Evidence map›Paper›PMID 39127865›Full record

ArticleJournal of natural medicines2024

Isolation of C-29 oxygenated oleanane triterpenoids and a (+)-muurolene type sesquiterpenoid from the fruiting bodies of Fuscoporia torulosa and their bioactivities.

Tatsuro Yoneyama, Chian Chen, Yoshihiro Ichimura, Katsuyuki Nakashima, Hiromichi Kenmoku, Hiroshi Imagawa, Akemi Umeyama, Masaaki Noji

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Article in Journal of natural medicines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Tatsuro YoneyamaFaculty of Pharmaceutical Science, Tokushima Bunri University, 180 Nishihamaboji, Yamashiro-cho, Tokushima, Tokushima, 770-8514, Japan. yoneyama@ph.bunri-u.ac.jp.ORCID http://orcid.org/0000-0001-7306-9015
Chian ChenFaculty of Pharmaceutical Science, Tokushima Bunri University, 180 Nishihamaboji, Yamashiro-cho, Tokushima, Tokushima, 770-8514, Japan.
Yoshihiro IchimuraFaculty of Pharmaceutical Science, Tokushima Bunri University, 180 Nishihamaboji, Yamashiro-cho, Tokushima, Tokushima, 770-8514, Japan.
Katsuyuki NakashimaFaculty of Pharmaceutical Science, Tokushima Bunri University, 180 Nishihamaboji, Yamashiro-cho, Tokushima, Tokushima, 770-8514, Japan.
Hiromichi KenmokuFaculty of Pharmaceutical Science, Tokushima Bunri University, 180 Nishihamaboji, Yamashiro-cho, Tokushima, Tokushima, 770-8514, Japan.
Hiroshi ImagawaFaculty of Pharmaceutical Science, Tokushima Bunri University, 180 Nishihamaboji, Yamashiro-cho, Tokushima, Tokushima, 770-8514, Japan.
Akemi UmeyamaFaculty of Pharmaceutical Science, Tokushima Bunri University, 180 Nishihamaboji, Yamashiro-cho, Tokushima, Tokushima, 770-8514, Japan.
Masaaki NojiFaculty of Pharmaceutical Science, Tokushima Bunri University, 180 Nishihamaboji, Yamashiro-cho, Tokushima, Tokushima, 770-8514, Japan.

Funding

Japan Society for the Promotion of Science 19K16402
6 · The paper itself

Abstract

Basidiomycetes with a wide variety of skeletons of secondary metabolites can be expected to be the source of new interesting biological compounds. During our research on basidiomycetes, two new C-29 oxygenated oleanane-type triterpenes (1 and 2) and torulosacid (3), a muurolene type sesquiterpenoid with a five-membered ether ring along with nine known compounds (4-12), were isolated from the MeOH extract of the fruiting bodies of Fuscoporia torulosa. The structures of 1-3 were determined by NMR and HREIMS analysis. Further studies on the stereochemistry of 3 were conducted using X-ray crystallographic analysis and comparison of experimental and calculated ECD spectra. In the antimicrobial assay of isolates, 1, 7, and 9 showed growth inhibitory activity against methicillin-resistant Staphylococcus aureus and other gram-positive strains. Isolation of oleanane type triterpenes from fungi including basidiomycetes, is a unique report that could lead to further isolation of new compounds and the discovery of unique biosynthetic enzymes.

Indexed as

Fruiting Bodies, FungalMicrobial Sensitivity TestsSesquiterpenesAnti-Bacterial AgentsBasidiomycotaCrystallography, X-RayMethicillin-Resistant Staphylococcus aureusMolecular StructureOleanolic AcidTriterpenesAnti-Bacterial AgentsoleananeOleanolic AcidSesquiterpenesTriterpenesAntimicrobial activityBasidiomycetesFuscoporia torulosa(+)-Muurolene type sesquiterpenoidOleanane type triterpenoid

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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.