Exact Mass: 246.081

Exact Mass Matches: 246.081

Found 500 metabolites which its exact mass value is equals to given mass value 246.081, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Marmesin

(2S)-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one

C14H14O4 (246.0892)


Marmesin is a member of psoralens and a tertiary alcohol. 2-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one is a natural product found in Zanthoxylum beecheyanum, Zanthoxylum arnottianum, and other organisms with data available. Nodakenetin is found in wild celery. Nodakenetin is a constituent of Angelica species Constituent of Angelica subspecies Nodakenetin is found in wild celery. (+)-marmesin is a marmesin. It is an enantiomer of a nodakenetin. Marmesin is a natural product found in Coronilla scorpioides, Clausena dunniana, and other organisms with data available. S-(+)-Marmesin is a natural coumarin, exhibiting COX-2/5-LOX dual inhibitory activity. (+)-Marmesin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=13849-08-6 (retrieved 2024-09-04) (CAS RN: 13849-08-6). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

Aegelinol

2-butenoic acid, 2-methyl-, (7S)-7,8-dihydro-8,8-dimethyl-2-oxo-2H,6H-benzo(1,2-b:5,4-b)dipyran-7-yl ester, (2Z)-

C14H14O4 (246.0892)


Decursinol is an organic heterotricyclic compound that is 7,8-dihydro-2H,6H-pyrano[3,2-g]chromen-2-one substituted by a beta-hydroxy group at position 7 and two methyl groups at position 8. It is isolated from the roots of Angelica gigas and has been found to possess significant inhibitory activity against acetylcholinesterase enzyme (EC 3.1.1.7). It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor, an antineoplastic agent, an analgesic and a metabolite. It is an organic heterotricyclic compound, a delta-lactone, a secondary alcohol and a cyclic ether. Decursinol is a natural product found in Smyrniopsis aucheri, Phlojodicarpus villosus, and other organisms with data available. Aegelinol is found in fruits. Aegelinol is obtained from Aegle marmelos (bael fruit). obtained from Aegle marmelos (bael fruit). Aegelinol is found in fruits. D020536 - Enzyme Activators (±)-Decursinol is a potent FtsZ inhibitor. (±)-Decursinol inhibits B. anthracis FtsZ polymerization with an IC50 of 102 μM[1]. (±)-Decursinol is a potent FtsZ inhibitor. (±)-Decursinol inhibits B. anthracis FtsZ polymerization with an IC50 of 102 μM[1]. Decursinol, isolated from the roots of Angelica gigas, possesses antinociceptive effect with orally bioavailability. Decursinol possesses anti-tumor and anti-metastasis activity[1]. Decursinol, isolated from the roots of Angelica gigas, possesses antinociceptive effect with orally bioavailability. Decursinol possesses anti-tumor and anti-metastasis activity[1].

   

Nodakenetic

7H-Furo[3,2g][1]-benzopyran-7-one, (-2,3-dihydro-2-(1-hydroxy-1-hydroxymethylethyl)-, (R)

C14H14O4 (246.0892)


Nodakenetic, also known as (-)-marmesin or marmesin, (R)-isomer, is a member of the class of compounds known as psoralens. Psoralens are organic compounds containing a psoralen moiety, which consists of a furan fused to a chromenone to for 7H-furo[3,2-g]chromen-7-one. Nodakenetic is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Nodakenetic can be found in wild celery, which makes nodakenetic a potential biomarker for the consumption of this food product. Nodakenetin is a marmesin with R-configuration. It has a role as a plant metabolite, a rat metabolite and a xenobiotic metabolite. It is an enantiomer of a (+)-marmesin. Nodakenetin is a natural product found in Zanthoxylum beecheyanum, Melicope barbigera, and other organisms with data available. Nodakenetin, isolated from Angelica decursiva, possesses antioxidant anti-inflammatory activities. Nodakenetin has the potential to be an antiarthritic and nerve tonic[1][2]. Nodakenetin, isolated from Angelica decursiva, possesses antioxidant anti-inflammatory activities. Nodakenetin has the potential to be an antiarthritic and nerve tonic[1][2]. S-(+)-Marmesin is a natural coumarin, exhibiting COX-2/5-LOX dual inhibitory activity. S-(+)-Marmesin is a natural coumarin, exhibiting COX-2/5-LOX dual inhibitory activity. S-(+)-Marmesin is a natural coumarin, exhibiting COX-2/5-LOX dual inhibitory activity.

   

Columbianetin

2H-Furo[2,3-h]-1-benzopyran-2-one, 8,9-dihydro-8-(1-hydroxy-1-methylethyl)-, (S)-(+)-

C14H14O4 (246.0892)


D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins (S)-columbianetin is the (S)-(+)-enantiomer of columbianetin. It is an enantiomer of a (R)-columbianetin. Columbianetin is a natural product found in Campylotropis hirtella, Prangos tschimganica, and other organisms with data available. (+)-Columbianetin is an isomer of Columbianetin. Columbianetin is a phytoalexin associated with celery (Apium graveolens) resistance to pathogens during storage. Columbianetin exhibits excellent anti-fungal and anti-inflammatory activity[1][2]. (+)-Columbianetin is an isomer of Columbianetin. Columbianetin is a phytoalexin associated with celery (Apium graveolens) resistance to pathogens during storage. Columbianetin exhibits excellent anti-fungal and anti-inflammatory activity[1][2]. (+)-Columbianetin is an isomer of Columbianetin. Columbianetin is a phytoalexin associated with celery (Apium graveolens) resistance to pathogens during storage. Columbianetin exhibits excellent anti-fungal and anti-inflammatory activity[1][2]. (+)-Columbianetin is an isomer of Columbianetin. Columbianetin is a phytoalexin associated with celery (Apium graveolens) resistance to pathogens during storage. Columbianetin exhibits excellent anti-fungal and anti-inflammatory activity[1][2].

   

Torachrysone

1-(6-Methoxy-3-methyl-1,8-bis(oxidanyl)naphthalen-2-yl)ethanone

C14H14O4 (246.0892)


Torachrysone is a member of naphthols. Torachrysone is a natural product found in Rheum palmatum, Rumex japonicus, and other organisms with data available. Isolated from seeds of Cassia tora (charota). Torachrysone is found in coffee and coffee products, herbs and spices, and pulses. Torachrysone is found in coffee and coffee products. Torachrysone is isolated from seeds of Cassia tora (charota).

   

N-Acetyltryptophan

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

C13H14N2O3 (246.1004)


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

   

Floxuridine

5-fluoro-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,3,4-tetrahydropyrimidine-2,4-dione

C9H11FN2O5 (246.0652)


An antineoplastic antimetabolite that is metabolized to fluorouracil when administered by rapid injection. Floxuridine is available as a sterile, nonpyrogenic, lyophilized powder for reconstitution. When administered by slow, continuous, intra-arterial infusion, it is converted to floxuridine monophosphate. It has been used to treat hepatic metastases of gastrointestinal adenocarcinomas and for palliation in malignant neoplasms of the liver and gastrointestinal tract. [PubChem] L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01B - Antimetabolites > L01BC - Pyrimidine analogues C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents Floxuridine (5-Fluorouracil 2'-deoxyriboside) is a?pyrimidine?analog?and known as an?oncology antimetabolite. Floxuridine inhibits Poly(ADP-Ribose) polymerase and induces DNA damage by activating the ATM and ATR checkpoint signaling pathways in vitro. Floxuridine is a extreamly potent inhibitor for S. aureus infection and induces cell apoptosis[1][2]. Floxuridine has antiviral effects against HSV and CMV[3].

   

Methylphenobarbital

5-Ethyl-1-methyl-5-phenyl-2,4,6(1H,3H,5H)-pyrimidinetrione

C13H14N2O3 (246.1004)


Methylphenobarbital is only found in individuals that have used or taken this drug. It is a barbiturate that is metabolized to phenobarbital. It has been used for similar purposes, especially in epilepsy, but there is no evidence mephobarbital offers any advantage over phenobarbital. [PubChem]Methylphenobarbital binds at a distinct binding site associated with a Cl- ionopore at the GABAA receptor, increasing the duration of time for which the Cl- ionopore is open. The post-synaptic inhibitory effect of GABA in the thalamus is, therefore, prolonged. D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants > D006993 - Hypnotics and Sedatives N - Nervous system > N03 - Antiepileptics > N03A - Antiepileptics > N03AA - Barbiturates and derivatives C78272 - Agent Affecting Nervous System > C29756 - Sedative and Hypnotic > C67084 - Barbiturate D018377 - Neurotransmitter Agents > D018682 - GABA Agents > D018757 - GABA Modulators D002491 - Central Nervous System Agents > D000927 - Anticonvulsants

   

5'-Deoxy-5-fluorouridine

1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-methyloxolan-2-yl]-5-fluoro-4-hydroxy-1,2-dihydropyrimidin-2-one

C9H11FN2O5 (246.0652)


5-Deoxy-5-fluorouridine is a metabolite of capecitabine. Capecitabine (Xeloda, Roche) is an orally-administered chemotherapeutic agent used in the treatment of metastatic breast and colorectal cancers. Capecitabine is a prodrug, that is enzymatically converted to 5-fluorouracil in the tumor, where it inhibits DNA synthesis and slows growth of tumor tissue. (Wikipedia) D002491 - Central Nervous System Agents > D000697 - Central Nervous System Stimulants > D019167 - Appetite Stimulants C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents Same as: D01309 Doxifluridine has anticancer activity. Doxifluidine is a 5-FU prodrug. Doxifluridine is a thymidine synthase inhibitor. Doxifluridine can enhance tumor inhibition by synergizing with a variety of drugs[1][2][3].

   

N-[(4-Chlorophenyl)methyl]-N-ethyl-2-pyridinamine

N-[(4-Chlorophenyl)methyl]-N-ethyl-2-pyridinamine

C14H15ClN2 (246.0924)


   

(2~{S})-3-(2-oxidanylsulfanyl-1~{H}-imidazol-4-yl)-2-(trimethyl-$l^{4}-azanyl)propanoic acid

(2~{S})-3-(2-oxidanylsulfanyl-1~{H}-imidazol-4-yl)-2-(trimethyl-$l^{4}-azanyl)propanoic acid

C9H16N3O3S+ (246.0912)


   

Naphazoline hydrochloride

Naphazoline hydrochloride (Naphcon)

C14H15ClN2 (246.0924)


C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C87053 - Adrenergic Agonist D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists D019141 - Respiratory System Agents > D014663 - Nasal Decongestants D002317 - Cardiovascular Agents > D014662 - Vasoconstrictor Agents Naphazoline (Naphthazoline) hydrochloride is a potent α-adrenergic receptor agonist. Naphazoline hydrochloride reduces vascular hyperpermeability and promotes vasoconstriction. Naphazoline hydrochloride reduces the levels of inflammatory factors (TNF-α, IL-1β and IL-6), cytokines (IFN-γ and IL-4), IgE, GMCSF, and NGF。Naphazoline hydrochloride can be used for non-bacterial conjunctivitis research[1][2].

   

7-hydroxy-8-(2-hydroxy-3-methylbut-3-en-1-yl)-2H-chromen-2-one

7-hydroxy-8-(2-hydroxy-3-methylbut-3-en-1-yl)-2H-chromen-2-one

C14H14O4 (246.0892)


   

7-hydroxy-6-(3-hydroxy-3-methylbut-1-en-1-yl)-2H-chromen-2-one

7-hydroxy-6-(3-hydroxy-3-methylbut-1-en-1-yl)-2H-chromen-2-one

C14H14O4 (246.0892)


   

7,8-dihydroxy-6-(3-methylbut-2-en-1-yl)-2H-chromen-2-one

7,8-dihydroxy-6-(3-methylbut-2-en-1-yl)-2H-chromen-2-one

C14H14O4 (246.0892)


   

N2-Oxalylarginine

5-carbamimidamido-2-(carboxyformamido)pentanoic acid

C8H14N4O5 (246.0964)


Constituent of the shoots of apple and pear trees (Malus subspecies). N2-Oxalylarginine is found in malus (crab apple) and pomes. N2-Oxalylarginine is found in pomes. N2-Oxalylarginine is a constituent of the shoots of apple and pear trees (Malus species).

   

Nigellicine

1-hydroxy-3-methyl-6H,7H,8H,9H-10λ⁵-pyridazino[1,2-a]indazol-10-ylium-11-carboxylate

C13H14N2O3 (246.1004)


Nigellicine is found in herbs and spices. Nigellicine is an alkaloid from the seeds of Nigella sativa (black cumin

   

Corticrocin

(2Z,4E,6Z,8E,10E,12Z)-tetradeca-2,4,6,8,10,12-hexaenedioic acid

C14H14O4 (246.0892)


Isolated from paprika (Capsicum annuum). Corticrocin is found in many foods, some of which are yellow bell pepper, orange bell pepper, herbs and spices, and red bell pepper. Corticrocin is found in herbs and spices. Corticrocin is isolated from paprika (Capsicum annuum

   

Dihydrowyerone acid

(2Z)-3-[5-(hept-2-ynoyl)furan-2-yl]prop-2-enoic acid

C14H14O4 (246.0892)


Dihydrowyerone acid is found in pulses. Dihydrowyerone acid is a constituent of broad bean Vicia faba infected with Botrytis species. Constituent of broad bean Vicia faba infected with Botrytis subspecies Dihydrowyerone acid is found in pulses.

   

5,6-Dihydrouridine

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

C9H14N2O6 (246.0852)


Dihydrouridine is a pyrimidine which is the result of adding two hydrogen atoms to a uridine. Dihydrouridine is found only in tRNA molecules. An inhibitor of nucleotide metabolism. [HMDB] Dihydrouridine (abbreviated as D,[1] DHU, or UH2) is a pyrimidine nucleoside which is the result of adding two hydrogen atoms to a uridine, making it a fully saturated pyrimidine ring with no remaining double bonds. D is found in tRNA and rRNA molecules as a nucleoside; the corresponding nucleobase is 5,6-dihydrouracil. Because it is non-planar, D disturbs the stacking interactions in helices and destabilizes the RNA structure. D also stabilizes the C2’-endo sugar conformation, which is more flexible than the C3’-endo conformation; this effect is propagated to the 5’-neighboring residue. Thus, while pseudouridine and 2’-O-methylations stabilize the local RNA structure, D does the opposite.[2] The tRNAs of organisms that grow at low temperatures (psychrophiles) have high 5,6-dihydrouridine levels (40-70\\\% more on average) which provides the necessary local flexibility of the tRNA at or below the freezing point.[3] Dihydrouridine. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=5627-05-4 (retrieved 2024-07-01) (CAS RN: 5627-05-4). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). 5,6-Dihydrouridine is a modified base found in conserved positions in the D-loop of tRNA in Bacteria, Eukaryota, and some Archaea. 5,6-Dihydrouridine is a modified base found in conserved positions in the D-loop of tRNA in Bacteria, Eukaryota, and some Archaea.

