5,8,11-EICOSATRIYNOIC ACID

CCCCCCCCC#CCC#CCC#CCCCC(O)=O

InChIKey=OWYNLPMPYBYKJP-UHFFFAOYSA-N

InChI=1S/C20H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h2-8,11,14,17-19H2,1H3,(H,21,22)

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Targets

Primary Target	Pharmacology	Condition	Potency
lipoxygenase 1 Target ID: lipoxygenase Sources: https://www.ncbi.nlm.nih.gov/pubmed/6106018 \| https://www.ncbi.nlm.nih.gov/pubmed/8048084	Inhibitor 8297
leukotriene C4 biosynthesis 1 Target ID: leukotriene C4 biosynthesis Sources: https://www.ncbi.nlm.nih.gov/pubmed/6106018	Inhibitor 8297

PubMed

Title	Date	PubMed
Inhibition of leukotriene C and leukotriene D biosynthesis.	1980 Sep 10	6106018
Inhibition of mammalian hepatic glutathione S-transferases by acetylenic fatty acids.	1994 Aug	8048084
Elevated 12-lipoxygenase activity in the spontaneously hypertensive rat.	1997 Apr	9128202

Substance Class	Chemical Created by `admin` on `Fri Dec 15 18:09:49 GMT 2023` Edited by `admin` on `Fri Dec 15 18:09:49 GMT 2023`
Record UNII	R7EU6LY7HJ
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

5,8,11-EICOSATRIYNOIC ACID

Common Name

English

ICOSA-5,8,11-TRIYNOIC ACID

Common Name

English

5,8,11-EICOSATRIYNOICACID

Common Name

English

EICOSATRIYNOIC ACID, 5,8,11-

Common Name

English

Code System Code Type Description

CAS

13488-22-7