Discovery and Structure Elucidation of a New Polyketide‐Derived Tetrahydropyran‐Containing Conjugated Fatty Acid Derivative Isolated From Typhonium blumei

ABSTRACT A chemical investigation of the 95% EtOH extract of Typhonium blumei led to the isolation of a new polyketide‐derived tetrahydropyran‐containing conjugated fatty acid derivative ( 1 ), together with four known compounds ( 2 – 5 ). The structure of compound 1 was elucidated through comprehensive spectroscopic analyses, including 1D and 2D NMR spectra ( 1 H NMR, 13 C NMR, DEPT, HSQC, HMBC, COSY, and NOESY), as well as HR‐ESI‐MS data. Its absolute configuration was further established by ECD calculation. The biosynthetic pathway for compound 1 was postulated. In addition, all the isolated compounds ( 1 – 5 ) were tested for their cytotoxic activities.

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Publication Details

Journal
Magnetic Resonance in Chemistry
Published
2026-10-30
DOI
https://doi.org/10.1002/mrc.70150
Primary Topic
Phytochemistry and Biological Activities
Type
article
Field-Weighted Citation Impact
0.00

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article

Discovery and Structure Elucidation of a New Polyketide‐Derived Tetrahydropyran‐Containing Conjugated Fatty Acid Derivative Isolated From Typhonium blumei

Yaling Deng, Kaifeng Hu, Weijia Hu, Xiaomei Yu et al.
Magnetic Resonance in Chemistry
Phytochemistry and Biological Activities
article

Discovery and Structure Elucidation of a New Polyketide‐Derived Tetrahydropyran‐Containing Conjugated Fatty Acid Derivative Isolated From Typhonium blumei

Yaling Deng, Kaifeng Hu, Weijia Hu, Xiaomei Yu, Tao Wang, Yu Hu, Qi Zhang, Bowen Zhang, Lu Dai
article en

Abstract

ABSTRACT A chemical investigation of the 95% EtOH extract of Typhonium blumei led to the isolation of a new polyketide‐derived tetrahydropyran‐containing conjugated fatty acid derivative ( 1 ), together with four known compounds ( 2 – 5 ). The structure of compound 1 was elucidated through comprehensive spectroscopic analyses, including 1D and 2D NMR spectra ( 1 H NMR, 13 C NMR, DEPT, HSQC, HMBC, COSY, and NOESY), as well as HR‐ESI‐MS data. Its absolute configuration was further established by ECD calculation. The biosynthetic pathway for compound 1 was postulated. In addition, all the isolated compounds ( 1 – 5 ) were tested for their cytotoxic activities.

Magnetic Resonance in Chemistry
Chengdu University of Traditional Chinese Medicine (CN)
National Natural Science Foundation of China, Chengdu University of Traditional Chinese Medicine, Foundation for Innovative Research Groups of the National Natural Science Foundation of China
Openalex Percentile: Top 15%
Phytochemistry and Biological Activities
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