   

Aspartylhydroxyproline

(2S,4R)-1-[(2S)-2-amino-3-carboxypropanoyl]-4-hydroxypyrrolidine-2-carboxylic acid

C9H14N2O6 (246.0852)


Aspartylhydroxyproline is a dipeptide found in urine (PMID: 3782411). It is likely a proteolytic breakdown product of collagen. Aspartylhydroxyproline belongs to the family of peptides. These are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by the formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another. L-alpha-Aspartyl-L-hydroxyproline is a dipeptide found in urine (PMID: 3782411). It is likely a proteolytic breakdown product of collagen. [HMDB]

   

Asparaginylasparagine

(2S)-2-[(2S)-2-amino-3-carbamoylpropanamido]-3-carbamoylpropanoic acid

C8H14N4O5 (246.0964)


Asparaginylasparagine is a dipeptide composed of two asparagine residues. It is an incomplete breakdown product of protein digestion or protein catabolism. Some dipeptides are known to have physiological or cell-signaling effects although most are simply short-lived intermediates on their way to specific amino acid degradation pathways following further proteolysis.

   

cyclic 6-Hydroxymelatonin

1-{6-hydroxy-5-methoxy-1H,2H,3H,8H-pyrrolo[2,3-b]indol-1-yl}ethan-1-one

C13H14N2O3 (246.1004)


cyclic 6-Hydroxymelatonin is a metabolite of melatonin. Melatonin Listen/ˌmɛləˈtoʊnɪn/, also known chemically as N-acetyl-5-methoxytryptamine, is a naturally occurring compound found in animals, plants, and microbes. In animals, circulating levels of the hormone melatonin vary in a daily cycle, thereby allowing the entrainment of the circadian rhythms of several biological functions. (Wikipedia)

   

1-(3,4-Dihydroxy-5-methyl-2-oxolanyl)-5-fluoropyrimidine-2,4-dione

1-(3,4-dihydroxy-5-methyloxolan-2-yl)-5-fluoro-1,2,3,4-tetrahydropyrimidine-2,4-dione

C9H11FN2O5 (246.0652)


   

8,9-Dihydro-8-(1-hydroxy-1-methylethyl)-2H-furo[2,3-h]1-benzopyran-2-one

8,9-Dihydro-8-(1-hydroxy-1-methylethyl)-2H-furo[2,3-h]1-benzopyran-2-one

C14H14O4 (246.0892)


   

3-Phenylacetylamino-2,6-piperidinedione

N-(2,6-dioxopiperidin-3-yl)-2-phenylacetamide

C13H14N2O3 (246.1004)


   

5-Ethyl-5-p-tolylbarbituric acid

5-ethyl-5-(4-methylphenyl)-1,3-diazinane-2,4,6-trione

C13H14N2O3 (246.1004)


   

5-Fluoro-1-[(2R,4R,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]pyrimidine-2,4-dione

5-Fluoro-1-[(2R,4R,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]pyrimidine-2,4-dione

C9H11FN2O5 (246.0652)


   

5,6-Dihydro-5-azacytidine

6-amino-3-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,3,4-tetrahydro-1,3,5-triazin-2-one

C8H14N4O5 (246.0964)


   

5,6-Dihydro-5'-azacytidine

4-amino-1-[3,4-dihydroxy-5-(hydroxyamino)oxolan-2-yl]-1,2,5,6-tetrahydropyrimidin-2-one

C8H14N4O5 (246.0964)


   

5'-Deoxy-5'-fluorouridine

1-[5-(fluoromethyl)-3,4-dihydroxyoxolan-2-yl]-1,2,3,4-tetrahydropyrimidine-2,4-dione

C9H11FN2O5 (246.0652)


   

Hydrazinecarbothioamide,2-[2-[2-(aminothioxomethyl)-2-methylhydrazinylidene]propylidene]-N-methyl-

Hydrazinecarbothioamide,2-[2-[2-(aminothioxomethyl)-2-methylhydrazinylidene]propylidene]-N-methyl-

C7H14N6S2 (246.0721)


   

Coumarin A

7-[(4-hydroxy-3-methylbut-1-en-1-yl)oxy]-2H-chromen-2-one

C14H14O4 (246.0892)


   

Diallyl phthalate

1,2-bis(prop-2-en-1-yl) benzene-1,2-dicarboxylate

C14H14O4 (246.0892)


   

indolepropionylglycine

2-[3-(1H-indol-2-yl)propanoylamino]acetic acid

C13H14N2O3 (246.1004)


   

N-Acetyl-D-tryptophan

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

C13H14N2O3 (246.1004)


   

S-Nitrosocaptopril

1-[2-Methyl-3-(nitrososulphanyl)propanoyl]pyrrolidine-2-carboxylic acid

C9H14N2O4S (246.0674)


   

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

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

C9H14N2O6 (246.0852)


   

Glycylglycylglycylglycine

2-{[2-({2-[(2-amino-1-hydroxyethylidene)amino]-1-hydroxyethylidene}amino)-1-hydroxyethylidene]amino}acetate

C8H14N4O5 (246.0964)


   

trioxyethylene dimethacrylate

2-{[(2-methylprop-2-enoyl)peroxy]peroxy}ethyl 2-methylprop-2-enoic acid

C10H14O7 (246.0739)


D013501 - Surface-Active Agents > D011092 - Polyethylene Glycols D001697 - Biomedical and Dental Materials

   

(+)-marmesin

3-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one

C14H14O4 (246.0892)


(+)-marmesin is a member of the class of compounds known as psoralens. Psoralens are organic compounds containing a psoralen moiety, which consists of a furan fused to a chromenone to for 7H-furo[3,2-g]chromen-7-one (+)-marmesin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (+)-marmesin can be found in a number of food items such as common wheat, mango, broad bean, and rubus (blackberry, raspberry), which makes (+)-marmesin a potential biomarker for the consumption of these food products.

   

benzyl-6-hydroxy-2-cyclohexene-on-oyl

Benzyl 1-hydroxy-6-oxocyclohex-2-ene-1-carboxylic acid

C14H14O4 (246.0892)


Benzyl-6-hydroxy-2-cyclohexene-on-oyl, also known as benzyl-hch, is a member of the class of compounds known as benzyloxycarbonyls. Benzyloxycarbonyls are organic compounds containing a carbonyl group substituted with a benzyloxyl group. Benzyl-6-hydroxy-2-cyclohexene-on-oyl is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Benzyl-6-hydroxy-2-cyclohexene-on-oyl can be found in a number of food items such as sunflower, american pokeweed, tea, and black cabbage, which makes benzyl-6-hydroxy-2-cyclohexene-on-oyl a potential biomarker for the consumption of these food products.

   

Hydroxykavain

Hydroxykavain

C14H14O4 (246.0892)


   
   

7-Hydroxy-6-(2-(R)-hydroxy-3-methylbut-3-enyl)coumarin

7-Hydroxy-6-(2-(R)-hydroxy-3-methylbut-3-enyl)coumarin

C14H14O4 (246.0892)


   

Dihydrooxyresveratrol

2,3,4,5-Tetrahydroxystilbene

C14H14O4 (246.0892)


   
   

Norpinguisanolide

Norpinguisanolide

C14H14O4 (246.0892)


   

fraxinellonone

fraxinellonone

C14H14O4 (246.0892)


   

6-(4-hydroxy-3-methyl-2-butenyl)-7-hydroxy coumarin

6-(4-hydroxy-3-methyl-2-butenyl)-7-hydroxy coumarin

C14H14O4 (246.0892)


   

Isoarnottinin

Isoarnottinin

C14H14O4 (246.0892)


   
   

Mansouramycin C

Mansouramycin C

C12H10N2O4 (246.0641)


   

Hyrtioerectine B

Hyrtioerectine B

C13H14N2O3 (246.1004)


   

Dihydropiceatannol

3,3,4,5-Tetrahydroxybibenzyl

C14H14O4 (246.0892)


   

Phaeochromycin E

Phaeochromycin E

C14H14O4 (246.0892)


   
   

2-Methoxy-4-oxo-6-phenyl-hexa-2,5-dienoic acid methyl ester

2-Methoxy-4-oxo-6-phenyl-hexa-2,5-dienoic acid methyl ester

C14H14O4 (246.0892)


   

2-hydroxy-3 ,6-dimethyl-5-( 1-oxo-2,4-hexadienyl)-1 ,4-benzoquinone

2-hydroxy-3 ,6-dimethyl-5-( 1-oxo-2,4-hexadienyl)-1 ,4-benzoquinone

C14H14O4 (246.0892)


   

Mansorin III

Mansorin III

C14H14O4 (246.0892)


   

Hibiscoquinone B

Hibiscoquinone B

C14H14O4 (246.0892)


   

anisocoumarin B

anisocoumarin B

C14H14O4 (246.0892)


   

Antrocinnamomin C

Antrocinnamomin C

C14H14O4 (246.0892)


   

(R)-(+)-7-Hydroxy-8-(2-hydroxy-3-methyl-3-butenyl)-2H-1-benzopyran-2-one

(R)-(+)-7-Hydroxy-8-(2-hydroxy-3-methyl-3-butenyl)-2H-1-benzopyran-2-one

C14H14O4 (246.0892)


   

DIALLYL PHTHALATE

POLY(DIALLYL PHTHALATE)

C14H14O4 (246.0892)


CONFIDENCE standard compound; INTERNAL_ID 8370

   

N-(3-Indolylacetyl)-L-alanine

N-(3-Indolylacetyl)-L-alanine

C13H14N2O3 (246.1004)


   

N-(6-methoxyquinolin-8-yl)alanine

N-(6-methoxyquinolin-8-yl)alanine

C13H14N2O3 (246.1004)


   

DTXSID70837683

DTXSID70837683

C14H14O4 (246.0892)


   

Lomatin

Lomatin

C14H14O4 (246.0892)


Origin: Plant, Coumarins

   

UNII-3U9JG90P8B

UNII-3U9JG90P8B

C14H14O4 (246.0892)


   

CHEMBL221291

CHEMBL221291

C14H14O4 (246.0892)


   

6-deoxyhaplopinol|7-[(E)-3-methyl-4-hydroxy-2-butenyloxy]coumarin

6-deoxyhaplopinol|7-[(E)-3-methyl-4-hydroxy-2-butenyloxy]coumarin

C14H14O4 (246.0892)


   

Demethylnieshoutin

Demethylnieshoutin

C14H14O4 (246.0892)


   
   

Platypodantherone

Platypodantherone

C14H14O4 (246.0892)


   

4,5,6-trimethoxy-2-naphthaldehyde

4,5,6-trimethoxy-2-naphthaldehyde

C14H14O4 (246.0892)


   
   

Dihydropinosylvindiol

Dihydropinosylvindiol

C14H14O4 (246.0892)


   

DTXSID60996152

DTXSID60996152

C14H14O4 (246.0892)


   

aspergillusol

aspergillusol

C14H14O4 (246.0892)


   

4-Hydroxy-2-methoxy-5-(1-oxo-2,4-hexadienyl)-benzaldehyde

4-Hydroxy-2-methoxy-5-(1-oxo-2,4-hexadienyl)-benzaldehyde

C14H14O4 (246.0892)


   
   

Garcibiphenyl C

Garcibiphenyl C

C14H14O4 (246.0892)


   

isotorachrysone

isotorachrysone

C14H14O4 (246.0892)


   
   

Quinolonic acid

Quinolonic acid

C12H10N2O4 (246.0641)


   

1-(5-formyl-2-hydroxy-4-methoxyphenyl)-E,E-2,4-hexadien-1-one|5-Formyl-2-hydroxy-4-methoxy-(E,E)-sorbophenon|5-formyl-2-hydroxyl-4-methoxy-(E,E)-sorbophenone

1-(5-formyl-2-hydroxy-4-methoxyphenyl)-E,E-2,4-hexadien-1-one|5-Formyl-2-hydroxy-4-methoxy-(E,E)-sorbophenon|5-formyl-2-hydroxyl-4-methoxy-(E,E)-sorbophenone

C14H14O4 (246.0892)


   

Umbelliferone-(3-hydroxymethyl-1t.-buten-1-yl)-ether|Umbelliferone-<3-hydroxymethyl-1t.-buten-1-yl>-ether

Umbelliferone-(3-hydroxymethyl-1t.-buten-1-yl)-ether|Umbelliferone-<3-hydroxymethyl-1t.-buten-1-yl>-ether

C14H14O4 (246.0892)


   
   

Tetrahydrocyperaquinone

Tetrahydrocyperaquinone

C14H14O4 (246.0892)


   

UEPYGMLWWBFEIC-UHFFFAOYSA-

UEPYGMLWWBFEIC-UHFFFAOYSA-

C14H14O4 (246.0892)


   

bis-(4-hydroxybenzyl)sulfide

bis-(4-hydroxybenzyl)sulfide

C14H14O2S (246.0714)


An organic sulfide that consists of two 4-hydroxybenzyl groups covalently bound to a central sulfur atom. It is isolated from Gastrodia elata and Pleuropterus ciliinervis and exhibits neoroprotective activity.

   

(1,1-Biphenyl)-3,4-diol, 4,5-dimethoxy-

(1,1-Biphenyl)-3,4-diol, 4,5-dimethoxy-

C14H14O4 (246.0892)


   

Eriosematin A

Eriosematin A

C14H14O4 (246.0892)


   

Multistatin

Multistatin

C14H14O4 (246.0892)


   

Methyl 2-(5-acetyl-2,3-dihydrobenzofuran-2-yl)propenoate

Methyl 2-(5-acetyl-2,3-dihydrobenzofuran-2-yl)propenoate

C14H14O4 (246.0892)


   

UNII-B6E1JXI8DF

UNII-B6E1JXI8DF

C14H14O4 (246.0892)


   

acetic acid (2E,8Z)-10-acetoxydeca-2,8-diene-4,6-diyn-1-yl ester

acetic acid (2E,8Z)-10-acetoxydeca-2,8-diene-4,6-diyn-1-yl ester

C14H14O4 (246.0892)


   

(-)-(1R,3S)-7-hydroxy-1-methyl-2,3,4,9-tetrahydro-1H-beta-carboline-3-carboxylic acid|brunnein B

(-)-(1R,3S)-7-hydroxy-1-methyl-2,3,4,9-tetrahydro-1H-beta-carboline-3-carboxylic acid|brunnein B

C13H14N2O3 (246.1004)


   

6-acetyl-8-methoxy-2,3-dimethylchromen-4-one

6-acetyl-8-methoxy-2,3-dimethylchromen-4-one

C14H14O4 (246.0892)


   

Caerulomycin G

Caerulomycin G

C13H14N2O3 (246.1004)


A pyridine alkaloid that is 2,2-bipyridine substituted at position 6 by a hydroxymethyl group and at positions 3 and 4 by methoxy groups respectively. Isolated from the marine-derived actinomycete Actinoalloteichus cyanogriseus, it exhibits antineoplastic activity.

