Planta Med 2012; 78(18): 1962-1966
DOI: 10.1055/s-0032-1327895
Natural Product Chemistry
Letters
Georg Thieme Verlag KG Stuttgart · New York

Neuroprotective Lignans from the Stems of Schisandra glaucescens

Heng-Yi Yu
1   Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Faculty of Pharmacy, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Peopleʼs Republic of China
,
Cui Hao
1   Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Faculty of Pharmacy, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Peopleʼs Republic of China
,
Fan-Yu Meng
1   Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Faculty of Pharmacy, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Peopleʼs Republic of China
,
Xue Li
1   Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Faculty of Pharmacy, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Peopleʼs Republic of China
,
Zu-Yu Chen
1   Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Faculty of Pharmacy, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Peopleʼs Republic of China
,
Xi Liang
1   Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Faculty of Pharmacy, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Peopleʼs Republic of China
,
Han-Li Ruan
1   Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Faculty of Pharmacy, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Peopleʼs Republic of China
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Publikationsverlauf

received 08. Februar 2012
revised 26. Juli 2012

accepted 08. Oktober 2012

Publikationsdatum:
13. November 2012 (online)

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Abstract

Two new tetrahydrofuran lignans, schiglaucin A and B (12), together with eight known analogues (310), were isolated from the stems of Schisandra glaucescens Diels. Their structures were elucidated on the basis of spectroscopic techniques (HRESIMS, UV, IR, NMR, and CD experiments). All of the compounds were tested for their neuroprotective activities against H2O2- and CoCl2-induced cell injuries in SH-SY5Y cells, respectively. Compounds 110 showed significant neuroprotective effects against H2O2-induced SH-SY5Y cell death, while compounds 15 and 810 exhibited significant neuroprotective effects against CoCl2-induced SH-SY5Y cell injury.

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