Product Data Sheet

Selexipag-d7

Catalog No. A63102

main product photo
Selexipag-d7 is a deuterium-labeled derivative of Selexipag, a highly potent and orally bioavailable agonist of the prostacyclin (PGI2) receptor, also known as the IP receptor. This stable isotope-labeled form is valuable for pharmacokinetic studies and metabolic profiling, enhancing the understanding of drug metabolism and dynamics in biological systems. Selexipag-d7 is particularly relevant in research focused on pulmonary arterial hypertension and cardiovascular diseases, supporting the development of targeted therapies.
Chemical Information
Catalog NumA63102
M. Wt503.66
FormulaC26H25D7N4O4S
Purity>98%
Storageat -20 °C 3 years (powder form); at -20 °C 6 months (Solution base)
CAS No.1265295-21-3
Synonyms
SMILESCS(NC(COCCCCN(C1=CN=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N1)C(C([2H])([2H])[2H])([2H])C([2H])([2H])[2H])=O)(=O)=O
Biological Activity
DescriptionSelexipag-d7 is a deuterium-labeled derivative of Selexipag, a highly potent and orally bioavailable agonist of the prostacyclin (PGI2) receptor, also known as the IP receptor. This stable isotope-labeled form is valuable for pharmacokinetic studies and metabolic profiling, enhancing the understanding of drug metabolism and dynamics in biological systems. Selexipag-d7 is particularly relevant in research focused on pulmonary arterial hypertension and cardiovascular diseases, supporting the development of targeted therapies.
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SHIPPING AND STORAGE
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