   

4,4-Biguaiacol

4,4-Biguaiacol

C14H14O4 (246.0892)


   

[1,1-Biphenyl]-2,2-diol, 6,6-dimethoxy-

[1,1-Biphenyl]-2,2-diol, 6,6-dimethoxy-

C14H14O4 (246.0892)


   

cyclo-L-Pro-L-Tyr

cyclo-L-Pro-L-Tyr

C13H14N2O3 (246.1004)


   

coniochaetone C

coniochaetone C

C14H14O4 (246.0892)


   

citrinolactone D

citrinolactone D

C14H14O4 (246.0892)


   

5-methoxy-6-methyl-biphenyl-3,4,3-triol

5-methoxy-6-methyl-biphenyl-3,4,3-triol

C14H14O4 (246.0892)


   

hyrtioreticulin D

hyrtioreticulin D

C13H14N2O3 (246.1004)


   

1-(p-hydroxybenzyl-)-2-methoxybenzene-3,4-diol|stenocephol

1-(p-hydroxybenzyl-)-2-methoxybenzene-3,4-diol|stenocephol

C14H14O4 (246.0892)


   

Ehreticoumarin

Ehreticoumarin

C14H14O4 (246.0892)


   
   

phthalidochromene|phthalidochromine

phthalidochromene|phthalidochromine

C14H14O4 (246.0892)


   

(R)-(+)-7-(2,3-epoxy-3-methylbutoxy)coumarin|(R)-(+)-7-(2,3-epoxy-3-methylbutoxy)-coumarin

(R)-(+)-7-(2,3-epoxy-3-methylbutoxy)coumarin|(R)-(+)-7-(2,3-epoxy-3-methylbutoxy)-coumarin

C14H14O4 (246.0892)


   

7-methoxyplatypterophthalide

7-methoxyplatypterophthalide

C14H14O4 (246.0892)


   

4,5,8-Trimethoxy-2-naphthaldehyd

4,5,8-Trimethoxy-2-naphthaldehyd

C14H14O4 (246.0892)


   

2,3,4-Trihydroxy-5,6-dimethyldiphenyl ether

2,3,4-Trihydroxy-5,6-dimethyldiphenyl ether

C14H14O4 (246.0892)


   

AKOS000277841

AKOS000277841

C14H14O4 (246.0892)


   

Cordyol C

Cordyol C

C14H14O4 (246.0892)


A catechol that is 5-methylbenzene-1,2-diol bearing a 3-hydroxy-5-methylphenoxy substituent at position 3.

   

Di-Me ether-6,7-Dihydroxy-2,3-dimethyl-1,4-naphthoquinone

Di-Me ether-6,7-Dihydroxy-2,3-dimethyl-1,4-naphthoquinone

C14H14O4 (246.0892)


   
   

compound 7 [PMID: 21334791]

compound 7 [PMID: 21334791]

C14H14O4 (246.0892)


   

9-hydroxycaleteucrin

9-hydroxycaleteucrin

C14H14O4 (246.0892)


   

3-Hydroxy-7-hydroxy-8-(3-methyl-2-butenyl)-2H-1-benzopyran-2-one

3-Hydroxy-7-hydroxy-8-(3-methyl-2-butenyl)-2H-1-benzopyran-2-one

C14H14O4 (246.0892)


   

8-(2-Thienyl)-3t,5t-octadien-7-in-1-ol-acetat|Ac-(3E,5E)-8-(2-Thienyl)-3,5-octadien-7-yl-1-ol

8-(2-Thienyl)-3t,5t-octadien-7-in-1-ol-acetat|Ac-(3E,5E)-8-(2-Thienyl)-3,5-octadien-7-yl-1-ol

C14H14O2S (246.0714)


   

5-acetyl-2-isopropylidene-6-methoxy-benzofuran-3-one

5-acetyl-2-isopropylidene-6-methoxy-benzofuran-3-one

C14H14O4 (246.0892)


   
   

7-(2-hydroxy-3-methylbut-3-epoxy)-coumarin

7-(2-hydroxy-3-methylbut-3-epoxy)-coumarin

C14H14O4 (246.0892)


   

6-(Prenyloxy)-7-hydroxy-2H-1-benzopyran-2-one

6-(Prenyloxy)-7-hydroxy-2H-1-benzopyran-2-one

C14H14O4 (246.0892)


   
   

2-hydroxyaucuparin

2-hydroxyaucuparin

C14H14O4 (246.0892)


   
   

2-[(2-methylsulfanyl)hexyl]maleate

2-[(2-methylsulfanyl)hexyl]maleate

C11H18O4S (246.0926)


   

benzyl 1-hydroxy-6-oxocyclohex-2-ene-1-carboxylate

benzyl 1-hydroxy-6-oxocyclohex-2-ene-1-carboxylate

C14H14O4 (246.0892)


   
   

Aegelinol

12-hydroxy-13,13-dimethyl-4,14-dioxatricyclo[8.4.0.0³,⁸]tetradeca-1(10),2,6,8-tetraen-5-one

C14H14O4 (246.0892)


Aegelinol is a member of coumarins. Aegelinol is a natural product found in Phlojodicarpus villosus and Angelica gigas with data available. Aegelinol is found in fruits. Aegelinol is obtained from Aegle marmelos (bael fruit). obtained from Aegle marmelos (bael fruit). Aegelinol is found in fruits. (±)-Decursinol is a potent FtsZ inhibitor. (±)-Decursinol inhibits B. anthracis FtsZ polymerization with an IC50 of 102 μM[1]. (±)-Decursinol is a potent FtsZ inhibitor. (±)-Decursinol inhibits B. anthracis FtsZ polymerization with an IC50 of 102 μM[1].

   

Indole-3-acetyl-L-alanine

N-(3-Indolylacetyl)-L-alanine

C13H14N2O3 (246.1004)


Annotation level-1

   

(2S)-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one

NCGC00178117-02!(2S)-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one

C14H14O4 (246.0892)


   

8-(2-hydroxypropan-2-yl)-8,9-dihydrofuro[2,3-h]chromen-2-one

NCGC00384660-01!8-(2-hydroxypropan-2-yl)-8,9-dihydrofuro[2,3-h]chromen-2-one

C14H14O4 (246.0892)


   

2-acetamido-3-(1H-indol-3-yl)propanoic acid

NCGC00180645-03!2-acetamido-3-(1H-indol-3-yl)propanoic acid

C13H14N2O3 (246.1004)


   

PRI_247.1079_16.2

PRI_247.1079_16.2

C13H14N2O3 (246.1004)


CONFIDENCE Tentative identification: most likely structure (Level 3); INTERNAL_ID 1602 INTERNAL_ID 1602; CONFIDENCE Tentative identification: most likely structure (Level 3)

   

nodakenetin

nodakenetin

C14H14O4 (246.0892)


Nodakenetin, isolated from Angelica decursiva, possesses antioxidant anti-inflammatory activities. Nodakenetin has the potential to be an antiarthritic and nerve tonic[1][2]. Nodakenetin, isolated from Angelica decursiva, possesses antioxidant anti-inflammatory activities. Nodakenetin has the potential to be an antiarthritic and nerve tonic[1][2].

   

N-Acetyltryptophan

N-Acetyl-DL-tryptophan

C13H14N2O3 (246.1004)


An N-acetylamino acid that is the N-acetyl derivative of tryptophan. Ac-DL-Trp-OH is an endogenous metabolite. Ac-DL-Trp-OH is an endogenous metabolite. N-Acetyl-L-tryptophan is an endogenous metabolite.

   

C14H14O4_2H-Pyran-2-one, 5,6-dihydro-5-hydroxy-4-methoxy-6-[(E)-2-phenylethenyl]-, (5S,6S)

NCGC00169621-02_C14H14O4_2H-Pyran-2-one, 5,6-dihydro-5-hydroxy-4-methoxy-6-[(E)-2-phenylethenyl]-, (5S,6S)-

C14H14O4 (246.0892)


   

(2S,3S)-3-hydroxy-4-methoxy-2-[(E)-2-phenylethenyl]-2,3-dihydropyran-6-one

(2S,3S)-3-hydroxy-4-methoxy-2-[(E)-2-phenylethenyl]-2,3-dihydropyran-6-one

C14H14O4 (246.0892)


   

8-(2-hydroxypropan-2-yl)-8,9-dihydrofuro[2,3-h]chromen-2-one [IIN-based on: CCMSLIB00000848272]

NCGC00384660-01!8-(2-hydroxypropan-2-yl)-8,9-dihydrofuro[2,3-h]chromen-2-one [IIN-based on: CCMSLIB00000848272]

C14H14O4 (246.0892)


   

8-(2-hydroxypropan-2-yl)-8,9-dihydrofuro[2,3-h]chromen-2-one [IIN-based: Match]

NCGC00384660-01!8-(2-hydroxypropan-2-yl)-8,9-dihydrofuro[2,3-h]chromen-2-one [IIN-based: Match]

C14H14O4 (246.0892)


   
   

N-Acetyl-D-tryptophan

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

C13H14N2O3 (246.1004)


D004791 - Enzyme Inhibitors > D011480 - Protease Inhibitors

   

N-Acetyl-tryptophan; LC-tDDA; CE10

N-Acetyl-tryptophan; LC-tDDA; CE10

C13H14N2O3 (246.1004)


   

N-Acetyl-tryptophan; LC-tDDA; CE20

N-Acetyl-tryptophan; LC-tDDA; CE20

C13H14N2O3 (246.1004)


   

N-Acetyl-tryptophan; LC-tDDA; CE30

N-Acetyl-tryptophan; LC-tDDA; CE30

C13H14N2O3 (246.1004)


   

N-Acetyl-tryptophan; LC-tDDA; CE40

N-Acetyl-tryptophan; LC-tDDA; CE40

C13H14N2O3 (246.1004)


   

N-Acetyl-tryptophan; AIF; CE0; CorrDec

N-Acetyl-tryptophan; AIF; CE0; CorrDec

C13H14N2O3 (246.1004)


   

N-Acetyl-tryptophan; AIF; CE10; CorrDec

N-Acetyl-tryptophan; AIF; CE10; CorrDec

C13H14N2O3 (246.1004)


   

N-Acetyl-tryptophan; AIF; CE30; CorrDec

N-Acetyl-tryptophan; AIF; CE30; CorrDec

C13H14N2O3 (246.1004)


   

N-Acetyl-tryptophan; AIF; CE0; MS2Dec

N-Acetyl-tryptophan; AIF; CE0; MS2Dec

C13H14N2O3 (246.1004)


   

N-Acetyl-tryptophan; AIF; CE10; MS2Dec

N-Acetyl-tryptophan; AIF; CE10; MS2Dec

C13H14N2O3 (246.1004)


   

N-Acetyl-tryptophan; AIF; CE30; MS2Dec

N-Acetyl-tryptophan; AIF; CE30; MS2Dec

C13H14N2O3 (246.1004)


   

N-(3-INDOLYLACETYL)-ALANINE

N-(3-INDOLYLACETYL)-ALANINE

C13H14N2O3 (246.1004)


   

Imidazolidine-deoxycytidine

Imidazolidine-deoxycytidine

C9H14N2O6 (246.0852)


   

Gly Gly Gly Gly

2-{2-[2-(2-aminoacetamido)acetamido]acetamido}acetic acid

C8H14N4O5 (246.0964)


   

Didesmethylchlorpheniramine

Didesmethylchlorpheniramine

C14H15ClN2 (246.0924)


   
   
   
   
   

DIHYDRO-OBLIQUIN

DIHYDRO-OBLIQUIN

C14H14O4 (246.0892)


   

56-Dihydrouridine

1-b-D-Ribofuranosylhydrouracil, Dihydrouridine , dihydro-1-b-D-Ribofuranosyl-2,4(1H,3H)-pyrimidinedione

C9H14N2O6 (246.0852)


5,6-Dihydrouridine is a modified base found in conserved positions in the D-loop of tRNA in Bacteria, Eukaryota, and some Archaea. 5,6-Dihydrouridine is a modified base found in conserved positions in the D-loop of tRNA in Bacteria, Eukaryota, and some Archaea.

   

a-Asp-Hyp

L-alpha-Aspartyl-L-hydroxyproline

C9H14N2O6 (246.0852)


   

Asn-asn

2-(2-amino-3-carbamoylpropanamido)-3-carbamoylpropanoic acid

C8H14N4O5 (246.0964)


A dipeptide formed from two L-asparagine units.

   

N2-Oxalylarginine

5-carbamimidamido-2-(carboxyformamido)pentanoic acid

C8H14N4O5 (246.0964)


   

Aegelinol

12-hydroxy-13,13-dimethyl-4,14-dioxatricyclo[8.4.0.0^{3,8}]tetradeca-1(10),2,6,8-tetraen-5-one

C14H14O4 (246.0892)


(±)-Decursinol is a potent FtsZ inhibitor. (±)-Decursinol inhibits B. anthracis FtsZ polymerization with an IC50 of 102 μM[1]. (±)-Decursinol is a potent FtsZ inhibitor. (±)-Decursinol inhibits B. anthracis FtsZ polymerization with an IC50 of 102 μM[1].

