Drug Information
Drug General Information | Top | |||
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Drug ID |
D0J5KK
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Former ID |
DNC006880
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Drug Name |
1-adamantan-1-yl-3-piperidin-4-yl-urea
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Synonyms |
ASN 06482309; 1-Adamantan-1-yl-3-piperidin-4-yl-urea; CHEMBL215356; AC1MLKMS; SCHEMBL8234307; BDBM50191891; AKOS000794965
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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 |
C16H27N3O
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Canonical SMILES |
C1CNCCC1NC(=O)NC23CC4CC(C2)CC(C4)C3
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InChI |
1S/C16H27N3O/c20-15(18-14-1-3-17-4-2-14)19-16-8-11-5-12(9-16)7-13(6-11)10-16/h11-14,17H,1-10H2,(H2,18,19,20)
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InChIKey |
NWWZZPCDHOXVSZ-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 | Synthesis and SAR of conformationally restricted inhibitors of soluble epoxide hydrolase. Bioorg Med Chem Lett. 2006 Oct 1;16(19):5212-6. |
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