Affiliation:
1. Unidad Académica de Ciencias Químicas, Universidad Autónoma de Zacatecas, 98160, Zacatecas, Zac. México
2. Facultad de Ciencias Químicas, Universidad Autónoma de San Luis Potosí, 78210, San Luis Potosí, SLP, México
Abstract
Abstract:
The therapeutic potential of the benzimidazole nucleus has been recognized since 1944, and
it is an important heterocycle system due to its presence in a wide range of bioactive compounds such
as antiviral, anticancer, antibacterial, and so on, where optimization of substituents in this class of
pharmacophore has resulted in many drugs. Its broad biological activity stems from physicochemical
properties such as hydrogen bond donor-acceptor capability, π→π stacking interactions, coordination
bonds with metals as ligands and hydrophobic interactions; properties that allow them to easily bind
with a series of biomolecules, including enzymes and nucleic acids, causing a growing interest in these
types of molecules. This review aims to present an overview to leading benzimidazole derivatives, as
well as to show the importance of the nature and type of substituents at the N1, C2, and C5(6) positions
when they are biologically evaluated, which can lead to obtaining potent drug candidate with a
significant range of biological activities.
Funder
Consejo Nacional de Ciencia y Tecnología
Publisher
Bentham Science Publishers Ltd.
Subject
Drug Discovery,Pharmacology,General Medicine
Cited by
28 articles.
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