   

Corticrocin

(2Z,4E,6Z,8E,10E,12Z)-tetradeca-2,4,6,8,10,12-hexaenedioic acid

C14H14O4 (246.0892)


   

Dihydrowyerone acid

(2Z)-3-[5-(hept-2-ynoyl)furan-2-yl]prop-2-enoic acid

C14H14O4 (246.0892)


   

4,4-dimethyl[1,1-biphenyl]-2,2,5,5-tetrol

4,4-dimethyl[1,1-biphenyl]-2,2,5,5-tetrol

C14H14O4 (246.0892)


   

2,2-diacetamidopentanedioic acid

2,2-diacetamidopentanedioic acid

C9H14N2O6 (246.0852)


   

1,2-BIS(PHENYLPHOSPHINO)ETHANE

1,2-BIS(PHENYLPHOSPHINO)ETHANE

C14H16P2 (246.0727)


   

Benzamide, 5-fluoro-2-hydroxy-N-(5-methyl-2-pyridinyl)- (9CI)

Benzamide, 5-fluoro-2-hydroxy-N-(5-methyl-2-pyridinyl)- (9CI)

C13H11FN2O2 (246.0805)


   

1,4-PHENYLENEDIACRYLIC ACID DIMETHYL ESTER

1,4-PHENYLENEDIACRYLIC ACID DIMETHYL ESTER

C14H14O4 (246.0892)


   

3-[(3-fluorobenzyl)oxy]benzoic acid

3-[(3-fluorobenzyl)oxy]benzoic acid

C14H11FO3 (246.0692)


   

Bis(4-methoxyphenyl) sulfide

Bis(4-methoxyphenyl) sulfide

C14H14O2S (246.0714)


   

5-(2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-2H-PYRAZOLE-3-CARBOXYLIC ACID

5-(2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-2H-PYRAZOLE-3-CARBOXYLIC ACID

C12H10N2O4 (246.0641)


   

4-amino-2-(furan-2-carbonylamino)benzoic acid

4-amino-2-(furan-2-carbonylamino)benzoic acid

C12H10N2O4 (246.0641)


   

1-(4-Chlorobenzyl)piperazine hydrochloride

1-(4-Chlorobenzyl)piperazine hydrochloride

C11H16Cl2N2 (246.069)


   

2-[(3-Fluorophenoxy)methyl]benzoic acid

2-[(3-Fluorophenoxy)methyl]benzoic acid

C14H11FO3 (246.0692)


   

Methyl 4,5-dimethoxy-2-naphthoate

Methyl 4,5-dimethoxy-2-naphthoate

C14H14O4 (246.0892)


   

METHYL 5,6-DIHYDROXY-2-PHENYLPYRIMIDINE-4-CARBOXYLATE

METHYL 5,6-DIHYDROXY-2-PHENYLPYRIMIDINE-4-CARBOXYLATE

C12H10N2O4 (246.0641)


   

3-(ISOINDOLIN-2-YL)PROPAN-1-AMINE DIHYDROCHLORIDE

3-(ISOINDOLIN-2-YL)PROPAN-1-AMINE DIHYDROCHLORIDE

C11H16Cl2N2 (246.069)


   

3-amino-4-(4-morpholino)benzotrifluoride

3-amino-4-(4-morpholino)benzotrifluoride

C11H13F3N2O (246.098)


   

2-(hydroxymethyl)-6-methyl-3-phenylmethoxypyran-4-one

2-(hydroxymethyl)-6-methyl-3-phenylmethoxypyran-4-one

C14H14O4 (246.0892)


   

2-Amino-4-(3,4-dimethylphenyl)thiophene-3-carboxamide

2-Amino-4-(3,4-dimethylphenyl)thiophene-3-carboxamide

C13H14N2OS (246.0827)


   

2-Amino-5-methyl-4-(4-methylphenyl)thiophene-3-carboxamide

2-Amino-5-methyl-4-(4-methylphenyl)thiophene-3-carboxamide

C13H14N2OS (246.0827)


   

di-p-tolyl sulfone

di-p-tolyl sulfone

C14H14O2S (246.0714)


   

dibenzyl sulfone

dibenzyl sulfone

C14H14O2S (246.0714)


   

Bis(4-methoxyphenyl)phosphine

Bis(4-methoxyphenyl)phosphine

C14H15O2P (246.081)


   

Ethyl 4-hydroxy-8-methoxy-2-naphthoate

Ethyl 4-hydroxy-8-methoxy-2-naphthoate

C14H14O4 (246.0892)


   

4-Ethoxy-5-methoxy-2-naphthoic acid

4-Ethoxy-5-methoxy-2-naphthoic acid

C14H14O4 (246.0892)


   

1-pyrenecarboxylic acid

1-pyrenecarboxylic acid

C17H10O2 (246.0681)


   

4,4-Thiobis(2-methylphenol)

4,4-Thiobis(2-methylphenol)

C14H14O2S (246.0714)


   

3-FLUORO-4-METHOXY-[1,1-BIPHENYL]-3-CARBOXYLIC ACID

3-FLUORO-4-METHOXY-[1,1-BIPHENYL]-3-CARBOXYLIC ACID

C14H11FO3 (246.0692)


   

ethyl 4-hydroxy-5-methoxynaphthalene-2-carboxylate

ethyl 4-hydroxy-5-methoxynaphthalene-2-carboxylate

C14H14O4 (246.0892)


   

Methyl 4,8-dimethoxy-2-naphthoate

Methyl 4,8-dimethoxy-2-naphthoate

C14H14O4 (246.0892)


   

Ethyl 4-hydroxy-6-methoxy-2-naphthoate

Ethyl 4-hydroxy-6-methoxy-2-naphthoate

C14H14O4 (246.0892)


   

2-(4-Fluorophenyl)-1-(2,4-dihydroxyphenyl)ethanone

2-(4-Fluorophenyl)-1-(2,4-dihydroxyphenyl)ethanone

C14H11FO3 (246.0692)


   

α-propargylhomoterephthalic acid dimethyl ester

α-propargylhomoterephthalic acid dimethyl ester

C14H14O4 (246.0892)


   

Zifrosilone

Zifrosilone

C11H13F3OSi (246.0688)


C471 - Enzyme Inhibitor > C47792 - Acetylcholinesterase Inhibitor

   

Glycylglycylglycylglycine

Glycylglycylglycylglycine

C8H14N4O5 (246.0964)


Tetraglycine is a oligopeptide composed of four glycine monomers[1].

   

SODIUM N-NONYL SULFATE

SODIUM N-NONYL SULFATE

C9H19NaO4S (246.0902)


   

methyl 2-oxo-5-propan-2-ylcyclohepta[b]furan-3-carboxylate

methyl 2-oxo-5-propan-2-ylcyclohepta[b]furan-3-carboxylate

C14H14O4 (246.0892)


   

3-(2-Fluorobenzyloxy)phenylboronic acid

3-(2-Fluorobenzyloxy)phenylboronic acid

C13H12BFO3 (246.0863)


   

3-(3-Fluorobenzyloxy)phenylboronic acid

3-(3-Fluorobenzyloxy)phenylboronic acid

C13H12BFO3 (246.0863)


   

4-(4-FLUOROBENZYLOXY)PHENYLBORONIC ACID

4-(4-FLUOROBENZYLOXY)PHENYLBORONIC ACID

C13H12BFO3 (246.0863)


   

(4-((2-Fluorobenzyl)oxy)phenyl)boronic acid

(4-((2-Fluorobenzyl)oxy)phenyl)boronic acid

C13H12BFO3 (246.0863)


   

[3-[(4-fluorophenyl)methoxy]phenyl]boronic acid

[3-[(4-fluorophenyl)methoxy]phenyl]boronic acid

C13H12BFO3 (246.0863)


   

2-FLUORO-5-METHOXY-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

2-FLUORO-5-METHOXY-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

C14H11FO3 (246.0692)


   

5-FLUORO-2-METHOXY-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

5-FLUORO-2-METHOXY-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

C14H11FO3 (246.0692)


   

Methyl 2-[4-(3-thienyl)phenyl]propanoate

Methyl 2-[4-(3-thienyl)phenyl]propanoate

C14H14O2S (246.0714)


   

1-(4-TRIFLUOROMETHOXYPHENYL)PIPERAZINE

1-(4-TRIFLUOROMETHOXYPHENYL)PIPERAZINE

C11H13F3N2O (246.098)


   

3-(2-phenylethynyl)-1-benzofuran-5-carbaldehyde

3-(2-phenylethynyl)-1-benzofuran-5-carbaldehyde

C17H10O2 (246.0681)


   

1-METHYL-2-[(PHENYLSULFONYL)METHYL]BENZENE

1-METHYL-2-[(PHENYLSULFONYL)METHYL]BENZENE

C14H14O2S (246.0714)


   

2-(1,3-benzodioxol-5-yl)-5-methyl-1H-imidazole-4-carboxylic acid

2-(1,3-benzodioxol-5-yl)-5-methyl-1H-imidazole-4-carboxylic acid

C12H10N2O4 (246.0641)


   

N-[(2R,3R,4R,5S,6R)-2-azido-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide

N-[(2R,3R,4R,5S,6R)-2-azido-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide

C8H14N4O5 (246.0964)


   

1-Pyrenylboronic acid

1-Pyrenylboronic acid

C16H11BO2 (246.0852)


   

5-(4-ISOPROPYLPHENYL)THIOPHENE-2-CARBOXYLIC ACID

5-(4-ISOPROPYLPHENYL)THIOPHENE-2-CARBOXYLIC ACID

C14H14O2S (246.0714)


   

2-Deoxy-2-fluorouridine

1-(2-Deoxy-2-fluoro-b-D-arabinofuranosyl)uracil

C9H11FN2O5 (246.0652)


C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite D000890 - Anti-Infective Agents > D000998 - Antiviral Agents D006133 - Growth Substances > D006131 - Growth Inhibitors 1-(2-Deoxy-2-fluoro-beta-D-arabinofuranosyl)uracil is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1]. 2'-Deoxy-2'-fluorouridine can be used as an intermediate for antiinfluenza virus agents synthesis[1].

   

Cyclic (p-methylbenzylidene)malonate2,2-propanediol

Cyclic (p-methylbenzylidene)malonate2,2-propanediol

C14H14O4 (246.0892)


   

1H-Imidazole-4-carboxylicacid,5-[(4-pyridinylamino)carbonyl]-,hydrazide

1H-Imidazole-4-carboxylicacid,5-[(4-pyridinylamino)carbonyl]-,hydrazide

C10H10N6O2 (246.0865)


   

2-(4-amino-1,2,5-oxadiazol-3-yl)-1-ethylimidazo[4,5-c]pyridin-7-ol

2-(4-amino-1,2,5-oxadiazol-3-yl)-1-ethylimidazo[4,5-c]pyridin-7-ol

C10H10N6O2 (246.0865)


   

(5-(BENZYLOXY)-2-FLUOROPHENYL)BORONIC ACID

(5-(BENZYLOXY)-2-FLUOROPHENYL)BORONIC ACID

C13H12BFO3 (246.0863)


   

4-prop-2-enyl-2,3-dihydro-1H-quinoxaline

4-prop-2-enyl-2,3-dihydro-1H-quinoxaline

C11H16Cl2N2 (246.069)


   

5,5-oxybis(5-oxopentanoic acid)

5,5-oxybis(5-oxopentanoic acid)

C10H14O7 (246.0739)


   

2-(4-Fluorobenzyloxy)phenylboronic acid

2-(4-Fluorobenzyloxy)phenylboronic acid

C13H12BFO3 (246.0863)


   

3-Benzyloxy-5-fluorophenylboronic acid

3-Benzyloxy-5-fluorophenylboronic acid

C13H12BFO3 (246.0863)


   

2-BENZYL-5,6-DIHYDROXY-PYRIMIDINE-4-CARBOXYLIC ACID

2-BENZYL-5,6-DIHYDROXY-PYRIMIDINE-4-CARBOXYLIC ACID

C12H10N2O4 (246.0641)


   

6-(4-Fluoro-2-methylphenyl)pyridazine-3-carboxylic acid hydrazide

6-(4-Fluoro-2-methylphenyl)pyridazine-3-carboxylic acid hydrazide

C12H11FN4O (246.0917)


   

6-(4-Fluoro-2-methylphenyl)pyridazine-3-carboxylic acid methyl ester

6-(4-Fluoro-2-methylphenyl)pyridazine-3-carboxylic acid methyl ester

C13H11FN2O2 (246.0805)


   

4-Methylumbelliferyl butyrate

Butanoic acid, 4-methyl-2-oxo-2H-1-benzopyran-7-yl ester

C14H14O4 (246.0892)


   

Diethyl (1,3-dioxo-1,3-propanediyl)biscarbamate

Diethyl (1,3-dioxo-1,3-propanediyl)biscarbamate

C9H14N2O6 (246.0852)


   

4-(4-hydroxy-2-methylphenyl)sulfanyl-3-methylphenol

4-(4-hydroxy-2-methylphenyl)sulfanyl-3-methylphenol

C14H14O2S (246.0714)


   

3-FLUORO-5-METHOXY-[1,1-BIPHENYL]-3-CARBOXYLIC ACID

3-FLUORO-5-METHOXY-[1,1-BIPHENYL]-3-CARBOXYLIC ACID

C14H11FO3 (246.0692)


   

4-FLUORO-3-METHOXY-[1,1-BIPHENYL]-3-CARBOXYLIC ACID

4-FLUORO-3-METHOXY-[1,1-BIPHENYL]-3-CARBOXYLIC ACID

C14H11FO3 (246.0692)


   

Benzhydryl 2-chloroethyl ether

Benzhydryl 2-chloroethyl ether

C15H15ClO (246.0811)


   

2-(3-FLUOROBENZYLOXY)PHENYLBORONIC ACID

2-(3-FLUOROBENZYLOXY)PHENYLBORONIC ACID

C13H12BFO3 (246.0863)


   

3-(Benzyloxy)-4-fluorophenylboronic acid

3-(Benzyloxy)-4-fluorophenylboronic acid

C13H12BFO3 (246.0863)


   

Ethyl 2,6-diaminohexanoate dihydrochloride

Ethyl 2,6-diaminohexanoate dihydrochloride

C8H20Cl2N2O2 (246.0902)


   

[2-(4-METHOXY-PHENYL)-5-OXO-CYCLOPENT-1-ENYL]-ACETIC ACID

[2-(4-METHOXY-PHENYL)-5-OXO-CYCLOPENT-1-ENYL]-ACETIC ACID

C14H14O4 (246.0892)


   

2,3-BUTANEDIONE DIOXIME SULFATE

2,3-BUTANEDIONE DIOXIME SULFATE

C6H18N2O6S (246.0886)


   

4-(3-Fluorobenzyloxy)phenylboronic acid

4-(3-Fluorobenzyloxy)phenylboronic acid

C13H12BFO3 (246.0863)


   

4-(4-AMINOANILINO)-4-OXOBUTANOIC ACID

4-(4-AMINOANILINO)-4-OXOBUTANOIC ACID

C13H14N2OS (246.0827)


   

4-[CYCLOHEXYL(METHYL)AMINO]-1-BUTANOL

4-[CYCLOHEXYL(METHYL)AMINO]-1-BUTANOL

C11H13F3N2O (246.098)


   

2-BENZYLOXY-6-FLUOROPHENYLBORONIC ACID

2-BENZYLOXY-6-FLUOROPHENYLBORONIC ACID

C13H12BFO3 (246.0863)


   

2-(4-FLUORO-BENZYLOXY)-BENZOIC ACID

2-(4-FLUORO-BENZYLOXY)-BENZOIC ACID

C14H11FO3 (246.0692)


   

(2-(Benzyloxy)-3-fluorophenyl)boronic acid

(2-(Benzyloxy)-3-fluorophenyl)boronic acid

C13H12BFO3 (246.0863)


   

Fluoranthene-3-boronic acid

Fluoranthene-3-boronic acid

C16H11BO2 (246.0852)


   

4-FLUORO-2-HYDROXY-4-METHOXYBENZOPHENONE

4-FLUORO-2-HYDROXY-4-METHOXYBENZOPHENONE

C14H11FO3 (246.0692)


   

