1020106-50-6Relevant articles and documents
Design, synthesis, and biological evaluation of novel alkenylthiophenes as potent and selective CB1 cannabinoid receptor antagonists
Tai, Chia-Liang,Hung, Ming-Shiu,Pawar, Vijay D.,Tseng, Shi-Liang,Song, Jen-Shin,Hsieh, Wan-Ping,Chiu, Hua-Hao,Wu, Hui-Chuan,Hsieh, Min-Tsang,Kuo, Chun-Wei,Hsieh, Chia-Chien,Tsao, Jing-Po,Chao, Yu-Sheng,Shia, Kak-Shan
supporting information; experimental part, p. 447 - 450 (2008/10/09)
A novel class of (5-(pent-1-enyl)thiophen-2-yl)pyrazole antagonists was discovered, many of which exhibited potent CB1 activity and good CB1/2 selectivity, suggesting that along with a 1,3-transposition of the carbonyl of the pyrazole 3-carboxamide, bioisosteric replacement of the conventional pyrazole 5-aryl group with a thienyl ring substituted with an appropriate alkenyl moiety is viable. The Royal Society of Chemistry 2008.
THIOPHENE COMPOUNDS
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Page/Page column 11, (2008/06/13)
This invention relates to thiophene compounds of formula (I) shown below: Each variable in formula (I) is defined in the specification. These compounds can be used to treat cannabinoid-receptor mediated disorders.