Affiliation:
1. Department of Drugs and Medicines, School of Pharmaceutical Sciences, Sao Paulo State University (UNESP),
Araraquara, SP, Brazil
Abstract
Mannich bases, synthesized through the reaction of an aldehyde, a primary or
secondary amine, and a compound bearing an acidic hydrogen atom, represent a versatile
class of scaffolds in medicinal chemistry. This review explores their broad spectrum
of biological activities, emphasizing their potential in combating infectious diseases.
With demonstrated efficacy against bacteria, fungi, and parasites, Mannich bases
stand out as promising candidates for the development of novel therapeutic agents. Their
versatility arises from the ability of their electronic, steric, and conformational parameters
to modulate receptor interactions, significantly expanding their applicability in drug
design. The review provides an in-depth analysis of the structure-activity relationship
(SAR) of Mannich bases, highlighting how specific structural modifications enhance
their biological activity. Additionally, it examines the lipophilic properties of these compounds,
offering key insights into their influence on pharmacokinetics and pharmacodynamics.
This understanding is essential for optimizing the development of novel therapeutics,
particularly for addressing challenging infectious diseases. By integrating these
aspects, this review underscores the pivotal role of Mannich bases in overcoming current
challenges in drug resistance and shaping the future of drug discovery and development.
Publisher
Bentham Science Publishers Ltd.