1-Hexyl-3-methylimidazolium Bromide

1-Hexyl-3-methylimidazolium Bromide

C10H19BrN2 (246.0732)


   

Diallyl terephthalate

Diallyl terephthalate

C14H14O4 (246.0892)


   

3-PHENYL-5-PIPERAZINO-1,2,4-THIADIAZOLE

3-PHENYL-5-PIPERAZINO-1,2,4-THIADIAZOLE

C12H14N4S (246.0939)


   

O-Methylisourea hemisulfate

O-Methylisourea hemisulfate

C4H14N4O6S (246.0634)


   

1-(4-Fluorophenyl)-1,1-dimethoxy-4-chlorobutane

1-(4-Fluorophenyl)-1,1-dimethoxy-4-chlorobutane

C12H16ClFO2 (246.0823)


   

4-(Benzyloxy)-2-fluorophenylboronic acid

4-(Benzyloxy)-2-fluorophenylboronic acid

C13H12BFO3 (246.0863)


   

Hydroxychloroquine Impurity F

Hydroxychloroquine Impurity F

C14H15ClN2 (246.0924)


   

4-((4-ETHYNYLPHENYL)ETHYNYL)BENZOIC ACID

4-((4-ETHYNYLPHENYL)ETHYNYL)BENZOIC ACID

C17H10O2 (246.0681)


   

4-(3-Trifluoromethylphenoxy)tetrahydro-2H-pyran

4-(3-Trifluoromethylphenoxy)tetrahydro-2H-pyran

C12H13F3O2 (246.0868)


   

1-(1-Borono-1-phenylmethyl)-1H-pyrazole-4-boronic acid

1-(1-Borono-1-phenylmethyl)-1H-pyrazole-4-boronic acid

C10H12B2N2O4 (246.0983)


   

Azanidazole

Azanidazole

C10H10N6O2 (246.0865)


G - Genito urinary system and sex hormones > G01 - Gynecological antiinfectives and antiseptics > G01A - Antiinfectives and antiseptics, excl. combinations with corticosteroids > G01AF - Imidazole derivatives P - Antiparasitic products, insecticides and repellents > P01 - Antiprotozoals > P01A - Agents against amoebiasis and other protozoal diseases > P01AB - Nitroimidazole derivatives C254 - Anti-Infective Agent > C276 - Antiparasitic Agent > C277 - Antiprotozoal Agent

   

2-(3-Phenyl-1H-1,2,4-triazol-5-yl)benzonitrile

2-(3-Phenyl-1H-1,2,4-triazol-5-yl)benzonitrile

C15H10N4 (246.0905)


   

TRIETHYOXY-2-THIENYLSILANE

TRIETHYOXY-2-THIENYLSILANE

C10H18O3SSi (246.0746)


   

2-Fluoro-5-methoxybiphenyl-3-carboxylic acid

2-Fluoro-5-methoxybiphenyl-3-carboxylic acid

C14H11FO3 (246.0692)


   

2-FLUORO-3-METHOXY-[1,1-BIPHENYL]-3-CARBOXYLIC ACID

2-FLUORO-3-METHOXY-[1,1-BIPHENYL]-3-CARBOXYLIC ACID

C14H11FO3 (246.0692)


   

N-METHYL-L-VALINE

N-METHYL-L-VALINE

C12H10N2O4 (246.0641)


   

[ethoxy(phenyl)phosphoryl]benzene

[ethoxy(phenyl)phosphoryl]benzene

C14H15O2P (246.081)


   

Diallyl Isophthalate

Diallyl Isophthalate

C14H14O4 (246.0892)


   

N-(4-[(THIOPHEN-2-YLMETHYL)-AMINO]-PHENYL)-ACETAMIDE

N-(4-[(THIOPHEN-2-YLMETHYL)-AMINO]-PHENYL)-ACETAMIDE

C13H14N2OS (246.0827)


   

Diethyl (4-fluorobenzyl)phosphonate

Diethyl (4-fluorobenzyl)phosphonate

C11H16FO3P (246.0821)


   

4-Benzyloxy-2-fluorobenzoic acid

4-Benzyloxy-2-fluorobenzoic acid

C14H11FO3 (246.0692)


   

Phenol,4,4-[1,2-ethanediylbis(oxy)]bis-

Phenol,4,4-[1,2-ethanediylbis(oxy)]bis-

C14H14O4 (246.0892)


   

1-BENZYL-1H-IMIDAZOLE-4,5-DICARBOXYLIC ACID

1-BENZYL-1H-IMIDAZOLE-4,5-DICARBOXYLIC ACID

C12H10N2O4 (246.0641)


   

(R)-M-METHYL-A-PHENETHYLAMIN

(R)-M-METHYL-A-PHENETHYLAMIN

C9H14N2O4S (246.0674)


   

2-Fluoro-4-methoxybiphenyl-3-carboxylic acid

2-Fluoro-4-methoxybiphenyl-3-carboxylic acid

C14H11FO3 (246.0692)


   

3-Deoxy-3-fluorouridine

3-Deoxy-3-fluorouridine

C9H11FN2O5 (246.0652)


   

Methoxymethyldiphenylphosphine oxide

Methoxymethyldiphenylphosphine oxide

C14H15O2P (246.081)


   

3-phenyl-[1,2,4]triazolo[3,4-a]phthalazine

3-phenyl-[1,2,4]triazolo[3,4-a]phthalazine

C15H10N4 (246.0905)


   

4-Benzyloxy-3-fluorobenzoic acid

4-Benzyloxy-3-fluorobenzoic acid

C14H11FO3 (246.0692)


   

5-Methyl-4-(4-methylphenyl)thiophene-3-carbohydrazide

5-Methyl-4-(4-methylphenyl)thiophene-3-carbohydrazide

C13H14N2OS (246.0827)


   

4-[(3-FLUOROBENZYL)OXY]BENZENECARBOXYLIC ACID

4-[(3-FLUOROBENZYL)OXY]BENZENECARBOXYLIC ACID

C14H11FO3 (246.0692)


   

4-[(2-Fluorobenzyl)oxy]benzoic acid

4-[(2-Fluorobenzyl)oxy]benzoic acid

C14H11FO3 (246.0692)


   

[2-(Benzyloxy)-4-fluorophenyl]boronic acid

[2-(Benzyloxy)-4-fluorophenyl]boronic acid

C13H12BFO3 (246.0863)


   

[2-(Benzyloxy)-5-fluorophenyl]boronic acid

[2-(Benzyloxy)-5-fluorophenyl]boronic acid

C13H12BFO3 (246.0863)


   

Ftalofyne

Phthalofyne

C14H14O4 (246.0892)


C254 - Anti-Infective Agent > C276 - Antiparasitic Agent > C250 - Antihelminthic Agent

   

3-(3-TRIFLUOROMETHYL-PHENYL)-PROPIONIC ACID ETHYL ESTER

3-(3-TRIFLUOROMETHYL-PHENYL)-PROPIONIC ACID ETHYL ESTER

C12H13F3O2 (246.0868)


   
   

Mafenide Acetate

Mafenide Acetate

C9H14N2O4S (246.0674)


D004791 - Enzyme Inhibitors > D002257 - Carbonic Anhydrase Inhibitors C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents

   

2-[4-(4-fluorophenoxy)phenyl]acetic acid

2-[4-(4-fluorophenoxy)phenyl]acetic acid

C14H11FO3 (246.0692)


   

TRANS-1-(BROMOETHYL)-4-PENTYLCYCLOHEXANE

TRANS-1-(BROMOETHYL)-4-PENTYLCYCLOHEXANE

C12H23Br (246.0983)


   

Benzenemethanol,2,2-thiobis-

Benzenemethanol,2,2-thiobis-

C14H14O2S (246.0714)


   

1,4-Naphthoquinone, 2-(butylthio)-

1,4-Naphthoquinone, 2-(butylthio)-

C14H14O2S (246.0714)


   

INDENO[2,1-B]CHROMENE-6-CARBOXALDEHYDE

INDENO[2,1-B]CHROMENE-6-CARBOXALDEHYDE

C17H10O2 (246.0681)


   

1H-1,2,4-Triazole-3-carboxamide,N-(2,3-dihydro-1,4-benzodioxin-6-yl)-(9CI)

1H-1,2,4-Triazole-3-carboxamide,N-(2,3-dihydro-1,4-benzodioxin-6-yl)-(9CI)

C11H10N4O3 (246.0753)


   

1-(BICYCLO[3.1.0]HEXAN-3-YL)-6-(METHYLTHIO)-1H-PYRAZOLO[3,4-D]PYRIMIDINE

1-(BICYCLO[3.1.0]HEXAN-3-YL)-6-(METHYLTHIO)-1H-PYRAZOLO[3,4-D]PYRIMIDINE

C12H14N4S (246.0939)


   

2-(BENZYLOXY)-4-FLUOROBENZOIC ACID

2-(BENZYLOXY)-4-FLUOROBENZOIC ACID

C14H11FO3 (246.0692)


   

METHYL 5-OXO-3,5-DIHYDRO-2H-OXAZOLO[2,3-B]QUINAZOLINE-8-CARBOXYLATE

METHYL 5-OXO-3,5-DIHYDRO-2H-OXAZOLO[2,3-B]QUINAZOLINE-8-CARBOXYLATE

C12H10N2O4 (246.0641)


   

methyl 4-fluoro-3-phenoxybenzoate

methyl 4-fluoro-3-phenoxybenzoate

C14H11FO3 (246.0692)


   

3,4-DIFLUORO-3,4-DIMETHYLBENZOPHENONE

3,4-DIFLUORO-3,4-DIMETHYLBENZOPHENONE

C15H12F2O (246.0856)


   

ethyl 5-oxo-3-pyridin-4-yl-2H-1,2,4-triazine-6-carboxylate

ethyl 5-oxo-3-pyridin-4-yl-2H-1,2,4-triazine-6-carboxylate

C11H10N4O3 (246.0753)


   

Aminoguanidine hemisulfate

Aminoguanidine hemisulfate

C2H14N8O4S (246.0859)


   

5-(4-amino-phenylcarbamoyl)-3h-imidazole-4-carboxylic acid

5-(4-amino-phenylcarbamoyl)-3h-imidazole-4-carboxylic acid

C11H10N4O3 (246.0753)


   

3,4-DIFLUORO-3,5-DIMETHYLBENZOPHENONE

3,4-DIFLUORO-3,5-DIMETHYLBENZOPHENONE

C15H12F2O (246.0856)


   

1,2-BIS(2-HYDROXYPHENOXY)ETHANE

1,2-BIS(2-HYDROXYPHENOXY)ETHANE

C14H14O4 (246.0892)


   

2-Pyrenecarboxylic acid

2-Pyrenecarboxylic acid

C17H10O2 (246.0681)


   

9H-Carbazol-3-amine,9-ethyl-, hydrochloride (1:1)

9H-Carbazol-3-amine,9-ethyl-, hydrochloride (1:1)

C14H15ClN2 (246.0924)


   

2-[4-(trifluoromethyl)phenoxy]oxane

2-[4-(trifluoromethyl)phenoxy]oxane

C12H13F3O2 (246.0868)


   

2-METHYL-5-(1,2,3,4-TETRAHYDROXYBUTYL)-3-FUROIC ACID

2-METHYL-5-(1,2,3,4-TETRAHYDROXYBUTYL)-3-FUROIC ACID

C10H14O7 (246.0739)


   

ethyl 5-oxo-3-pyridin-2-yl-2H-1,2,4-triazine-6-carboxylate

ethyl 5-oxo-3-pyridin-2-yl-2H-1,2,4-triazine-6-carboxylate

C11H10N4O3 (246.0753)


   

Disodium sebacate

Disodium sebacate

C10H16Na2O4 (246.0844)


   

1-[2-(2-Hydroxyethoxy)ethyl]piperazine 2HCl

1-[2-(2-Hydroxyethoxy)ethyl]piperazine 2HCl

C8H20Cl2N2O2 (246.0902)


   

3-FLUORO-4-METHOXY-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

3-FLUORO-4-METHOXY-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

C14H11FO3 (246.0692)


   

N-Cyclopropyl-2-nitro-4-(trifluoromethyl)aniline

N-Cyclopropyl-2-nitro-4-(trifluoromethyl)aniline

C10H9F3N2O2 (246.0616)


   

MAFENAMIDE ACETATE

MAFENAMIDE ACETATE

C9H14N2O4S (246.0674)


   

3-(4-Chloro-4-biphenylyl)-1-propanol

3-(4-Chloro-4-biphenylyl)-1-propanol

C15H15ClO (246.0811)


   

2-(Chloromethyl)benzyl 2-methylphenyl ether

2-(Chloromethyl)benzyl 2-methylphenyl ether

C15H15ClO (246.0811)


   

1-Bromocyclododecane

1-Bromocyclododecane

C12H23Br (246.0983)


   

3-[5-(4-methoxy-phenyl)-furan-2-yl]-propionic acid

3-[5-(4-methoxy-phenyl)-furan-2-yl]-propionic acid

C14H14O4 (246.0892)


   

3-[(4-FLUOROBENZYL)OXY]BENZOIC ACID

3-[(4-FLUOROBENZYL)OXY]BENZOIC ACID

C14H11FO3 (246.0692)


   

4-MORPHOLINO-3-(TRIFLUOROMETHYL)ANILINE

4-MORPHOLINO-3-(TRIFLUOROMETHYL)ANILINE

C11H13F3N2O (246.098)


   

Nifurpirinol

Nifurpirinol

C12H10N2O4 (246.0641)


C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent

   

gallium,propan-2-olate

gallium,propan-2-olate

C9H21GaO3 (246.0746)


   

2-diphenylphosphanylethanethiol

2-diphenylphosphanylethanethiol

C14H15PS (246.0632)


   

1,1,1,2,2-Pentafluoro-6,6-dimethyl-3,5-heptanedione

1,1,1,2,2-Pentafluoro-6,6-dimethyl-3,5-heptanedione

C9H11F5O2 (246.0679)


   

4-Amino-2,5-dimethoxy-N-methylbenzenesulphonamide

4-Amino-2,5-dimethoxy-N-methylbenzenesulphonamide

C9H14N2O4S (246.0674)


   

2-(4-methoxyphenoxy)-3-nitropyridine

2-(4-methoxyphenoxy)-3-nitropyridine

C12H10N2O4 (246.0641)


   

ethyl 2-cyano-3-(3-nitrophenyl)acrylate

ethyl 2-cyano-3-(3-nitrophenyl)acrylate

C12H10N2O4 (246.0641)


   

1,2-bis(3-hydroxyphenoxy)ethane

1,2-bis(3-hydroxyphenoxy)ethane

C14H14O4 (246.0892)


   

