxy-4-methoxyphenyl)-8,16-dimethoxy-3-oxo-4-oxa-1-azapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-2(11),5(10),6,8,12,14,16,18-octaen-7-yl]oxidanesulfonic acid

C28H23NO11S (581.0992)

11,25-diisopropyl-4-methyl-8,22-bis(sec-butyl)-3,17-dioxa-13,27-dithia-7,10,21,24,29,30,31,32-octaazapentacyclo[24.2.1.1²,⁵.1¹²,¹⁵.1¹⁶,¹⁹]dotriaconta-1(28),2(32),6,9,12(31),14,16(30),20,23,26(29)-decaene-6,9,20,23-tetrol

C35H50N8O6S2 (742.3295)

2-(3,5-diiodo-4-methoxyphenyl)ethanimidic acid

C9H9I2NO2 (416.8723)

(4s,7r,8s,11r,18s,21r,22s,25r)-11-benzyl-4-[(2s)-butan-2-yl]-18,25-diisopropyl-7,21-dimethyl-6,20-dioxa-13,27-dithia-3,10,17,24,29,30,31,32-octaazapentacyclo[24.2.1.1⁵,⁸.1¹²,¹⁵.1¹⁹,²²]dotriaconta-1(28),2,5(32),9,12(31),14,16,19(30),23,26(29)-decaene-2,9,16,23-tetrol

C39H50N8O6S2 (790.3295)

(2s,8s,15s,22r,25s,26r)-8,15-dibenzyl-10,17,24-trihydroxy-22-isopropyl-26-methyl-27-oxa-13,20-dithia-6,9,16,23,28,29,30-heptaazapentacyclo[23.2.1.1¹¹,¹⁴.1¹⁸,²¹.0²,⁶]triaconta-1(28),9,11,14(30),16,18,21(29),23-octaen-7-one

C38H41N7O5S2 (739.261)

n-[2-(3,4-dihydroxyphenyl)ethenyl]guanidine

C9H11N3O2 (193.0851)

10,14-bis(3,4-dihydroxyphenyl)-12-[2-(3,4-dihydroxyphenyl)ethyl]-5,6,18,19-tetrahydroxy-12-azapentacyclo[11.8.0.0²,¹¹.0³,⁸.0¹⁶,²¹]henicosa-1,3,5,7,10,13,16,18,20-nonaene-9,15-dione

C40H27NO12 (713.1533)

15-bromo-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-3-amine

C14H16BrN3OS (353.0197)

(5r,7r)-4,11,12,13-tetrakis(3,5-dibromo-4-hydroxyphenyl)-1,6,8-trioxadispiro[4.1.4⁷.2⁵]trideca-3,10,12-triene-2,9-dione

C34H14Br8O9 (1197.4105)

(2s)-n-[(6s,7s,10s,11s,15s,17r,20r,25as)-8,11,18-trihydroxy-15-isopropyl-3-[(4-methoxyphenyl)methyl]-2,6,17-trimethyl-20-(2-methylpropyl)-1,4,13,16,21-pentaoxo-10-(sec-butyl)-3h,6h,7h,10h,11h,12h,15h,17h,20h,23h,24h,25h,25ah-pyrrolo[2,1-f]1,15-dioxa-4,7,10,20-tetraazacyclotricosan-7-yl]-2-{1-[(2s)-1-(2-hydroxypropanoyl)pyrrolidin-2-yl]-n-methylformamido}-4-methylpentanimidic acid

C57H89N7O15 (1111.6416)

5-bromo-2-methylpyrido[3,4-b]indol-6-ol

C12H9BrN2O (275.9898)

(3e,7z,11e)-3,7,11-trimethylbicyclo[12.2.2]octadeca-1(16),3,7,11,14(18)-pentaene-15,17-dione

C21H26O2 (310.1933)

(2s,3r)-2-aminododecan-3-ol

C12H27NO (201.2093)

5-methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol

C28H26N4O4 (482.1954)

(3e,7e,11z,14s)-4,8,12-trimethylbicyclo[12.2.2]octadeca-1(16),3,7,11-tetraene-15,17-dione

C21H28O2 (312.2089)

2-(3-hydroxy-3,7-dimethyloct-6-en-1-yl)benzene-1,4-diol

C16H24O3 (264.1725)

n-[2-(3,5-dibromo-4-hydroxyphenyl)ethenyl]-3-(4-hydroxyphenyl)-2-methoxyprop-2-enamide

C18H15Br2NO4 (466.9368)

n-{3-[(2s,5z)-5-[(3,5-dibromo-4-methoxyphenyl)methylidene]-4-hydroxy-2h-1,3-oxazol-2-yl]propyl}guanidine

C15H18Br2N4O3 (459.9746)

(4s,11s,18s)-4,11,18-triisopropyl-7-methyl-6,13-dioxa-20-thia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),7,9,12(23),14,16,19(22)-nonaene-2,9,16-triol

C25H32N6O5S (528.2155)

3-hydroxy-4-[(1-hydroxy-2-{6-[(3e)-2-hydroxypent-3-en-1-yl]-4-methyloxan-2-yl}ethylidene)amino]-n-(3-{8-[(4e)-6-hydroxy-3,5-dimethylhept-4-en-1-yl]-3-methyl-1,7-dioxaspiro[5.5]undecan-2-yl}propyl)-2-methylbutanimidic acid

C40H70N2O8 (706.5132)

(2s)-n-[(2e,4e)-5-[(2s,3s,4e,6e,8s,11z,13e,16s,17e,19e,21r,22e)-8,16-dimethoxy-3,12,18,21-tetramethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,17,19,22-heptaen-2-yl]-2-methylhexa-2,4-dien-1-yl]-2-[(hydroxymethylidene)amino]-3-(sulfooxy)propanimidic acid

C40H58N2O10S (758.3812)

(1r,4r,5s,8r,15r,18r,19s,22s)-4,18-dimethyl-8,22-bis(2-methylpropyl)-3,17-dioxa-10,24,30,31-tetrathia-7,14,21,28,33,34,35,36-octaazahexacyclo[13.13.4.1²,⁵.1⁹,¹².1¹⁶,¹⁹.1²³,²⁶]hexatriaconta-2(36),6,9(35),11,13,16(34),20,23(33),25,27-decaene-6,13,20,27-tetrol

C32H42N8O6S4 (762.211)

2-[(1s,6s)-6-(2-methoxypropan-2-yl)-3-methylcyclohex-2-en-1-yl]benzene-1,4-diol

C17H24O3 (276.1725)

(14r,16r)-14-hydroxy-16-isopropyl-15-oxa-2,12,18-triazahexacyclo[11.8.1.1¹⁴,¹⁸.0³,⁸.0⁹,²².0²¹,²³]tricosa-1,3(8),4,6,9(22),10,12,21(23)-octaen-17-one

C22H19N3O3 (373.1426)

