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Marine indole alkaloid diversity and bioactivity. What do we know and what are we missing?

Journal

NATURAL PRODUCT REPORTS
Volume -, Issue -, Pages -

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2np00085g

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This article presents a meta-analysis of the biological activities of 2048 marine indole alkaloids (MIAs) and highlights the underexplored bioactivity potentials of most published MIAs. Despite the majority of MIAs not exhibiting cytotoxic or antimicrobial activity, there is still a focus on evaluating structurally related analogues using these assays. Cheminformatics analyses reveal that some MIAs possess potent and diverse activities, and many analogues that were previously only tested in cellular toxicity assays could be better utilized to generate structure-activity relationships for the treatment of emerging diseases. Shifting the focus to non-toxic disease targets could maximize the potential of MIAs for drug discovery.
Covering: marine indole alkaloids (n = 2048) and their reported bioactivities up to the end of 2021 Despite increasing numbers of marine natural products (MNPs) reported each year, most have only been examined for cytotoxic, antibacterial, and/or antifungal biological activities with the majority found to be inactive in these assays. In this context, why are natural products continuing to be examined in assays they are unlikely to show significant activity in, and what targets might be more useful for expanding knowledge of their biologically relevant chemical space? We have undertaken a meta-analysis of the biological activities for 2048 marine indole alkaloids (MIAs), a diverse sub-class of MNPs reported up to the end of 2021, and this has highlighted that the bioactivity potentials for up to 86% of published MIAs remains underexplored and/or undefined. Although most published MIAs are not cytotoxic or antimicrobial, there is a continued focus on using these assays to evaluate new structurally related analogues. Using cheminformatics analyses, the chemical diversity of the 2048 MIAs were clustered using fragment based fingerprints and their reported bioactivity potency towards specific disease targets was assessed for structure activity trends. These analyses showed that there are groups of MIAs that possess potent and diverse activities and that many analogues, previously tested only in cellular toxicity assays, could be better exploited to generate structure activity relationships associated with leads to treat emerging diseases. A collection of indole drug and drug-lead structures from non-natural sources were also incorporated into the dataset providing complementary bioactivity profiles that were further used to predict underexplored areas of potential new activity and to better direct future testing of MIAs. Our findings clearly suggest the biological evaluation of MIAs continues to be conducted on a narrow range of bioassays and disease targets, and that shifting the focus to non-toxic disease targets should provide expanded knowledge of biologically relevant chemical space aimed at maximising the potential of MIAs for drug discovery.

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