New C22-related terpenoid from Formosan marine sponge Lendenfeldia sp.

A new C₂₂ furanoterpenoid, lendenfurone A ( 1 ), was isolated from the Formosan marine sponge Lendenfeldia sp. C₂₂ furanoterpenoids are rare among sponge-derived natural products, with only two compounds (furodendin and dehydrofurodendin) reported to date. The structure of 1 was elucidated by NMR spectroscopy and HRESIMS, and the absolute configuration was established by specific optical rotation (SOR) prediction and confirmed through DFT-based NMR calculations with DP4⁺ analysis. Although compound 1 showed no significant anti-osteoclastogenic activity in PMA/RANKL-induced THP-1 cells, it exhibited no cytotoxicity. The unique scaffold of lendenfurone A may serve as a promising lead for future pharmacological studies. • A new C₂₂ furanoterpenoid, lendenfurone A, was isolated from Lendenfeldia sp. • Structure elucidation was confirmed by NMR, HRESIMS, and DP4⁺ analysis. • Lendenfurone A has a unique scaffold and shows no cytotoxicity or bioactivity.

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Publication Details

Journal
Phytochemistry Letters
Published
2026-01-02
DOI
https://doi.org/10.1016/j.phytol.2025.104106
Primary Topic
Marine Sponges and Natural Products
Type
article
Field-Weighted Citation Impact
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article

New C22-related terpenoid from Formosan marine sponge Lendenfeldia sp.

Yu-Cheng Chen, Yun-Shiuan Chen, Bo‐Rong Peng, Kuei-Hung Lai et al.
Phytochemistry Letters
Marine Sponges and Natural Products
article

New C22-related terpenoid from Formosan marine sponge Lendenfeldia sp.

Yu-Cheng Chen, Yun-Shiuan Chen, Bo‐Rong Peng, Kuei-Hung Lai, Quoc Vu Pham, Hsin-Wei Wang, Yu-Chia Chang, Jui-Hsin Su, You-Song Cheng, Mei-Hsien Lee
article en

Abstract

A new C₂₂ furanoterpenoid, lendenfurone A ( 1 ), was isolated from the Formosan marine sponge Lendenfeldia sp. C₂₂ furanoterpenoids are rare among sponge-derived natural products, with only two compounds (furodendin and dehydrofurodendin) reported to date. The structure of 1 was elucidated by NMR spectroscopy and HRESIMS, and the absolute configuration was established by specific optical rotation (SOR) prediction and confirmed through DFT-based NMR calculations with DP4⁺ analysis. Although compound 1 showed no significant anti-osteoclastogenic activity in PMA/RANKL-induced THP-1 cells, it exhibited no cytotoxicity. The unique scaffold of lendenfurone A may serve as a promising lead for future pharmacological studies. • A new C₂₂ furanoterpenoid, lendenfurone A, was isolated from Lendenfeldia sp. • Structure elucidation was confirmed by NMR, HRESIMS, and DP4⁺ analysis. • Lendenfurone A has a unique scaffold and shows no cytotoxicity or bioactivity.

Phytochemistry LettersVol. 71
Chang Gung University of Science and Technology (TW), National Sun Yat-sen University (TW), National Yang Ming Chiao Tung University (TW), Taipei Medical University Hospital (TW), National Museum of Marine Biology and Aquarium (TW), Taipei Medical University (TW)
Life below water
Openalex Percentile: Top 98%
Marine Sponges and Natural Products
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New C22-related terpenoid from Formosan marine sponge Lendenfeldia sp. — Yu-Cheng Chen, Yun-Shiuan Chen, et al. · Phytochemistry Letters (2026) | TGRS Research Map | TGRS