(16r,20r,21s)-17-hydroxy-13-methoxy-20,21-dimethyl-1,11,18-triazahexacyclo[10.9.2.0²,⁷.0⁸,²³.0¹⁵,²².0¹⁶,²⁰]tricosa-2,4,6,8(23),9,11,13,15(22),17-nonaen-19-one

C23H19N3O3 (385.1426)

2-amino-6-{[1-hydroxy-3-(3h-imidazol-4-yl)prop-2-en-1-ylidene]amino}hexanoic acid

C12H18N4O3 (266.1379)

n-{2-[11-(methylsulfanyl)-12-oxo-8,14-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadeca-1(17),2(7),3,5,8,10,13,15-octaen-10-yl]ethyl}ethanimidic acid

C20H17N3O2S (363.1041)

(2r)-n-[(3s,6r,7s,10r,11s,15s,17r,20s,25as)-10-[(2s)-butan-2-yl]-8,11,18-trihydroxy-15-isopropyl-3-[(4-methoxyphenyl)methyl]-2,6,17-trimethyl-20-(2-methylpropyl)-1,4,13,16,21-pentaoxo-3h,6h,7h,10h,11h,12h,15h,17h,20h,23h,24h,25h,25ah-pyrrolo[2,1-f]1,15-dioxa-4,7,10,20-tetraazacyclotricosan-7-yl]-4-methyl-2-(methylamino)pentanimidic acid

C49H78N6O12 (942.5677)

7-methoxy-3,11,21-triazapentacyclo[12.7.0.0²,¹⁰.0⁴,⁹.0¹⁵,²⁰]henicosa-1(14),2,4,6,8,10,12,15(20),16,18-decaene

C19H13N3O (299.1059)

(3r,4s,6s,9as)-4-methyl-6-[(1e,3e)-octa-1,3-dien-1-yl]-octahydro-1h-quinolizin-3-yl acetate

C20H33NO2 (319.2511)

({5-hexyl-7-oxo-decahydropyrrolo[2,1-j]quinolin-3-yl}methyl)sulfanylcarbonitrile

C20H32N2OS (348.2235)

3a,7,8,9b-tetrahydroxy-1-(6-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-1h,2h,3h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-5-one

C27H42O6 (462.2981)

7-bromo-3-(2-imino-1h-pyrimidin-4-yl)-1h-indol-4-ol

C12H9BrN4O (303.996)

4,8,12-trimethylbicyclo[12.2.2]octadeca-1(16),3,7,11,14,17-hexaene-2,15,17-triol

C21H28O3 (328.2038)

n-{3,35-dichloro-12-hydroxy-10-isopropyl-8,37,40-trioxa-4,11,22,34,39-pentaazadecacyclo[27.6.1.1²,⁵.1⁶,⁹.1¹⁵,¹⁹.1¹⁸,²¹.0⁷,²⁰.0²⁰,²⁴.0²³,²⁸.0³³,³⁶]tetraconta-1(35),2,4,6,9(39),11,15,17,19(38),23(28),24,26,29(36),30,32-pentadecaen-13-yl}-2-hydroxy-3-methylbutanimidic acid

C40H34Cl2N6O6 (764.1917)

17-hydroxy-3,7,11-trimethylbicyclo[12.2.2]octadeca-3,7,11,14(18)-tetraen-15-one

C21H30O2 (314.2246)

9-benzyl-4,11,18,27-tetrahydroxy-16,25-diisopropyl-2-(sec-butyl)-7,14,30-trithia-3,10,17,23,26,31,32,33-octaazapentacyclo[26.2.1.1⁵,⁸.1¹²,¹⁵.0¹⁹,²³]tritriaconta-1(31),3,8(33),10,12,15(32),17,26,28-nonaen-24-one

C39H50N8O5S3 (806.3066)

7-hydroxy-12-(3-hydroxy-4-methoxyphenyl)-8,16,17-trimethoxy-4-oxa-1-azapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-5,7,9,12,14,16,18,20-octaen-3-one

C29H25NO8 (515.158)

1-[6,14,25-trihydroxy-18-(6-hydroxy-3,5-dimethylhept-4-en-1-yl)-8,15,23-trimethyl-2,17,28-trioxa-13,26-diazatricyclo[14.7.4.1⁶,⁹]octacosa-13,25-dien-3-yl]pent-3-en-2-one

C40H68N2O8 (704.4975)

(2s,3r)-3-hydroxy-4-({1-hydroxy-2-[(2s,3s,6r)-3-methyl-6-(2-oxopentyl)oxan-2-yl]ethylidene}amino)-n-{3-[(2r,3s,6s,8s)-8-[(3s,4e,6s)-6-hydroxy-3,5-dimethylhept-4-en-1-yl]-3-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]propyl}-2-methylbutanimidic acid

C40H70N2O8 (706.5132)

n-[(2r,3s)-3-(acetyloxy)dodecan-2-yl]ethanimidic acid

C16H31NO3 (285.2304)

3-amino-15-bromo-7-oxa-5-thia-8,18-diazatetracyclo[9.7.0.0²,⁸.0¹²,¹⁷]octadeca-1(11),12,14,16-tetraen-14-ol

C14H16BrN3O2S (369.0147)

18-(acetyloxy)-12-[3-(acetyloxy)-4-methoxyphenyl]-8,16,17-trimethoxy-3-oxo-4-oxa-1-azapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-2(11),5(10),6,8,12,14(19),15,17,20-nonaen-7-yl acetate

C35H29NO12 (655.169)

(12e,19e,21e)-24-[(3e)-5-[2-(2,3-dimethyloxiran-2-yl)-1,3-thiazol-4-yl]-2-hydroxy-4-methylpent-3-en-2-yl]-8,16,17-trihydroxy-11-(hydroxymethyl)-18-methoxy-3,6,9,15,19,23-hexamethyl-2,10-dioxo-1-oxacyclotetracosa-12,19,21-trien-3-yl 3-hydroxy-2-methylbutanoate

C49H77NO13S (919.5115)

24-{5-[2-(2,3-dimethyloxiran-2-yl)-1,3-thiazol-4-yl]-2-hydroxy-4-methylpent-3-en-2-yl}-8,16,17-trihydroxy-11-(hydroxymethyl)-18-methoxy-3,6,9,15,19,23-hexamethyl-2,10-dioxo-1-oxacyclotetracosa-12,19,21-trien-3-yl 3-hydroxy-2-methylbutanoate

C49H77NO13S (919.5115)

(4s,5r)-4-hydroxy-4-(hydroxymethyl)-5-[(2e)-1-hydroxypenta-2,4-dien-2-yl]cyclopent-2-en-1-one

C11H14O4 (210.0892)

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

C30H30Br2N6O (648.0848)

n-(4-{7-bromo-9-hydroxypyrido[3,4-b]indol-1-yl}butyl)guanidine

C16H18BrN5O (375.0695)

n-{2-[2-carbamimidamido-3-(3,4-dihydroxyphenyl)-2,3-dihydro-1,4-benzodioxin-6-yl]ethenyl}guanidine

