Progress in the Synthesis and Biological Activities of the Calothrixin and Topyrone Natural Products

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Authors: Aboudramane Koné, Marie-Aimée Penayori, Coulibaly, S eacute raphin Kati Coulibaly
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Abstract

Natural products represent a rich source of structurally diverse and biologically potent compounds. Among these are the calothrixins (cyanobacterial indolo[3,2-j]phenanthridine alkaloids) and the topyrones (fungal anthraquinone-type polyketides). While originating from different kingdoms of life and possessing distinct overall architectures, both scaffold families share a crucial quinone pharmacophore that is intrinsically linked to their potent cytotoxic activities, often involving DNA interaction and reactive oxygen species (ROS) generation. This review provides a comprehensive overview of the progress in the total synthesis and biological characterization of these two intriguing natural product classes. We discuss the various synthetic strategies developed to access their complex cores.

Fields of Study & Subjects

Synthesis and bioactivity of alkaloids Isoquinoline Alkaloid Synthesis Cyclization and Aryne Chemistry

Publication details

Journal / source
ChemRxiv
Publication date
2 March 2026
Language
EN
Document type
Preprint