
European Journal of Medicinal Chemistry p. 133 - 139 (1995)
Update date:2022-08-03
Topics:
Colotta, V.
Cecchi, L.
Catarzi, D.
Filacchioni, G.
Martini, C.
et al.
The syntheses, A%1 and A2a adenosine receptor affinities and structure-activity relationships of some 2-aryl-1,2,4-triazolo<1,5-a>quinoxalines, 2-arylimidazo<1,2-a>quinoxalines, 1-arylimidazo<1,5-a>quinoxalines are reported and compared with that of a previously reported 2-phenylpyrazolo<1,5-a>quinoxaline.The results show that some triazoloquinoxalines are potent and specific A1 adenosine receptor ligands and that the replacement of either nitrogen at position 1 or 3 of the triazoloquinoxaline moiety with a CH brought about a decrease in affinity at both adenosine receptors. adenosine receptor ligand / 1,2,4-triazolo<1,5-a>quinoxaline / imidazo<1,2-a>quinoxaline / imidazo<1,5-a>quinoxaline / tricyclic heteroaromatic system
View MoreZHEJIANG CHEMICAL INDUSTRY INSTITUTE TECHNOLOGY CO.,LTD(expird)
Contact:86-575-82730298
Address:shangyu
Hangzhou Showland Technology Co., Ltd.
Contact:86-571-88920516
Address:ROOM2118,NO.553,WENSAN ROAD,HANGZHOU,CHINA
Jiangsu Dacheng Pharmaceutical and Chemical Co.,Ltd
Contact:+86-0517-87036900
Address:Chuzhou Chemical park, Huai'an, Jiangsu Province
Tangshan Moneide Trading Co., Ltd.
Contact:+86-315-8309571
Address:2-7-420 Jidong Building Materials Commercial Center, Tangshan, Hebei, 064000 China
Arshine Pharmaceutical Co., Limited
website:http://www.cnarshine.com
Contact:0731-88503671
Address:Room 1109.Block C3, Lugu Enterprise Plaza,No.27 Wenxuan Road,Changsha National Hi-Tech Industrial Development Zone,Hunan ,P.R.China
Doi:10.1002/jhet.5570320334
(1995)Doi:10.1002/adsc.201300698
(2013)Doi:10.1039/DT9950002469
(1995)Doi:10.1021/ja01191a051
(1948)Doi:10.1139/v63-323
(1963)Doi:10.1021/jo01148a001
(1950)