C18H20N6O4 (384.1546)

n-[(4s)-4-(5-bromo-1h-indol-3-yl)-3,4,5,6-tetrahydropyrimidin-2-yl]ethanimidic acid

C14H15BrN4O (334.0429)

(6e,10e)-3,9-dihydroxy-n-{2-hydroxy-3-[(3-{8-[(4e)-6-hydroxy-3,5-dimethylhept-4-en-1-yl]-3-methyl-1,7-dioxaspiro[5.5]undecan-2-yl}propyl)-c-hydroxycarbonimidoyl]-3-methylpropyl}-4-methyldodeca-6,10-dienimidic acid

C40H70N2O8 (706.5132)

(2s)-n-[(3s,6s,7s,10r,11r,15s,17r,20s,25ar)-10-[(2s)-butan-2-yl]-8,11,18-trihydroxy-15-isopropyl-3-[(4-methoxyphenyl)methyl]-2,6,17-trimethyl-20-(2-methylpropyl)-1,4,13,16,21-pentaoxo-3h,6h,7h,10h,11h,12h,15h,17h,20h,23h,24h,25h,25ah-pyrrolo[2,1-f]1,15-dioxa-4,7,10,20-tetraazacyclotricosan-7-yl]-2-{1-[(2r)-1-[(2s)-2-hydroxypropanoyl]pyrrolidin-2-yl]-n-methylformamido}-4-methylpentanimidic acid

C57H89N7O15 (1111.6416)

{5-hexyl-decahydro-1h-pyrrolo[2,1-j]quinolin-3-yl}methanol

C19H35NO (293.2719)

10-(3-hydroxyphenyl)-19-azahexacyclo[20.2.2.1⁸,¹⁹.0²,⁷.0¹⁰,¹⁸.0¹¹,¹⁶]heptacosa-1(25),2,4,6,8(27),11,13,15,22(26),23-decaene-5,12,14,24-tetrol

C32H27NO5 (505.1889)

(2s,3r,7z)-2-aminohexadeca-7,15-dien-3-ol

C16H31NO (253.2406)

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

C15H9BrN4O2 (355.9909)

5-hexyl-3-(methoxymethyl)-decahydropyrrolo[2,1-j]quinolin-7-one

C20H35NO2 (321.2668)

n-[3-(acetyloxy)octadeca-6,9,12,15-tetraen-2-yl]ethanimidic acid

C22H35NO3 (361.2617)

(2s,25s)-8,15-dibenzyl-10,17,24-trihydroxy-22-isopropyl-26-methyl-27-oxa-13,20-dithia-6,9,16,23,28,29,30-heptaazapentacyclo[23.2.1.1¹¹,¹⁴.1¹⁸,²¹.0²,⁶]triaconta-1(28),9,11,14(30),16,21(29),23-heptaen-7-one

C38H43N7O5S2 (741.2767)

11,12,18,23-tetrahydroxy-5-methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaen-16-one

C28H24N4O7 (528.1645)

({5-butyl-7-oxo-decahydropyrrolo[2,1-j]quinolin-3-yl}methyl)sulfanylcarbonitrile

C18H28N2OS (320.1922)

n-[(1r,4z,8s,13e)-1-hydroxy-8-{[(2r,3r,4r,5r,6r)-4-hydroxy-5-[(1s)-2-hydroxy-1-{[(2s,4s,5s,6r)-4-hydroxy-6-methyl-5-(methylsulfanyl)oxan-2-yl]oxy}ethyl]-3-{[(2s,4s,5s)-5-(isopropylamino)-4-methoxyoxan-2-yl]oxy}-6-methyl-5-(methylsulfanyl)oxan-2-yl]oxy}-13-{2-[(methylsulfanyl)disulfanyl]ethylidene}-11-oxobicyclo[7.3.1]trideca-4,9-dien-2,6-diyn-10-yl]methoxycarboximidic acid

C43H62N2O14S5 (990.2804)

(2s)-2-{[(2s)-1-hydroxy-2-[(2-methylbut-3-en-2-yl)amino]-3-phenylpropylidene]amino}-n-[(1s)-2-methyl-1-(1,3-thiazol-2-yl)propyl]-3-phenylpropanimidic acid

C30H38N4O2S (518.2715)

n-(3-hydroxydodecan-2-yl)ethanimidic acid

C14H29NO2 (243.2198)

(1r,8r,11s,14r,21r,24s)-8-benzyl-21-[(2r)-butan-2-yl]-11,24-bis[(1r)-1-hydroxyethyl]-6,19,28,29-tetrathia-2,9,12,15,22,25,31,32-octaazatetracyclo[12.12.4.1⁴,⁷.1¹⁷,²⁰]dotriaconta-2,4,7(32),9,12,15,17,20(31),22,25-decaene-3,10,13,16,23,26-hexol

C35H44N8O8S4 (832.2165)

11-bromo-4-(methanesulfinylmethyl)-3-methyl-1,3,6-triazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-12-ol

C16H16BrN3O2S (393.0147)

(1s,2r,5r,6r,9r,10r,13s,15s)-5-[(2r,5r)-5,6-dimethylheptan-2-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol

C28H46O3 (430.3447)

(2s,5s,8s,14s,17s,20s)-14-benzyl-4,7,16,19-tetrahydroxy-2,5-diisopropyl-17-[(1r)-1-[(2-methylbut-3-en-2-yl)oxy]ethyl]-22-thia-3,6,12,15,18,23-hexaazatricyclo[18.2.1.0⁸,¹²]tricosa-1(23),3,6,15,18-pentaen-13-one

C36H52N6O6S (696.3669)

6,10-dimethyl-5-(6-methyl-5-methylideneheptan-2-yl)-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol

C28H44O3 (428.329)

(2z)-3-(4-hydroxyphenyl)-2-methoxyprop-2-enimidic acid

C10H11NO3 (193.0739)

bis(3,5-dibromo-4-hydroxyphenyl)furan-2,5-dione

C16H6Br4O5 (593.6949)

6,7-dibromo-8-methoxy-4-oxo-1h-quinoline-2-carboxylic acid

C11H7Br2NO4 (374.8742)

n-[(1e,3e,5r)-5-[(2r,4z,6e,10r,11r,12z,14r,18z)-11,14-dihydroxy-10-(c-hydroxycarbonimidoyloxy)-4-methyl-20-oxo-1-oxacycloicosa-4,6,12,18-tetraen-2-yl]-3-methylhexa-1,3-dien-1-yl]-3-methylbut-2-enimidic acid

C33H48N2O7 (584.3461)

7,18-dihydroxy-12-(3-hydroxy-4-methoxyphenyl)-8,16,17-trimethoxy-4-oxa-1-azapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-2(11),5(10),6,8,12,14(19),15,17-octaen-3-one

C29H25NO9 (531.1529)

{2-[8,9-dimethoxy-7-(methylsulfanyl)-1,2,3,4,5-benzopentathiepin-6-yl]ethyl}dimethylamine

