Drug Information
Drug General Information | Top | |||
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Drug ID |
D0I0YE
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Former ID |
DNC009858
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Drug Name |
N-[3,3-Bis-(4-fluorophenyl)-propyl]-benzamide
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Synonyms |
N-(3,3-diphenylpropyl)benzamide; CHEMBL556303; AC1LOGD3; Oprea1_468003; N-[3,3-Bis-(4-fluorophenyl)-propyl]-benzamide; SCHEMBL5948102; MolPort-001-492-275; ZINC995229; STK448927; BDBM50297396; AKOS003256160; MCULE-7987321913; ST50916006
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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 |
C22H21NO
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Canonical SMILES |
C1=CC=C(C=C1)C(CCNC(=O)C2=CC=CC=C2)C3=CC=CC=C3
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InChI |
1S/C22H21NO/c24-22(20-14-8-3-9-15-20)23-17-16-21(18-10-4-1-5-11-18)19-12-6-2-7-13-19/h1-15,21H,16-17H2,(H,23,24)
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InChIKey |
NSSSSHDNQFPODZ-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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