Synthesis and evaluation of 3-anilino-quinoxalinones as glycogen phosphorylase inhibitors
摘要:
A series of 3-anilino-quinoxalinones has been identified as a new class of glycogen phosphorylase inhibitors. The lead compound I was identified through high throughput screening as well as through pharmacophore-based electronic screening. Modifications were made to the scaffold of 1 to produce novel analogues, some of which are 25 times more potent than the lead compound. (c) 2005 Elsevier Ltd. All rights reserved.
Synthesis and evaluation of 3-anilino-quinoxalinones as glycogen phosphorylase inhibitors
摘要:
A series of 3-anilino-quinoxalinones has been identified as a new class of glycogen phosphorylase inhibitors. The lead compound I was identified through high throughput screening as well as through pharmacophore-based electronic screening. Modifications were made to the scaffold of 1 to produce novel analogues, some of which are 25 times more potent than the lead compound. (c) 2005 Elsevier Ltd. All rights reserved.
The invention features quinoxalinones, pharmaceutical compositions containing them and methods of using them to treat, for example, diabetes.
这项发明涉及喹喔啉酮,包含它们的药物组合物以及使用它们治疗糖尿病等疾病的方法。
(3-OXO-3,4-DIHYDRO-QUINOXALIN-2-YL-AMINO)-BENZAMIDE DERIVATIVES AND RELATED COMPOUNDS AS GLYCOGEN PHOSPHORYLASE INHIBITORS FOR THE TREATMENT OF DIABETES AND OBESITY
申请人:JANSSEN PHARMACEUTICA N.V.
公开号:EP1711184B1
公开(公告)日:2007-07-18
Synthesis and evaluation of 3-anilino-quinoxalinones as glycogen phosphorylase inhibitors
作者:Joseph Dudash、Yongzheng Zhang、John B. Moore、Richard Look、Yin Liang、Mary Pat Beavers、Bruce R. Conway、Philip J. Rybczynski、Keith T. Demarest
DOI:10.1016/j.bmcl.2005.07.021
日期:2005.11
A series of 3-anilino-quinoxalinones has been identified as a new class of glycogen phosphorylase inhibitors. The lead compound I was identified through high throughput screening as well as through pharmacophore-based electronic screening. Modifications were made to the scaffold of 1 to produce novel analogues, some of which are 25 times more potent than the lead compound. (c) 2005 Elsevier Ltd. All rights reserved.