Basic information Safety Supplier Related

5,6BETA-DIHYDRO PGI2

Basic information Safety Supplier Related

5,6BETA-DIHYDRO PGI2 Basic information

Product Name:
5,6BETA-DIHYDRO PGI2
Synonyms:
  • 6BETA-PROSTAGLANDIN I1
  • 6S,9ALPHA-EPOXY-11ALPHA,15S-DIHYDROXY-PROST-13E-EN-1-OIC ACID
  • 5,6BETA-DIHYDRO PGI2
  • 5,6-dihydroprostacyclin
  • (6S,13E,15S)-6,9α-Epoxy-11α,15-dihydroxyprost-13-en-1-oic acid
  • RJADQDXZYFCVHV-CBIPHORWSA-N
  • Prost-13-en-1-oic acid, 6,9-epoxy-11,15-dihydroxy-, (6S,9α,11α,13E,15S)- (9CI)
  • 6β-Prostaglandin I1
CAS:
62770-50-7
MF:
C20H34O5
MW:
354.48
Mol File:
62770-50-7.mol
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5,6BETA-DIHYDRO PGI2 Chemical Properties

storage temp. 
Store at -20°C
solubility 
DMF: >10 mg/ml; DMSO: >5 mg/ml; Ethanol: >20 mg/ml; PBS pH 7.2: >80 μg/ml
form 
A crystalline solid
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5,6BETA-DIHYDRO PGI2 Usage And Synthesis

Description

6β-PGI1 is a stable PGI2 analog resistant to hydrolysis in aqueous solutions. 6β-PGI1 has a much longer half-life than PGI2, but a greatly reduced molar potency for receptor mediated function. 6β-PGI1 has a Kact for adenylate cyclase in NCB-20 cells of 4.2 μM compared with 18 nM for PGI2. The potency for vasodilation and inhibition of platelet aggregation is about 1% of PGI2.1,2

Definition

ChEBI: 6-Prostaglandin I1 is a prostanoid.

References

1. Whittle, B.J.R., Moncada, S., Whiting, F., et al. Carbacyclin — a potent stable prostacyclin analogue for the inhibition of platelet aggregation Prostaglandins 19(4),605-627(1980).
2. Blair, I.A., Hensby, C.N., and MacDermot, J. Prostacyclin-dependent activation of adenylate cyclase in a neuronal somatic cell hybrid: Prostanoid structure-activity relationships Br. J. Pharmac. 69(3),519-525(1980).

5,6BETA-DIHYDRO PGI2Supplier

Shanghai Hongye Biotechnology Co. Ltd
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400-9205774
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Hangzhou Synstar pharmaceutical Technology CO.,Ltd
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ChemeGen(Shanghai) Biotechnology Co.,Ltd.
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Shanghai Yifei Biotechnology Co. , Ltd.
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TargetMol Chemicals Inc.
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