Drug Information
Drug General Information | Top | |||
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Drug ID |
D09IQS
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Former ID |
DNC004105
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Drug Name |
4-Methyl-pyridine
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Synonyms |
4-METHYLPYRIDINE; 4-Picoline; 108-89-4; Pyridine, 4-methyl-; p-Picoline; gamma-Picoline; p-Methylpyridine; 4-methyl-pyridine; gamma-Methylpyridine; Ba 35846; UNII-TJD6V9SSO7; .gamma.-Picoline; NSC 18252; 4-Mepy; CCRIS 1723; .gamma.-Methylpyridine; HSDB 5386; EINECS 203-626-4; TJD6V9SSO7; AI3-24111; CHEBI:32547; FKNQCJSGGFJEIZ-UHFFFAOYSA-N; 4-Picoline, 99%; DSSTox_CID_1892; DSSTox_RID_76389; DSSTox_GSID_21892; 4-methyl pyridine; CAS-108-89-4; gamma-picolin; 4-Pyridylmethyl; 4-pi-coline; para-Methylpyridine; Methyl, 4-pyridinyl-; 4-Picoline
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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 |
C6H7N
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Canonical SMILES |
CC1=CC=NC=C1
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InChI |
1S/C6H7N/c1-6-2-4-7-5-3-6/h2-5H,1H3
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InChIKey |
FKNQCJSGGFJEIZ-UHFFFAOYSA-N
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CAS Number |
CAS 108-89-4
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PubChem Compound ID | ||||
ChEBI ID |
CHEBI:32547
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Target and Pathway | Top | |||
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Target(s) | Thromboxane-A synthase (TBXAS1) | Target Info | Inhibitor | [1] |
BioCyc | C20 prostanoid biosynthesis | |||
KEGG Pathway | Arachidonic acid metabolism | |||
Metabolic pathways | ||||
Platelet activation | ||||
Pathwhiz Pathway | Arachidonic Acid Metabolism | |||
WikiPathways | Prostaglandin Synthesis and Regulation | |||
Arachidonic acid metabolism | ||||
Phase 1 - Functionalization of compounds | ||||
Eicosanoid Synthesis |
References | Top | |||
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REF 1 | Highly selective inhibitors of thromboxane synthetase. 2. Pyridine derivatives. J Med Chem. 1981 Oct;24(10):1149-55. |
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