[EN] MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR [FR] MODULATEURS DU RÉGULATEUR DE LA CONDUCTANCE TRANSMEMBRANAIRE DE LA MUCOVISCIDOSE
[EN] MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR [FR] MODULATEURS DU RÉGULATEUR DE LA CONDUCTANCE TRANSMEMBRANAIRE DE LA MUCOVISCIDOSE
AZEPANE DERIVATIVES AND METHODS OF TREATING HEPATITIS B INFECTIONS
申请人:Novira Therapeutics, Inc.
公开号:US20150197493A1
公开(公告)日:2015-07-16
Provided herein are compounds useful for the treatment of HBV infection in a subject in need thereof, pharmaceutical compositions thereof, and methods of inhibiting, suppressing, or preventing HBV infection in the subject.
Catalytic Ring Expansions of Cyclic Alcohols Enabled by Proton-Coupled Electron Transfer
作者:Kuo Zhao、Kenji Yamashita、Joseph E. Carpenter、Trevor C. Sherwood、William R. Ewing、Peter T. W. Cheng、Robert R. Knowles
DOI:10.1021/jacs.9b03973
日期:2019.6.5
the modular ringexpansion of cyclic aliphatic alcohols. In this work, proton-coupled electron transfer activation of an allylic alcohol substrate affords an alkoxy radical intermediate that undergoes subsequent C-C bond cleavage to furnish an enone and a tethered alkyl radical. Recombination of this alkyl radical with the revealed olefin acceptor in turn produces a ring-expanded ketone product. The
我们在这里报告了一种用于环状脂肪醇模块化扩环的催化方法。在这项工作中,烯丙醇底物的质子耦合电子转移活化提供烷氧基自由基中间体,该中间体经历随后的 CC 键断裂以提供烯酮和系链烷基自由基。该烷基与暴露的烯烃受体的重组又产生扩环的酮产物。这种 CC 键形成事件的区域选择性可以通过烯烃底物上的取代基可靠地控制,提供了一种以选择性方式将简单的 N 元环底物转化为 n+1 或 n+2 环加合物的方法。
[EN] CARBOXAMIDES AS UBIQUITIN-SPECIFIC PROTEASE INHIBITORS<br/>[FR] CARBOXAMIDES UTILISÉES EN TANT QU'INHIBITEURS DE PROTÉASE SPÉCIFIQUE DE L'UBIQUITINE
申请人:FORMA THERAPEUTICS INC
公开号:WO2019032863A1
公开(公告)日:2019-02-14
The present disclosure relates to modulators, such as inhibitors, of at least one pathway chosen from USP28 and USP25, pharmaceutical compositions comprising the inhibitors, and methods of using the inhibitors. The modulators, such as inhibitors, of at least one pathway chosen from USP28 and USP25 can be useful in the treatment of cancers, among other ailments.
Heterocyclic compounds, which are inhibitors of the enzyme DPP-IV
申请人:——
公开号:US20020161001A1
公开(公告)日:2002-10-31
The present invention relates to therapeutically active and selective inhibitors of the enzyme DPP-IV, pharmaceutical compositions comprising the compounds and the use of such compounds for and the manufacture of medicaments for treating diseases that are associated with proteins which are subject to inactivation by DPP-IV, such as type 2 diabetes and obesity, as well as methods for treating diseases that are associated with proteins which are subject to inactivation by DPP-IV, such as type 2 diabetes and obesity
AZEPANE DERIVATIVES AND METHODS OF TREATING HEPATITIS B INFECTIONS
申请人:Novira Therapeutics, Inc.
公开号:US20150197533A1
公开(公告)日:2015-07-16
Provided herein are compounds useful for the treatment of HBV infection in a subject in need thereof, pharmaceutical compositions thereof, and methods of inhibiting, suppressing, or preventing HBV infection in the subject.