5-(2,5-DIMETHYLPHENOXYMETHYL)FURAN-2-CARBOXYLICACID

5-(2,5-DIMETHYLPHENOXYMETHYL)FURAN-2-CARBOXYLICACID

C14H14O4 (246.0892)


   

[4-(Benzyloxy)-3-fluorophenyl]boronic acid

[4-(Benzyloxy)-3-fluorophenyl]boronic acid

C13H12BFO3 (246.0863)


   

1beta-D-Ribofuranosyl-5-fluoropyrimidin-2(1H)-one

1beta-D-Ribofuranosyl-5-fluoropyrimidin-2(1H)-one

C9H11FN2O5 (246.0652)


   

Pyruvaldehyde bis(N4,N4-dimethylthiosemicarbazone)

Pyruvaldehyde bis(N4,N4-dimethylthiosemicarbazone)

C7H14N6S2 (246.0721)


   

1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,3-diazinane-2,4-dione

1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,3-diazinane-2,4-dione

C9H14N2O6 (246.0852)


   

1-[5-(Fluoromethyl)-3,4-dihydroxyoxolan-2-yl]pyrimidine-2,4-dione

1-[5-(Fluoromethyl)-3,4-dihydroxyoxolan-2-yl]pyrimidine-2,4-dione

C9H11FN2O5 (246.0652)


   

N-(4-methyl-2-nitrophenyl)furan-2-carboxamide

N-(4-methyl-2-nitrophenyl)furan-2-carboxamide

C12H10N2O4 (246.0641)


   

N-(5-methyl-3-isoxazolyl)-1,3-benzodioxole-5-carboxamide

N-(5-methyl-3-isoxazolyl)-1,3-benzodioxole-5-carboxamide

C12H10N2O4 (246.0641)


   

5-chloro-2-methyl-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole

5-chloro-2-methyl-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole

C14H15ClN2 (246.0924)


   

2-[(2-Cyclopropyl-2-oxoethyl)thio]-4,6-dimethyl-3-pyridinecarbonitrile

2-[(2-Cyclopropyl-2-oxoethyl)thio]-4,6-dimethyl-3-pyridinecarbonitrile

C13H14N2OS (246.0827)


   

Glycyl-asparaginyl-glycine

Glycyl-asparaginyl-glycine

C8H14N4O5 (246.0964)


   

Cysteine-beta-naphthylamide

Cysteine-beta-naphthylamide

C13H14N2OS (246.0827)


   

1-(4-Chlorophenyl)-2-phenylpropan-2-ol

1-(4-Chlorophenyl)-2-phenylpropan-2-ol

C15H15ClO (246.0811)


   

S-(1-Ethyl-2,5-dioxopyrrolidin-3-yl)-L-cysteine

S-(1-Ethyl-2,5-dioxopyrrolidin-3-yl)-L-cysteine

C9H14N2O4S (246.0674)


   

(E)-5-(8-Oxo-5,6,7,8-tetrahydropyrrolo[2,3-c]azepin-4(1H)-ylidene)imidazolidine-2,4-dione

(E)-5-(8-Oxo-5,6,7,8-tetrahydropyrrolo[2,3-c]azepin-4(1H)-ylidene)imidazolidine-2,4-dione

C11H10N4O3 (246.0753)


   

2-(beta-D-Glucopyranosyl)-5-methyl-1,3,4-oxadiazole

2-(beta-D-Glucopyranosyl)-5-methyl-1,3,4-oxadiazole

C9H14N2O6 (246.0852)


   

4-Butyl-5-propyl-1,3-selenazol-2-amine

4-Butyl-5-propyl-1,3-selenazol-2-amine

C10H18N2Se (246.0635)


   

Floxuridine

Floxuridine

C9H11FN2O5 (246.0652)


L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01B - Antimetabolites > L01BC - Pyrimidine analogues C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents Floxuridine (5-Fluorouracil 2'-deoxyriboside) is a?pyrimidine?analog?and known as an?oncology antimetabolite. Floxuridine inhibits Poly(ADP-Ribose) polymerase and induces DNA damage by activating the ATM and ATR checkpoint signaling pathways in vitro. Floxuridine is a extreamly potent inhibitor for S. aureus infection and induces cell apoptosis[1][2]. Floxuridine has antiviral effects against HSV and CMV[3].

   

Doxifluridine

1-[(4S,5R)-3,4-dihydroxy-5-methyl-2-oxolanyl]-5-fluoropyrimidine-2,4-dione

C9H11FN2O5 (246.0652)


D002491 - Central Nervous System Agents > D000697 - Central Nervous System Stimulants > D019167 - Appetite Stimulants C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents Same as: D01309 Doxifluridine has anticancer activity. Doxifluidine is a 5-FU prodrug. Doxifluridine is a thymidine synthase inhibitor. Doxifluridine can enhance tumor inhibition by synergizing with a variety of drugs[1][2][3].

   

Marmesin

7H-Furo[3,2g][1]-benzopyran-7-one, (-2,3-dihydro-2-(1-hydroxy-1-hydroxymethylethyl)-, (R)

C14H14O4 (246.0892)


Nodakenetin is a marmesin with R-configuration. It has a role as a plant metabolite, a rat metabolite and a xenobiotic metabolite. It is an enantiomer of a (+)-marmesin. Nodakenetin is a natural product found in Zanthoxylum beecheyanum, Melicope barbigera, and other organisms with data available. A marmesin with R-configuration. (+)-marmesin is a marmesin. It is an enantiomer of a nodakenetin. Marmesin is a natural product found in Coronilla scorpioides, Clausena dunniana, and other organisms with data available. Nodakenetin, isolated from Angelica decursiva, possesses antioxidant anti-inflammatory activities. Nodakenetin has the potential to be an antiarthritic and nerve tonic[1][2]. Nodakenetin, isolated from Angelica decursiva, possesses antioxidant anti-inflammatory activities. Nodakenetin has the potential to be an antiarthritic and nerve tonic[1][2]. S-(+)-Marmesin is a natural coumarin, exhibiting COX-2/5-LOX dual inhibitory activity. S-(+)-Marmesin is a natural coumarin, exhibiting COX-2/5-LOX dual inhibitory activity. S-(+)-Marmesin is a natural coumarin, exhibiting COX-2/5-LOX dual inhibitory activity.

   

Torachrysone

1-(1,8-dihydroxy-6-methoxy-3-methyl-naphthalen-2-yl)ethanone

C14H14O4 (246.0892)


   

Marmesine

7H-Furo[3,2g][1]-benzopyran-7-one, (-2,3-dihydro-2-(1-hydroxy-1-hydroxymethylethyl)-, (R)

C14H14O4 (246.0892)


Nodakenetin, isolated from Angelica decursiva, possesses antioxidant anti-inflammatory activities. Nodakenetin has the potential to be an antiarthritic and nerve tonic[1][2]. Nodakenetin, isolated from Angelica decursiva, possesses antioxidant anti-inflammatory activities. Nodakenetin has the potential to be an antiarthritic and nerve tonic[1][2].

   

decursinol

(7S)-7-hydroxy-8,8-dimethyl-6,7-dihydropyrano[5,6-g]chromen-2-one

C14H14O4 (246.0892)


D020536 - Enzyme Activators Decursinol, isolated from the roots of Angelica gigas, possesses antinociceptive effect with orally bioavailability. Decursinol possesses anti-tumor and anti-metastasis activity[1]. Decursinol, isolated from the roots of Angelica gigas, possesses antinociceptive effect with orally bioavailability. Decursinol possesses anti-tumor and anti-metastasis activity[1].

   

3-Hydroxy-4-methoxy-2-(2-phenylethenyl)-2,3-dihydropyran-6-one

3-Hydroxy-4-methoxy-2-(2-phenylethenyl)-2,3-dihydropyran-6-one

C14H14O4 (246.0892)


   

4,4-Biphenyldiol, 3,3-dimethoxy-

4,4-Biphenyldiol, 3,3-dimethoxy-

C14H14O4 (246.0892)


   

(Z)-2-(6-methylsulfanylhexyl)but-2-enedioic acid

(Z)-2-(6-methylsulfanylhexyl)but-2-enedioic acid

C11H18O4S (246.0926)


   
   

1-[3,4-Dihydroxy-5-(hydroxyamino)oxolan-2-yl]-4-imino-1,3-diazinan-2-one

1-[3,4-Dihydroxy-5-(hydroxyamino)oxolan-2-yl]-4-imino-1,3-diazinan-2-one

C8H14N4O5 (246.0964)


   

2-Propan-2-yl-2,3-dihydropyrano[2,3-g][1,4]benzodioxin-7-one

2-Propan-2-yl-2,3-dihydropyrano[2,3-g][1,4]benzodioxin-7-one

C14H14O4 (246.0892)


   

N-(4,5-dihydro-1,3-thiazol-2-yl)-3-(4-methylphenyl)acrylamide

N-(4,5-dihydro-1,3-thiazol-2-yl)-3-(4-methylphenyl)acrylamide

C13H14N2OS (246.0827)


   

4-(1,3-Benzodioxol-5-ylhydrazinylidene)pyrazole-3,5-diamine

4-(1,3-Benzodioxol-5-ylhydrazinylidene)pyrazole-3,5-diamine

C10H10N6O2 (246.0865)


   

Asparagylasparagine

Asparagylasparagine

C8H14N4O5 (246.0964)


   

1-(2,6-Dimethylphenyl)-3-thiophen-2-ylurea

1-(2,6-Dimethylphenyl)-3-thiophen-2-ylurea

C13H14N2OS (246.0827)


   

3-(4-methyl-1,3-dioxan-2-yl)-4H-chromen-4-one

3-(4-methyl-1,3-dioxan-2-yl)-4H-chromen-4-one

C14H14O4 (246.0892)


   

p-Hydroxykavain

p-Hydroxykavain

C14H14O4 (246.0892)


   
   
   

1-(2-Amino-3-carboxypropanoyl)-4-hydroxypyrrolidine-2-carboxylic acid

1-(2-Amino-3-carboxypropanoyl)-4-hydroxypyrrolidine-2-carboxylic acid

C9H14N2O6 (246.0852)


   

N-carbamoyl-L-tryptophanate

N-carbamoyl-L-tryptophanate

C12H12N3O3- (246.0879)


   

GS4012 free base(1+)

GS4012 free base(1+)

C14H16NOS+ (246.0953)


   

6-[(E)-3-hydroxybut-1-enyl]-7-methoxychromen-2-one

6-[(E)-3-hydroxybut-1-enyl]-7-methoxychromen-2-one

C14H14O4 (246.0892)


   

8-[(3,3-Dimethyloxiran-2-yl)methyl]-7-hydroxychromen-2-one

8-[(3,3-Dimethyloxiran-2-yl)methyl]-7-hydroxychromen-2-one

C14H14O4 (246.0892)


   

Ethyl piperate

Ethyl piperate

C14H14O4 (246.0892)


   

(5S,6S)-5,6-Dihydro-5-hydroxy-4-methoxy-6-[(E)-2-phenylethenyl]-2H-pyran-2-one

(5S,6S)-5,6-Dihydro-5-hydroxy-4-methoxy-6-[(E)-2-phenylethenyl]-2H-pyran-2-one

C14H14O4 (246.0892)


   

Smirino

2-butenoic acid, 2-methyl-, (7S)-7,8-dihydro-8,8-dimethyl-2-oxo-2H,6H-benzo(1,2-b:5,4-b)dipyran-7-yl ester, (2Z)-

C14H14O4 (246.0892)


Decursinol is an organic heterotricyclic compound that is 7,8-dihydro-2H,6H-pyrano[3,2-g]chromen-2-one substituted by a beta-hydroxy group at position 7 and two methyl groups at position 8. It is isolated from the roots of Angelica gigas and has been found to possess significant inhibitory activity against acetylcholinesterase enzyme (EC 3.1.1.7). It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor, an antineoplastic agent, an analgesic and a metabolite. It is an organic heterotricyclic compound, a delta-lactone, a secondary alcohol and a cyclic ether. Decursinol is a natural product found in Smyrniopsis aucheri, Phlojodicarpus villosus, and other organisms with data available. An organic heterotricyclic compound that is 7,8-dihydro-2H,6H-pyrano[3,2-g]chromen-2-one substituted by a beta-hydroxy group at position 7 and two methyl groups at position 8. It is isolated from the roots of Angelica gigas and has been found to possess significant inhibitory activity against acetylcholinesterase enzyme (EC 3.1.1.7). D020536 - Enzyme Activators Decursinol, isolated from the roots of Angelica gigas, possesses antinociceptive effect with orally bioavailability. Decursinol possesses anti-tumor and anti-metastasis activity[1]. Decursinol, isolated from the roots of Angelica gigas, possesses antinociceptive effect with orally bioavailability. Decursinol possesses anti-tumor and anti-metastasis activity[1].

   

(-)-Columbianetin

(-)-Columbianetin

C14H14O4 (246.0892)


D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins

   

benzyl-6-hydroxy-2-cyclohexene-on-oyl

benzyl-6-hydroxy-2-cyclohexene-on-oyl

C14H14O4 (246.0892)


   

5-Fluoro-2-deoxyuridine

5-Fluoro-2-deoxyuridine

C9H11FN2O5 (246.0652)


   

L-alpha-Aspartyl-L-hydroxyproline

L-alpha-Aspartyl-L-hydroxyproline

C9H14N2O6 (246.0852)


   

L-cysteine 2-naphthylamide

L-cysteine 2-naphthylamide

C13H14N2OS (246.0827)


An L-cysteine derivative that is the amide obtained by formal condensation of the carboxy group of L-cysteine with the amino group of 2-naphthylamine.

   
   
   

sAJM589

sAJM589

C16H10N2O (246.0793)


sAJM589 is a Myc inhibitor which potently disrupts the Myc-Max heterodimer with an IC50 of 1.8 μM[1].

