1-Benzylbenzimidazoles: The discovery of a novel series of bradykinin B1 receptor antagonists
摘要:
The design, synthesis, and structure-activity studies of a novel series of BK B-1 receptor antagonists based on a 1-benzylbenzimidazole chemotype are described. A number of compounds, for example, 38g, with excellent affinity for the cynomolgus macaque and rat bradykinin B-1 receptor were discovered. (C) 2008 Elsevier Ltd. All rights reserved.
Inhibitors of low molecular weight protein tyrosine phosphatase (LMPTP) and uses thereof
申请人:Sanford Burnham Prebys Medical Discovery Institute
公开号:US11066420B2
公开(公告)日:2021-07-20
Protein tyrosine phosphatases (PTPs) are key regulators of metabolism and insulin signaling. As a negative regulator of insulin signaling, the low molecular weight protein tyrosine phosphatase (LMPTP) is a target for insulin resistance and related conditions. Described herein are compounds capable of modulating the level of activity of low molecular weight protein tyrosine phosphatase (LMPTP) and compositions, and methods of using these compounds and compositions.
INHIBITORS OF LOW MOLECULAR WEIGHT PROTEIN TYROSINE PHOSPHATASE (LMPTP) AND USES THEREOF
申请人:Sanford Burnham Prebys Medical Discovery Institute
公开号:US20200055875A1
公开(公告)日:2020-02-20
Protein tyrosine phosphatases (PTPs) are key regulators of metabolism and insulin signaling. As a negative regulator of insulin signaling, the low molecular weight protein tyrosine phosphatase (LMPTP) is a target for insulin resistance and related conditions. Described herein are compounds capable of modulating the level of activity of low molecular weight protein tyrosine phosphatase (LMPTP) and compositions, and methods of using these compounds and compositions.
1-Benzylbenzimidazoles: The discovery of a novel series of bradykinin B1 receptor antagonists
作者:Qin Guo、Jayaraman Chandrasekhar、David Ihle、David J. Wustrow、Bertrand L. Chenard、James E. Krause、Alan Hutchison、Dawn Alderman、Charles Cheng、Daniel Cortright、Daniel Broom、Mark T. Kershaw、Jean Simmermacher-Mayer、Yao Peng、Kevin J. Hodgetts
DOI:10.1016/j.bmcl.2008.08.014
日期:2008.9
The design, synthesis, and structure-activity studies of a novel series of BK B-1 receptor antagonists based on a 1-benzylbenzimidazole chemotype are described. A number of compounds, for example, 38g, with excellent affinity for the cynomolgus macaque and rat bradykinin B-1 receptor were discovered. (C) 2008 Elsevier Ltd. All rights reserved.