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ChemicalBook--->CAS DataBase List--->53319-30-5

53319-30-5

53319-30-5 Structure

53319-30-5 Structure
IdentificationBack Directory
[Name]

8-iso-16-cyclohexyl-tetranor Prostaglandin E2
[CAS]

53319-30-5
[Synonyms]

8-iso-16-cyclohexyl-tetranor Prostaglandin E2
5-Heptenoic acid, 7-[2-(4-cyclohexyl-3-hydroxy-1-butenyl)-3-hydroxy-5-oxocyclopentyl]-, [1R-[1α(Z),2β(1E,3R*),3α]]- (9CI)
[Molecular Formula]

C22H34O5
[MDL Number]

MFCD12912331
[MOL File]

53319-30-5.mol
[Molecular Weight]

378.5
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 50 mg/ml; DMSO: 50 mg/ml; Ethanol: 50 mg/ml; PBS (pH 7.2): 1 mg/ml
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS07,GHS08
[Signal word ]

Danger
[Hazard statements ]

H225-H319-H360-H336
[Precautionary statements ]

P201-P202-P210-P240-P241-P242-P243-P261-P264-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P308+P313-P312-P337+P313-P370+P378-P403+P233-P403+P235-P405-P501
Hazard InformationBack Directory
[Description]

8-iso Prostaglandin E2 (8-iso PGE2) is one of several isoprostanes produced from polyunsaturated fatty acids during lipid peroxidation.1 8-iso-16-cyclohexyl-tetranor PGE2 is a synthetic analog of 8-iso PGE2. There are no published studies on the pharmacological properties of 8-iso-16-cyclohexyl-tetranor PGE2.
[References]

1. Morrow, J.D., Minton, T.A., Mukundan, C.R., et al. Free radical-induced generation of isoprostanes in vivo. Evidence for the formation of D-ring and E-ring isoprostanes J. Biol. Chem. 269,4317-4326(1994).
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