C13H19NO2S6 (412.974)

1-(3,4-dihydroxyphenyl)-3-[2-(3,4-dihydroxyphenyl)ethyl]-7,8-dihydroxychromeno[3,4-b]pyrrol-4-one

C25H19NO8 (461.1111)

(2r)-hexadeca-3,5,10,13-tetraen-2-amine

C16H27N (233.2143)

(2s,3s,4as,5s,8ar)-2-methyl-5-[(1e,3e)-octa-1,3-dien-1-yl]-decahydroquinolin-3-ol

C18H31NO (277.2406)

(4s,7s,8s,11r,18r,21s,22s,25s)-11-benzyl-4,18-bis[(2r)-butan-2-yl]-7,21,25-trimethyl-6,20-dioxa-13,27-dithia-3,10,17,24,29,30,31,32-octaazapentacyclo[24.2.1.1⁵,⁸.1¹²,¹⁵.1¹⁹,²²]dotriaconta-1(28),2,5(32),9,12(31),14,16,19(30),23,26(29)-decaene-2,9,16,23-tetrol

C38H48N8O6S2 (776.3138)

4,11,18-triisopropyl-7-methyl-6,13-dioxa-20-thia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),14,16,19(22)-octaene-2,9,16-triol

C25H34N6O5S (530.2311)

10-bromo-11-methoxy-4,6-dimethyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),9,12,14-tetraene

C17H21BrN2O (348.0837)

n-[(2s,3r,6z,9z,12z,15z)-3-(acetyloxy)octadeca-6,9,12,15-tetraen-2-yl]ethanimidic acid

C22H35NO3 (361.2617)

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

C17H24N4O5 (364.1747)

(2r,4r,5s)-5-amino-2-[(3e,5z)-trideca-3,5-dien-1-yl]piperidin-4-ol

C18H34N2O (294.2671)

(4r)-11-bromo-3-methyl-4-[(methylsulfanyl)methyl]-1,3,6-triazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-12-ol

C16H16BrN3OS (377.0197)

n-[2-(3-bromo-4-methoxyphenyl)ethenyl]-3-(4-hydroxyphenyl)-2-methoxyprop-2-enamide

C19H18BrNO4 (403.0419)

3-bromo-5-[(3-bromo-4-hydroxyphenyl)methylidene]-4-(3-chloro-4-hydroxyphenyl)furan-2-one

C17H9Br2ClO4 (469.8556)

(16r,20s,23r)-17-hydroxy-13-methoxy-20,23-dimethyl-1,11,18-triazahexacyclo[10.8.2.1¹⁶,²⁰.0²,⁷.0⁸,²².0¹⁵,²¹]tricosa-2,4,6,8(22),9,11,13,15(21),17-nonaen-19-one

C23H19N3O3 (385.1426)

(4r,5s,8s,11s,18r,19s,22s,25r)-11-benzyl-22-[(2s)-butan-2-yl]-8-isopropyl-4,18,25-trimethyl-3,17-dioxa-13,27-dithia-7,10,21,24,29,30,31,32-octaazapentacyclo[24.2.1.1²,⁵.1¹²,¹⁵.1¹⁶,¹⁹]dotriaconta-1(28),2(32),6,9,12(31),14,16(30),20,23,26(29)-decaene-6,9,20,23-tetrol

C37H46N8O6S2 (762.2982)

(2r,4r,5r,6s)-4-amino-5-methoxy-6-methyl-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol

C27H24N4O4 (468.1797)

1-{7-bromo-9h-pyrido[3,4-b]indol-1-yl}-2-phenylethanone

C19H13BrN2O (364.0211)

8-amino-3,10,19-triazapentacyclo[10.7.1.0²,⁷.0⁹,²⁰.0¹³,¹⁸]icosa-1(19),2,7,9(20),11,13(18),14,16-octaen-6-one

C17H12N4O (288.1011)

methyl (21s,22s)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-(3-oxo-3-{[(2e)-3,7,11,15-tetramethylhexadec-2-en-1-yl]oxy}propyl)-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate

C55H74N4O5 (870.5659)

(2r,3r,4as,5s,8ar)-5-[(5s)-5-hydroxyoctyl]-2-methyl-decahydroquinolin-3-yl (2e)-oct-2-enoate

C26H47NO3 (421.3556)

(2s)-n-[(2e,4e)-5-[(2s,3s,4e,6e,8s,11z,13e,16s,17e,19e,21r,22e)-8,16-dimethoxy-3,12,18,21,23-pentamethyl-24-oxo-1-oxacyclotetracosa-4,6,11,13,17,19,22-heptaen-2-yl]-2-methylhexa-2,4-dien-1-yl]-3-hydroxy-2-[(hydroxymethylidene)amino]propanimidic acid

C41H60N2O7 (692.44)

(3r,5s,7r,7ar,11ar)-5-butyl-3-[(cyanosulfanyl)methyl]-decahydro-1h-pyrrolo[2,1-j]quinolin-7-yl acetate

C20H32N2O2S (364.2184)

n-(2-methoxy-2-{12-oxo-8,14-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadeca-1(17),2(7),3,5,8,10,13,15-octaen-10-yl}ethyl)-3-methylbut-2-enimidic acid

C23H21N3O3 (387.1583)

2-{pyrido[3,4-b]indol-2-yl}benzoic acid

C18H12N2O2 (288.0899)

(4r,4as,6s,8as)-4,6-dihydroxy-2-[(1r,2r,3r)-2-(2-hydroxyethyl)-2-methyl-3-[(2r)-6-methylheptan-2-yl]cyclopentyl]-8a-methyl-4,4a,5,6,7,8-hexahydronaphthalen-1-one

C27H46O4 (434.3396)

4-amino-5-methoxy-6-methyl-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol

C27H24N4O4 (468.1797)

(2s,3r,4ar,4br,6ar,7r,10ar)-2,3-dihydroxy-7-[(2r)-6-hydroxy-6-methylheptan-2-yl]-4a,6a-dimethyl-2h,3h,4h,4bh,5h,6h,7h,8h,9h,11h-indeno[1,7a-a]naphthalene-10,12-dione

C27H42O5 (446.3032)

7-bromo-4-oxo-1h-quinoline-2-carboxylic acid

C10H6BrNO3 (266.9531)

4-(3-bromo-4-hydroxyphenyl)-5-[(3-bromo-4-hydroxyphenyl)methylidene]furan-2-one

C17H10Br2O4 (435.8946)

14-hydroxy-16-isopropyl-15-oxa-2,12,18-triazahexacyclo[11.8.1.1¹⁴,¹⁸.0³,⁸.0⁹,²².0²¹,²³]tricosa-1,3(8),4,6,9(22),10,12,21(23)-octaen-17-one

C22H19N3O3 (373.1426)

5-(5-ethyl-6-methylheptan-2-yl)-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol

C29H48O3 (444.3603)

