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D8008

Sigma-Aldrich

7,7-Dimethyl-(5Z,8Z)-eicosadienoic acid

≥95%

Synonym(s):

DEDA

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About This Item

Empirical Formula (Hill Notation):
C22H40O2
CAS Number:
89560-01-0
Molecular Weight:
336.55
MDL number:
MFCD00133010
UNSPSC Code:
12352202
PubChem Substance ID:
24278388

biological source

synthetic (organic)

Assay

≥95%

form

liquid

storage temp.

−20°C

SMILES string

CCCCCCCCCCC\C=C/C(C)(C)\C=C/CCCC(O)=O

InChI

1S/C22H40O2/c1-4-5-6-7-8-9-10-11-12-13-16-19-22(2,3)20-17-14-15-18-21(23)24/h16-17,19-20H,4-15,18H2,1-3H3,(H,23,24)/b19-16-,20-17-

InChI key

AGKRHAILCPYNFH-DUQSFWPASA-N

Gene Information

human ... ADORA2A(135) , ADORA2B(136)

Biochem/physiol Actions

Inhibitor of phospholipase A2 and lipoxygenase. Inhibits endogenous synthesis of leukotrienes.

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Activity of the epithelial Na+ channel (ENaC) is the limiting step for discretionary Na+ reabsorption in the cortical collecting duct. Xenopus laevis kidney A6 cells were used to investigate the effects of cytosolic phospholipase A2 (cPLA2) activity on Na+ transport.
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Neurochemical research, 28(2), 319-326 (2003-03-01)
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M D Lister et al.
The Journal of biological chemistry, 264(15), 8520-8528 (1989-05-25)
In order to ascertain the role of phospholipase A2 (PLA2) in the release of arachidonic acid for eicosanoid biosynthesis, we have characterized a Ca2+-dependent PLA2 from P388D1 cells, evaluated inhibitors of its activity, and correlated the effects of these inhibitors
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