Kerry R, Scrutton M C
Br J Pharmacol. 1983 Jun;79(2):401-7. doi: 10.1111/j.1476-5381.1983.tb11012.x.
781094 (2-(2(1, 4-benzodioxanyl))-2-imidazoline hydrochloride) is a potent competitive inhibitor of the aggregatory responses of human platelets induced by adrenaline (pA2 = 7.3) and UK-14304. 781094 is a more potent inhibitor of the pro-aggregatory response to clonidine than of that to methoxamine. The alpha 2/alpha 1-adrenoceptor selectivity ratio is 11.4. 781094 is a potent inhibitor of the binding of [3H]-dihydroergocryptine to platelet lysates. 781094 has no effect on the aggregatory responses of human platelets induced by adenosine-5'-pyrophosphate (ADP), 5-hydroxytryptamine, thrombin, U-46619, or arginine-vasopressin provided that the platelet-rich plasma does not exhibit enhanced responsiveness. In some instances high concentrations of 781094 potentiate the aggregatory response to collagen. In platelet-rich plasma which exhibits enhanced responsiveness, 781094 causes partial inhibition of the aggregatory responses to 5-hydroxytryptamine, ADP and vasopressin at concentrations similar to those required to inhibit the response to adrenaline. 781094 acts as a specific antagonist for the responses mediated by human platelet alpha-adrenoceptors and exhibits moderate selectivity for the alpha 2-adrenoceptors on this cell.
781094(2-(2(1,4-苯并二氧杂环己基))-2-咪唑啉盐酸盐)是一种强效竞争性抑制剂,可抑制肾上腺素(pA2 = 7.3)和UK-14304诱导的人血小板聚集反应。781094对可乐定促聚集反应的抑制作用比对甲氧明的更强。α2/α1肾上腺素能受体选择性比值为11.4。781094是[3H]-二氢麦角隐亭与血小板裂解物结合的强效抑制剂。只要富血小板血浆没有表现出增强的反应性,781094对腺苷-5'-焦磷酸(ADP)、5-羟色胺、凝血酶、U-46619或精氨酸加压素诱导的人血小板聚集反应没有影响。在某些情况下,高浓度的781094会增强对胶原蛋白的聚集反应。在反应性增强的富血小板血浆中,781094在抑制肾上腺素反应所需的类似浓度下,会部分抑制对5-羟色胺、ADP和加压素的聚集反应。781094作为人血小板α-肾上腺素能受体介导反应的特异性拮抗剂,对该细胞上的α2-肾上腺素能受体表现出中等选择性。