Details
Stereochemistry | ACHIRAL |
Molecular Formula | C11H14O2 |
Molecular Weight | 178.2277 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)CCCCC1=CC=CC=C1
InChI
InChIKey=BYHDDXPKOZIZRV-UHFFFAOYSA-N
InChI=1S/C11H14O2/c12-11(13)9-5-4-8-10-6-2-1-3-7-10/h1-3,6-7H,4-5,8-9H2,(H,12,13)
Molecular Formula | C11H14O2 |
Molecular Weight | 178.2277 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Metabolism of dietary procyanidins in rats. | 2003 Oct 15 |
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The inhibition of the high sensitive peripheral nerve soluble esterases by mipafox. A new mathematical processing for the kinetics of inhibition of esterases by organophosphorus compounds. | 2004 Jun 15 |
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Molecular characterization of extracellular medium-chain-length poly(3-hydroxyalkanoate) depolymerase genes from Pseudomonas alcaligenes strains. | 2005 Jun |
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Induction and quantification of phenylacyl-CoA ligase enzyme activities in Pseudomonas putida CA-3 grown on aromatic carboxylic acids. | 2005 Oct 15 |
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4-Phenylbutyrate restores the functionality of a misfolded mutant low-density lipoprotein receptor. | 2007 Apr |
|
Specificity of procaine and ester hydrolysis by human, minipig, and rat skin and liver. | 2007 Nov |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:50:01 GMT 2023
by
admin
on
Fri Dec 15 18:50:01 GMT 2023
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Record UNII |
XYJ5U8LCQ8
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Record Status |
Validated (UNII)
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Record Version |
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