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27376-76-7

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27376-76-7 Structure

27376-76-7 Structure
IdentificationBack Directory
[Name]

13,14-DIHYDRO-15-KETO PROSTAGLANDIN F2ALPHA
[CAS]

27376-76-7
[Synonyms]

PGFM
Prostaglandin FM
13,14-Dihydro-15-oxo-PGF2α
13,14-Dihydro-15-ketoPGF2α
VKTIONYPMSCHQI-XAGFEHLVSA-N
13,14-dihydro-15-keto PGF2a
13,14-Dihydro-15-ketodinoprost
15-Ketodihydroprostaglandin F2α
13,14-Dihydro-15-keto-pgf2alpha
15-Keto-13,14-dihydro-pgf2alpha
13,14-Dihydro-15-oxoprostaglandin f
13,14-Dihydro-15-ketoprostaglandin f
13,14-dihydro-15-ketoprostaglandin F2A
13,14-dihydro-15-keto Prostaglandin F2α
15-keto-13,14-dihydroprostaglandinf2alpha
13,14-DIHYDRO-15-KETO PROSTAGLANDIN F2ALPHA
PROSTAGLANDIN F2-ALPHA, (13;14-DIH-15-KETO)
13,14-DIHYDRO-15-KETO PROSTAGLANDIN F2ALPHA 99%
(5Z)-9α,11α-Dihydroxy-15-oxoprost-5-en-1-oic acid
9ALPHA,11ALPHA-DIHYDROXY-15-OXO-PROST-5Z-EN-1-OIC ACID
13,14-dihydro-15-keto Prostaglandin F2 MaxSpecStandard
13,14-dihydro-15-keto Prostaglandin F2α MaxSpec? Standard
Prost-5-en-1-oic acid, 9,11-dihydroxy-15-oxo-, (5Z,9α,11α)-
13,14-dihydro-15-keto Prostaglandin F2α Lipid Maps MS Standard
(5Z,9alpha,11 alpha)-9,11-Dihydroxy-15-oxoprost-5-en-1-oic acid
(Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-(3-oxooctyl)cyclopentyl]hept-5-enoic acid
[Molecular Formula]

C20H34O5
[MDL Number]

MFCD00135243
[MOL File]

27376-76-7.mol
[Molecular Weight]

354.48
Chemical PropertiesBack Directory
[storage temp. ]

−20°C
[solubility ]

DMF: >100 mg/ml (from PGF2a); DMSO: >100 mg/ml (from PGF2a); Ethanol: >100 mg/ml (from PGF2a); PBS pH 7.2: >10 mg/ml (from PGF2a)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H312-H332-H302
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P261-P271-P304+P340-P312-P280-P302+P352-P312-P322-P363-P501
[Hazard Codes ]

Xn
[Risk Statements ]

20/21/22
[Safety Statements ]

22-36
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

13,14-Dihydro-15-ketoPGF2α is a metabolite of PGF2α that binds bovine acetylcholine esterase.
[Definition]

ChEBI: A prostaglandin Falpha obtained by formal oxidation of the 15-hydroxy group and hydrogenation of the 13,14-double bond of prostaglandin F2alpha.
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