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ChemicalBook--->CAS DataBase List--->89847-02-9

89847-02-9

89847-02-9 Structure

89847-02-9 Structure
IdentificationBack Directory
[Name]

9BETA,11ALPHA,15S-TRIHYDROXY-PROSTA-5Z,13E-DIEN-1-OIC ACID, TRIS (HYDROXYMETHYL)AMINOMETHANE SALT
[CAS]

89847-02-9
[Synonyms]

9BETA-PGF2ALPHA (TROMETHAMINE SALT)
Prostaglandin F2β (tromethamine salt)
PROSTAGLANDIN F2BETA TROMETHAMINE SALT
9BETA,11ALPHA,15S-TRIHYDROXY-PROSTA-5Z,13E-DIEN-1-OIC ACID, TRIS (HYDROXYMETHYL)AMINOMETHANE SALT
2-amino-2-(hydroxymethyl)propane-1,3-diol (Z)-7-((1R,2R,3R,5R)-3,5-dihydroxy-2-((S,E)-3-hydroxyoct-1-en-1-yl)cyclopentyl)hept-5-enoate
[Molecular Formula]

C24H45NO8
[MDL Number]

MFCD00135236
[MOL File]

89847-02-9.mol
[Molecular Weight]

475.62
Chemical PropertiesBack Directory
[solubility ]

Acetone: >5 mg/ml (from PGF2a THAM); Acetonitrile: >5 mg/ml (from PGF2a THAM); DMSO: >50 mg/ml (from PGF2a THAM); Ethanol: >50 mg/ml (from PGF2a THAM); Methanol: >100 mg/ml (from PGF2a THAM); PBS pH 7.2: >25 mg/ml (from PGF2a THAM)
[form ]

A crystalline solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07,GHS08
[Signal word ]

Danger
[Hazard statements ]

H302-H360
[Precautionary statements ]

P201-P202-P264-P270-P280-P301+P312-P330-P308+P313-P405-P501
Hazard InformationBack Directory
[Description]

Prostaglandin F (PGF) (tromethamine salt) is a derivative of PGF with increased water solubility. PGF is the 9β-hydroxy stereoisomer of PGF2α . It is much less active than PGF in antifertility and bronchoconstrictor activities. PGF exhibits bronchodilating activity in guinea pigs and cats and antagonizes the bronchoconstrictor activity of PGF.
[Uses]

(5R)-Dinoprost tromethamine (Prostaglandin F2β tromethamine) is a metabolite produced by the metabolism of arachidonic acid cyclooxygenase. (5R)-Dinoprost tromethamine induces dose-dependent release of hexosaccharide containing mucin[1][2].
[References]

[1] Lamont JT, et, al. Cysteamine and prostaglandin F2 beta stimulate rat gastric mucin release. Gastroenterology. 1983 Feb;84(2):306-13. PMID:6184259
[2] Jang Y, et, al. Molecular mechanisms underlying the actions of arachidonic acid-derived prostaglandins on peripheral nociception. J Neuroinflammation. 2020 Jan 22;17(1):30. DOI:10.1186/s12974-020-1703-1
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