Three New Steroids from the Roots of <i>Marsdenia tenacissima</i>

Three undescribed pregnane steroids, 12β-O-4-hydroxybenzoyl tenacigenin D (1), 12β-O-4-hydroxybenzoyl tenacigenin A (2), and 11α-nicotinoyl-17β-marsdenin (3), along with two known analogues (4 and 5), were isolated from the roots of Marsdenia tenacissima. Their structures were elucidated using one- and two-dimensional NMR, high-resolution electron ionization-mass spectrometry, single-crystal X-ray diffraction data, and experimental and density-functional-theory-calculated electronic circular dichroism measurements. All isolated compounds were evaluated for their cytotoxic activities against human lung cancer cells (A549), ovarian carcinoma cells (SKOV-3), gastric cancer cells (MGC 803) and breast cancer cells (MCF-7). Notably, 3 exhibited significant cytotoxic activity against both A549 (median inhibitory concentration (IC<sub>50</sub>)=16.79 μM) and SKOV-3 (IC<sub>50</sub>=12.30 μM) cells while exhibiting moderate cytotoxicity on MGC803 and MCF-7 cells.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2024-08-30
DOI
https://doi.org/10.1002/cbdv.202401801
Primary Topic
Phytochemistry and Bioactive Compounds
Type
article
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article

Three New Steroids from the Roots of Marsdenia tenacissima

Hong‐Tao Xu, Ming‐Hui Fan, Jinling Liu, M.‐H. Yang et al.
Chemistry & Biodiversity
Phytochemistry and Bioactive Compounds
article

Three New Steroids from the Roots of Marsdenia tenacissima

Hong‐Tao Xu, Ming‐Hui Fan, Jinling Liu, M.‐H. Yang, Dan‐Dan Mu
article en

Abstract

Three undescribed pregnane steroids, 12β-O-4-hydroxybenzoyl tenacigenin D (1), 12β-O-4-hydroxybenzoyl tenacigenin A (2), and 11α-nicotinoyl-17β-marsdenin (3), along with two known analogues (4 and 5), were isolated from the roots of Marsdenia tenacissima. Their structures were elucidated using one- and two-dimensional NMR, high-resolution electron ionization-mass spectrometry, single-crystal X-ray diffraction data, and experimental and density-functional-theory-calculated electronic circular dichroism measurements. All isolated compounds were evaluated for their cytotoxic activities against human lung cancer cells (A549), ovarian carcinoma cells (SKOV-3), gastric cancer cells (MGC 803) and breast cancer cells (MCF-7). Notably, 3 exhibited significant cytotoxic activity against both A549 (median inhibitory concentration (IC<sub>50</sub>)=16.79 μM) and SKOV-3 (IC<sub>50</sub>=12.30 μM) cells while exhibiting moderate cytotoxicity on MGC803 and MCF-7 cells.

Chemistry & BiodiversityVol. 21(12)
Shanghai Innovative Research Center of Traditional Chinese Medicine (CN), Shanghai University of Traditional Chinese Medicine (CN), Xinjiang Uygur Autonomous Region Uygur Medicine Hospital (CN), Zhengzhou People's Hospital (CN)
Openalex Percentile: Top 93%
Phytochemistry and Bioactive Compounds
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