ChemicalBook--->CAS DataBase List--->79551-84-1

79551-84-1

79551-84-1 Structure

79551-84-1 Structure
IdentificationBack Directory
[Name]

20-carboxyarachidonic acid
[CAS]

79551-84-1
[Synonyms]

20-carboxyarachidonic acid
(5Z,8Z,11Z,14Z)-icosatetraenedioic acid
5(Z),8(Z),11(Z),14(Z)-eicosatetraenedioic acid
[Molecular Formula]

C20H30O4
[MOL File]

79551-84-1.mol
[Molecular Weight]

334.45
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

0.1 M Na2CO3: 1.5 mg/ml; DMF: 100 mg/ml; DMSO: 100 mg/ml; Ethanol: 100 mg/ml
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H319
[Precautionary statements ]

P210-P233-P240-P241-P242-P243-P264-P280-P303+P361+P353-P305+P351+P338-P337+P313-P370+P378-P403+P235-P501
Hazard InformationBack Directory
[Description]

20-carboxy Arachidonic acid (20-COOH-AA) is the major metabolite of 20-HETE that is produced in renal tubular epithelial, endothelial, and microvascular smooth muscle cell cultures. This ω-oxidation conversion can take place using purified alcohol dehydrogenases three and four or by microsomes containing recombinant human CYP4F3B. Like 20-HETE, 20-COOH-AA inhibits ion transport in the kidneys. It also produces vasorelaxation of porcine coronary microvessels constricted with endothelin. 20-COOH-AA binds to isolated ligand binding domains of peroxisome proliferator-activated receptor α (PPARα) (Kd = 0.87 ± 0.12 μM) and PPARγ (Kd = 1.7 ± 0.5 μM), and is a dual activator of PPARα and PPARγ in a transiently transfected COS-7 cell reporter system.
[Uses]

20-carboxy Arachidonic Acid is a PPARα and PPARγ activator.
[Definition]

ChEBI: An alpha,omega-dicarboxylic acid that is (5Z,8Z,11Z,14Z)-icosatetraene in which the two methyl groups are replaced by carboxy groups.
[storage]

Store at -20°C
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