Naturally Occurring Alkaloids, Derivatives, and Semi-synthetic Modifications as Lead Compounds for the Development of New Anti-Trypanosoma cruzi Agents

被引:1
|
作者
Fernandez, Lucia Raquel [1 ,2 ]
Musikant, Daniel [3 ]
Edreira, Martin M. [3 ,4 ,5 ]
机构
[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Quim Organ, Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, Unidad Microanal & Metodos Fis Aplicados Quim Org, CONICET, UMYMFOR, Buenos Aires, DF, Argentina
[3] Univ Buenos Aires, Dept Quim Biol, Fac Ciencias Exactas & Nat, Buenos Aires, DF, Argentina
[4] Univ Buenos Aires, Inst Quim Biol, Fac Ciencias Exactas Nat IQUIBICEN, CONICET, RA-1428 Buenos Aires, DF, Argentina
[5] Univ Pittsburgh, Sch Med, Dept Pharmacol & Chem Biol, Pittsburgh, PA USA
关键词
Alkaloids; Trypanosoma cruzi; Synthetic modifications; Antiparasitic activity; 7,3'-COUPLED NAPHTHYLISOQUINOLINE ALKALOIDS; IN-VITRO; ANTIAUSTERITY ACTIVITIES; ANTIPROTOZOAL ACTIVITY; TRYPANOCIDAL ACTIVITY; QUINOLINE ALKALOIDS; A-D; LIANA; SUSCEPTIBILITY; BENZNIDAZOLE;
D O I
10.1007/s40588-021-00163-x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Purpose of Review Despite recent advances, Chagas disease is still a public health issue that requires more efforts in order to develop efficient and safe drugs. Plants and fungi are the main source for semi-synthetic natural-inspired new molecules to treat human illness. In the present work, we summarize the main findings of natural-derived and semi-synthetic alkaloids against Trypanosoma cruzi. Recent Findings Over the last 10 years, at least seven alkaloids groups with structural modifications, including 130 molecules and almost 100 semi-synthetic compounds derived from natural alkaloids, including hybrids molecules, modifications of aliphatic chain extension, chemical groups, and heteroatoms, were analyzed for its toxicity over parasites and mammalian cells. Summary According to the available data, there are a good number of promising natural and/or semi-synthetic alkaloids that would meet the criteria to become candidates in the drug discovery process against Trypanosoma cruzi parasites. Main scaffolds that deserve special attention are natural quinolones, isoquinolines, and semi-synthetic hybrids molecules.
引用
收藏
页码:68 / 86
页数:19
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