Title
Indole and Benzimidazole Bichalcophenes: Synthesis, DNA Binding and Antiparasitic Activity
Author
Abdelbasset A. Farahat, Mohamed A. Ismail, Arvind Kumar, Tanja Wenzlerd, Reto Brund, Ananya Paul, W. David Wilson, David W. Boykin
Year
2018
Journal
European Journal of Medicinal Chemistry
Abstract
A novel series of indole and benzimidazole bichalcophene diamidine derivatives were prepared to study their antimicrobial activity against the tropical parasites causing African sleeping sickness and malaria. The dicyanoindoles needed to synthesize the target diamidines were obtained through Stille coupling reactions while the bis-cyanobenzimidazoles intermediates were made via condensation/cyclization reactions of different aldehydes with 4-cyano-1,2-diaminobenzene. Different amidine synthesis methodologies namely, lithium bis-trimethylsilylamide (LiN[Si(CH3)3]2) and Pinner methods were used to prepare the diamidines. Both types (indole and benzimidazole) derivatives of the new diamidines bind strongly with the DNA minor groove and generally show excellent in vitro antitrypanosomal activity. The diamidino-indole derivatives also showed excellent in vitro antimalarial activity while their benzimidazole counterparts were generally less active. Compound 7c was highly active in vivo and cured all mice infected with Trypanosoma brucei rhodesiense, a model that mimics the acute stage of African sleeping sickness, at a low dose of 4 × 5 mg/kg i.p. and hence 7c is more potent in vivo than pentamidine.
Instrument
J-810
Keywords
Induced circular dichroism, DNA binding, Biochemistry, Medicinal