Chemical Formula: C13H12N2O
Chemical Formula C13H12N2O
Found 62 metabolite its formula value is C13H12N2O
Harmine
C13H12N2O (212.09495819999998)
Harmine is a harmala alkaloid in which the harman skeleton is methoxy-substituted at C-7. It has a role as a metabolite, an anti-HIV agent and an EC 1.4.3.4 (monoamine oxidase) inhibitor. It derives from a hydride of a harman. Harmine is a natural product found in Thalictrum foetidum, Acraea andromacha, and other organisms with data available. Alkaloid isolated from seeds of PEGANUM HARMALA; ZYGOPHYLLACEAE. It is identical to banisterine, or telepathine, from Banisteria caapi and is one of the active ingredients of hallucinogenic drinks made in the western Amazon region from related plants. It has no therapeutic use, but (as banisterine) was hailed as a cure for postencephalitic PARKINSON DISEASE in the 1920s. D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D006213 - Hallucinogens Harmine is found in fruits. Harmine is an alkaloid from Passiflora edulis (passionfruit A harmala alkaloid in which the harman skeleton is methoxy-substituted at C-7. D004791 - Enzyme Inhibitors > D008996 - Monoamine Oxidase Inhibitors C471 - Enzyme Inhibitor > C667 - Monoamine Oxidase Inhibitor CONFIDENCE Reference Standard (Level 1); NaToxAq - Natural Toxins and Drinking Water Quality - From Source to Tap (https://natoxaq.ku.dk) [Raw Data] CB043_Harmine_pos_40eV_CB000020.txt [Raw Data] CB043_Harmine_pos_50eV_CB000020.txt [Raw Data] CB043_Harmine_pos_10eV_CB000020.txt [Raw Data] CB043_Harmine_pos_30eV_CB000020.txt [Raw Data] CB043_Harmine_pos_20eV_CB000020.txt CONFIDENCE standard compound; INTERNAL_ID 2884 [Raw Data] CB043_Harmine_neg_50eV_000013.txt [Raw Data] CB043_Harmine_neg_30eV_000013.txt [Raw Data] CB043_Harmine_neg_10eV_000013.txt [Raw Data] CB043_Harmine_neg_20eV_000013.txt [Raw Data] CB043_Harmine_neg_40eV_000013.txt Harmine is a natural dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) inhibitor with anticancer and anti-inflammatory activities. Harmine has a high affinity of 5-HT2A serotonin receptor, with an Ki of 397 nM[1]. Harmine is a natural dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) inhibitor with anticancer and anti-inflammatory activities. Harmine has a high affinity of 5-HT2A serotonin receptor, with an Ki of 397 nM[1]. Harmine is a natural dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) inhibitor with anticancer and anti-inflammatory activities. Harmine has a high affinity of 5-HT2A serotonin receptor, with an Ki of 397 nM[1].
Carbanilide
C13H12N2O (212.09495819999998)
Carbanilide is found in fruits. Carbanilide is isolated from coconut mil
Salicyaldehyde
C13H12N2O (212.09495819999998)
Salicyaldehyde, also known as salicylaldehyde phenylhydrazone, is a member of the class of compounds known as phenylhydrazines. Phenylhydrazines are compounds containing a phenylhydrazide moiety, which consists of a hydrazide substituent attached to a phenyl group. Salicyaldehyde is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Salicyaldehyde can be found in chinese cinnamon, which makes salicyaldehyde a potential biomarker for the consumption of this food product.
9-acetamido-3,4-dihydropyrido-(3,4-b)-indole|9-Acetyl-3,4-dihydro-beta-carboline
C13H12N2O (212.09495819999998)
Harmine
C13H12N2O (212.09495819999998)
Origin: Plant; SubCategory_DNP: Alkaloids derived from tryptophan, beta-Carboline alkaloids, Indole alkaloids D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D006213 - Hallucinogens D004791 - Enzyme Inhibitors > D008996 - Monoamine Oxidase Inhibitors C471 - Enzyme Inhibitor > C667 - Monoamine Oxidase Inhibitor Annotation level-1 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.622 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.620 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.613 Harmine is a natural dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) inhibitor with anticancer and anti-inflammatory activities. Harmine has a high affinity of 5-HT2A serotonin receptor, with an Ki of 397 nM[1]. Harmine is a natural dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) inhibitor with anticancer and anti-inflammatory activities. Harmine has a high affinity of 5-HT2A serotonin receptor, with an Ki of 397 nM[1]. Harmine is a natural dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) inhibitor with anticancer and anti-inflammatory activities. Harmine has a high affinity of 5-HT2A serotonin receptor, with an Ki of 397 nM[1].
