Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D07HSQ
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| Former ID |
DNC007096
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| Drug Name |
1-adamantan-1-yl-3-((R)-1-phenyl-ethyl)-urea
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| Synonyms |
CHEMBL222080; 1-adamantan-1-yl-3-((R)-1-phenyl-ethyl)-urea
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
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Download2D MOL |
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| Formula |
C19H26N2O
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| Canonical SMILES |
CC(C1=CC=CC=C1)NC(=O)NC23CC4CC(C2)CC(C4)C3
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| InChI |
1S/C19H26N2O/c1-13(17-5-3-2-4-6-17)20-18(22)21-19-10-14-7-15(11-19)9-16(8-14)12-19/h2-6,13-16H,7-12H2,1H3,(H2,20,21,22)/t13-,14?,15?,16?,19?/m1/s1
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| InChIKey |
ODVZFEPLOWORBJ-PGBRGIIUSA-N
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|
| REF 1 | Solid-phase combinatorial approach for the optimization of soluble epoxide hydrolase inhibitors. Bioorg Med Chem Lett. 2006 Nov 15;16(22):5773-7. | |||
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