Evidence map›Paper›PMID 42870210›Full record

ReviewJournal of natural medicines2026

Exploration of bioactive natural products from tropical plant genetic resources: from diversity to functional seeds.

Hiroshi Morita, Yusuke Hirasawa, Toshio Kaneda

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In one paragraph

Review in Journal of natural medicines, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Hiroshi MoritaFaculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41, Shinagawa-Ku, Tokyo, 142-8501, Japan. moritah@hoshi.ac.jp.
Yusuke HirasawaFaculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41, Shinagawa-Ku, Tokyo, 142-8501, Japan.
Toshio KanedaFaculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41, Shinagawa-Ku, Tokyo, 142-8501, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural products derived from higher plants continue to represent an important source of structurally diverse and biologically active molecules for drug discovery. In particular, tropical plant genetic resources provide a rich reservoir of unique secondary metabolites owing to their exceptional biodiversity. Through long-term collaborative studies conducted mainly in Southeast Asia, extensive collections of tropical plant materials were screened for diverse biological activities, leading to the discovery of numerous bioactive natural products. Early phytochemical studies on medicinal plants such as Eurycoma longifolia, a well-known traditional herbal medicine widely used in Malaysia and Indonesia, also contributed to the establishment of our research platform for tropical natural product discovery. This review summarizes representative studies on structurally unique compounds isolated from tropical plant resources and highlights their biological activities and mechanisms of action. Representative examples include ceramicines, limonoids from Chisocheton ceramicus with anti-lipid droplet accumulation activity, calofolic acids from Calophyllum scriblitifolium exhibiting vasorelaxant effects through PI3K-PKA signaling modulation, cassiarins, alkaloids from Cassia siamea with potent antimalarial activity, bisindole alkaloids from Leuconotis species inducing autophagy through AKT-mTOR pathway inhibition, cyclolinopeptides from flaxseed suppressing osteoclast differentiation via the c-Fos/RANK axis, celogentins, bicyclic peptides from Celosia argentea inhibiting tubulin polymerization, and mollugin derivatives from Rubia species targeting TLR4-mediated inflammatory signaling pathways. These studies demonstrate that tropical plant-derived natural products possess remarkable structural diversity and act on biologically relevant molecular targets. Furthermore, several cases illustrate the importance of mechanistic analysis and structural modification for the optimization of pharmacological activity. Collectively, this review highlights the significance of biodiversity-driven natural product exploration as a strategy for identifying functional seeds for future drug discovery.

Indexed as

Bioactive natural productsBiodiversity-driven drug discoveryMechanism-based pharmacologyStructure–activity relationshipTropical plant genetic resources

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.