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Anti-RAFLS Triterpenoids and Hepatoprotective Lignans From the Leaves of Tujia Ethnomedicine Kadsura heteroclita (Xuetong)

A pair of 3,4-seco-cycloartane triterpenoid isomers with a rare peroxy bridge, namely, xuetonins A and B (1 and 2), four new lignans xuetonlignans A–D (3–6), a new sesquiterpene xuetonpene (7), and a new natural product xuetonin C (8), along with 43 known compounds, were obtained from the leaves of...

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Autores principales: Wang, Mengyun, Jiang, Sai, Hussain, Nusrat, Zafar, Salman, Xie, Qingling, Huang, Feibing, Mao, Linxi, Li, Bin, Jian, Yuqing, Wang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127087/
https://www.ncbi.nlm.nih.gov/pubmed/35620653
http://dx.doi.org/10.3389/fchem.2022.878811
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author Wang, Mengyun
Jiang, Sai
Hussain, Nusrat
Zafar, Salman
Xie, Qingling
Huang, Feibing
Mao, Linxi
Li, Bin
Jian, Yuqing
Wang, Wei
author_facet Wang, Mengyun
Jiang, Sai
Hussain, Nusrat
Zafar, Salman
Xie, Qingling
Huang, Feibing
Mao, Linxi
Li, Bin
Jian, Yuqing
Wang, Wei
author_sort Wang, Mengyun
collection PubMed
description A pair of 3,4-seco-cycloartane triterpenoid isomers with a rare peroxy bridge, namely, xuetonins A and B (1 and 2), four new lignans xuetonlignans A–D (3–6), a new sesquiterpene xuetonpene (7), and a new natural product xuetonin C (8), along with 43 known compounds, were obtained from the leaves of Tujia ethnomedicine, Kadsura heteroclita. Their structures and configurations were determined with the help of a combination of 1D- and 2D-NMR, HRESIMS spectra, electronic circular dichroism (ECD), and X-ray diffraction data. Compounds 2, 10, 13–15, and 17–19 showed moderate-to-potent activity against rheumatoid arthritis fibroblast-like synoviocytes (RAFLS) with IC(50) values of 19.81 ± 0.26, 12.73 ± 0.29, 5.70 ± 0.24, 9.25 ± 0.79, 5.66 ± 0.52, 11.91 ± 0.44, 13.22 ± 0.27, and 15.94 ± 0.36 μM, respectively. Furthermore, compounds 22, 25, and 31 exhibited significant hepatoprotective effects against N-acetyl-p-aminophenol (APAP)–induced toxicity in HepG2 cells at 10 μM, and the cell viability increased by 12.93, 25.23, and 13.91%, respectively, compared with that in the model group (cf. bicyclol, 12.60%).
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spelling pubmed-91270872022-05-25 Anti-RAFLS Triterpenoids and Hepatoprotective Lignans From the Leaves of Tujia Ethnomedicine Kadsura heteroclita (Xuetong) Wang, Mengyun Jiang, Sai Hussain, Nusrat Zafar, Salman Xie, Qingling Huang, Feibing Mao, Linxi Li, Bin Jian, Yuqing Wang, Wei Front Chem Chemistry A pair of 3,4-seco-cycloartane triterpenoid isomers with a rare peroxy bridge, namely, xuetonins A and B (1 and 2), four new lignans xuetonlignans A–D (3–6), a new sesquiterpene xuetonpene (7), and a new natural product xuetonin C (8), along with 43 known compounds, were obtained from the leaves of Tujia ethnomedicine, Kadsura heteroclita. Their structures and configurations were determined with the help of a combination of 1D- and 2D-NMR, HRESIMS spectra, electronic circular dichroism (ECD), and X-ray diffraction data. Compounds 2, 10, 13–15, and 17–19 showed moderate-to-potent activity against rheumatoid arthritis fibroblast-like synoviocytes (RAFLS) with IC(50) values of 19.81 ± 0.26, 12.73 ± 0.29, 5.70 ± 0.24, 9.25 ± 0.79, 5.66 ± 0.52, 11.91 ± 0.44, 13.22 ± 0.27, and 15.94 ± 0.36 μM, respectively. Furthermore, compounds 22, 25, and 31 exhibited significant hepatoprotective effects against N-acetyl-p-aminophenol (APAP)–induced toxicity in HepG2 cells at 10 μM, and the cell viability increased by 12.93, 25.23, and 13.91%, respectively, compared with that in the model group (cf. bicyclol, 12.60%). Frontiers Media S.A. 2022-05-10 /pmc/articles/PMC9127087/ /pubmed/35620653 http://dx.doi.org/10.3389/fchem.2022.878811 Text en Copyright © 2022 Wang, Jiang, Hussain, Zafar, Xie, Huang, Mao, Li, Jian and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Wang, Mengyun
Jiang, Sai
Hussain, Nusrat
Zafar, Salman
Xie, Qingling
Huang, Feibing
Mao, Linxi
Li, Bin
Jian, Yuqing
Wang, Wei
Anti-RAFLS Triterpenoids and Hepatoprotective Lignans From the Leaves of Tujia Ethnomedicine Kadsura heteroclita (Xuetong)
title Anti-RAFLS Triterpenoids and Hepatoprotective Lignans From the Leaves of Tujia Ethnomedicine Kadsura heteroclita (Xuetong)
title_full Anti-RAFLS Triterpenoids and Hepatoprotective Lignans From the Leaves of Tujia Ethnomedicine Kadsura heteroclita (Xuetong)
title_fullStr Anti-RAFLS Triterpenoids and Hepatoprotective Lignans From the Leaves of Tujia Ethnomedicine Kadsura heteroclita (Xuetong)
title_full_unstemmed Anti-RAFLS Triterpenoids and Hepatoprotective Lignans From the Leaves of Tujia Ethnomedicine Kadsura heteroclita (Xuetong)
title_short Anti-RAFLS Triterpenoids and Hepatoprotective Lignans From the Leaves of Tujia Ethnomedicine Kadsura heteroclita (Xuetong)
title_sort anti-rafls triterpenoids and hepatoprotective lignans from the leaves of tujia ethnomedicine kadsura heteroclita (xuetong)
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127087/
https://www.ncbi.nlm.nih.gov/pubmed/35620653
http://dx.doi.org/10.3389/fchem.2022.878811
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