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从中国红豆杉细胞培养物中分离得到的四种新的紫杉烷类化合物。

Four new minor taxanes from cell cultures of Taxus chinensis.

作者信息

Xie Dan, Jia Hong-Ting, Zhang Yi, Zou Jian-Hua, Yin Da-Li, Chen Xiao-Guang, Yan Yu-Ning, Dai Jun-Gui

机构信息

Key Laboratory of Biosynthesis of Natural Drugs, Peking Union Medical College, Ministry of Public Health and Key Laboratory of Bioactive Substances and Resources Utilization, Ministry of Education, Institute of Materia Medica, Chinese Academy of Medical Sciences, Beijing, China.

出版信息

J Asian Nat Prod Res. 2009 Jun;11(6):490-7. doi: 10.1080/10286020902882143.

Abstract

Four new minor taxanes (1-4) have been isolated from Ts-19 cell cultures of Taxus chinensis together with five known taxanes (5-9) by silica gel chromatography combined with semi-preparative HPLC chromatography. On the basis of the analyses of the chemical and spectroscopic (IR, MS, 1D, and 2D NMR) data, the structures of new compounds were elucidated as 5alpha-hydroxy-2alpha,10beta-diacetoxy-14beta-(3-hydroxy-2-methyl-butyryl)oxytaxa-4(20),11-diene (1), 2alpha,5alpha,10beta-triacetoxy-14beta-(2-hydroxy-propionyl)oxytaxa-4(20),11-diene (2), 2alpha,5alpha,10beta-triacetoxy-14beta-(2-hydroxy-3-methyl-butyryl)oxytaxa-4(20),11-diene (3), and 2alpha-benzoxy-4alpha,9alpha,10beta,13alpha-tetraacetoxytax-11-ene (4), respectively. Compounds 1-5 were pharmacologically evaluated for their cytotoxicities against five human cancer cell lines (HCT-8, Bel-7402, BGC-823, A549, and A2780) and their reversing activity towards multi-drug resistance A549/taxol tumor cell line, and the results showed that all of the tested compounds exhibited very low cytotoxicities, while compound 4 possessed twice the reversing activity as that of verapamil at 10 muM.

摘要

通过硅胶柱色谱结合半制备高效液相色谱,从中国红豆杉Ts-19细胞培养物中分离得到4个新的紫杉烷类化合物(1-4)以及5个已知的紫杉烷类化合物(5-9)。基于化学和光谱(红外、质谱、一维和二维核磁共振)数据的分析,确定新化合物的结构分别为5α-羟基-2α,10β-二乙酰氧基-14β-(3-羟基-2-甲基丁酰基)氧基紫杉-4(20),11-二烯(1)、2α,5α,10β-三乙酰氧基-14β-(2-羟基丙酰基)氧基紫杉-4(20),11-二烯(2)、2α,5α,10β-三乙酰氧基-14β-(2-羟基-3-甲基丁酰基)氧基紫杉-4(20),11-二烯(3)和2α-苄氧基-4α,9α,10β,13α-四乙酰氧基紫杉-11-烯(4)。对化合物1-5进行了药理活性评价,考察它们对5种人类癌细胞系(HCT-8、Bel-7402、BGC-823、A549和A2780)的细胞毒性以及对多药耐药A549/紫杉醇肿瘤细胞系的逆转活性,结果表明所有测试化合物均表现出极低的细胞毒性,而化合物4在10 μM时的逆转活性是维拉帕米的两倍。

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