HIFJCPQKFCZDDL-UGQITTIWSA-N

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HIFJCPQKFCZDDL-UGQITTIWSA-N Basic information
Product Name:HIFJCPQKFCZDDL-UGQITTIWSA-N
Synonyms:HIFJCPQKFCZDDL-UGQITTIWSA-N;Pentanoic acid, 5-[(3aS,4R,5R,6aS)-hexahydro-5-hydroxy-4-[(1E,3S)-3-hydroxy-4-methyl-1-octen-6-ynyl]-2(1H)-pentalenylidene]-, (5Z)- (9CI);6,9α-methylene-11α,15S-dihydroxy-16-methyl-prosta-5Z,13E-dien-18-yn-1-oic acid;Iloprost Impurity 40;(Z)-Iloprost
CAS:82889-99-4
MF:C22H32O4
MW:360.49
EINECS:
Product Categories:
Mol File:82889-99-4.mol
HIFJCPQKFCZDDL-UGQITTIWSA-N Structure
HIFJCPQKFCZDDL-UGQITTIWSA-N Chemical Properties
Boiling point 539.2±50.0 °C(Predicted)
density 1.210±0.06 g/cm3(Predicted)
solubility DMF: 30 mg/ml; DMSO: 25 mg/ml; Ethanol: 30 mg/ml; PBS (pH 7.2): 1 mg/ml
pka4.77±0.10(Predicted)
Safety Information
MSDS Information
HIFJCPQKFCZDDL-UGQITTIWSA-N Usage And Synthesis
Description5-cis Iloprost is the C-5 cis-isomer of iloprost, a second generation structural analog of prostaglandin I2 (prostacyclin). Iloprost displays ten-fold greater potency than the first generation stable prostacyclin analogs, typified by carbaprostacyclin.1 There are no published studies of the pharmacological properties of 5-cis iloprost.
Uses(Z)-Iloprost ((Z)-Ciloprost; (Z)-ZK 36374) is a vasodilator that prevents heparin-induced platelet activation[1][2][3].
References1. Schrr, K., Darius, H., Matzky, R., et al. The antiplatelet and cardiovascular actions of a new carbacyclin derivative (ZK36374) — equipotent to PGI2 in vitro Naunyn Schmiedebergs Arch. Pharmacol. 316(3),252-255(1981).
HIFJCPQKFCZDDL-UGQITTIWSA-N Preparation Products And Raw materials
Tag:HIFJCPQKFCZDDL-UGQITTIWSA-N(82889-99-4) Related Product Information
5-cis-15(R)-Iloprost 15(R)-ILOPROST ILOPROST Iloprost-d4 15-keto Iloprost Human IgG1, kappa Isotype Control