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AB120908

U-51605, PGI2 and TXA2 synthase inhibitor

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(1 Publication)

MW 332.49 g/mol, Purity >98%. Selective inhibitor of PGI2 synthase (IC50 = 2 μM) and TXA2 synthase. PGH2 analog. Partial agonist at TP receptors.
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Chemical Structure - U-51605, PGI2 and TXA2 synthase inhibitor (AB120908)
  • Chemical Structure

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Chemical Structure - U-51605, PGI2 and TXA2 synthase inhibitor (AB120908)

2D chemical structure image of ab120908, U-51605, PGI2 and TXA2 synthase inhibitor

Key facts

CAS number

64192-56-9

Purity

>98%

Form

Liquid

form

Molecular weight

332.49 g/mol

Nature

Synthetic

Biological description

Selective inhibitor of PGI2 synthase (IC50 = 2 μM) and TXA2 synthase. PGH2 analog. Partial agonist at TP receptors.

Isomeric smiles

CCCCCC/C=C/[C@H]1C2N=NC(C2)C1C/C=CCCCC(=O)O

IUPAC Name

9α,11α-Azoprosta-5Z,13E-dien-1-oic acid

Properties and storage information

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
-20°C|-80°C
Appropriate long-term storage conditions
-20°C|-80°C
Storage information
Store under desiccating conditions

Product protocols

Publications (1)

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Vascular pharmacology 106:46-53 PubMed29471140

2018

Activation of endothelial TrkB receptors induces relaxation of resistance arteries.

Applications

Unspecified application

Species

Unspecified reactive species

P Totoson,M Pedard,C Marie,C Demougeot
View all publications

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