Drug Information
Drug General Information | Top | |||
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Drug ID |
D0D0KT
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Former ID |
DNC009865
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Drug Name |
N-(3-Phenyl-propyl)-nicotinamide
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Synonyms |
N-(3-phenylpropyl)pyridine-3-carboxamide; CHEMBL560538; N-(3-Phenyl-propyl)-nicotinamide; AC1NEVG1; SCHEMBL4182430; MolPort-001-620-971; ZINC2736778; BDBM50297409; STK440753; AKOS003254198; MCULE-2570363469; N-(3-phenylpropyl)-3-pyridylcarboxamide
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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 |
C15H16N2O
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Canonical SMILES |
C1=CC=C(C=C1)CCCNC(=O)C2=CN=CC=C2
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InChI |
1S/C15H16N2O/c18-15(14-9-5-10-16-12-14)17-11-4-8-13-6-2-1-3-7-13/h1-3,5-7,9-10,12H,4,8,11H2,(H,17,18)
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InChIKey |
DGVNUZBITSWBPL-UHFFFAOYSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Soluble epoxide hydrolase (EPHX2) | Target Info | Inhibitor | [1] |
KEGG Pathway | Arachidonic acid metabolism | |||
Metabolic pathways | ||||
Peroxisome | ||||
Pathwhiz Pathway | Arachidonic Acid Metabolism | |||
WikiPathways | Metapathway biotransformation | |||
Arachidonate Epoxygenase / Epoxide Hydrolase | ||||
Arachidonic acid metabolism |
References | Top | |||
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REF 1 | Structure-based optimization of arylamides as inhibitors of soluble epoxide hydrolase. J Med Chem. 2009 Oct 8;52(19):5880-95. |
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