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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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Images

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

Publications

Key facts

CAS number
64192-56-9
Purity
> 98%
Form
Liquid
Molecular weight
332.49 g/mol
Nature
Synthetic

Target data

Recommended products

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.

Key facts

Purity
> 98%
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

Storage

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 promise

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1 product image

  • Chemical Structure - U-51605, PGI2 and TXA2 synthase inhibitor (ab120908), expandable thumbnail

    Chemical Structure - U-51605, PGI2 and TXA2 synthase inhibitor (ab120908)

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

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Product protocols

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