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Hybrid Compounds as Direct Multitarget Ligands: A Review
Michelle de Oliveira Pedrosa1, Rayssa Marques Duarte da Cruz1, Jessika de Oliveira Viana1
1Laboratory of Synthesis and Drug Delivery, Department of Biological Science, State University of Paraiba, Joao Pessoa, PB,. Brazil.
Molecular hybridization combines pharmacophores into single molecules for enhanced drug design. This review covers its recent applications in developing novel anti-inflammatory, antimicrobial, anticancer, and antiprotozoal agents.
Area of Science:
- Medicinal Chemistry
- Drug Design
Background:
- Molecular hybridization is a rational drug design strategy.
- It involves combining pharmacophoric units from different bioactive compounds into a single molecule.
- The goal is to achieve improved drug properties and efficacy.
Purpose of the Study:
- To review molecular hybridization and multitarget profiling in rational drug design.
- To highlight applications in designing novel hybrid compounds.
- Focus on anti-inflammatory, antimicrobial, anticancer, and antiprotozoal activities over the last six years.
Main Methods:
- Literature review of molecular hybridization and multitarget profiling.
- Analysis of applications in drug discovery.
- Focus on studies published within the last six years.
Main Results:
- Molecular hybridization has shown promise for multifactorial diseases like Alzheimer's, Parkinson's, cancer, inflammation, and hypertension.
- Hybrid compounds can exhibit enhanced affinity, efficacy, and selectivity.
- Potential for dual modes of action and reduced side effects.
Conclusions:
- Molecular hybridization is a valuable approach for developing novel therapeutics.
- It offers advantages such as improved pharmacokinetic/pharmacodynamic profiles and reduced drug resistance.
- The review highlights successful applications in anti-inflammatory, antimicrobial, anticancer, and antiprotozoal drug discovery.
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