   

(3s)-3-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-7-one

(3s)-3-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-7-one

C14H14O4 (246.0892)


   

7-hydroxy-6-[(2z)-4-hydroxy-3-methylbut-2-en-1-yl]chromen-2-one

7-hydroxy-6-[(2z)-4-hydroxy-3-methylbut-2-en-1-yl]chromen-2-one

C14H14O4 (246.0892)


   

7-hydroxy-6-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]chromen-2-one

7-hydroxy-6-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]chromen-2-one

C14H14O4 (246.0892)


   

6-hydroxy-8,9,9-trimethyl-8h-furo[2,3-h]chromen-2-one

6-hydroxy-8,9,9-trimethyl-8h-furo[2,3-h]chromen-2-one

C14H14O4 (246.0892)


   

5-[2-(3,4-dihydroxyphenyl)ethyl]benzene-1,3-diol

5-[2-(3,4-dihydroxyphenyl)ethyl]benzene-1,3-diol

C14H14O4 (246.0892)


   

7-{[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]oxy}chromen-2-one

7-{[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]oxy}chromen-2-one

C14H14O4 (246.0892)


   

1-(3,4-dihydroxy-5-methoxynaphthalen-2-yl)propan-2-one

1-(3,4-dihydroxy-5-methoxynaphthalen-2-yl)propan-2-one

C14H14O4 (246.0892)


   

6-methoxy-7-[(2-methylprop-1-en-1-yl)oxy]chromen-2-one

6-methoxy-7-[(2-methylprop-1-en-1-yl)oxy]chromen-2-one

C14H14O4 (246.0892)


   

(1r,2s,4e,5s,5's)-4-(hexa-2,4-diyn-1-ylidene)-3,6-dioxaspiro[bicyclo[3.1.0]hexane-2,2'-oxan]-5'-ol

(1r,2s,4e,5s,5's)-4-(hexa-2,4-diyn-1-ylidene)-3,6-dioxaspiro[bicyclo[3.1.0]hexane-2,2'-oxan]-5'-ol

C14H14O4 (246.0892)


   

4-amino-n-(2,6-dihydroxypyrimidin-4-yl)benzenecarboximidic acid

4-amino-n-(2,6-dihydroxypyrimidin-4-yl)benzenecarboximidic acid

C11H10N4O3 (246.0753)


   

methyl 2-(5-acetyl-2,3-dihydro-1-benzofuran-2-yl)prop-2-enoate

methyl 2-(5-acetyl-2,3-dihydro-1-benzofuran-2-yl)prop-2-enoate

C14H14O4 (246.0892)


   

7-methoxy-8-[(1e)-3-oxobut-1-en-1-yl]-3,4-dihydro-1-benzopyran-2-one

7-methoxy-8-[(1e)-3-oxobut-1-en-1-yl]-3,4-dihydro-1-benzopyran-2-one

C14H14O4 (246.0892)


   

7-hydroxy-6-(2-(r)-hydroxy-3-methylbut-3-enyl)coumarin

NA

C14H14O4 (246.0892)


{"Ingredient_id": "HBIN013250","Ingredient_name": "7-hydroxy-6-(2-(r)-hydroxy-3-methylbut-3-enyl)coumarin","Alias": "NA","Ingredient_formula": "C14H14O4","Ingredient_Smile": "CC(=C)C(CC1=C(C=C2C(=C1)C=CC(=O)O2)O)O","Ingredient_weight": "246.26 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "10196","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "12050842","DrugBank_id": "NA"}

   

9alpha-Hydroxyfraxinellone

(3R,3aR,6R)-3-(3-furyl)-6-hydroxy-3a,7-dimethyl-3,4,5,6-tetrahydroisobenzofuran-1-one; 3-Furan-3-yl-6-hydroxy-3a,7-dimethyl-3a,4,5,6-tetrahydro-3H-isobenzofuran-1-one; 1(3H)-isobenzofuranone, 3-(3-furanyl)-3a,4,5,6-tetrahydro-6-hydroxy-3a,7-dimethyl-, (3R,3aR,6R)-; (3R,3aR,6R)-3-furan-3-yl-6-hydroxy-3a,7-dimethyl-3,4,5,6-tetrahydro-2-benzofuran-1-one; rel-(3R,3aR,6R)-3-(3-furyl)-6-hydroxy-3a,7-dimethyl-3a,4,5,6-tetrahydro-2-benzofuran-1(3H)-one; InChI=1/C14H16O4/c1-8-10(15)3-5-14(2)11(8)13(16)18-12(14)9-4-6-17-7-9/h4,6-7,10,12,15H,3,5H2,1-2H3/t10-,12+,14-/m1/s; (-)-(3R,3aR,6R)-3-(3'-Furanyl)-3a,7-dimethyl-6-hydroxy-1,3,3a,4,5,6-hexahydrobenzo[c]furan-1-one

C14H14O4 (246.0892)


{"Ingredient_id": "HBIN014048","Ingredient_name": "9alpha-Hydroxyfraxinellone","Alias": "(3R,3aR,6R)-3-(3-furyl)-6-hydroxy-3a,7-dimethyl-3,4,5,6-tetrahydroisobenzofuran-1-one; 3-Furan-3-yl-6-hydroxy-3a,7-dimethyl-3a,4,5,6-tetrahydro-3H-isobenzofuran-1-one; 1(3H)-isobenzofuranone, 3-(3-furanyl)-3a,4,5,6-tetrahydro-6-hydroxy-3a,7-dimethyl-, (3R,3aR,6R)-; (3R,3aR,6R)-3-furan-3-yl-6-hydroxy-3a,7-dimethyl-3,4,5,6-tetrahydro-2-benzofuran-1-one; rel-(3R,3aR,6R)-3-(3-furyl)-6-hydroxy-3a,7-dimethyl-3a,4,5,6-tetrahydro-2-benzofuran-1(3H)-one; InChI=1/C14H16O4/c1-8-10(15)3-5-14(2)11(8)13(16)18-12(14)9-4-6-17-7-9/h4,6-7,10,12,15H,3,5H2,1-2H3/t10-,12+,14-/m1/s; (-)-(3R,3aR,6R)-3-(3'-Furanyl)-3a,7-dimethyl-6-hydroxy-1,3,3a,4,5,6-hexahydrobenzo[c]furan-1-one","Ingredient_formula": "C14H14O4","Ingredient_Smile": "CC1=C2C(=O)OC(C2(CCC1O)C)C3=COC=C3","Ingredient_weight": "246.26","OB_score": "75.49531473","CAS_id": "128475-17-2","SymMap_id": "SMIT07908","TCMID_id": "NA","TCMSP_id": "MOL006259","TCM_ID_id": "NA","PubChem_id": "636856","DrugBank_id": "NA"}

   

(1s)-6-hydroxy-1-methoxy-8-methyl-1h,2h,3h-cyclopenta[c]isochromen-5-one

(1s)-6-hydroxy-1-methoxy-8-methyl-1h,2h,3h-cyclopenta[c]isochromen-5-one

C14H14O4 (246.0892)


   

7-hydroxy-8,8-dimethyl-6h,7h-pyrano[3,2-g]chromen-2-one

7-hydroxy-8,8-dimethyl-6h,7h-pyrano[3,2-g]chromen-2-one

C14H14O4 (246.0892)


   

7,8-dihydroxy-5-isopropyl-3-methylnaphthalene-1,2-dione

7,8-dihydroxy-5-isopropyl-3-methylnaphthalene-1,2-dione

C14H14O4 (246.0892)


   

7-hydroxy-6-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]chromen-2-one

7-hydroxy-6-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]chromen-2-one

C14H14O4 (246.0892)


   

9-hydroxy-8,8-dimethyl-9h,10h-pyrano[2,3-h]chromen-2-one

9-hydroxy-8,8-dimethyl-9h,10h-pyrano[2,3-h]chromen-2-one

C14H14O4 (246.0892)


   

7-hydroxy-8-[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]chromen-2-one

7-hydroxy-8-[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]chromen-2-one

C14H14O4 (246.0892)


   

(8s)-6-hydroxy-8,9,9-trimethyl-8h-furo[2,3-h]chromen-2-one

(8s)-6-hydroxy-8,9,9-trimethyl-8h-furo[2,3-h]chromen-2-one

C14H14O4 (246.0892)


   

3-methyl-4-[(1e,3e,5e)-6-methyl-7-oxoocta-1,3,5-trien-1-yl]furan-2,5-dione

3-methyl-4-[(1e,3e,5e)-6-methyl-7-oxoocta-1,3,5-trien-1-yl]furan-2,5-dione

C14H14O4 (246.0892)


   

8-hydroxy-7-[(3-methylbut-2-en-1-yl)oxy]chromen-2-one

8-hydroxy-7-[(3-methylbut-2-en-1-yl)oxy]chromen-2-one

C14H14O4 (246.0892)


   

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

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

C13H14N2OS (246.0827)


   

7-hydroxy-6-[(1e)-3-hydroxy-3-methylbut-1-en-1-yl]chromen-2-one

7-hydroxy-6-[(1e)-3-hydroxy-3-methylbut-1-en-1-yl]chromen-2-one

C14H14O4 (246.0892)


   

7-methoxy-11-(prop-1-en-2-yl)-4,10-dioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-5-one

7-methoxy-11-(prop-1-en-2-yl)-4,10-dioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-5-one

C14H14O4 (246.0892)


   

(11s)-7-methoxy-11-(prop-1-en-2-yl)-4,10-dioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-5-one

(11s)-7-methoxy-11-(prop-1-en-2-yl)-4,10-dioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-5-one

C14H14O4 (246.0892)


   

(8r)-8-(hydroxymethyl)-8-methyl-9h,10h-pyrano[2,3-h]chromen-2-one

(8r)-8-(hydroxymethyl)-8-methyl-9h,10h-pyrano[2,3-h]chromen-2-one

C14H14O4 (246.0892)


   

5,8-dihydroxy-3-[(1e)-pent-1-en-1-yl]isochromen-1-one

5,8-dihydroxy-3-[(1e)-pent-1-en-1-yl]isochromen-1-one

C14H14O4 (246.0892)


   

6-hydroxy-7-[(3-methylbut-2-en-1-yl)oxy]chromen-2-one

6-hydroxy-7-[(3-methylbut-2-en-1-yl)oxy]chromen-2-one

C14H14O4 (246.0892)


   

1-(3,5-dihydroxy-4-methoxynaphthalen-2-yl)propan-2-one

1-(3,5-dihydroxy-4-methoxynaphthalen-2-yl)propan-2-one

C14H14O4 (246.0892)


   

2-[(2e,4e)-hexa-2,4-dienoyl]-5-hydroxy-3,6-dimethylcyclohexa-2,5-diene-1,4-dione

2-[(2e,4e)-hexa-2,4-dienoyl]-5-hydroxy-3,6-dimethylcyclohexa-2,5-diene-1,4-dione

C14H14O4 (246.0892)


   

2,3-dimethoxy-7-methyl-5h-benzo[7]annulene-1,4-dione

2,3-dimethoxy-7-methyl-5h-benzo[7]annulene-1,4-dione

C14H14O4 (246.0892)


   

(2e)-3-(2,2-dimethyl-4-oxo-3h-1-benzopyran-6-yl)prop-2-enoic acid

(2e)-3-(2,2-dimethyl-4-oxo-3h-1-benzopyran-6-yl)prop-2-enoic acid

C14H14O4 (246.0892)


   

3,7-dihydroxy-8-(3-methylbut-2-en-1-yl)chromen-2-one

3,7-dihydroxy-8-(3-methylbut-2-en-1-yl)chromen-2-one

C14H14O4 (246.0892)


   

5-hydroxy-7-[(3-methylbut-2-en-1-yl)oxy]chromen-2-one

5-hydroxy-7-[(3-methylbut-2-en-1-yl)oxy]chromen-2-one

C14H14O4 (246.0892)


   

7-hydroxy-8-(4-hydroxy-3-methylbut-2-en-1-yl)chromen-2-one

7-hydroxy-8-(4-hydroxy-3-methylbut-2-en-1-yl)chromen-2-one

C14H14O4 (246.0892)


   

5,5'-dimethoxy-[1,1'-biphenyl]-2,2'-diol

5,5'-dimethoxy-[1,1'-biphenyl]-2,2'-diol

C14H14O4 (246.0892)


   

(4-oxo-2-propylchromen-5-yl)acetic acid

(4-oxo-2-propylchromen-5-yl)acetic acid

C14H14O4 (246.0892)


   

2-(hexa-2,4-dienoyl)-5-hydroxy-3,6-dimethylcyclohexa-2,5-diene-1,4-dione

2-(hexa-2,4-dienoyl)-5-hydroxy-3,6-dimethylcyclohexa-2,5-diene-1,4-dione

C14H14O4 (246.0892)


   

3-hydroxy-4-methoxy-[2,2'-bipyridine]-6-carboxylic acid

3-hydroxy-4-methoxy-[2,2'-bipyridine]-6-carboxylic acid

C12H10N2O4 (246.0641)


   

7-hydroxy-8-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]chromen-2-one

7-hydroxy-8-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]chromen-2-one

C14H14O4 (246.0892)


   

4,5,6-trimethoxynaphthalene-2-carbaldehyde

4,5,6-trimethoxynaphthalene-2-carbaldehyde

C14H14O4 (246.0892)


   

4-methoxy-7,7-dimethyl-1h-furo[3,4-f]chromen-3-one

4-methoxy-7,7-dimethyl-1h-furo[3,4-f]chromen-3-one

C14H14O4 (246.0892)


   

methyl 2-[(2s)-5-acetyl-2,3-dihydro-1-benzofuran-2-yl]prop-2-enoate

methyl 2-[(2s)-5-acetyl-2,3-dihydro-1-benzofuran-2-yl]prop-2-enoate

C14H14O4 (246.0892)


   

(9r)-5,9-dihydroxy-2,4-dimethyl-7h,8h,9h-naphtho[1,2-b]furan-6-one

(9r)-5,9-dihydroxy-2,4-dimethyl-7h,8h,9h-naphtho[1,2-b]furan-6-one

C14H14O4 (246.0892)


   

(1r,2s,5s,5's)-4-(hexa-2,4-diyn-1-ylidene)-3,6-dioxaspiro[bicyclo[3.1.0]hexane-2,2'-oxan]-5'-ol

(1r,2s,5s,5's)-4-(hexa-2,4-diyn-1-ylidene)-3,6-dioxaspiro[bicyclo[3.1.0]hexane-2,2'-oxan]-5'-ol

C14H14O4 (246.0892)


   

1-[6-hydroxy-7-methoxy-2-(prop-1-en-2-yl)-1-benzofuran-5-yl]ethanone

1-[6-hydroxy-7-methoxy-2-(prop-1-en-2-yl)-1-benzofuran-5-yl]ethanone

C14H14O4 (246.0892)


   

5-[(1r,2s)-1,2-dihydroxy-2-phenylethyl]benzene-1,3-diol

5-[(1r,2s)-1,2-dihydroxy-2-phenylethyl]benzene-1,3-diol

C14H14O4 (246.0892)


   

(2e,8z)-10-(acetyloxy)deca-2,8-dien-4,6-diyn-1-yl acetate

(2e,8z)-10-(acetyloxy)deca-2,8-dien-4,6-diyn-1-yl acetate

C14H14O4 (246.0892)


   

7-[(2-hydroxy-3-methylbut-3-en-1-yl)oxy]chromen-2-one

7-[(2-hydroxy-3-methylbut-3-en-1-yl)oxy]chromen-2-one

C14H14O4 (246.0892)


   

6-[(2s)-3,3-dimethyloxiran-2-yl]-7-methoxychromen-2-one

6-[(2s)-3,3-dimethyloxiran-2-yl]-7-methoxychromen-2-one

C14H14O4 (246.0892)


   

