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D2154

5,6-Dehydroarachidonic acid

≥98%, ethanol solution

Synonym(s):

5,6-dehydro AA, cis-8,11,14-Eicosatrien-5-ynoic acid

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Pack SizeSKUAvailabilityPrice
100 μg
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$534.00

About This Item

Empirical Formula (Hill Notation):
C20H30O2
CAS Number:
Molecular Weight:
302.45
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352211
EC Number:
200-578-6
MDL number:

$534.00


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Quality Level

assay

≥98%

form

ethanol solution

shipped in

wet ice

storage temp.

−20°C

SMILES string

CCCCC\C=C/C\C=C/C\C=C/CC#CCCCC(O)=O

InChI

1S/C20H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h6-7,9-10,12-13H,2-5,8,11,14,17-19H2,1H3,(H,21,22)/b7-6-,10-9-,13-12-

InChI key

GIOQWSLKUVKKAO-QNEBEIHSSA-N

General description

An analog of arachidonic acid in which the 5,6 double bond has been replaced with an acetylene group.

Biochem/physiol Actions

Inhibits 5-lipoxygenase of guinea pig leukocytes with an IC50 of 10 μM. In extracts of rat basophilic leukemia cells preincubated with 5,6-dehydro AA, the Ki for the conversion of arachidonic acid to 5-HPETE is 15 μM.

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This Item
181198735000SML1395
assay

≥98%

assay

≥99% (TLC and GC)

assay

≥97% (CP)

assay

≥98.5% (GC)

storage temp.

−20°C

storage temp.

−70°C

storage temp.

−20°C

storage temp.

−20°C

shipped in

wet ice

shipped in

dry ice

shipped in

dry ice

shipped in

dry ice

form

ethanol solution

form

oil

form

liquid

form

waxy solid

Quality Level

200

Quality Level

100

Quality Level

200

Quality Level

200


pictograms

FlameExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

62.6 °F - closed cup

flash_point_c

17 °C - closed cup



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Strong suppression by mononuclear leukocytes from human newborns on maternal leukocytes: mediation by prostaglandins.
S A Johnsen et al.
Clinical immunology and immunopathology, 23(3), 606-615 (1982-06-01)
E Razin et al.
Journal of immunology (Baltimore, Md. : 1950), 133(2), 938-945 (1984-08-01)
The quantitative relationships between the secretion of a granule-associated mediator, beta-hexosaminidase, and the oxidative metabolism of arachidonic acid by the 5-lipoxygenase pathway were analyzed for a homogeneous population of T cell-dependent, bone marrow-derived, murine mast cells. The mast cells were
H H Tai et al.
Biochemistry, 19(9), 1989-1993 (1980-04-29)
[5,6-3H]arachidonic acid has been prepared by catalytic reduction of eicosa-cis-8,11,14-trien-5-ynoic acid (IV) over Lindlar catalyst. When either [5,6-3H]arachidonic acid or [5,6-3H]PGH2 is converted into PGI2 by swine aortic microsomes, the tritium at C-6 is lost to the medium. Thus, the



Global Trade Item Number

SKUGTIN
D2154-25UG04061838070678
D2154-100UG04061837896828

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