Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D0K0OR
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| Former ID |
DNC013508
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| Drug Name |
1-(5-(pyridin-2-yl)oxazol-2-yl)octan-1-one
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| Synonyms |
CHEMBL175021; 1-(5-(pyridin-2-yl)oxazol-2-yl)octan-1-one; SCHEMBL3197441; VLJKBQYNIDBQEJ-UHFFFAOYSA-N; BDBM50163176
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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 |
C16H20N2O2
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| Canonical SMILES |
CCCCCCCC(=O)C1=NC=C(O1)C2=CC=CC=N2
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| InChI |
1S/C16H20N2O2/c1-2-3-4-5-6-10-14(19)16-18-12-15(20-16)13-9-7-8-11-17-13/h7-9,11-12H,2-6,10H2,1H3
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| InChIKey |
VLJKBQYNIDBQEJ-UHFFFAOYSA-N
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|
| REF 1 | Inhibitors of proteases and amide hydrolases that employ an alpha-ketoheterocycle as a key enabling functionality. Bioorg Med Chem. 2008 Feb 15;16(4):1562-95. | |||
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