5-PHENYLVALERIC ACID

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

Structure Search

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)

HIDE SMILES / InChI

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
Specificity of procaine and ester hydrolysis by human, minipig, and rat skin and liver.	2007-11	17664252
Inter-individual variability in esterases in human liver.	2007-09-15	17651701
4-Phenylbutyrate restores the functionality of a misfolded mutant low-density lipoprotein receptor.	2007-04	17408384
Structure and polymer form of poly-3-hydroxyalkanoates produced by Pseudomonas oleovorans grown with mixture of sodium octanoate/undecylenic acid and sodium octanoate/5-phenylvaleric acid.	2007-01-30	16919325
Effects of chromophore orientation and molecule conformation on surface-enhanced Raman scattering studied with alkanoic acids and colloidal silver nanoparticles.	2006-12-21	17190569
Induction and quantification of phenylacyl-CoA ligase enzyme activities in Pseudomonas putida CA-3 grown on aromatic carboxylic acids.	2005-10-15	16165317
Molecular characterization of extracellular medium-chain-length poly(3-hydroxyalkanoate) depolymerase genes from Pseudomonas alcaligenes strains.	2005-06	15995648
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.	2004-06-15	15177652
Metabolism of dietary procyanidins in rats.	2003-10-15	14556848
Properties of phenyl valerate esterase activities from chicken serum are comparable with soluble esterases of peripheral nerves in relation with organophosphorus compounds inhibition.	2003-04-30	12765233
Intracellular degradation of two structurally different polyhydroxyalkanoic acids accumulated in Pseudomonas putida and Pseudomonas citronellolis from mixtures of octanoic acid and 5-phenylvaleric acid.	2001-12-10	11718820
Paraoxon sensitive phenylvalerate hydrolase in assessing the severity of acute paraoxon poisoning.	2001	11327223

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:21:57 GMT 2025` Edited by `admin` on `Mon Mar 31 19:21:57 GMT 2025`
Record UNII	XYJ5U8LCQ8
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

5-PHENYLVALERIC ACID

Systematic Name

English

NSC-65637

Preferred Name

English

VALERIC ACID, 5-PHENYL-

Common Name

English

BENZENEPENTANOIC ACID

Systematic Name

English

.DELTA.-PHENYLVALERIC ACID

Systematic Name

English

VALERIC ACID, .DELTA.-PHENYL-

Common Name

English

Code System Code Type Description

DRUG BANK

DB04051