7-hydroxy-6-(4-hydroxy-3-methylbut-2-en-1-yl)chromen-2-one

7-hydroxy-6-(4-hydroxy-3-methylbut-2-en-1-yl)chromen-2-one

C14H14O4 (246.0892)


   

5,8-dihydroxy-3-(pent-1-en-1-yl)isochromen-1-one

5,8-dihydroxy-3-(pent-1-en-1-yl)isochromen-1-one

C14H14O4 (246.0892)


   

7,8-dihydroxy-4-isopropyl-6-methylnaphthalene-1,2-dione

7,8-dihydroxy-4-isopropyl-6-methylnaphthalene-1,2-dione

C14H14O4 (246.0892)


   

(8r)-10-hydroxy-4,8,12-trimethyl-2,6-dioxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),4,9(13),10-tetraen-3-one

(8r)-10-hydroxy-4,8,12-trimethyl-2,6-dioxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),4,9(13),10-tetraen-3-one

C14H14O4 (246.0892)


   

3-(c-hydroxycarbonimidoyl)-1-methyl-4-oxoquinoline-2-carboxylic acid

3-(c-hydroxycarbonimidoyl)-1-methyl-4-oxoquinoline-2-carboxylic acid

C12H10N2O4 (246.0641)


   

(9r)-9-hydroxy-8,8-dimethyl-9h,10h-pyrano[2,3-h]chromen-2-one

(9r)-9-hydroxy-8,8-dimethyl-9h,10h-pyrano[2,3-h]chromen-2-one

C14H14O4 (246.0892)


   

2-(hydroxymethyl)-9-methoxy-4-methyl-3-benzoxepine-1-carbaldehyde

2-(hydroxymethyl)-9-methoxy-4-methyl-3-benzoxepine-1-carbaldehyde

C14H14O4 (246.0892)


   

(1s)-8-hydroxy-1-methoxy-6-methyl-1h,2h,3h-cyclopenta[b]chromen-9-one

(1s)-8-hydroxy-1-methoxy-6-methyl-1h,2h,3h-cyclopenta[b]chromen-9-one

C14H14O4 (246.0892)


   

(9s)-9-hydroxy-8,8-dimethyl-9h,10h-pyrano[2,3-h]chromen-2-one

(9s)-9-hydroxy-8,8-dimethyl-9h,10h-pyrano[2,3-h]chromen-2-one

C14H14O4 (246.0892)


   

3-(furan-2-yl)-3a,7-dimethyl-4,5-dihydro-3h-2-benzofuran-1,6-dione

3-(furan-2-yl)-3a,7-dimethyl-4,5-dihydro-3h-2-benzofuran-1,6-dione

C14H14O4 (246.0892)


   

3',5'-dimethoxy-[1,1'-biphenyl]-2,4'-diol

3',5'-dimethoxy-[1,1'-biphenyl]-2,4'-diol

C14H14O4 (246.0892)


   

7-{[(2r)-3,3-dimethyloxiran-2-yl]methoxy}chromen-2-one

7-{[(2r)-3,3-dimethyloxiran-2-yl]methoxy}chromen-2-one

C14H14O4 (246.0892)


   

7-methoxy-8-(3-oxobut-1-en-1-yl)-3,4-dihydro-1-benzopyran-2-one

7-methoxy-8-(3-oxobut-1-en-1-yl)-3,4-dihydro-1-benzopyran-2-one

C14H14O4 (246.0892)


   

5-(1,2-dihydroxy-2-phenylethyl)benzene-1,3-diol

5-(1,2-dihydroxy-2-phenylethyl)benzene-1,3-diol

C14H14O4 (246.0892)


   

8-(1,2-dihydroxy-3-methylbut-3-en-1-yl)chromen-2-one

8-(1,2-dihydroxy-3-methylbut-3-en-1-yl)chromen-2-one

C14H14O4 (246.0892)


   

6-[(3,5-dihydroxyphenyl)methyl]-2,3-dimethylpyran-4-one

6-[(3,5-dihydroxyphenyl)methyl]-2,3-dimethylpyran-4-one

C14H14O4 (246.0892)


   

(8r)-8-hydroxy-4,8,12-trimethyl-2,6-dioxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),4,9(13),10-tetraen-3-one

(8r)-8-hydroxy-4,8,12-trimethyl-2,6-dioxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),4,9(13),10-tetraen-3-one

C14H14O4 (246.0892)


   

(1r,9r,11s,14s)-9,14-dimethyl-4,12-dioxatetracyclo[9.2.1.0¹,⁹.0³,⁷]tetradeca-3(7),5-diene-8,13-dione

(1r,9r,11s,14s)-9,14-dimethyl-4,12-dioxatetracyclo[9.2.1.0¹,⁹.0³,⁷]tetradeca-3(7),5-diene-8,13-dione

C14H14O4 (246.0892)


   

(-)-decursinol

(-)-decursinol

C14H14O4 (246.0892)


   

7-[(4-hydroxy-3-methylbut-2-en-1-yl)oxy]chromen-2-one

7-[(4-hydroxy-3-methylbut-2-en-1-yl)oxy]chromen-2-one

C14H14O4 (246.0892)


   

10-(acetyloxy)deca-2,8-dien-4,6-diyn-1-yl acetate

10-(acetyloxy)deca-2,8-dien-4,6-diyn-1-yl acetate

C14H14O4 (246.0892)


   

5-hydroxy-7-methyl-2-(3-oxobutyl)chromen-4-one

5-hydroxy-7-methyl-2-(3-oxobutyl)chromen-4-one

C14H14O4 (246.0892)


   

8-hydroxy-1-methoxy-6-methyl-1h,2h,3h-cyclopenta[b]chromen-9-one

8-hydroxy-1-methoxy-6-methyl-1h,2h,3h-cyclopenta[b]chromen-9-one

C14H14O4 (246.0892)


   

3-[(2s)-butan-2-yl]-4-(4-hydroxyphenyl)furan-2,5-dione

3-[(2s)-butan-2-yl]-4-(4-hydroxyphenyl)furan-2,5-dione

C14H14O4 (246.0892)


   

methyl (2e,5e)-2-methoxy-4-oxo-6-phenylhexa-2,5-dienoate

methyl (2e,5e)-2-methoxy-4-oxo-6-phenylhexa-2,5-dienoate

C14H14O4 (246.0892)


   

6-hydroxy-1-methoxy-8-methyl-1h,2h,3h-cyclopenta[c]isochromen-5-one

6-hydroxy-1-methoxy-8-methyl-1h,2h,3h-cyclopenta[c]isochromen-5-one

C14H14O4 (246.0892)


   

7-hydroxy-5-methyl-2-(2-oxobutyl)chromen-4-one

7-hydroxy-5-methyl-2-(2-oxobutyl)chromen-4-one

C14H14O4 (246.0892)


   

4-[(2e,4e)-hexa-2,4-dienoyl]-5-hydroxy-3,6-dimethylcyclohexa-3,5-diene-1,2-dione

4-[(2e,4e)-hexa-2,4-dienoyl]-5-hydroxy-3,6-dimethylcyclohexa-3,5-diene-1,2-dione

C14H14O4 (246.0892)


   

5-[(2e,4e)-hexa-2,4-dienoyl]-4-hydroxy-2-methoxybenzaldehyde

5-[(2e,4e)-hexa-2,4-dienoyl]-4-hydroxy-2-methoxybenzaldehyde

C14H14O4 (246.0892)


   

7-methoxy-8-(3-oxobutyl)chromen-2-one

7-methoxy-8-(3-oxobutyl)chromen-2-one

C14H14O4 (246.0892)


   

3',4'-dimethoxy-[1,1'-biphenyl]-3,4-diol

3',4'-dimethoxy-[1,1'-biphenyl]-3,4-diol

C14H14O4 (246.0892)


   

3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione

3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione

C14H14O4 (246.0892)


   

5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)chromen-4-one

5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)chromen-4-one

C14H14O4 (246.0892)


   

7-{[(1e,3r)-4-hydroxy-3-methylbut-1-en-1-yl]oxy}chromen-2-one

7-{[(1e,3r)-4-hydroxy-3-methylbut-1-en-1-yl]oxy}chromen-2-one

C14H14O4 (246.0892)


   

(2z,8z)-10-(acetyloxy)deca-2,8-dien-4,6-diyn-1-yl acetate

(2z,8z)-10-(acetyloxy)deca-2,8-dien-4,6-diyn-1-yl acetate

C14H14O4 (246.0892)


   

methyl 2-methoxy-4-oxo-6-phenylhexa-2,5-dienoate

methyl 2-methoxy-4-oxo-6-phenylhexa-2,5-dienoate

C14H14O4 (246.0892)


   

3-[(2r)-2-hydroxypropyl]-8-methoxynaphthalene-1,2-dione

3-[(2r)-2-hydroxypropyl]-8-methoxynaphthalene-1,2-dione

C14H14O4 (246.0892)


   

7-hydroxy-6-[(1z)-3-hydroxy-3-methylbut-1-en-1-yl]chromen-2-one

7-hydroxy-6-[(1z)-3-hydroxy-3-methylbut-1-en-1-yl]chromen-2-one

C14H14O4 (246.0892)


   

3,5-dimethoxy-[1,1'-biphenyl]-4,4'-diol

3,5-dimethoxy-[1,1'-biphenyl]-4,4'-diol

C14H14O4 (246.0892)


   

(1r,9r,11r,14s)-9,14-dimethyl-4,12-dioxatetracyclo[9.2.1.0¹,⁹.0³,⁷]tetradeca-3(7),5-diene-8,13-dione

(1r,9r,11r,14s)-9,14-dimethyl-4,12-dioxatetracyclo[9.2.1.0¹,⁹.0³,⁷]tetradeca-3(7),5-diene-8,13-dione

C14H14O4 (246.0892)


   

7-hydroxy-6-(2-hydroxy-3-methylbut-3-en-1-yl)chromen-2-one

7-hydroxy-6-(2-hydroxy-3-methylbut-3-en-1-yl)chromen-2-one

C14H14O4 (246.0892)


   

4-(hexa-2,4-dienoyl)-5-hydroxy-3,6-dimethylcyclohexa-3,5-diene-1,2-dione

4-(hexa-2,4-dienoyl)-5-hydroxy-3,6-dimethylcyclohexa-3,5-diene-1,2-dione

C14H14O4 (246.0892)


   

7-hydroxy-8-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]chromen-2-one

7-hydroxy-8-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]chromen-2-one

C14H14O4 (246.0892)


   

methyl 4-oxo-2-propylchromene-5-carboxylate

methyl 4-oxo-2-propylchromene-5-carboxylate

C14H14O4 (246.0892)


   

7-[(3,3-dimethyloxiran-2-yl)methoxy]chromen-2-one

7-[(3,3-dimethyloxiran-2-yl)methoxy]chromen-2-one

C14H14O4 (246.0892)


   

7-hydroxy-8-[(3-methylbut-2-en-1-yl)oxy]chromen-2-one

7-hydroxy-8-[(3-methylbut-2-en-1-yl)oxy]chromen-2-one

C14H14O4 (246.0892)


   

5-acetyl-6-methoxy-2-(propan-2-ylidene)-1-benzofuran-3-one

5-acetyl-6-methoxy-2-(propan-2-ylidene)-1-benzofuran-3-one

C14H14O4 (246.0892)


   

8-(hydroxymethyl)-8-methyl-9h,10h-pyrano[2,3-h]chromen-2-one

8-(hydroxymethyl)-8-methyl-9h,10h-pyrano[2,3-h]chromen-2-one

C14H14O4 (246.0892)


   

(3r,3ar)-3-(furan-2-yl)-3a,7-dimethyl-4,5-dihydro-3h-2-benzofuran-1,6-dione

(3r,3ar)-3-(furan-2-yl)-3a,7-dimethyl-4,5-dihydro-3h-2-benzofuran-1,6-dione

C14H14O4 (246.0892)


   

(1r)-8-hydroxy-1-methoxy-6-methyl-1h,2h,3h-cyclopenta[b]chromen-9-one

(1r)-8-hydroxy-1-methoxy-6-methyl-1h,2h,3h-cyclopenta[b]chromen-9-one

C14H14O4 (246.0892)


   

3-[3-hydroxy-5-(hydroxymethyl)phenoxy]-5-methylphenol

3-[3-hydroxy-5-(hydroxymethyl)phenoxy]-5-methylphenol

C14H14O4 (246.0892)


   

1-{10-methoxy-5-methylidene-3,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-11-yl}ethanone

1-{10-methoxy-5-methylidene-3,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-11-yl}ethanone

C14H14O4 (246.0892)


   

7-hydroxy-6-[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]chromen-2-one

7-hydroxy-6-[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]chromen-2-one

C14H14O4 (246.0892)


   

7-hydroxy-8-[(1r)-1-hydroxy-3-methylbut-3-en-1-yl]chromen-2-one

7-hydroxy-8-[(1r)-1-hydroxy-3-methylbut-3-en-1-yl]chromen-2-one

C14H14O4 (246.0892)


   

3-(furan-3-yl)-3a,7-dimethyl-4,5-dihydro-3h-2-benzofuran-1,6-dione

3-(furan-3-yl)-3a,7-dimethyl-4,5-dihydro-3h-2-benzofuran-1,6-dione

C14H14O4 (246.0892)


   

1-(1,6-dihydroxy-8-methoxy-3-methylnaphthalen-2-yl)ethanone

1-(1,6-dihydroxy-8-methoxy-3-methylnaphthalen-2-yl)ethanone

C14H14O4 (246.0892)


   

6-butanoyl-7-methoxychromen-2-one

6-butanoyl-7-methoxychromen-2-one

C14H14O4 (246.0892)


   

6,8-dihydroxy-3-(penta-1,3-dien-1-yl)-3,4-dihydro-2-benzopyran-1-one

6,8-dihydroxy-3-(penta-1,3-dien-1-yl)-3,4-dihydro-2-benzopyran-1-one

C14H14O4 (246.0892)


   

4-(3-hydroxy-5-methylphenoxy)-5-methylbenzene-1,3-diol

4-(3-hydroxy-5-methylphenoxy)-5-methylbenzene-1,3-diol

C14H14O4 (246.0892)


   

5-[(4z)-8-hydroxy-1h,5h,6h-pyrrolo[2,3-c]azepin-4-ylidene]imidazole-2,4-diol

5-[(4z)-8-hydroxy-1h,5h,6h-pyrrolo[2,3-c]azepin-4-ylidene]imidazole-2,4-diol

C11H10N4O3 (246.0753)


   

6,8-dihydroxy-3-[(1e,3e)-penta-1,3-dien-1-yl]-3,4-dihydro-2-benzopyran-1-one

6,8-dihydroxy-3-[(1e,3e)-penta-1,3-dien-1-yl]-3,4-dihydro-2-benzopyran-1-one

C14H14O4 (246.0892)