Hit-to-Lead studies: The discovery of potent adamantane amide P2X7 receptor antagonists
摘要:
A Hit-to-Lead optimisation programme was carried out on the adamantane high throughput screening hit I resulting in the discovery of a number of potent P2X(7) antagonists. (C) 2003 Elsevier Ltd. All rights reserved.
DOI:
10.1016/j.bmcl.2003.08.034
作为产物:
描述:
1-金刚烷甲胺 、 2-氯-3-硝基苯甲酸 以to give the title compound as a yellow solid (1.7 g)的产率得到2-Chloro-3-nitro-N-(tricyclo[3.3.1.13.7]dec-1-ylmethyl)-benzamide
The invention provides adamantane derivatives, a process for their preparation, pharmaceutical compositions containing them, a process for preparing the pharmaceutical compositions, and their use in therapy.
The invention provides adamantane derivatives, a process for their preparation, pharmaceutical compositions containing them, a process for preparing the pharmaceutical compositions, and their use in therapy.
The invention provides adamantane derivatives, a process for their preparation, pharmaceutical compositions containing them, a process for preparing the pharmaceutical compositions, and their use in therapy.