(1s,2r,5r,6r,9r,10r,13s,15s)-5-[(2r,3e,5s)-5,6-dimethylhept-3-en-2-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol

C28H44O3 (428.329)

4-methyl-2-(methylamino)-n-{8,11,18-trihydroxy-15-isopropyl-3-[(4-methoxyphenyl)methyl]-2,6,17-trimethyl-20-(2-methylpropyl)-1,4,13,16,21-pentaoxo-10-(sec-butyl)-3h,6h,7h,10h,11h,12h,15h,17h,20h,23h,24h,25h,25ah-pyrrolo[2,1-f]1,15-dioxa-4,7,10,20-tetraazacyclotricosan-7-yl}pentanimidic acid

C49H78N6O12 (942.5677)

(2r,3s,4s,6s)-2-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),16,20(27),21(26),22,24-decaene-3,16-diol

C27H24N4O3 (452.1848)

7-hydroxy-3-[2-(2-hydroxyethyl)-2-methyl-3-(6-methylheptan-2-yl)cyclopentyl]-4a-methyl-1ah,5h,6h,7h,8h-naphtho[1,8a-b]oxiren-4-one

C27H44O4 (432.3239)

4-[(2s)-2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-2-carboxyethyl]-1,3-dimethyl-5-(methylsulfanyl)-2h-imidazol-2-yl

C18H20BrN4O3S (451.0439)

1,5,6-trichloro-2-(dichloromethyl)-6-methylocta-1,3,7-triene

C10H11Cl5 (305.9303)

(10s,18s)-10-(3-hydroxyphenyl)-19-azahexacyclo[20.2.2.1⁸,¹⁹.0²,⁷.0¹⁰,¹⁸.0¹¹,¹⁶]heptacosa-1(25),2,4,6,8(27),11,13,15,22(26),23-decaene-5,12,14,24-tetrol

C32H27NO5 (505.1889)

5-butyl-3-[(cyanosulfanyl)methyl]-decahydro-1h-pyrrolo[2,1-j]quinolin-7-yl acetate

C20H32N2O2S (364.2184)

5,12,14-tris(acetyloxy)-10-[3-(acetyloxy)phenyl]-19-azahexacyclo[20.2.2.1⁸,¹⁹.0²,⁷.0¹⁰,¹⁸.0¹¹,¹⁶]heptacosa-1(25),2,4,6,8(27),11,13,15,22(26),23-decaen-24-yl acetate

C42H37NO10 (715.2417)

2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-3-(2-iminoimidazolidin-4-yl)propanoic acid

C15H16BrN5O3 (393.0436)

1,7-dimethyl (2e,5s,6s)-6-[(1r,2r,4s,5s)-1-(acetyloxy)-5-[(2s,4s,6s,8r,10s)-8-(acetyloxy)-4,10-dimethyl-8-(2-oxopropyl)-1,7-dioxaspiro[5.5]undecan-2-yl]-4-methyl-2,5-bis[(3-methylbutanoyl)oxy]pentyl]-2-methyl-5-(propanoyloxy)hept-2-enedioate

C47H74O17 (910.4926)

(12br)-1h,2h,3h,4h,6h,7h,12h,12bh-indolo[2,3-a]quinolizine

C15H18N2 (226.147)

(2s,8s,11s,15s,18r,22r,25r,26r)-8,15-dibenzyl-10,17,24-trihydroxy-22-isopropyl-26-methyl-27-oxa-13,20-dithia-6,9,16,23,28,29,30-heptaazapentacyclo[23.2.1.1¹¹,¹⁴.1¹⁸,²¹.0²,⁶]triaconta-1(28),9,14(30),16,21(29),23-hexaen-7-one

C38H45N7O5S2 (743.2923)

5-amino-2-(trideca-6,8-dien-1-yl)piperidin-4-ol

C18H34N2O (294.2671)

3-[11-ethyl-16-(hydroxymethyl)-12,17,21,26-tetramethyl-4-oxo-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1(23),2(6),5(26),8,10,12,14,16,18(24),19-decaen-22-yl]propanoic acid

C32H34N4O4 (538.258)

(2r)-n-[(3s,6r,7s,10r,11s,15s,17r,20s,25as)-15-[(2r)-butan-2-yl]-10-[(2s)-butan-2-yl]-8,11,18-trihydroxy-3-[(4-methoxyphenyl)methyl]-2,6,17-trimethyl-20-(2-methylpropyl)-1,4,13,16,21-pentaoxo-3h,6h,7h,10h,11h,12h,15h,17h,20h,23h,24h,25h,25ah-pyrrolo[2,1-f]1,15-dioxa-4,7,10,20-tetraazacyclotricosan-7-yl]-2-{1-[(2s)-1-[(2s)-2-hydroxypropanoyl]pyrrolidin-2-yl]-n-methylformamido}-4-methylpentanimidic acid

C58H91N7O15 (1125.6573)

(5z)-5-[(3-bromo-4-methoxyphenyl)methylidene]-4-(4-hydroxyphenyl)furan-2-one

C18H13BrO4 (371.9997)

(2r,4r,5s)-5-amino-2-[(3e,5e)-trideca-3,5-dien-1-yl]piperidin-4-ol

C18H34N2O (294.2671)

11-amino-4-bromo-8,14-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadeca-1(17),2(7),3,5,8,10,13,15-octaen-12-one

C15H8BrN3O (324.9851)

9-acetyl-7-bromopyrido[3,4-b]indol-6-yl acetate

C15H11BrN2O3 (345.9953)

4,18-dimethyl-8,22-bis(2-methylpropyl)-3,17-dioxa-10,24,30,31-tetrathia-7,14,21,28,33,34,35,36-octaazahexacyclo[13.13.4.1²,⁵.1⁹,¹².1¹⁶,¹⁹.1²³,²⁶]hexatriaconta-2(36),6,9(35),11,13,16(34),20,23(33),25,27-decaene-6,13,20,27-tetrol

C32H42N8O6S4 (762.211)

2-(2-hydroxyethyl)-1,6-dioxaspiro[4.5]dec-8-en-4-one

C10H14O4 (198.0892)

n-[3-(acetyloxy)hexadec-15-en-2-yl]ethanimidic acid

C20H37NO3 (339.2773)

{[(3r,5s,7ar,11ar)-5-hexyl-7-oxo-decahydropyrrolo[2,1-j]quinolin-3-yl]methyl}sulfanylcarbonitrile

C20H32N2OS (348.2235)

12-[(1s,14e,21r,22r,24s)-13-hydroxy-24-[(3-methylbutanoyl)oxy]-10-oxo-9,26,27-trioxa-12-azatricyclo[19.4.1.1¹,²²]heptacosa-12,14-dien-8-yl]-3-[(sulfooxy)methyl]-1,5,13-trioxa-2-azatridecane-1,13-disulfonic acid

C38H66N2O20S3 (966.3371)

