Selexipag
From Infogalactic: the planetary knowledge core
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Names | |
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IUPAC name
2-{4-[(5,6-diphenylpyrazin-2-yl)(propan-2-yl)amino]butoxy}-N-(methanesulfonyl)acetamide
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Other names
ACT-293987, NS-304
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Identifiers | |
475086-01-2 ![]() |
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ChEBI | CHEBI:90844 ![]() |
ChEMBL | ChEMBL238804 ![]() |
ChemSpider | 8089417 ![]() |
7552 | |
Jmol 3D model | Interactive image |
KEGG | D09994 ![]() |
PubChem | 9913767 |
UNII | P7T269PR6S ![]() |
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Properties | |
C26H32N4O4S | |
Molar mass | 496.6 g·mol−1 |
Vapor pressure | {{{value}}} |
Pharmacology | |
ATC code | B01 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references | |
Selexipag (brand name Uptravi) is a drug developed by Actelion for the treatment of pulmonary arterial hypertension (PAH). Selexipag and its active metabolite, ACT-333679 (or MRE-269, the free carboxylic acid), are agonists of the prostacyclin receptor, which leads to vasodilation in the pulmonary circulation.[1]
File:MRE 269 skeletal.svg
ACT-333679 or MRE-269, the active metabolite of selexipag
History
The US FDA granted selexipag Orphan Drug status for PAH.[2] It was approved by the US FDA on 22 December 2015.[2] The expected price for the drug in the US is $160,000 to $170,000 per patient before rebates.[3]
See also
- Epoprostenol, another name for prostacyclin
- Analogues of prostacyclin:
References
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ 2.0 2.1 New Drug Approved for Rare Lung Disorder. PPN. 23 Dec 2015 Has link to GRIPHON study results
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
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