Relcovaptan
From Self-sufficiency
220px | |
Systematic (IUPAC) name | |
---|---|
1-({(2R,3S)-5-chloro-3-(2-chlorophenyl)-1-[(3,4-dimethoxyphenyl)sulfonyl]-3-hydroxy-2,3-dihydro-1H-indol-2-yl}carbonyl)-L-prolinamide | |
Identifiers | |
CAS Number | 150375-75-0 |
ATC code | none |
PubChem | CID 60943 |
Synonyms | (2S)-1-[(2R,3S)-5-chloro-3-(2-chlorophenyl)-1-(3,4-dimethoxyphenyl)sulfonyl-3-hydroxy-2H-indole-2-carbonyl]pyrrolidine-2-carboxamide |
Chemical data | |
Formula | C28H27Cl2N3O7S |
Molar mass | 620.501[[Script error: No such module "String".]] |
Script error: No such module "collapsible list". |
Relcovaptan (SR-49059) is a non-peptide inhibitor of the antidiuretic hormone (vasopressin) receptor, selective for the V1a subtype.[1] It has shown positive initial results in tests against Raynaud's disease, dysmenorrhoea, and tocolysis,[2] although it is not yet approved for clinical use.
References
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45px | This hormonal preparation article is a stub. You can help ssf by expanding it. |
- ↑ Lemmens-Gruber R, Kamyar M. Vasopressin antagonists. Cellular and Molecular Life Sciences. 2006 Aug;63(15):1766-79. PMID 16794787
- ↑ Decaux G, Soupart A, Vassart G. Non-peptide arginine-vasopressin antagonists: the vaptans. Lancet. 2008 May 10;371(9624):1624-32. PMID 18468546
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