Darusentan
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Revision as of 22:31, 10 September 2010 by حسن علي البط (Talk) (Adding category Category:Phenol ethers (using HotCat))
| File:Darusentan.png | |
| Systematic (IUPAC) name | |
|---|---|
|
(2S)-2-(4,6-Dimethoxypyrimidin-2-yl)oxy-3-methoxy-3,3-di(phenyl)propanoic acid | |
| Clinical data | |
| Routes of administration | Oral |
| Pharmacokinetic data | |
| Metabolism | Hepatic |
| Biological half-life | 12.5 hours |
| Identifiers | |
| CAS Number | 171714-84-4 |
| ATC code | none |
| PubChem | CID 177236 |
| Chemical data | |
| Formula | C22H22N2O6 |
| Molar mass | 410.42 g/mol[[Script error: No such module "String".]] |
| Script error: No such module "collapsible list". | |
Darusentan (LU-135252; HMR-4005) is a endothelin receptor antagonist. Gilead Colorado, a subsidiary of Gilead Sciences,[1] under license from Abbott Laboratories, is developing darusentan for the potential treatment of uncontrolled hypertension.
In June 2003, Myogen licensed the compound from Abbott for its application in the cancer field.[2]
In May 2007, a randomized, double-blind, active control, parallel assignment, safety and efficacy phase III trial was initiated in subjects who had completed the maintenance period of the DAR-312 study.
References
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