design, synthesis and biological evaluation of 3’,4’,5 ... · *corresponding author: dr. guotao...
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Design, synthesis and biological evaluation of 3’,4’,5’-trimethoxy
flavonoid benzimidazole derivatives as potential anti-tumor agents
Zhe Wanga,1, Xiangping Denga,1, Runde Xionga, Shujuan Xionga, Juan Liua, Xuan Caoa,
Xiaoyong Leia, Yanming Chenb, Xing Zhenga,*, Guotao Tanga,*
aInstitute of Pharmacy and Pharmacology, Hunan Province Cooperative Innovation
Center for Molecular Target New Drug Study, University of South China, Hengyang, C
hina,
bMu Dan Jiang You Bo Pharmacertical Co.Ltd, Mudanjiang, China
*Corresponding Author: Dr. Guotao Tang, Ph.D. Dr .Xing Zheng, Ph.D
Corresponding author at:
Guotao Tang, Xing Zheng, Institute of Pharmacy and Pharmacology, University of
South China, Hengyang, Hunan, 421001,People’s Republic of China.
E-mail adress: [email protected] (Guotao Tang), [email protected] (Xing Zheng)
1 These authors contributed equally to this work.
Electronic Supplementary Material (ESI) for MedChemComm.This journal is © The Royal Society of Chemistry 2017
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Table of contents 1H NMR and 13C NMR spectra of compound 4a……………………….………….….2 1H NMR and 13C NMR spectra of compound 4b…………………….…….…….……3 1H NMR and 13C NMR spectra of compound 4c……………………………….……..4 1H NMR and 13C NMR spectra of compound 5……………………….………………5 1H NMR and 13C NMR spectra of compound 6…………………….…………………6 1H NMR and 13C NMR spectra of compound 7………………….……………………7 1H NMR and 13C NMR spectra of compound 8……………….……………...….……8 1H NMR and 13C NMR spectra of compound 9……………….………………………9 1H NMR and 13C NMR spectra of compound 10…………………………….………10 1H NMR and 13C NMR spectra of compound 11……………………….……………11 1H NMR and 13C NMR spectra of compound 12…………………….………………12 1H NMR and 13C NMR spectra of compound 13………………….…………………13 1H NMR and 13C NMR spectra of compound 14…………….………………………14 1H NMR and 13C NMR spectra of compound 15………….…………………………15 1H NMR and 13C NMR spectra of compound 16……………………………….……16 1H NMR and 13C NMR spectra of compound 17………….…………………………17 1H NMR and 13C NMR spectra of compound 18………………………….…………18 1H NMR and 13C NMR spectra of compound 19…………………….………………19 1H NMR and 13C NMR spectra of compound 20……………………………….……20 1H NMR and 13C NMR spectra of compound 21………………………………….…21 1H NMR and 13C NMR spectra of compound 22………………………….…………22 1H NMR and 13C NMR spectra of compound 23…………………….………………23 1H NMR and 13C NMR spectra of compound 24……………………………….……24 1H NMR and 13C NMR spectra of compound 25……………………………….……25 1H NMR and 13C NMR spectra of compound 26…………………….………………26 1H NMR and 13C NMR spectra of compound 27……………………………….……27 1H NMR and 13C NMR spectra of compound 28……………………………….……28
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1H NMR of compound 4a
13C NMR of compound 4a
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1H NMR of compound 4b
13C NMR of compound 4b
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1H NMR of compound 4c
13C NMR of compound 4c
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1H NMR of compound 5
13C NMR of compound 5
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1H NMR of compound 6
13C NMR of compound 5
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1H NMR of compound 7
13C NMR of compound 7
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1H NMR of compound 8
13C NMR of compound 8
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1H NMR of compound 9
13C NMR of compound 9
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1H NMR of compound 10
13C NMR of compound 10
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1H NMR of compound 11
13C NMR of compound 11
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1H NMR of compound 12
13C NMR of compound 12
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1H NMR of compound 13
13C NMR of compound 13
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1H NMR of compound 14
13C NMR of compound 14
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1H NMR of compound 15
13C NMR of compound 15
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1H NMR of compound 16
13C NMR of compound 16
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1H NMR of compound 17
13C NMR of compound 17
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1H NMR of compound 18
13C NMR of compound 18
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1H NMR of compound 19
13C NMR of compound 19
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1H NMR of compound 20
13C NMR of compound 20
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1H NMR of compound 21
13C NMR of compound 21
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1H NMR of compound 22
13C NMR of compound 22
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1H NMR of compound 23
13C NMR of compound 23
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1H NMR of compound 24
13C NMR of compound 24
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1H NMR of compound 25
13C NMR of compound 25
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1H NMR of compound 26
13C NMR of compound 26
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1H NMR of compound 27
13C NMR of compound 27
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1H NMR of compound 28
13C NMR of compound 28