Volume 38, Issue 8 pp. 812-816
Concise Report

Structurally Interesting Diarymethane Derivatives from Securidaca inappendiculata

Bin Zhou

Bin Zhou

State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai, 201203 China

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Yan Wu

Yan Wu

State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai, 201203 China

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Lishe Gan

Lishe Gan

College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, Zhejiang, 310058 China

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Seema Dalal

Seema Dalal

Department of Biochemistry, MC 0308, Virginia Tech, Blacksburg, Virginia 24061, United States, Department of Biochemistry and Molecular Biology, and Center for Tropical and Emerging Global Diseases (CTEGD), University of Georgia, Athens, Georgia, 30602 United States

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Maria B. Cassera

Maria B. Cassera

Department of Biochemistry, MC 0308, Virginia Tech, Blacksburg, Virginia 24061, United States, Department of Biochemistry and Molecular Biology, and Center for Tropical and Emerging Global Diseases (CTEGD), University of Georgia, Athens, Georgia, 30602 United States

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Jianmin Yue

Corresponding Author

Jianmin Yue

State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai, 201203 China

E-mail: [email protected]Search for more papers by this author
First published: 13 March 2020
Citations: 9

Summary of main observation and conclusion

Securines A—E, three dimeric diarymethane derivatives (13) and two enantiomeric diarymethane derivative monomers (4 and 5), were isolated and characterized from the medicinal plant Securidaca inappendiculata. Compounds 1 and 2 are a pair of enantiomeric diarymethane derivative dimers, and compound 3 is a mesomeric diarymethane derivative dimer. Their structures were determined by a combination of spectroscopic data, X-ray crystallography, electronic circular dichroism (ECD) analysis, and computational ECD calculations. Dimeric compounds 13 showed moderate antiplasmodial activities with IC50 values of 0.9, 1.4, and 1.5 μM, respectively.

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