Drug Information
Drug General Information | Top | |||
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Drug ID |
D0UV8T
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Former ID |
DNC010090
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Drug Name |
4-(1H-1,2,3-triazol-5-yl)pyridine
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Synonyms |
(4-pyridyl)triazole; 4-(1H-1,2,3-triazol-5-yl)pyridine; SCHEMBL4806159; CHEMBL364898; ZINC27317; BDBM17472; 1,2,3-triazole analogue, 28; AKOS027406024
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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 |
C7H6N4
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Canonical SMILES |
C1=CN=CC=C1C2=NNN=C2
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InChI |
1S/C7H6N4/c1-3-8-4-2-6(1)7-5-9-11-10-7/h1-5H,(H,9,10,11)
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InChIKey |
KEFBRERBEDJOQZ-UHFFFAOYSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Indoleamine 2,3-dioxygenase 1 (IDO1) | Target Info | Inhibitor | [1] |
BioCyc | Superpathway of tryptophan utilization | |||
Tryptophan degradation | ||||
L-kynurenine degradation | ||||
Tryptophan degradation to 2-amino-3-carboxymuconate semialdehyde | ||||
NAD de novo biosynthesis | ||||
KEGG Pathway | Tryptophan metabolism | |||
Metabolic pathways | ||||
African trypanosomiasis | ||||
NetPath Pathway | TSLP Signaling Pathway | |||
IL5 Signaling Pathway | ||||
TGF_beta_Receptor Signaling Pathway | ||||
Pathwhiz Pathway | Tryptophan Metabolism | |||
Reactome | Tryptophan catabolism | |||
WikiPathways | Tryptophan metabolism | |||
Metabolism of amino acids and derivatives |
References | Top | |||
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REF 1 | Rational design of indoleamine 2,3-dioxygenase inhibitors. J Med Chem. 2010 Feb 11;53(3):1172-89. |
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