Drug Information
Drug General Information | |||||
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Drug ID |
D04UEN
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Former ID |
DNC008163
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Drug Name |
1,1,1-trifluoro-3-(octylsulfinyl)propan-2-one
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Drug Type |
Small molecular drug
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Indication | Discovery agent | Investigative | [1] | ||
Structure |
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Download2D MOL |
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Formula |
C11H19F3O2S
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Canonical SMILES |
CCCCCCCCS(=O)CC(=O)C(F)(F)F
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InChI |
1S/C11H19F3O2S/c1-2-3-4-5-6-7-8-17(16)9-10(15)11(12,13)14/h2-9H2,1H3
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InChIKey |
WVDSELHSQAACKS-UHFFFAOYSA-N
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PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | Fatty-acid amide hydrolase | Target Info | Inhibitor | [1] | |
Liver carboxylesterase | Target Info | Inhibitor | [1] | ||
BioCyc Pathway | Anandamide degradation | ||||
KEGG Pathway | Retrograde endocannabinoid signalinghsa00983:Drug metabolism - other enzymes | ||||
Metabolic pathways | |||||
PANTHER Pathway | Anandamide degradation | ||||
Pathway Interaction Database | E2F transcription factor network | ||||
WikiPathways | NRF2 pathway | ||||
Nuclear Receptors Meta-Pathway | |||||
Heroin metabolism | |||||
Irinotecan Pathway | |||||
Fluoropyrimidine Activity | |||||
Phase I biotransformations, non P450 | |||||
References | |||||
REF 1 | Bioorg Med Chem. 2008 Feb 15;16(4):2114-30. Epub 2007 Nov 26.Influence of sulfur oxidation state and steric bulk upon trifluoromethyl ketone (TFK) binding kinetics to carboxylesterases and fatty acid amide hydrolase (FAAH). | ||||
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