Verma A, Snyder S H
Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Mol Pharmacol. 1988 Dec;34(6):800-5.
We have examined organ and species variations in interactions of porphyrins with peripheral-type benzodiazepine receptors and explored structure-activity requirements for porphyrin-receptor interactions. Whereas potency of the benzodiazepine RO5-4864 varies several orders of magnitude in competing for receptors in different organs and species, effects of porphyrins and the isoquinoline carboxamide PK11195 are relatively constant. The structural requirements determining porphyrin affinity for benzodiazepine binding sites are fairly strict. The most potent porphyrins are those with prominent physiological functions.
我们研究了卟啉与外周型苯二氮䓬受体相互作用中的器官和物种差异,并探索了卟啉 - 受体相互作用的构效关系。虽然苯二氮䓬RO5 - 4864在不同器官和物种中竞争受体的效力相差几个数量级,但卟啉和异喹啉甲酰胺PK11195的作用相对恒定。决定卟啉对苯二氮䓬结合位点亲和力的结构要求相当严格。最有效的卟啉是那些具有显著生理功能的卟啉。