Novel benzimidazole derivatives as selective CB2 agonists
摘要:
The preparation and evaluation of a novel class of CB2 agonists based on a benzimidazole moiety are reported. They showed binding affinities up to 1 nM towards the CB2 receptor with partial to full agonist potencies. They also demonstrated good to excellent selectivity (> 1000-fold) over the CB1 receptor. (C) 2008 Elsevier Ltd. All rights reserved.
DOI:
10.1016/j.bmcl.2008.05.073
作为产物:
描述:
N-{4-[(cyclopropylmethyl)amino]-3-nitrophenyl}acetamide 在
钯 作用下,
以
乙酸乙酯 为溶剂,
以After work up, isolated the desired product (5.5 g, 89%)的产率得到N-{3-amino-4-[(cyclopropylmethyl)amino]phenyl}acetamide
BICYCLICALLY SUBSTITUTED URACILS AND THE USE THEREOF
申请人:BAYER PHARMA AKTIENGESELLSCHAFT
公开号:US20150148340A1
公开(公告)日:2015-05-28
The present application relates to novel bicyclically substituted uracil derivatives, to processes for preparation thereof, to the use thereof alone or in combinations for treatment and/or prophylaxis of diseases, and to the use thereof for production of medicaments for treatment and/or prophylaxis of diseases.
Compounds of general formula (I), are disclosed and claimed in the present application, as well as salts and pharmaceutical compositions comprising the novel compounds and their use in therapy, in particular in the management of pain.
1
Bicyclically substituted uracils and the use thereof
申请人:Bayer Pharma Aktiengesellschaft
公开号:US10300062B2
公开(公告)日:2019-05-28
The present application relates to novel bicyclically substituted uracil derivatives, to processes for preparation thereof, to the use thereof alone or in combinations for treatment and/or prophylaxis of diseases, and to the use thereof for production of medicaments for treatment and/or prophylaxis of diseases.