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Three new cytotoxic stilbene dimers from paphiopedilum dianthum
Three new stilbene dimers, paphiodianthins A-C (1-3), and nine known stilbenes, lignan and flavonoids (4-12) were isolated from the roots and leaves of Paphiopedilum dianthum (Orchidaceae). The structures of new compounds were elucidated from their NMR, HRESIMS and IR spectroscopic data. Cytotoxic a...
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Published in: | Natural product research 2023-11, Vol.37 (21), p.3685-3693 |
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creator | Lertnitikul, Nonthalert Liangsakul, Jatupol Jianmongkol, Suree Suttisri, Rutt |
description | Three new stilbene dimers, paphiodianthins A-C (1-3), and nine known stilbenes, lignan and flavonoids (4-12) were isolated from the roots and leaves of Paphiopedilum dianthum (Orchidaceae). The structures of new compounds were elucidated from their NMR, HRESIMS and IR spectroscopic data. Cytotoxic activity of all isolated compounds was evaluated by in vitro MTT assay against two human cancer cell lines (MCF-7, Caco-2), doxorubicin-resistant and mitoxantrone-resistant MCF-7 sublines, as well as a normal cell line (NIH/3T3). Stilbenes 1, 3, 10 and 11 were strongly cytotoxic to both cancer cell lines with IC
50
values ranging from 0.50 to 4.51 µM. Compounds 1, 10 and 11 were also active against chemotherapy-resistant MCF-7 sublines. |
doi_str_mv | 10.1080/14786419.2022.2101049 |
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50
values ranging from 0.50 to 4.51 µM. Compounds 1, 10 and 11 were also active against chemotherapy-resistant MCF-7 sublines.</description><subject>Cancer</subject><subject>Chemotherapy</subject><subject>Cytotoxicity</subject><subject>Dimers</subject><subject>Doxorubicin</subject><subject>Flavonoids</subject><subject>Lignans</subject><subject>Mitoxantrone</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Orchidaceae</subject><subject>Paphiopedilum dianthum</subject><subject>Stilbene</subject><subject>stilbenes</subject><subject>Tumor cell lines</subject><issn>1478-6419</issn><issn>1478-6427</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kE9LxDAQxYMouK5-BKHgxUtrJk2T5qSy-A8WvKznkE0TNkvb1KRl3W9vy64ePHiaYea9mccPoWvAGeAS3wHlJaMgMoIJyQhgwFScoNk0Txkl_PS3B3GOLmLcYkygKIoZul9tgjFJa3aJ3ve-919OJ7F39dq0JqlcY0JMbPBN0qlu43xnKlcPzbhRbb8Zmkt0ZlUdzdWxztHH89Nq8Zou31_eFo_LVFMo-5QrrTgtdEnA8CIfw4Cxua0UZ2AFACMFw8pSTjBlORXKiHzNLbWCcaZKyOfo9nC3C_5zMLGXjYva1LVqjR-iJEwAZZgBH6U3f6RbP4R2TCdJyXPA0_9RVRxUOvgYg7GyC65RYS8Bywmr_MEqJ6zyiHX0PRx8rrU-NGrnQ13JXu1rH2xQrXZR5v-f-AZ8Snz5</recordid><startdate>20231102</startdate><enddate>20231102</enddate><creator>Lertnitikul, Nonthalert</creator><creator>Liangsakul, Jatupol</creator><creator>Jianmongkol, Suree</creator><creator>Suttisri, Rutt</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7T7</scope><scope>7TK</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20231102</creationdate><title>Three new cytotoxic stilbene dimers from paphiopedilum dianthum</title><author>Lertnitikul, Nonthalert ; Liangsakul, Jatupol ; Jianmongkol, Suree ; Suttisri, Rutt</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-7aca745c821e7534781ef3fda761f91162560af472046349ae93b7f4f9676a813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Cancer</topic><topic>Chemotherapy</topic><topic>Cytotoxicity</topic><topic>Dimers</topic><topic>Doxorubicin</topic><topic>Flavonoids</topic><topic>Lignans</topic><topic>Mitoxantrone</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Orchidaceae</topic><topic>Paphiopedilum dianthum</topic><topic>Stilbene</topic><topic>stilbenes</topic><topic>Tumor cell lines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lertnitikul, Nonthalert</creatorcontrib><creatorcontrib>Liangsakul, Jatupol</creatorcontrib><creatorcontrib>Jianmongkol, Suree</creatorcontrib><creatorcontrib>Suttisri, Rutt</creatorcontrib><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Natural product research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lertnitikul, Nonthalert</au><au>Liangsakul, Jatupol</au><au>Jianmongkol, Suree</au><au>Suttisri, Rutt</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Three new cytotoxic stilbene dimers from paphiopedilum dianthum</atitle><jtitle>Natural product research</jtitle><date>2023-11-02</date><risdate>2023</risdate><volume>37</volume><issue>21</issue><spage>3685</spage><epage>3693</epage><pages>3685-3693</pages><issn>1478-6419</issn><eissn>1478-6427</eissn><abstract>Three new stilbene dimers, paphiodianthins A-C (1-3), and nine known stilbenes, lignan and flavonoids (4-12) were isolated from the roots and leaves of Paphiopedilum dianthum (Orchidaceae). The structures of new compounds were elucidated from their NMR, HRESIMS and IR spectroscopic data. Cytotoxic activity of all isolated compounds was evaluated by in vitro MTT assay against two human cancer cell lines (MCF-7, Caco-2), doxorubicin-resistant and mitoxantrone-resistant MCF-7 sublines, as well as a normal cell line (NIH/3T3). Stilbenes 1, 3, 10 and 11 were strongly cytotoxic to both cancer cell lines with IC
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source | Taylor and Francis Science and Technology Collection |
subjects | Cancer Chemotherapy Cytotoxicity Dimers Doxorubicin Flavonoids Lignans Mitoxantrone NMR Nuclear magnetic resonance Orchidaceae Paphiopedilum dianthum Stilbene stilbenes Tumor cell lines |
title | Three new cytotoxic stilbene dimers from paphiopedilum dianthum |
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