4-Methoxy-1-methyl-9h-pyrido[3,4-b]indole
C13H12N2O (212.09495819999998)
1-Methoxymethyl-β-carboline
C13H12N2O (212.09495819999998)
1-(methoxymethyl)-9H-pyrido[3,4-b]indole is a natural product found in Eurycoma longifolia with data available.
7-methoxy-1-methyl-9H-pyrido[3,4-b]indole
C13H12N2O (212.09495819999998)
2-imidazol-1-yl-3,4-dihydro-2H-naphthalen-1-one
C13H12N2O (212.09495819999998)
3-PHENYL-6,7-DIHYDRO-1H-INDAZOL-4(5H)-ONE
C13H12N2O (212.09495819999998)
4-HYDROXYBIPHENYL-4-CARBOXIMIDAMIDE
C13H12N2O (212.09495819999998)
BIPHENYL-3-CARBOXYLIC ACID HYDRAZIDE
C13H12N2O (212.09495819999998)
4-(2-FURYL)-2,3-DIHYDRO-1H-1,5-BENZODIAZEPINE
C13H12N2O (212.09495819999998)
Benzamide,N-(3-methyl-2-pyridinyl)-
C13H12N2O (212.09495819999998)
4-oxo-8-propan-2-yl-1H-quinoline-3-carbonitrile
C13H12N2O (212.09495819999998)
Phenol,4-methyl-2-(2-phenyldiazenyl)-
C13H12N2O (212.09495819999998)
N-(4-methoxyphenyl)-1-pyridin-4-ylmethanimine
C13H12N2O (212.09495819999998)
(2-aminophenyl)(phenyl)methanone oxime
C13H12N2O (212.09495819999998)
Salicylaldehyde phenylhydrazone
C13H12N2O (212.09495819999998)
8-Isopropyl-4-oxo-1,4-dihydro-3-quinolinecarbonitrile
C13H12N2O (212.09495819999998)
4-PHENYL-3,4-DIHYDROPYRROLO[1,2-A]PYRAZIN-1(2H)-ONE
C13H12N2O (212.09495819999998)
4-Biphenylcarboxylic acid hydrazide
C13H12N2O (212.09495819999998)
N-(4-METHYL-PYRIDIN-3-YL)-BENZAMIDE
C13H12N2O (212.09495819999998)
(1-methyl-9H-pyrido[3,4-b]indol-3-yl)methanol
C13H12N2O (212.09495819999998)
2-((3-OXOCYCLOHEX-1-ENYL)AMINO)BENZENECARBONITRILE
C13H12N2O (212.09495819999998)
5-[(1-Indolyl)Methyl]-3-Methylisoxazole
C13H12N2O (212.09495819999998)
Cordysinin D
C13H12N2O (212.09495819999998)
A member of the class of beta-carbolines that is beta-carboline substituted by a 1-hydroxyethyl group at position 1 (the S enantiomer). It has been isolated from the mycelia of Cordyceps sinensis.
Cordysinin C
C13H12N2O (212.09495819999998)
A member of the class of beta-carbolines that is beta-carboline substituted by a 1-hydroxyethyl group at position 1 (the R enantiomer). It has been isolated from the mycelia of Cordyceps sinensis.
Yageine
C13H12N2O (212.09495819999998)
D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D006213 - Hallucinogens D004791 - Enzyme Inhibitors > D008996 - Monoamine Oxidase Inhibitors C471 - Enzyme Inhibitor > C667 - Monoamine Oxidase Inhibitor Harmine is a natural dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) inhibitor with anticancer and anti-inflammatory activities. Harmine has a high affinity of 5-HT2A serotonin receptor, with an Ki of 397 nM[1]. Harmine is a natural dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) inhibitor with anticancer and anti-inflammatory activities. Harmine has a high affinity of 5-HT2A serotonin receptor, with an Ki of 397 nM[1]. Harmine is a natural dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) inhibitor with anticancer and anti-inflammatory activities. Harmine has a high affinity of 5-HT2A serotonin receptor, with an Ki of 397 nM[1].
N-benzoyl-1-methylpyridin-4(1H)-imine
C13H12N2O (212.09495819999998)
1,3-Diphenylurea
C13H12N2O (212.09495819999998)
A member of the class of phenylureas that is urea in which one of the hydrogens of each amino group is replaced by a phenyl group. It is present in coconut milk (Cocos nucifera).
SIRT-IN-3
C13H12N2O (212.09495819999998)
SIRT-IN-3 is a potent SIRT inhibitor, with an IC50 of 17 μM for SIRT1. SIRT-IN-3 shows about 4-fold and 14-fold selectivity for SIRT1 over SIRT2 and SIRT3, respectively (IC50 of 74 μM and 235 μM for SIRT2 and SIRT3, respectively)[1].