Chemical constituents from Schisandra sphenanthera and their cytotoxic activity

Nguyen Thi Mai; Vu Van Doan; Hoang Thi Tuyet Lan; Bui Thi Mai Anh; Nguyen Huy Hoang; Bui Huu Tai; Nguyen Xuan Nhiem; Pham Hai Yen; Seon Ju Park; Yohan Seo; Wan Namkung; Seung Hyun Kim; Phan Van Kiem

doi:10.1080/14786419.2019.1700247

Chemical constituents from Schisandra sphenanthera and their cytotoxic activity

Nguyen Thi Mai, Vu Van Doan, Hoang Thi Tuyet Lan, Bui Thi Mai Anh, Nguyen Huy Hoang, Bui Huu Tai, Nguyen Xuan Nhiem, Pham Hai Yen, Seon Ju Park, Yohan Seo, Wan Namkung, Seung Hyun Kim, Phan Van Kiem

Department of Pharmacy

Research output: Contribution to journal › Article › peer-review

Abstract

Extensive phytochemical investigation of Schisandra sphenanthera leaves resulted in the isolation of six highly oxygenated nortriterpenoids (1–6) and five lignans (7–11) including a new pre-schisanartane-type, schisandrathera A (1), a new dibenzocyclooctadiene glycoside, schisandrathera B (7) and two new lignans, schisandrathera C (8) and schisandrathera D (9). Their chemical structures including absolute configurations were determined extensively by means of HR-ESI-MS, NMR, and ECD spectra. In addition, all isolated compounds were tested for cytotoxic activity against PC3 (prostate cancer) and MCF7 (breast cancer) cell lines. Among these compounds, schirubrisin B (3) showed strong cytotoxic effect on both PC3 and MCF7 cell lines with IC₅₀ values of 3.21 ± 0.68, 13.30 ± 0.68 μM, respectively, whereas ten remaining compounds were found to be less effective in the investigated models.

Original language	English
Journal	Natural Product Research
DOIs	https://doi.org/10.1080/14786419.2019.1700247
Publication status	Accepted/In press - 2019

Bibliographical note

Publisher Copyright:
© 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.

All Science Journal Classification (ASJC) codes

Analytical Chemistry
Biochemistry
Plant Science
Organic Chemistry

UN SDGs

This output contributes to the following Sustainable Development Goal(s)

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10.1080/14786419.2019.1700247

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@article{fbe49739c1d6424895d65e17982b01f6,

title = "Chemical constituents from Schisandra sphenanthera and their cytotoxic activity",

abstract = "Extensive phytochemical investigation of Schisandra sphenanthera leaves resulted in the isolation of six highly oxygenated nortriterpenoids (1–6) and five lignans (7–11) including a new pre-schisanartane-type, schisandrathera A (1), a new dibenzocyclooctadiene glycoside, schisandrathera B (7) and two new lignans, schisandrathera C (8) and schisandrathera D (9). Their chemical structures including absolute configurations were determined extensively by means of HR-ESI-MS, NMR, and ECD spectra. In addition, all isolated compounds were tested for cytotoxic activity against PC3 (prostate cancer) and MCF7 (breast cancer) cell lines. Among these compounds, schirubrisin B (3) showed strong cytotoxic effect on both PC3 and MCF7 cell lines with IC50 values of 3.21 ± 0.68, 13.30 ± 0.68 μM, respectively, whereas ten remaining compounds were found to be less effective in the investigated models.",

author = "Mai, {Nguyen Thi} and Doan, {Vu Van} and Lan, {Hoang Thi Tuyet} and Anh, {Bui Thi Mai} and Hoang, {Nguyen Huy} and Tai, {Bui Huu} and Nhiem, {Nguyen Xuan} and Yen, {Pham Hai} and Park, {Seon Ju} and Yohan Seo and Wan Namkung and Kim, {Seung Hyun} and Kiem, {Phan Van}",

note = "Publisher Copyright: {\textcopyright} 2019, {\textcopyright} 2019 Informa UK Limited, trading as Taylor & Francis Group.",

year = "2019",

doi = "10.1080/14786419.2019.1700247",

language = "English",

journal = "Natural Product Research",

issn = "1478-6419",

publisher = "Taylor and Francis Ltd.",

}

Chemical constituents from Schisandra sphenanthera and their cytotoxic activity. / Mai, Nguyen Thi; Doan, Vu Van; Lan, Hoang Thi Tuyet; Anh, Bui Thi Mai; Hoang, Nguyen Huy; Tai, Bui Huu; Nhiem, Nguyen Xuan; Yen, Pham Hai; Park, Seon Ju; Seo, Yohan; Namkung, Wan ; Kim, Seung Hyun; Kiem, Phan Van.

In: Natural Product Research, 2019.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - Chemical constituents from Schisandra sphenanthera and their cytotoxic activity

AU - Mai, Nguyen Thi

AU - Doan, Vu Van

AU - Lan, Hoang Thi Tuyet

AU - Anh, Bui Thi Mai

AU - Hoang, Nguyen Huy

AU - Tai, Bui Huu

AU - Nhiem, Nguyen Xuan

AU - Yen, Pham Hai

AU - Park, Seon Ju

AU - Seo, Yohan

AU - Namkung, Wan

AU - Kim, Seung Hyun

AU - Kiem, Phan Van

PY - 2019

Y1 - 2019

N2 - Extensive phytochemical investigation of Schisandra sphenanthera leaves resulted in the isolation of six highly oxygenated nortriterpenoids (1–6) and five lignans (7–11) including a new pre-schisanartane-type, schisandrathera A (1), a new dibenzocyclooctadiene glycoside, schisandrathera B (7) and two new lignans, schisandrathera C (8) and schisandrathera D (9). Their chemical structures including absolute configurations were determined extensively by means of HR-ESI-MS, NMR, and ECD spectra. In addition, all isolated compounds were tested for cytotoxic activity against PC3 (prostate cancer) and MCF7 (breast cancer) cell lines. Among these compounds, schirubrisin B (3) showed strong cytotoxic effect on both PC3 and MCF7 cell lines with IC50 values of 3.21 ± 0.68, 13.30 ± 0.68 μM, respectively, whereas ten remaining compounds were found to be less effective in the investigated models.

AB - Extensive phytochemical investigation of Schisandra sphenanthera leaves resulted in the isolation of six highly oxygenated nortriterpenoids (1–6) and five lignans (7–11) including a new pre-schisanartane-type, schisandrathera A (1), a new dibenzocyclooctadiene glycoside, schisandrathera B (7) and two new lignans, schisandrathera C (8) and schisandrathera D (9). Their chemical structures including absolute configurations were determined extensively by means of HR-ESI-MS, NMR, and ECD spectra. In addition, all isolated compounds were tested for cytotoxic activity against PC3 (prostate cancer) and MCF7 (breast cancer) cell lines. Among these compounds, schirubrisin B (3) showed strong cytotoxic effect on both PC3 and MCF7 cell lines with IC50 values of 3.21 ± 0.68, 13.30 ± 0.68 μM, respectively, whereas ten remaining compounds were found to be less effective in the investigated models.

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DO - 10.1080/14786419.2019.1700247

M3 - Article

C2 - 31829042

AN - SCOPUS:85076426086

JO - Natural Product Research

JF - Natural Product Research

SN - 1478-6419

ER -

Chemical constituents from Schisandra sphenanthera and their cytotoxic activity

Abstract

Bibliographical note

All Science Journal Classification (ASJC) codes

UN SDGs

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