Cytotoxic biotransformed products from cinobufagin by Mucor spinosus and Aspergillus niger
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作者:
He, XJ
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Jinan Univ, Inst Tradit Chinese Med & Nat Prod, Guangzhou 510632, Peoples R ChinaJinan Univ, Inst Tradit Chinese Med & Nat Prod, Guangzhou 510632, Peoples R China
He, XJ
[1
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Tang, JS
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机构:Jinan Univ, Inst Tradit Chinese Med & Nat Prod, Guangzhou 510632, Peoples R China
Tang, JS
Qiao, AM
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机构:Jinan Univ, Inst Tradit Chinese Med & Nat Prod, Guangzhou 510632, Peoples R China
Qiao, AM
Wang, GH
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机构:Jinan Univ, Inst Tradit Chinese Med & Nat Prod, Guangzhou 510632, Peoples R China
Wang, GH
Jiang, MM
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机构:Jinan Univ, Inst Tradit Chinese Med & Nat Prod, Guangzhou 510632, Peoples R China
Jiang, MM
Liu, RH
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机构:Jinan Univ, Inst Tradit Chinese Med & Nat Prod, Guangzhou 510632, Peoples R China
Liu, RH
Yao, XS
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机构:Jinan Univ, Inst Tradit Chinese Med & Nat Prod, Guangzhou 510632, Peoples R China
Yao, XS
机构:
[1] Jinan Univ, Inst Tradit Chinese Med & Nat Prod, Guangzhou 510632, Peoples R China
[2] Cornell Univ, Dept Food Sci, Ithaca, NY 14853 USA
[3] Shenyang Pharmaceut Univ, Dept Nat Prod Chem, Shenyang 110016, Peoples R China
[4] Shenyang Pharmaceut Univ, Dept Pharmacol, Shenyang 110016, Peoples R China
Cinobufagin (1) was one of important cardenolidal steroids and major components of Chan'Su, a famous traditional Chinese medicine. Bioconversion of cinobufagin by the fungi of Mucor spinosus and Aspergillus niger were investigated. Nine bioconversion products were obtained from M. spinosus and seven products from A. niger. Their structures were elucidated by high-resolution fast atom bombardment mass spectroscopy (HR-FAB-MS), extensive NMR techniques, including H-1 NMR, C-13 NMR, DEPT, H-1-H-1 correlation spectroscopy (COSY), two-dimensional nuclear Overhauser effect correlation spectroscopy (NOESY), heteronuclear multiple quantum coherence (HMQC) and heteronuclear multiple bond coherence (HMBC). The in vitro cytotoxic activities against human hepatoma cells (HepG2, SMMC-7221 and BEL-7402) and human leukemia cells (K562, HL-60 and HEL) of all bioconversion products were determined by the MTT method, and their structure-activity relationships (SAR) were discussed. (c) 2006 Elsevier Inc. All rights reserved.