Details
Stereochemistry | RACEMIC |
Molecular Formula | C13H14N2O2 |
Molecular Weight | 230.2625 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H]1N[C@@H](CC2=C1NC3=CC=CC=C23)C(O)=O
InChI
InChIKey=ZUPHXNBLQCSEIA-HQJQHLMTSA-N
InChI=1S/C13H14N2O2/c1-7-12-9(6-11(14-7)13(16)17)8-4-2-3-5-10(8)15-12/h2-5,7,11,14-15H,6H2,1H3,(H,16,17)/t7-,11+/m1/s1
Molecular Formula | C13H14N2O2 |
Molecular Weight | 230.2625 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
(1R,3S)-1-methyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid (MTCA) is a β-carboline indole alkaloid naturally occurring in plants, foods, insects, and endogenously in mammals and humans. It exerts antioxidant and antithrombotic properties. MTCA is thought to be a possible causative substance of eosinophilia-myalgia syndrome associated with ingestion of L-tryptophan.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8517786
Curator's Comment: 1-Methyl-tetrahydro-beta-carboline-3-carboxylic acid (MTCA) is brain penetrant in rats. No human data available.
Originator
Sources: http://pubs.acs.org/doi/10.1021/jm00262a027
Curator's Comment: reference retrieved from https://www.ncbi.nlm.nih.gov/pubmed/6574460
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL204 Sources: https://www.ncbi.nlm.nih.gov/pubmed/27997749 |
0.39 µM [Ki] | ||
Target ID: CHEMBL244 Sources: https://www.ncbi.nlm.nih.gov/pubmed/27997749 |
0.43 µM [Ki] | ||
Target ID: CHEMBL1929 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22957895 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
---|---|---|
Presence of 1-methyl-1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid, a precursor of a mutagenic nitroso compound, in soy sauce. | 1983 May |
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Endogenous formation of 1-methyl-1,2,3,4-tetrahydro-beta-carboline-3- carboxylic acid in man as the possible causative substance of eosinophilia-myalgia syndrome associated with ingestion of L-tryptophan. | 1991 |
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Accumulation of 1-methyl-tetrahydro-beta-carboline-3-carboxylic acid in blood and organs of rat. A possible causative substance of eosinophilia-myalgia syndrome associated with ingestion of L-tryptophan. | 1993 |
|
1-methyl-1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid and 1,2, 3,4-tetrahydro-beta-carboline-3-carboxylic acid in fruits. | 1999 Dec |
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Tetrahydro-beta-carbolines, potential neuroactive alkaloids, in chocolate and cocoa. | 2000 Oct |
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Investigation of the tuber constituents of maca (Lepidium meyenii Walp.). | 2002 Sep 25 |
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Increased level of tetrahydro-beta-carboline derivatives in short-term fermented garlic. | 2006 Dec |
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The Methyltetrahydro-{beta}-Carbolines in Maca (Lepidium meyenii). | 2009 Sep |
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Inhibition of platelet aggregation and thrombosis by indole alkaloids isolated from the edible insect Protaetia brevitarsis seulensis (Kolbe). | 2017 Jun |
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Manipulation of the Precursor Supply in Yeast Significantly Enhances the Accumulation of Prenylated β-Carbolines. | 2017 Jun 16 |
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Chemical Constituents from the Flower of Hosta plantaginea with Cyclooxygenases Inhibition and Antioxidant Activities and Their Chemotaxonomic Significance. | 2017 Oct 26 |
Patents
Sample Use Guides
rats: single oral dose 1.6 mg/kg or 10 mg/kg, chronic treatment with a 10 mg/kg dose for 6 weeks.
mice: 10-50 uM (iv)
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27997749
(1R,3S)-1-methyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid treatment resulted in a dose-dependent inhibition of TNF-a-induced secretion of PAI-1 from HUVECs, which was significant at 10-50lM
Substance Class |
Chemical
Created
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admin
on
Edited
Sat Dec 16 11:14:53 GMT 2023
by
admin
on
Sat Dec 16 11:14:53 GMT 2023
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Record UNII |
0QGP5V5JAT
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Record Status |
Validated (UNII)
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Record Version |
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