
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 MoreNantong Kaixin Pharma Chemical Co.,Ltd.
Contact:86-513-85250786
Address:2-1103 Huachen Mansion, 111 Gongnong Road,Nantong, Jiangsu, China
Contact:0572-2722882
Address:1201,F3,xinghuibandao,
Changzhou Kingyo Chemical Corporation Ltd.
website:http://www.kingyochem.com
Contact:+86-519-85105717
Address:19# Wuqing North Road, Changzhou , Jiangsu, China
Wuhan Kemi-Works Chemical Co., Ltd
website:http://www.kemiworks.com
Contact:86-27-85736489
Address:Rm. 1503, No. 164, Jianghan North Rd., Wuhan, 430022 China
ShenZhen InnoSyn Biotech Co.,Ltd
website:http://www.innosyns.com
Contact:+86-755-28351685
Address:Floor 5 & 6, Building A1, HAIKEXING Strategic Innovative Industrial Park, 16 BaoShan Road, PingShan District
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)