3-(Pyrrol-1-yl)phenylmethyl esters and intermediates
申请人:FMC Corporation
公开号:US04339457A1
公开(公告)日:1982-07-13
3-(Pyrrol-1-yl)phenylmethyl esters and intermediates having the general formula ##STR1## the use of the esters as pesticides, compositions thereof and a process for preparation are disclosed and exemplified.
[EN] 3-(PYRROL-1-YL)PHENYLMETHYL ESTERS AND INTERMEDIATES
申请人:FMC CORPORATION
公开号:WO1982001368A1
公开(公告)日:1982-04-29
(EN) 3-(Pyrrol-1-yl)phenylmethyl esters and intermediates having the general formula (FORMULA) the use of the esters as pesticides, compositions thereof and a process for preparation are disclosed and exemplified. (FR) 3-(pyrrole-1-yl)phenyl-methyle esters et produits intermediaires selon la formule generale (FORMULE) l'utilisation de ces esters comme pesticides, des compositions les contenant ainsi qu'un procede de preparation sont decrits et expliques par des exemples.
Identification of non-peptidic cysteine reactive fragments as inhibitors of cysteine protease rhodesain
作者:Danielle McShan、Stefan Kathman、Brittiney Lowe、Ziyang Xu、Jennifer Zhan、Alexander Statsyuk、Ifedayo Victor Ogungbe
DOI:10.1016/j.bmcl.2015.08.074
日期:2015.10
Rhodesain, the major cathepsin L-like cysteine protease in the protozoan Trypanosoma brucei rhodesiense, the causative agent of African sleeping sickness, is a well-validated drug target. In this work, we used a fragment-based approach to identify inhibitors of this cysteine protease, and identified inhibitors of T. brucei. To discover inhibitors active against rhodesain and T. brucei, we screened a library of covalent fragments against rhodesain and conducted preliminary SAR studies. We envision that in vitro enzymatic assays will further expand the use of the covalent tethering method, a simple fragment-based drug discovery technique to discover covalent drug leads. (C) 2015 Elsevier Ltd. All rights reserved.
PLUMMER, E. L.;PALMERE, R. M.
作者:PLUMMER, E. L.、PALMERE, R. M.
DOI:——
日期:——
3-(PYRROL-1-YL)PHENYLMETHYL ESTERS AND INTERMEDIATES