Press J B, Wright W B, Chan P S, Marsico J W, Haug M F, Tauber J, Tomcufcik A S
J Med Chem. 1986 May;29(5):816-9. doi: 10.1021/jm00155a036.
A series of N-[(1H-heteroaryl)alkyl]-1H-isoindole-1,3(2H)-diones were prepared as part of a continuing investigation into the biological properties of compounds that were both thromboxane synthetase inhibitors and potential antihypertensive agents. The most active thromboxane synthetase inhibition was found for the title imidazole derivatives wherein a hexyl or octyl chain separated the heterocyclic ends of the molecule (5,6) or with substitution on the isoindole portion of the molecule (18, 19, 21, 22, 25, 26). Compounds with shorter alkyl chain separations had good antihypertensive effects (1-5, 8-10, 19-22, 27-30). Butyl derivative 3 was chosen for further evaluation as a potential antihypertensive agent with thromboxane synthetase inhibitory properties.
作为对兼具血栓素合成酶抑制剂和潜在抗高血压药物特性的化合物生物学特性持续研究的一部分,制备了一系列N-[(1H-杂芳基)烷基]-1H-异吲哚-1,3(2H)-二酮。对于标题中的咪唑衍生物,发现其对血栓素合成酶的抑制活性最高,其中己基或辛基链分隔了分子的杂环末端(5,6),或者分子的异吲哚部分有取代基(18,19,21,22,25,26)。具有较短烷基链分隔的化合物具有良好的抗高血压作用(1-5,8-10,19-22,27-30)。选择丁基衍生物3作为具有血栓素合成酶抑制特性的潜在抗高血压药物进行进一步评估。