meroterpenoids

Meroterpenoids are a diverse class of natural compounds that originate from the partial biosynthesis of terpenoids, combined with other biosynthetic pathways such as polyketide, amino acid, or shikimate pathways. The term "meroterpenoid" derives from "mero," meaning part, and "terpenoid," indicating their mixed origin. These compounds are often characterized by complex structures featuring both terpenoid and non-terpenoid moieties, contributing to their wide range of biological activities.

Meroterpenoids are predominantly found in marine organisms, fungi, and plants. They exhibit a broad spectrum of bioactivities, including antimicrobial, anticancer, anti-inflammatory, and antiviral effects, making them of great interest in pharmaceutical research. Their structural diversity is partly due to various oxygenation, cyclization, and oxidation reactions during biosynthesis.

Biosynthetically, meroterpenoids typically involve the attachment of terpenoid units such as isoprene-derived skeletons to other molecular frameworks. For instance, they may incorporate polyketide-derived aromatic rings or amino acid derivatives, resulting in compounds with unique properties.

Research into meroterpenoids continues to expand, driven by their potential therapeutic applications and their role as chemical probes for understanding complex biosynthetic processes. Some well-known examples include amoebapyrroles, sesterterpenoids, and certain halogenated natural products. As natural products, they provide valuable scaffolds for synthetic modification and drug development.

Overall, meroterpenoids represent a fascinating intersection of multiple biosynthetic routes, contributing to the chemical diversity and biological significance of natural products.