Chemistry:Selepressin
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Short description: Chemical compound
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Other names | H-Cys(1)-Phe-Ile-hGln-Asn-Cys(1)-Pro-Orn(iPr)-Gly-NH2 |
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Formula | C46H73N13O11S2 |
Molar mass | 1048.29 g·mol−1 |
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Selepressin (INN) (code name FE-202158), also known as [Phe(2),Ile(3), Hgn(4),Orn(iPr)(8)]vasopressin) is a potent, highly selective, short-acting peptide full agonist of the vasopressin 1A receptor and analog of vasopressin which was under development by Ferring Pharmaceuticals for the treatment of vasodilatory hypotension in septic shock.[1][2][3][4]
The Phase 2b/3 adaptive trial (SEPSIS-ACT) was terminated in February 2018 for futility. The trial was halted prior to the initiation of the arm for the highest dosing regimen of 5.0 ng/kg/min.[5]
References
- ↑ Levin, Jeremy I (24 October 2014). Macrocycles in Drug Discovery. Royal Society of Chemistry. pp. 313–. ISBN 978-1-84973-701-2. https://books.google.com/books?id=t13YBAAAQBAJ&pg=PA313.
- ↑ Vincent, Jean-Louis (23 September 2012). Annual Update in Intensive Care and Emergency Medicine 2012. Springer Science & Business Media. pp. 80–. ISBN 978-3-642-25716-2. https://books.google.com/books?id=hLC_pIcizCgC&pg=PA80.
- ↑ Yearbook of Intensive Care and Emergency Medicine 2008. Springer Science & Business Media. 2 September 2008. pp. 427–. ISBN 978-3-540-77290-3. https://books.google.com/books?id=KXEdgwRXULMC&pg=PA427.
- ↑ "Pharmacological characterization of FE 202158, a novel, potent, selective, and short-acting peptidic vasopressin V1a receptor full agonist for the treatment of vasodilatory hypotension". The Journal of Pharmacology and Experimental Therapeutics 337 (3): 786–96. June 2011. doi:10.1124/jpet.111.178848. PMID 21411496.
- ↑ Clinical trial number NCT02508649 for "Selepressin Evaluation Programme for Sepsis-Induced Shock - Adaptive Clinical Trial" at ClinicalTrials.gov
Original source: https://en.wikipedia.org/wiki/Selepressin.
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