Sundberg R J, Biswas S, Kumar Murthi K, Rowe D, McCall J W, Dzimianski M T
Department of Parasitology, College of Veterinary Medicine, University of Georiga, Athens, Georgia 30602, USA.
J Med Chem. 1998 Oct 22;41(22):4317-28. doi: 10.1021/jm9803368.
A series of guanylhydrazone, amidine, and hydrazone derivatives of 2-phenylimidazo[1,2-a]pyridine have been prepared and evaluated for macrofilarial activity against Acanthocheilonema viteae and Brugia pahangi in jirds. Compounds with 4',6-bis-substitution by cyclic guanylhydrazone groups show activity. 4',6-Bis-amidines show some activity but are more toxic; 4'- or 6-monosubstituted compounds are inactive. 2,6-Bis-substituted compounds lacking the phenyl ring are inactive. 4',6-Bis-substituted compounds having additional double bonds inserted between the heterocyclic ring and the phenyl ring or between the substituent and the ring system show reduced activity.
已制备了一系列2-苯基咪唑并[1,2-a]吡啶的胍腙、脒和腙衍生物,并在沙鼠体内对其抗棘唇旋尾线虫和彭亨布鲁线虫的杀丝虫活性进行了评估。4',6-位被环状胍腙基团双取代的化合物具有活性。4',6-双脒显示出一定活性,但毒性更大;4'-或6-单取代的化合物无活性。缺少苯环的2,6-双取代化合物无活性。在杂环与苯环之间或取代基与环系之间插入额外双键的4',6-双取代化合物活性降低。