A New Acyclic Compound from the Medicinal Plant Tinospora sinensis

In this study, chemical investigation of the aerial parts of the medicinal plant Tinospora sinensis yielded five compounds (1-5), including a new acyclic compound (1) and four known compounds (2-5).Their structures were determined by extensive analysis of the spectroscopic data, including 1D ( 1 H and 13 C NMR) and 2D NMR data (HSQC, COSY, and HMBC).Compounds 3-5 were identified to be stearic acid (3), abscisic acid (4), and blumenol A (5) based on comparisons of the NMR data with those reported in the literature.The NMR data for 2-hydroxy methyl stearate (2) were reported for the first time in CDCl3 in this study.The compounds were evaluated for their antitumor potential against A549 cell line, while all were inactive (25 M).Besides, compound 1 demonstrated marginal inhibition (19.35%) of LPS-induced NO production in RAW 264.7 cells (50 M).

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Publication Details

Journal
Records of Natural Products
Published
2025-07-26
DOI
https://doi.org/10.25135/rnp.530.2505.3536
Primary Topic
Phytochemicals and Medicinal Plants
Type
article
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article

A New Acyclic Compound from the Medicinal Plant Tinospora sinensis

Mengying Zhang, Lijing Cai
1 links
Records of Natural Products
Phytochemicals and Medicinal Plants
article

A New Acyclic Compound from the Medicinal Plant Tinospora sinensis

Mengying Zhang, Lijing Cai
article en

Abstract

In this study, chemical investigation of the aerial parts of the medicinal plant Tinospora sinensis yielded five compounds (1-5), including a new acyclic compound (1) and four known compounds (2-5).Their structures were determined by extensive analysis of the spectroscopic data, including 1D ( 1 H and 13 C NMR) and 2D NMR data (HSQC, COSY, and HMBC).Compounds 3-5 were identified to be stearic acid (3), abscisic acid (4), and blumenol A (5) based on comparisons of the NMR data with those reported in the literature.The NMR data for 2-hydroxy methyl stearate (2) were reported for the first time in CDCl3 in this study.The compounds were evaluated for their antitumor potential against A549 cell line, while all were inactive (25 M).Besides, compound 1 demonstrated marginal inhibition (19.35%) of LPS-induced NO production in RAW 264.7 cells (50 M).

Records of Natural Products(5)
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