(8z,16e,21e,23e,27z)-9,17,24,28-tetramethyl-13,32,34,37-tetraoxopentacyclo[28.2.2.2¹¹,¹⁴.1⁵,¹⁹.0³,²⁰]heptatriaconta-1(33),5(35),8,11,14(36),16,21,23,27,30-decaene-20-carbaldehyde

C42H46O5 (630.3345)

(2s,8s,15r,22s,25s,26r)-8-benzyl-15-[(2s)-butan-2-yl]-10,17,24-trihydroxy-22-isopropyl-26-methyl-27-oxa-13,20-dithia-6,9,16,23,28,29,30-heptaazapentacyclo[23.2.1.1¹¹,¹⁴.1¹⁸,²¹.0²,⁶]triaconta-1(28),9,11,14(30),16,18,21(29),23-octaen-7-one

C35H43N7O5S2 (705.2767)

2-aminooctadeca-5,9,12,15-tetraen-3-ol

C18H31NO (277.2406)

methyl (2e,5s,6s,7r,8r,10s,11s)-7-(acetyloxy)-11-[(2s,4s,6s,10r)-8-[(1r)-1-hydroxy-2-oxopropyl]-4,10-dimethyl-1,7-dioxaspiro[5.5]undecan-2-yl]-2,6,10-trimethyl-8,11-bis[(3-methylbutanoyl)oxy]-5-(propanoyloxy)undec-2-enoate

C44H72O14 (824.4922)

2-amino-5-({[3-(4-hydroxyphenyl)-2-methoxyprop-2-enamido]methanimidoyl}amino)pentanoic acid

C16H22N4O5 (350.159)

1-{6-bromo-2-methyl-1h,3h,4h,9h-pyrido[3,4-b]indol-1-yl}-2-(4-methylphenyl)ethanamine

C21H24BrN3 (397.1153)

(4r,7r,8s,11s,18r,21r,22r,25r)-11-benzyl-4-[(2r)-butan-2-yl]-18-isopropyl-7,21,25-trimethyl-6,20-dioxa-13,27-dithia-3,10,17,24,29,30,31,32-octaazapentacyclo[24.2.1.1⁵,⁸.1¹²,¹⁵.1¹⁹,²²]dotriaconta-1(28),2,5(32),9,12(31),14,16,19(30),23,26(29)-decaene-2,9,16,23-tetrol

C37H46N8O6S2 (762.2982)

2-{2-[1-(1h-indol-3-yl)-2h,3h,4h,9h-pyrido[3,4-b]indol-1-yl]-1h-indol-3-yl}ethanamine

C29H27N5 (445.2266)

5-carbamimidamido-2-[(4-hydroxyphenyl)formamido]pentanoic acid

C13H18N4O4 (294.1328)

n-[(10s,11r)-10-[(2r)-butan-2-yl]-8,11,18-trihydroxy-15-isopropyl-3-[(4-methoxyphenyl)methyl]-2,6,17-trimethyl-20-(2-methylpropyl)-1,4,13,16,21-pentaoxo-3h,6h,7h,10h,11h,12h,15h,17h,20h,23h,24h,25h,25ah-pyrrolo[2,1-f]1,15-dioxa-4,7,10,20-tetraazacyclotricosan-7-yl]-4-methyl-2-(methylamino)pentanimidic acid

C49H78N6O12 (942.5677)

(4r,5s,8r,18r,22r)-4,18-dimethyl-8,22-bis(2-methylpropyl)-3,17-dioxa-10,24,30,31-tetrathia-7,14,21,28,33,34,35,36-octaazahexacyclo[13.13.4.1²,⁵.1⁹,¹².1¹⁶,¹⁹.1²³,²⁶]hexatriaconta-2(36),6,9(35),11,13,16(34),20,23(33),25,27-decaene-6,13,20,27-tetrol

C32H42N8O6S4 (762.211)

2-(3,7-dimethylocta-2,6-dien-1-yl)-6-methoxycyclohexa-2,5-diene-1,4-dione

C17H22O3 (274.1569)

12-(3,5-dimethoxyphenyl)-18-hydroxy-8,16,17-trimethoxy-4-oxa-1-azapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-2(11),5,7,9,12,14,16,18-octaen-7-yl acetate

C32H31NO9 (573.1999)

(4r)-11-bromo-4-[(r)-methanesulfinylmethyl]-3-methyl-1,3,6-triazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-5,7,9(16),10(15),11,13-hexaen-12-ol

C16H16BrN3O2S (393.0147)

6-hydroxy-20-imino-2,12,15-triazapentacyclo[11.7.1.0³,⁸.0⁹,²¹.0¹⁴,¹⁹]henicosa-1,3(8),4,6,9(21),10,12,14(19)-octaen-18-one

C18H12N4O2 (316.096)

(2r,3r,4as,5s,8ar)-5-[(5r)-5-hydroxyoctyl]-2-methyl-decahydroquinolin-3-yl (2e)-oct-2-enoate

C26H47NO3 (421.3556)

n-[(1r,4z,8s,13z)-1-hydroxy-8-{[(2r,3r,4r,5r,6r)-4-hydroxy-5-[(1s)-2-hydroxy-1-{[(2s,4s,5s,6r)-4-hydroxy-6-methyl-5-(methylsulfanyl)oxan-2-yl]oxy}ethyl]-3-{[(2s,4s,5s)-5-(isopropylamino)-4-methoxyoxan-2-yl]oxy}-6-methyl-5-(methylsulfanyl)oxan-2-yl]oxy}-13-{2-[(methylsulfanyl)disulfanyl]ethylidene}-11-oxobicyclo[7.3.1]trideca-4,9-dien-2,6-diyn-10-yl]methoxycarboximidic acid

C43H62N2O14S5 (990.2804)

2-[(2z)-7-hydroxy-3,7-dimethyloct-2-en-1-yl]-6-methoxycyclohexa-2,5-diene-1,4-dione

C17H24O4 (292.1675)

3-{[5-hydroxy-2-(1h-indole-3-carbonyl)-3h-imidazol-4-yl]methylidene}indol-6-ol

C21H14N4O3 (370.1066)

(3e,6r,7r,8e,10e,14z,23s,28z)-4,11,15,29-tetramethyl-19,33,35,37-tetraoxopentacyclo[29.2.2.1⁶,²⁵.1¹⁷,²¹.0⁷,²³]heptatriaconta-1(34),3,8,10,14,17,20,25(36),28,31-decaene-7-carbaldehyde

C42H46O5 (630.3345)

6-(3,7-dimethylocta-2,6-dien-1-yl)-7-methoxy-3,4-dihydro-2h-1λ⁶,4-benzothiazine-1,1,5,8-tetrone

C19H25NO5S (379.1453)

(1r,3as,7as)-3,3,6-trimethyl-3a,4,5,7a-tetrahydrospiro[2-benzofuran-1,1'-cyclohexan]-3'-ene-2',5'-dione

C16H20O3 (260.1412)

n-[2-(5,6-dibromo-1h-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3h-imidazole-2-carboximidic acid

