1265295-92-8
Chemical Structure
Selexipag-d6
Synonym(s): NS-304-d6;ACT-293987-d6
- CAS No.: 1265295-92-8
- Formula:C26H26D6N4O4S
- Molecular Weight:502.66
IUPAC Name: 2-(4-((5,6-diphenylpyrazin-2-yl)(propan-2-yl-1,1,1,3,3,3-d6)amino)butoxy)-N-(methylsulfonyl)acetamide
InChIKey: QXWZQTURMXZVHJ-WFGJKAKNSA-N
SMILES: O=C(NS(=O)(C)=O)COCCCCN(C1=NC(C2=CC=CC=C2)=C(C3=CC=CC=C3)N=C1)C(C([2H])([2H])[2H])C([2H])([2H])[2H]
Biological Activity: Selexipag-d6 is deuterium labeled Selexipag. Selexipag (NS-304) is an orally available and potent agonist for the Prostacyclin (PGI2) receptor (IP receptor).
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Selexipag-d6 | Selexipag-d6 is deuterium labeled Selexipag. Selexipag (NS-304) is an orally available and potent agonist for the Prostacyclin (PGI2) receptor (IP receptor). | |||||||||||||||||||||
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Selexipag (Standard) | ≥98% | Selexipag (Standard) is the analytical standard of Selexipag. This product is intended for research and analytical applications. Selexipag (NS-304) is an orally available and potent agonist for the Prostacyclin (PGI2) receptor (IP receptor). | ||||||||||||||||||||
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Selexipag-d7 | 98.44% | Selexipag-d7 is the deuterium labeled Selexipag. Selexipag (NS-304) is an orally available and potent agonist for the Prostacyclin (PGI2) receptor (IP receptor). | ||||||||||||||||||||
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Selexipag | 99.86% | Selexipag (NS-304) is an orally available and potent agonist for the Prostacyclin (PGI2) receptor (IP receptor). | ||||||||||||||||||||
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