Kebabian J W, Briggs C, Britton D R, Asin K, DeNinno M, MacKenzie R G, McKelvy J F, Schoenleber R
Abbott Laboratories, Neuroscience Research Division, Pharmaceutical Discovery, Abbott Park, Illinois 60064.
Am J Hypertens. 1990 Jun;3(6 Pt 2):40S-42S. doi: 10.1093/ajh/3.6.40s.
A68930 (5,6-dihydroxy-3-phenyl-1-aminomethyl-isochroman) is a potent (EC50 = 2.5 nmol/L) partial agonist at the D-1 dopamine receptor. In contrast, A68930 is a much weaker agonist (EC50 = 3,920 nmol/L) at the D-2 dopamine receptor. The orientation of the 3-phenyl substituent in the molecule is critical for the affinity and selectivity of the molecule towards the D-1 receptor in vitro and in vivo. The role of the D-1 receptor in the functioning of the basal ganglia is discussed.
A68930(5,6 - 二羟基 - 3 - 苯基 - 1 - 氨甲基异苯并二氢吡喃)是一种强效(EC50 = 2.5纳摩尔/升)的D - 1多巴胺受体部分激动剂。相比之下,A68930在D - 2多巴胺受体上是一种弱得多的激动剂(EC50 = 3920纳摩尔/升)。分子中3 - 苯基取代基的取向对于该分子在体外和体内对D - 1受体的亲和力和选择性至关重要。文中讨论了D - 1受体在基底神经节功能中的作用。