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大叶山楝根化学成分与细胞毒活性的研究 被引量:2

Studies on Chemical Compositions and Cytotoxicities from Roots of Aphanamixis grandifolia Bl.
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摘要 为了解大叶山楝(Aphanamixis grandifoliaBl.)根中的抗肿瘤活性成分,利用各种色谱技术从其95%乙醇提取物中分离得到9个化合物,经波谱分析分别鉴定为:7-hydroxycadalene (1)、dregeana-1(2)、4-oxopinoresinol (3)、4-ketopinoresinol (4)、6-deoxyjacareubin (5)、schleicheol 1(6)、豆甾醇(7)、β-谷甾醇(8)和胡萝卜苷(9)。其中化合物1~6为首次从山楝属植物中分离得到,并首次报道了化合物1的碳谱数据。生物活性测试结果表明,化合物1和5对慢性髓原白血病细胞K562有生长抑制活性,化合物1、5和6对人胃癌细胞SGC-7901有生长抑制活性。 In order to understand the antitumor active ingredients ofAphanamixis grandifoliaBl., nine compounds were isolated from 95% ethanol extract of its roots. They were identiifed as 7-hydroxycadalene (1), dregeana-1 (2), 4-oxopinoresinol (3), 4-ketopinoresinol (4), 6-deoxyjacareubin (5), schleicheol 1 (6), stigmasterol (7), β-sitosterol (8), and daucosterol (9) on the basis of spectral data. Compounds1–6 were isolated from the genusAphanamixis for the ifrst time, and the13C NMR spectral data of compound1 was reported for the ifrst time. Compounds1 and 5 showed inhibition of the proliferation of K562 cell line, and compounds1,5 and6 possessed inhibitory activity against SGC-7901 cell line.
出处 《热带亚热带植物学报》 CAS CSCD 北大核心 2015年第3期329-333,共5页 Journal of Tropical and Subtropical Botany
基金 公益性行业(农业)科研专项经费(201303117) 国家科技支撑计划课题(2013BAI11B04) 海南省重大科技项目(ZDZX2013008-4)资助
关键词 楝科 大叶山楝 化学成分 抗肿瘤活性 Meliaceae Aphanamixis grandifoliaBl. Chemical constituent Antitumor activity
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  • 1刘冬梅,李理,杨晓泉,梁世中.用牛津杯法测定益生菌的抑菌活力[J].食品研究与开发,2006,27(3):110-111. 被引量:274
  • 2广西壮族自治区中医药研究所.广西药用植物名录[M].南宁:广西人民出版社,1986.509.
  • 3Wu H F,Zhang X P,Wang Y,et al.Four new diterpenes from Aphanamixis polystachya[J].Fitoterapia,2013,90:126-131.
  • 4Triana J,Luis E J,Jose O J,et al.Chemotaxonomy of gonospermum and related genera[J].Phytochemistry,2010,71(5/6):627-634.
  • 5Goncalves O,Pereira R,Goncalves F,et al.Evaluation of the mutagenicity of sesquiterpenic compounds and their influence on the susceptibility towards antibiotics of two clinically relevant bacterial strains[J].Mutation Research-Genetic Toxicology and Environmental Mutagenesis,2011,723(1):18-25.
  • 6Zeng Q,Guan B,Qin J J,et al.2,3-Seco-and 3,4-seco-tirucallane triterpenoid derivatives from the stems of Aphanamixis grandifolia Blume[J].Phytochemistry,2012,80:148-155.
  • 7PACIFICO S, SCOGNAMIGLIO M, D'ABROSCA B, et al. Spectroscopiccharacterization and antiproliferative activity on HepG2 humanhepatoblastoma cells of flavonoid C-glycosides form Petrorhagiavelutina [J]. J Nat Prod, 2010, 73(12): 1973–1978. doi: 10.1021/np100255u.
  • 8DIAS T A, DUARTE C L, LIMA C F, et al. Superior anticanceractivity of halogenated chalcones and flavonols over the naturalflavonol quercetin [J]. Eurp J Med Chem, 2013, 65: 500–510. doi:10.1016/j.ejmech.2013.04.064.
  • 9MASUOKA N, MATSUDA M, KUBO I. Characterisation of theantioxidant activity of flavonoids [J]. Food Chem, 2012, 131(2): 541–545. doi: 10.1016/j.foodchem.2011.09.020.
  • 10GUN I. Antioxidant activity of food constituents: An overview [J].Arch Toxicol, 2012, 86(3): 345?91. doi: 10.1007/s00204-011-0774-2.

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