Advancing Bioactive Natural Products Through Synthesis and Structural Modification

Sara T. Radwan, Old Dominion University
Kyle Lambert, Old Dominion University
Karen Vargas, Old Dominion University

Abstract/Description/Artist Statement

Natural products represent an important reservoir of bioactive molecules with wide-ranging relevance to pharmaceutical, agricultural, and industrial fields. Owing to their structural diversity and varied biological functions, these compounds continue to inspire the development of new therapeutics and functional materials. This study examines the isolation, structural elucidation, and synthetic modification of selected biologically active natural products. Emphasis is placed on key chemical transformations, including targeted functional group modifications and strategic bond-forming reactions, aimed at improving compound stability, solubility, and biological performance. The synthesis and optimization of these natural product derivatives offer insight into structure–function relationships and highlight their potential utility across multiple applied contexts.

 

Advancing Bioactive Natural Products Through Synthesis and Structural Modification

Natural products represent an important reservoir of bioactive molecules with wide-ranging relevance to pharmaceutical, agricultural, and industrial fields. Owing to their structural diversity and varied biological functions, these compounds continue to inspire the development of new therapeutics and functional materials. This study examines the isolation, structural elucidation, and synthetic modification of selected biologically active natural products. Emphasis is placed on key chemical transformations, including targeted functional group modifications and strategic bond-forming reactions, aimed at improving compound stability, solubility, and biological performance. The synthesis and optimization of these natural product derivatives offer insight into structure–function relationships and highlight their potential utility across multiple applied contexts.