C21H24Br2N4O2 (522.0266)

(1s,4s,7r,8s,11s,14r,15s,18s,21r)-4,11,18-triisopropyl-7,14,21-trimethyl-6,13,20-trioxa-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-2,5(24),9,12(23),16,19(22)-hexaene-2,9,16-triol

C27H42N6O6 (546.3166)

1-(6-hydroxy-2-methylchromen-2-yl)-4-methylpentan-2-one

C16H20O3 (260.1412)

n-[(1s,2r,3r,4s)-3-carbamimidamido-2,4-bis(3,4-dihydroxyphenyl)cyclobutyl]guanidine

C18H22N6O4 (386.1702)

(6s)-6-[(1e)-2,6-dimethylhepta-1,5-dien-1-yl]-8-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-10-hydroxy-1,2,3,6-tetrahydro-7-oxa-4λ⁶-thia-1-azatetraphene-4,4,5,12-tetrone

C34H41NO6S (591.2654)

(2s)-2-[(3e,5e)-dodeca-3,5-dien-1-yl]-1-ethylpyrrolidine

C18H33N (263.2613)

3-(2-imino-1h-pyrimidin-4-yl)-1h-indol-4-ol

C12H10N4O (226.0855)

2-({1-hydroxy-2-[(3-methylbut-2-en-1-yl)amino]-3-phenylpropylidene}amino)-3-methyl-n-[2-methyl-1-(1,3-thiazol-2-yl)propyl]butanimidic acid

C26H38N4O2S (470.2715)

5-(2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-2-carboxyethyl)-1,3-dimethyl-4-(methylsulfanyl)imidazol-1-ium

[C18H20BrN4O3S]+ (451.0439)

2-{6,7-dibromo-9h-pyrido[3,4-b]indol-1-yl}-4,5-dihydro-3h-pyrrole

C15H11Br2N3 (390.932)

n-[2-(2-iminoimidazolidin-4-yl)ethyl]-9h-pyrido[3,4-b]indole-3-carboxamide

C17H18N6O (322.1542)

4-(5-bromo-1-methoxyindol-3-yl)-1,3-diazinan-2-imine

C13H15BrN4O (322.0429)

(2r,3s,5e,9z,12z,15z)-2-aminooctadeca-5,9,12,15-tetraen-3-ol

C18H31NO (277.2406)

4,8-dihydroxy-n-[2-(4-hydroxyphenyl)ethenyl]quinoline-2-carboximidic acid

C18H14N2O4 (322.0954)

(4s,7r,8s,11r,18s,21r,22s,25r)-4,18-bis[(2s)-butan-2-yl]-11,25-diisopropyl-7,21-dimethyl-6,20-dioxa-13,27-dithia-3,10,17,24,29,30,31,32-octaazapentacyclo[24.2.1.1⁵,⁸.1¹²,¹⁵.1¹⁹,²²]dotriaconta-1(28),2,5(32),9,12(31),14,16,19(30),23,26(29)-decaene-2,9,16,23-tetrol

C36H52N8O6S2 (756.3451)

(2s,4r,5r)-5-amino-2-[(6e,8e)-trideca-6,8-dien-1-yl]piperidin-4-ol

C18H34N2O (294.2671)

(5z)-4-(3-bromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methylidene]furan-2-one

C17H9Br3O4 (513.8051)

11,25-diisopropyl-7-methyl-4,18-bis(sec-butyl)-6,20-dioxa-13,27-dithia-3,10,17,24,29,30,31,32-octaazapentacyclo[24.2.1.1⁵,⁸.1¹²,¹⁵.1¹⁹,²²]dotriaconta-1(28),2,5(32),9,12(31),14,16,19(30),23,26(29)-decaene-2,9,16,23-tetrol

C35H50N8O6S2 (742.3295)

4-amino-11,12,18-trihydroxy-5-methoxy-6-methyl-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaen-16-one

C27H22N4O6 (498.1539)

2-amino-3-({15-[(1r,7r)-7-[(5e)-7-ethoxy-7-oxohept-5-en-1-yl]-2-hydroxy-6,8-dioxabicyclo[3.2.1]octan-5-yl]pentadecyl}oxy)propoxysulfonic acid

C33H61NO10S (663.4016)

(4s,7r,8s,11r,18s,21r,22s,25r)-11-benzyl-4-[(2s)-butan-2-yl]-18-isopropyl-7,21,25-trimethyl-6,20-dioxa-13,27-dithia-3,10,17,24,29,30,31,32-octaazapentacyclo[24.2.1.1⁵,⁸.1¹²,¹⁵.1¹⁹,²²]dotriaconta-1(28),2,5(32),9,12(31),14,16,19(30),23,26(29)-decaene-2,9,16,23-tetrol

C37H46N8O6S2 (762.2982)

(4r)-4-(5-bromo-1h-indol-3-yl)-1,3-diazinan-2-imine

C12H13BrN4 (292.0324)

(z,2z,4e)-n-[(1e)-3-[(3r,7s,8e,10r,11z)-10,17-dihydroxy-7,11-dimethyl-1,5-dioxo-4,7,10,13-tetrahydro-3h-2,6-benzodioxacyclopentadecin-3-yl]prop-1-en-1-yl]-4-(methoxyimino)but-2-enimidic acid

C27H32N2O8 (512.2159)

n-[(2s,3r,11e)-3-(acetyloxy)hexadeca-11,15-dien-2-yl]ethanimidic acid

C20H35NO3 (337.2617)

8-{[2-(dimethylamino)ethyl]sulfanyl}-4,11-diazatetracyclo[8.7.1.0⁵,¹⁸.0¹²,¹⁷]octadeca-1(18),4,6,8,10,12,14,16-octaene-6,15-diol

C20H21N3O2S (367.1354)

7-bromo-9h-pyrido[3,4-b]indole

C11H7BrN2 (245.9793)

(3e,7e,10r)-4,8-dimethyl-10-(2-methylprop-1-en-1-yl)bicyclo[9.3.1]pentadeca-1(14),3,7,11-tetraene-13,15-dione

C21H26O2 (310.1933)

(2r,4r,5r,6s)-4-amino-11,12,18-trihydroxy-5-methoxy-6-methyl-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaen-16-one

C27H22N4O6 (498.1539)

10-(3-hydroxyphenyl)-19-azahexacyclo[20.2.2.1⁸,¹⁹.0²,⁷.0¹⁰,¹⁸.0¹¹,¹⁶]heptacosa-1(25),2,4,6,8(27),11,13,15,22(26),23-decaene-5,12,24-triol

C32H27NO4 (489.194)

methyl docosa-4,7,10,13,16,19-hexaenoate

C23H34O2 (342.2559)

n-[(2s,3r,9z)-3-(acetyloxy)hexadec-9-en-2-yl]ethanimidic acid

C20H37NO3 (339.2773)

3-chloro-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methylidene]furan-2-one

