Drug Information
Drug General Information | Top | |||
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Drug ID |
D0T8ZL
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Former ID |
DNC006528
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Drug Name |
3-(2-carboxy-3-mercaptopropyl)benzoic acid
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Synonyms |
Thiol-Based Inhibitor, 7a; CHEMBL206699; CTK8A8777; BDBM17764; AKOS015965664; 3-[2-carboxy-2-(sulfanylmethyl)ethyl]benzoic acid; 3-(2-CARBOXY-3-MERCAPTO-PROPYL)-BENZOIC ACID
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
Structure |
Download2D MOL |
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Formula |
C11H12O4S
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Canonical SMILES |
C1=CC(=CC(=C1)C(=O)O)CC(CS)C(=O)O
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InChI |
1S/C11H12O4S/c12-10(13)8-3-1-2-7(4-8)5-9(6-16)11(14)15/h1-4,9,16H,5-6H2,(H,12,13)(H,14,15)
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InChIKey |
LQVBVNPZOILYPX-UHFFFAOYSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Glutamate carboxypeptidase II (GCPII) | Target Info | Inhibitor | [1] |
KEGG Pathway | Alanine, aspartate and glutamate metabolism | |||
Metabolic pathways | ||||
Vitamin digestion and absorption | ||||
NetPath Pathway | TCR Signaling Pathway | |||
TNFalpha Signaling Pathway | ||||
Reactome | Amino acid synthesis and interconversion (transamination) | |||
WikiPathways | One Carbon Metabolism |
References | Top | |||
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REF 1 | Structural optimization of thiol-based inhibitors of glutamate carboxypeptidase II by modification of the P1' side chain. J Med Chem. 2006 May 18;49(10):2876-85. |
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