Drug Information
Drug General Information | Top | |||
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Drug ID |
D08ILW
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Former ID |
DNC014089
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Drug Name |
Cyclohexyl biphenyl-4-ylcarbamate
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Synonyms |
cyclohexyl biphenyl-4-ylcarbamate; CHEMBL541244; SCHEMBL12166742; URB602, 3k
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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 |
C19H21NO2
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Canonical SMILES |
C1CCC(CC1)OC(=O)NC2=CC=C(C=C2)C3=CC=CC=C3
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InChI |
1S/C19H21NO2/c21-19(22-18-9-5-2-6-10-18)20-17-13-11-16(12-14-17)15-7-3-1-4-8-15/h1,3-4,7-8,11-14,18H,2,5-6,9-10H2,(H,20,21)
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InChIKey |
SSVRRVRYQFRADL-UHFFFAOYSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Fatty acid amide hydrolase (FAAH) | Target Info | Inhibitor | [1] |
BioCyc | Anandamide degradation | |||
KEGG Pathway | Retrograde endocannabinoid signaling | |||
Panther Pathway | Anandamide degradation |
References | Top | |||
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REF 1 | The synthesis and biological evaluation of para-substituted phenolic N-alkyl carbamates as endocannabinoid hydrolyzing enzyme inhibitors. Eur J Med Chem. 2009 Jul;44(7):2994-3008. |
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