Selected Thoughts on Hydrophobicity in Drug Design
Lillian L. Lou, John C. Martin
Abstract
The fundamental aim of drug design in research and development is to invent molecules with selective affinity towards desired disease-associated targets. At the atomic loci of binding surfaces, systematic structural variations can define affinities between drug candidates and biomolecules, and thereby guide the optimization of safety, efficacy and pharmacologic properties. Hydrophobic interaction between biomolecules and drugs is integral to binding affinity and specificity. Examples of antiviral drug discovery are discussed.
Topics & Concepts
BiomoleculeBinding affinitiesDrugAffinitiesComputational biologyDrug discoveryChemistryNanotechnologyCombinatorial chemistryPharmacologyStereochemistryBiologyBiochemistryMaterials scienceReceptorClick Chemistry and ApplicationsMonoclonal and Polyclonal Antibodies ResearchHIV/AIDS drug development and treatment