Schaeffer J M, Blizzard T A, Ondeyka J, Goegelman R, Sinclair P J, Mrozik H
Department of Biochemical Parasitology, Merck Sharp & Dohme Research Laboratories, Rahway, NJ 07065.
Biochem Pharmacol. 1992 Feb 18;43(4):679-84. doi: 10.1016/0006-2952(92)90230-g.
Paraherquamide was identified recently as a potent anthelmintic agent. In this paper we describe the identification and characterization of a specific, high-affinity paraherquamide binding site in a membrane preparation isolated from the free-living nematode, Caenorhabditis elegans. [3H] Paraherquamide bound specifically to C. elegans membranes with an apparent dissociation constant, Kd, of 263 nM. A series of paraherquamide analogs were examined, and their relative affinity for the paraherquamide binding site correlated with their nematocidal activity. Phenothiazines were the only other class of anthelmintics tested which inhibited specific [3H]paraherquamide binding. These results suggest that the anthelmintic activity of paraherquamide and phenothiazine is mediated via an interaction with a common binding site.
副赫曲霉素最近被鉴定为一种有效的驱虫剂。在本文中,我们描述了从自由生活的线虫秀丽隐杆线虫分离的膜制剂中一种特异性、高亲和力的副赫曲霉素结合位点的鉴定和表征。[3H]副赫曲霉素与秀丽隐杆线虫膜特异性结合,其表观解离常数Kd为263 nM。研究了一系列副赫曲霉素类似物,它们对副赫曲霉素结合位点的相对亲和力与其杀线虫活性相关。吩噻嗪是测试的唯一一类其他驱虫剂,它抑制特异性[3H]副赫曲霉素结合。这些结果表明,副赫曲霉素和吩噻嗪的驱虫活性是通过与一个共同结合位点的相互作用介导的。