16-PHENYL TETRANOR PROSTAGLANDIN E2

16-PHENYL TETRANOR PROSTAGLANDIN E2 Suppliers list
Company Name: Hangzhou Synstar pharmaceutical Technology CO.,Ltd  
Tel: 0571-85361029
Email: synstar518@163.com
Products Intro: Product Name:16-phenyl tetranor Prostaglandin E2
CAS:38315-44-5
Purity:0.98 Package:100mg、500mg、1g、5g
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Email: marketing@targetmol.cn
Products Intro: Product Name:16-phenyl tetranor Prostaglandin E2
CAS:38315-44-5
Package:10mg;50mg
Company Name: Cayman Chemical Company  
Tel: (800) 364-9897
Email: cayman@caymanchem.com
Products Intro: Product Name:16-phenyl tetranor Prostaglandin E2
CAS:38315-44-5
Package:>99% Remarks:14770
16-PHENYL TETRANOR PROSTAGLANDIN E2 Basic information
Product Name:16-PHENYL TETRANOR PROSTAGLANDIN E2
Synonyms:9-OXO-11ALPHA-15S-DIHYDROXY-16-PHENYL-17,18,19,20-TETRANOR-PROSTA-5Z,13E-DIEN-1-OIC ACID;16-PHENYL TETRANOR PROSTAGLANDIN E2;DXWJXQSQVUJRNS-YYWARMNLSA-N;5-Heptenoic acid, 7-[(1R,2R,3R)-3-hydroxy-2-[(1E,3S)-3-hydroxy-4-phenyl-1-buten-1-yl]-5-oxocyclopentyl]-, (5Z)-
CAS:38315-44-5
MF:C22H28O5
MW:372.45
EINECS:
Product Categories:
Mol File:38315-44-5.mol
16-PHENYL TETRANOR PROSTAGLANDIN E2 Structure
16-PHENYL TETRANOR PROSTAGLANDIN E2 Chemical Properties
Boiling point 576.8±50.0 °C(Predicted)
density 1.235±0.06 g/cm3(Predicted)
solubility DMF: >100 mg/ml (from Fluprostenol); DMSO: >100 mg/ml (from Fluprostenol); Ethanol: >100 mg/ml (from Fluprostenol); PBS pH 7.2: >0.8 mg/ml
pka4.75±0.10(Predicted)
Safety Information
MSDS Information
16-PHENYL TETRANOR PROSTAGLANDIN E2 Usage And Synthesis
Description16-phenyl tetranor PGE2 is a metabolically stable synthetic analog of PGE2. 16-phenyl tetranor PGE2 is five times more potent than PGE2 in causing hypotension in dogs (0.1 μg/kg dose).1 It is comparable to PGE2 in inhibiting histamine-induced bronchoconstriction in conscious guinea pigs.1
DefinitionChEBI: 16-Phenyl-tetranor-PGE2 is a prostanoid.
References1. Johnson, M.R., Schaaf, T.K., Constantine, J.W., et al. Structure activity studies leading to a tissue-selective hypotensive prostaglandin analog, 13,14-dihydro-16-phenyl-ω-tetranor PGE2 Prostaglandins 20(3),515-520(1980).
16-PHENYL TETRANOR PROSTAGLANDIN E2 Preparation Products And Raw materials
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16-PHENYL TETRANOR PROSTAGLANDIN E2

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