Drug Information
Drug General Information | Top | |||
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Drug ID |
D05MTA
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Former ID |
DNC007615
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Drug Name |
1-adamantan-1-yl-3-(4-pentyloxycylclohexyl)urea
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Synonyms |
CHEMBL439577; CHEMBL2031926; 1-(1-adamantyl)-3-(4-pentoxycyclohexyl)urea; 1-adamantan-1-yl-3-(4-pentyloxycylclohexyl)urea; SCHEMBL3178050; BDBM50383478
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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 |
C22H38N2O2
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Canonical SMILES |
CCCCCOC1CCC(CC1)NC(=O)NC23CC4CC(C2)CC(C4)C3
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InChI |
1S/C22H38N2O2/c1-2-3-4-9-26-20-7-5-19(6-8-20)23-21(25)24-22-13-16-10-17(14-22)12-18(11-16)15-22/h16-20H,2-15H2,1H3,(H2,23,24,25)
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InChIKey |
VIWCJPKZDQYQRJ-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 | 1,3-disubstituted ureas functionalized with ether groups are potent inhibitors of the soluble epoxide hydrolase with improved pharmacokinetic prope... J Med Chem. 2007 Oct 18;50(21):5217-26. |
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