Two previously undescribed triterpenoid saponins from the roots and rhizomes of Caulophyllum robustum Maxim

Since ancient times, plants have provided humans with important bioactive compounds for the treatment of various diseases. Nine compounds were isolated from the roots and rhizomes of Caulophyllum robustum (a plant in the family Panaxaceae), including two new saponins C. Spanion A and C. Spanion B (1...

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Main Authors: Cong-Yu Zhang, Yu-Mei Wang, Peng-Cheng Qiu, Jia-Yu Feng, Bing-Wen Wang, Yu Cao, Yi-Sha Wei, Yi-Tong Zhou, Hai-Feng Tang, Yun-Yang Lu, Qian Zhang
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Chemistry
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Online Access:https://www.frontiersin.org/articles/10.3389/fchem.2024.1507891/full
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author Cong-Yu Zhang
Yu-Mei Wang
Peng-Cheng Qiu
Jia-Yu Feng
Bing-Wen Wang
Yu Cao
Yi-Sha Wei
Yi-Tong Zhou
Hai-Feng Tang
Yun-Yang Lu
Qian Zhang
author_facet Cong-Yu Zhang
Yu-Mei Wang
Peng-Cheng Qiu
Jia-Yu Feng
Bing-Wen Wang
Yu Cao
Yi-Sha Wei
Yi-Tong Zhou
Hai-Feng Tang
Yun-Yang Lu
Qian Zhang
author_sort Cong-Yu Zhang
collection DOAJ
description Since ancient times, plants have provided humans with important bioactive compounds for the treatment of various diseases. Nine compounds were isolated from the roots and rhizomes of Caulophyllum robustum (a plant in the family Panaxaceae), including two new saponins C. Spanion A and C. Spanion B (1-2) and seven known saponins (3-9). The cytotoxicity of these compounds on human cancer cell lines was analyzed using MTT method. Compounds 6 and 9 exhibit cytotoxicity towards these three types of human cancer cells (<10 μM). By utilizing the SEA platform for target prediction, a common tumor related target CD81 was identified. The molecular docking of saponins 1, 2, 6, and 9 with CD81 protein showed strong binding affinities ranging from -4.5 to -7.1 kcal/mol. Research has shown that these compounds can become potential anti-tumor drugs. Further research is still recommended to understand its exact molecular mechanism and toxicological effects.
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institution Kabale University
issn 2296-2646
language English
publishDate 2025-01-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Chemistry
spelling doaj-art-f561798872944a4f8e88b6d1fb6d13d62025-01-09T06:10:41ZengFrontiers Media S.A.Frontiers in Chemistry2296-26462025-01-011210.3389/fchem.2024.15078911507891Two previously undescribed triterpenoid saponins from the roots and rhizomes of Caulophyllum robustum MaximCong-Yu Zhang0Yu-Mei Wang1Peng-Cheng Qiu2Jia-Yu Feng3Bing-Wen Wang4Yu Cao5Yi-Sha Wei6Yi-Tong Zhou7Hai-Feng Tang8Yun-Yang Lu9Qian Zhang10Department of Chinese Materia Medica and Natural Medicines, School of Pharmacy, The Air Force Medical University, Xi’an, ChinaSchool of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, ChinaDepartment of Chinese Materia Medica and Natural Medicines, School of Pharmacy, The Air Force Medical University, Xi’an, ChinaSchool of Public Health, Health Science Center, Xi’an Jiaotong University, Xi’an, Shaanxi, ChinaDepartment of Chinese Materia Medica and Natural Medicines, School of Pharmacy, The Air Force Medical University, Xi’an, ChinaDepartment of Chinese Materia Medica and Natural Medicines, School of Pharmacy, The Air Force Medical University, Xi’an, ChinaSchool of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, ChinaSchool of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, ChinaDepartment of Chinese Materia Medica and Natural Medicines, School of Pharmacy, The Air Force Medical University, Xi’an, ChinaDepartment of Chinese Materia Medica and Natural Medicines, School of Pharmacy, The Air Force Medical University, Xi’an, ChinaDepartment of Chinese Materia Medica and Natural Medicines, School of Pharmacy, The Air Force Medical University, Xi’an, ChinaSince ancient times, plants have provided humans with important bioactive compounds for the treatment of various diseases. Nine compounds were isolated from the roots and rhizomes of Caulophyllum robustum (a plant in the family Panaxaceae), including two new saponins C. Spanion A and C. Spanion B (1-2) and seven known saponins (3-9). The cytotoxicity of these compounds on human cancer cell lines was analyzed using MTT method. Compounds 6 and 9 exhibit cytotoxicity towards these three types of human cancer cells (<10 μM). By utilizing the SEA platform for target prediction, a common tumor related target CD81 was identified. The molecular docking of saponins 1, 2, 6, and 9 with CD81 protein showed strong binding affinities ranging from -4.5 to -7.1 kcal/mol. Research has shown that these compounds can become potential anti-tumor drugs. Further research is still recommended to understand its exact molecular mechanism and toxicological effects.https://www.frontiersin.org/articles/10.3389/fchem.2024.1507891/fullCaulophyllum robustum MaximTriterpenoid saponinstructure identificationantitumor activitymolecular docking
spellingShingle Cong-Yu Zhang
Yu-Mei Wang
Peng-Cheng Qiu
Jia-Yu Feng
Bing-Wen Wang
Yu Cao
Yi-Sha Wei
Yi-Tong Zhou
Hai-Feng Tang
Yun-Yang Lu
Qian Zhang
Two previously undescribed triterpenoid saponins from the roots and rhizomes of Caulophyllum robustum Maxim
Frontiers in Chemistry
Caulophyllum robustum Maxim
Triterpenoid saponin
structure identification
antitumor activity
molecular docking
title Two previously undescribed triterpenoid saponins from the roots and rhizomes of Caulophyllum robustum Maxim
title_full Two previously undescribed triterpenoid saponins from the roots and rhizomes of Caulophyllum robustum Maxim
title_fullStr Two previously undescribed triterpenoid saponins from the roots and rhizomes of Caulophyllum robustum Maxim
title_full_unstemmed Two previously undescribed triterpenoid saponins from the roots and rhizomes of Caulophyllum robustum Maxim
title_short Two previously undescribed triterpenoid saponins from the roots and rhizomes of Caulophyllum robustum Maxim
title_sort two previously undescribed triterpenoid saponins from the roots and rhizomes of caulophyllum robustum maxim
topic Caulophyllum robustum Maxim
Triterpenoid saponin
structure identification
antitumor activity
molecular docking
url https://www.frontiersin.org/articles/10.3389/fchem.2024.1507891/full
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