Modification of the pyridine moiety of non-peptidyl indole GnRH receptor antagonists
摘要:
The synthesis of a number of indole GnRH antagonists is described. Oxidation of the pyridine ring nitrogen, combined with alkylation at the two position, led to a compound with an excellent in vitro activity profile as well as oral bioavailability in both rats and dogs. (C) 2002 Elsevier Science Ltd. All rights reserved.
Construction of cis - and trans -octahydroisoquinoline-7-ones via a tandem ring-opening and -closing strategy
摘要:
cis- and trans-Octahyroisoquiniolines can be efficiently constructed via a tandem ring-opening and -closing strategy. The precursors required to achieve this transformation are easily obtained by a Diets-Alder reaction followed by a stereoselective hydrogenation. (C) 2001 Elsevier Science Ltd. All rights reserved.
[EN] COMPOUNDS AND METHODS<br/>[FR] COMPOSÉS ET MÉTHODES
申请人:TEMPERO PHARMACEUTICALS INC
公开号:WO2013019682A1
公开(公告)日:2013-02-07
The present invention relates to novel retinoid-related orphan receptor gamma (RORγ) modulators and their use in the treatment of diseases mediated by RORy.
本发明涉及新型视黄醛酸相关孤儿受体γ(RORγ)调节剂及其在治疗由RORγ介导的疾病中的应用。
TALIK, T. ,, JR.;TALIK, Z., PR. NAUK. AE WROCLAWIU, 1984, N 278, 149-161
作者:TALIK, T. ,, JR.、TALIK, Z.
DOI:——
日期:——
Catalyst and process for hydrogenating olefinically unsaturated compound