Medetomidine analogs as α2-adrenergic ligands. 3. Synthesis and biological evaluation of a new series of medetomidine analogs and their potential binding …
…, JE De Los Angeles, MY He, JT Dalton…
Index: Zhang, Xiaoyan; De Los Angeles, Joseph E.; He, Mei-Ying; Dalton, James T.; Shams, Gamal; Lei, Longping; Patil, Popat N.; Feller, Dennis R.; Miller, Duane D.; Hsu, Fu-Lian Journal of Medicinal Chemistry, 1997 , vol. 40, # 19 p. 3014 - 3024
Full Text: HTML
Citation Number: 23
Abstract
The synthesis and the biological evaluation of a new series of medetomidine analogs are reported. The substitution pattern at the phenyl ring of the tetralin analogs had a distinct influence on the α2-adrenoceptor binding affinity. 4-Methylindan analog 6 was the most potent α2-adrenoceptor binding ligand among these 4-substituted imidazoles, and its α2- adrenoceptor selectivity was greater than the 5-methyl tetralin analog 4c. Ligand- ...
Related Articles:
[Morin,F.G.; Horton,W.J.; Grant,D.M. Journal of the American Chemical Society, 1983 , vol. 105, p. 3992]
[Newman et al. Journal of the American Chemical Society, 1953 , vol. 75, p. 347]
[Demole,E.; Enggist,P. Helvetica Chimica Acta, 1978 , vol. 61, p. 1335 - 1341]
[Munslow, William D.; Reusch, William Journal of Organic Chemistry, 1982 , vol. 47, # 26 p. 5096 - 5099]