C17H7Br4ClO4 (625.6766)

n-[(2r,3s)-3-(acetyloxy)dodecan-2-yl]methanimidic acid

C15H29NO3 (271.2147)

(3r)-3-[(2z,4e,6e,8e,10e,12e,14e,16e)-3-hydroxy-19-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16-octaen-18-ynoyl]-3,4,4-trimethylcyclopentan-1-one

C40H52O4 (596.3865)

(2r,3r,4s,5s)-2-(6-aminopurin-9-yl)-4-{[(2e)-3-(3h-imidazol-4-yl)prop-2-enoyl]oxy}-5-[(r)-methanesulfinylmethyl]oxolan-3-yl (2z)-3-(4-hydroxyphenyl)-2-methoxyprop-2-enoate

C27H27N7O8S (609.1642)

(2s,4r,5s)-5-amino-2-[(1e,3e,8e,10e)-pentadeca-1,3,8,10-tetraen-1-yl]piperidin-4-ol

C20H34N2O (318.2671)

4-(5,6-dibromo-1h-indol-3-yl)-1h-pyrimidin-2-imine

C12H8Br2N4 (365.9116)

n-(2-{6-oxa-4-thia-9,19-diazapentacyclo[10.7.1.0³,⁷.0⁸,²⁰.0¹³,¹⁸]icosa-1,3(7),8,10,12(20),13,15,17-octaen-2-yl}ethyl)ethanimidic acid

C20H17N3O2S (363.1041)

5,6,18,19-tetrahydroxy-9,15-dioxa-12-azapentacyclo[11.8.0.0²,¹¹.0³,⁸.0¹⁶,²¹]henicosa-1(13),2(11),3(8),4,6,16(21),17,19-octaene-10,14-dione

C18H9NO8 (367.0328)

(4s,7r,8s,11s,18s)-4,11,18-triisopropyl-7-methyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),9,12(23),14,16,19(22)-octaene-2,9,16-triol

C25H34N6O4S2 (546.2083)

(1r,3r,4r,7r,9r,10r,12r,13r,19r,21r,23s,27s)-4,9,23,27-tetrahydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]heptacosa-15,17-dien-3-yl butanoate

C30H46O10 (566.3091)

7,17-dihydroxy-12-(3-hydroxy-4-methoxyphenyl)-8,16-dimethoxy-4-oxa-1-azapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-2(11),5(10),6,8,12,14(19),15,17,20-nonaen-3-one

C28H21NO8 (499.1267)

2-(2-hydroxy-n-methylpropanamido)-4-methyl-n-{8,11,18-trihydroxy-3-[(4-methoxyphenyl)methyl]-2,6,17-trimethyl-20-(2-methylpropyl)-1,4,13,16,21-pentaoxo-15-propyl-10-(sec-butyl)-3h,6h,7h,10h,11h,12h,15h,17h,20h,23h,24h,25h,25ah-pyrrolo[2,1-f]1,15-dioxa-4,7,10,20-tetraazacyclotricosan-7-yl}pentanimidic acid

C52H82N6O14 (1014.5889)

3-[({[(1s)-1-[(4-carbamimidamidobutyl)-c-hydroxycarbonimidoyl]-3-methylbutyl]-c-hydroxycarbonimidoyl}methyl)(sulfo)amino]-n-(5-carbamimidamidopentyl)undecanimidic acid

C30H62N10O6S (690.4574)

(3e,7e,11z)-4,8,12-trimethylbicyclo[12.2.2]octadeca-1(16),3,7,11,14,17-hexaene-2,15,17-triol

C21H28O3 (328.2038)

7-bromo-1-(1h-pyrrol-2-yl)-9h-pyrido[3,4-b]indol-6-ol

C15H10BrN3O (327.0007)

(1r,3ar,7s,8r,9as,9bs,11ar)-3a,7,8,9b-tetrahydroxy-1-[(2r)-6-hydroxy-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-5-one

C27H42O6 (462.2981)

n-(3-{3h,4h,9h-pyrido[3,4-b]indol-1-yl}propyl)guanidine

C15H19N5 (269.164)

4,11,18-triisopropyl-7-methyl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexaazatetracyclo[17.2.1.1⁵,⁸.1¹²,¹⁵]tetracosa-1(21),2,5(24),7,9,12(23),14,16,19(22)-nonaene-2,9,16-triol

C25H32N6O4S2 (544.1926)

3-hydroxy-4-({1-hydroxy-2-[3-methyl-6-(2-oxopentyl)oxan-2-yl]ethylidene}amino)-n-(3-{8-[(4e)-6-hydroxy-3,5-dimethylhept-4-en-1-yl]-3-methyl-1,7-dioxaspiro[5.5]undecan-2-yl}propyl)-2-methylbutanimidic acid

C40H70N2O8 (706.5132)

(2s)-2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-3-(3h-imidazol-4-yl)propanoic acid

C15H13BrN4O3 (376.0171)

5-(5,6-dimethylheptan-2-yl)-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol

C28H46O3 (430.3447)

7-(4-methylpent-3-en-1-yl)-2h,3h,4h-1λ⁶-naphtho[2,3-b][1,4]thiazine-1,1,5,10-tetrone

C18H19NO4S (345.1035)

7-bromo-2-methylpyrido[3,4-b]indol-6-ol

C12H9BrN2O (275.9898)

n-(2-hydroxyundecyl)ethanimidic acid

C13H27NO2 (229.2042)

12-(3,4-dimethoxyphenyl)-7,18-dihydroxy-8,16,17-trimethoxy-4-oxa-1-azapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-2(11),5(10),6,8,12,14(19),15,17-octaen-3-one

C30H27NO9 (545.1686)

4-(3-bromo-4-hydroxyphenyl)-5-[(4-hydroxyphenyl)methylidene]furan-2-one

C17H11BrO4 (357.9841)

17-thia-1,11,14-triazahexacyclo[10.9.2.0²,⁷.0⁸,²³.0¹³,¹⁸.0¹⁹,²²]tricosa-2(7),3,5,8(23),9,11,13(18),14,19(22),20-decaen-15-ol

C19H11N3OS (329.0623)

n-{2-[(4s)-2-iminoimidazolidin-4-yl]ethyl}-9h-pyrido[3,4-b]indole-3-carboxamide

C17H18N6O (322.1542)

7-hydroxy-12-(3-hydroxy-4-methoxyphenyl)-8,16,17-trimethoxy-4-oxa-1-azapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-2(11),5(10),6,8,12,14,16,18-octaen-3-one

C29H25NO8 (515.158)

(12e,19z,21e)-24-[(3z)-5-[2-(2,3-dimethyloxiran-2-yl)-1,3-thiazol-4-yl]-2-hydroxy-4-methylpent-3-en-2-yl]-8,16,17-trihydroxy-18-methoxy-3,6,9,11,15,19,23-heptamethyl-2,10-dioxo-1-oxacyclotetracosa-12,19,21-trien-3-yl 3-hydroxy-2-methylbutanoate

C49H77NO12S (903.5166)