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54382-74-0

54382-74-0 Structure

54382-74-0 Structure
IdentificationBack Directory
[Name]

16-PHENOXY TETRANOR PROSTAGLANDIN E2
[CAS]

54382-74-0
[Synonyms]

LYXKJZCRLQWIIN-BYCQWZGOSA-N
16-PHENOXY TETRANOR PROSTAGLANDIN E2
9-OXO-11ALPHA,15R-DIHYDROXY-16-PHENOXY-17,18,19,20-TETRANOR-PROSTA-5Z,13E-DIEN-1-OIC ACID
[Molecular Formula]

C22H28O6
[MDL Number]

MFCD00797647
[MOL File]

54382-74-0.mol
[Molecular Weight]

388.45
Chemical PropertiesBack Directory
[Boiling point ]

605.1±55.0 °C(Predicted)
[density ]

1.256±0.06 g/cm3(Predicted)
[solubility ]

DMF: 100 mg/ml; DMSO: 100 mg/ml; Ethanol: 100 mg/ml; PBS (pH 7.2): 0.8 mg/ml
[pka]

4.75±0.10(Predicted)
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]

16-phenoxy tetranor PGE2 is the free acid form of sulprostone formed by the hydrolysis of the methylsulfonamide bond. 16-phenoxy tetranor PGE2 is a minor metabolite of sulprostone found in human plasma after parenteral administration of the drug.
[Uses]

16-phenoxy tetranor PGE2 is the free acid form of sulprostone formed by the hydrolysis of the methylsulfonamide bond.1 16-phenoxy tetranor PGE2 is a minor metabolite of sulprostone found in human plasma after parenteral administration of the drug.
[References]

[1] Kuhnz, et al. Identification of the major metabolites of the prostaglandin E2-analogue sulprostone in human plasma, and isolation from urine (in vivo) and liver perfusate (in vitro) of female guinea-pigs. Drug Metab. Dispos. 19(5), 920-925 (1991).
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