Xiao-Chi Ma, Xiulan Xin, Bao-jing Zhang, Sha Deng, Ji-hong Yao, Chang-yuan Wang, Jian Cui, Yan Tian, Ke-xin Liu
Index: J. Sep. Sci. 33(15) , 2272-7, (2010)
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An efficient separation method of using high-speed counter-current chromatography was successfully established to directly purify cytotoxic transformed products of cinobufagin by Cordyceps militaris. The two-phase solvent system composed of n-hexane-ethyl acetate-methanol-water (4:6:3:4, v/v) was used in high-speed counter-current chromatography. A total of 9 mg of 4beta,12alpha-dihydroxyl-cinobufagin (1), 15 mg of 12beta-hydroxyl-cinobufagin (2), 8 mg of 5beta-hydroxyl-cinobufagin (3), 12 mg of deacetylcinobufagin (4) and 6 mg of 3-keto-cinobufagin (5) were obtained in a one-step separation from 400 mg of the crude extract with purity of 98.7, 97.2, 90.6, 99.1 and 99.4%, respectively, as determined by HPLC. Their chemical structures were identified on the basis of (1)H-NMR and (13)C-NMR technology. All products (1-5) showed the potent activities against human carcinoma cervicis (Hela) and malignant melanoma (A375) cells in vitro.
Structure | Name/CAS No. | Molecular Formula | Articles |
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Cinobufagin
CAS:470-37-1 |
C26H34O6 |
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2008-07-01 [J. Nat. Prod. 71 , 1268-70, (2008)] |
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2010-07-01 [Nat. Prod. Commun. 5(7) , 1031-4, (2010)] |
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2012-02-01 [Bioorg. Med. Chem. Lett. 22(3) , 1459-63, (2012)] |
Bufothionine, a possible effective component in cinobufocini...
2012-06-01 [J. Ethnopharmacol. 141(2) , 692-700, (2012)] |
Qualitative and quantitative analysis of cinobufacini inject...
2013-02-01 [J. Sep. Sci. 36(3) , 492-502, (2013)] |
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