Synthesis of guanidino-N-alkylarginines by the use of polymeric pseudoureas
作者:Shlomo Pundak、Meir Wilchek
DOI:10.1021/jo00317a033
日期:1981.2
POTENT AND SELECTIVE INHIBITORS OF NAV1.3 AND NAV1.7
申请人:Amgen Inc.
公开号:EP2686340A2
公开(公告)日:2014-01-22
[EN] POTENT AND SELECTIVE INHIBITORS OF NAV1.3 AND NAV1.7<br/>[FR] INHIBITEURS PUISSANTS ET SÉLECTIFS DE NAV1.3 ET NAV1.7
申请人:MURRAY JUSTIN K
公开号:WO2012125973A2
公开(公告)日:2012-09-20
Disclosed is a composition of matter comprising an isolated polypeptide, which is a peripherally-restricted Nav1.7 inhibitor. In some disclosed embodiments, the isolated polypeptide is an inhibitor of Nav1.7 and/or Nav1.3. Other embodiments are conjugated embodiments of the inventive composition of matter and pharmaceutical compositions containing the inventive composition of matter. Isolated nucleic acids encoding some embodiments of inventive polypeptides and expression vectors, and recombinant host cells containing them are disclosed. A method of treating or preventing pain is also disclosed.
Nω-alkylnitrosocarbamoyl-α,ω-diaminocarboxylic acids. 1. Synthesis and antitumor activity of Nω-methylnitrosocarbamoyl-α,ω-diamino carboxylic acids
作者:G. L. Levit、L. B. Radina、V. P. Krasnov、V. F. Gopko、N. M. Peretolchina