Dual SNAr reaction in activated ortho-halonitrobenzene: direct synthesis of substituted 1,2,3,4-tetrahydroquinoxalines, 2,3-dihydro-1,4-benzoxazines, and 1,4-benzodioxines
BICYCLIC ACETYL-COA CARBOXYLASE INHIBITORS AND USES THEREOF
申请人:BARNES David Weninger
公开号:US20120028969A1
公开(公告)日:2012-02-02
The present invention provides compounds of formula (I);
or pharmaceutically acceptable salts thereof, wherein the variables are defined as herein. The present invention provides a method for manufacturing the compounds of formula (I), their therapeutic uses, combinations with other of pharmacologically active agents, and a pharmaceutical compositions.
The present invention provides cyclic depsipeptides of Formula (1), stereoisomers thereof, and veterinary acceptable salts thereof
wherein each of R
1
, R
2
, R
3
, R
4
, L
1
, and L
2
, are as defined herein. The present invention also contemplates compositions and methods of treatment as an endoparasiticide with a Formula (1) compound.
US8697739B2
申请人:——
公开号:US8697739B2
公开(公告)日:2014-04-15
US9789118B2
申请人:——
公开号:US9789118B2
公开(公告)日:2017-10-17
[EN] HETEROCYCLES AND USES THEREOF<br/>[FR] HÉTÉROCYCLES ET LEURS UTILISATIONS
申请人:[en]KUMQUAT BIOSCIENCES INC.
公开号:WO2022081912A2
公开(公告)日:2022-04-21
The present disclosure provides compounds and pharmaceutically acceptable salt thereof, and methods of using the same. The compounds and methods have a range of utilities as therapeutics, diagnostics, and research tools. In particular, the subject compositions and methods are useful for reducing signaling output of oncogenic proteins.