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哥纳香醇甲及其类似物的合成与抗肿瘤活性研究 被引量:6

STUDIES ON THE SYNTHESIS AND ANTITUMOR ACTIVITIESOF HOWIINOL A AND ITS ANALOGUES
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摘要 哥纳香醇甲(1)是从番荔枝科哥纳香属植物海南哥纳香的根和茎皮中分离得到的有明显抗肿瘤活性的化合物,本文以αD葡庚糖酸内酯为原料,经9步反应对其进行了不对称合成研究,总收率为133%。根据药物设计原理,设计合成了26个类似物,并进行了抗肿瘤活性筛选,初步结果表明大部分化合物体外对多种瘤株有不同程度的抑制作用。 Howiinol A(1), one of the active antitumor constituents from the root and stem bark of Goniothamus howii Meer. (Annonaceae) has been sythesized in nine steps from α-D-glucoheptonic γ-lactone with an over all yield of 13.3%. It shows that all data of the synthetic product are identical to those of the natural howiinol A, thus the absolute configuration of natural howiinol A is further confirmed as 1. In the search for new antitumor compounds with high potency, 26 analogues have been synthesized. In pharmacological tests most of them showed antitumor activities in vitro, some of them are significant.
出处 《药学学报》 CAS CSCD 北大核心 1998年第7期502-511,共10页 Acta Pharmaceutica Sinica
基金 国家自然科学基金 国家教委博士点基金
关键词 哥纳香醇甲 抗肿瘤活性 不对称合成 Howiinol A Antitumor agents Asymmetric synthesis
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参考文献3

  • 1陈若芸,药学学报,1998年,33卷,453页
  • 2于德泉,中国医学科学院中国协和医科大学年会学术论文集,1996年,260页
  • 3Shing T K M,J Chem Soc Perkin Trans,1992年,6卷,885页

同被引文献16

  • 1于利人,靳秋月,谢红,陈立军.Isogoniotriol衍生物对肿瘤细胞DNA的损伤[J].天津医药,2005,33(5):266-267. 被引量:1
  • 2Alkofahi A, Ma W W, Mackenzie A T, et al. Goniotriol from Goniothalamus giganteus [J]. Nat Prod, 1989, 52(6):1371-1373.
  • 3Mukai C, Hiral S, Hanaoka M. An optically active chromium(O)-complexed benzaldehyde derivative in organic synthesis:A highly stereo controlled total synthesis of (+)-goniofufurone [J]. Tetrahedron Lett, 1993, 34(38): 6081-6084.
  • 4Chen H, Zhou L E, Zhang Y J, et al. Synthesis and antitumor activities of p-C1 howiinol A and its analogues [J]. Chin Chem Lett, 1999, 10(6): 449-452.
  • 5Talapatra SK, Basu D, Deb T, et al.Structure & stereochemistry four new 5, 6-dihydro-2-pyrones from goniothalamussesquipedalis & goniothalamus girfithii [J]. Indian J Chem(Sect. B), 1985, 24 (1),29-34.
  • 6Shing TKM, Tsui HC, Zhou ZH. Stereoselective synthesis of2,4:5,6-Di-O-isopropylidene-1-C-Phenyl-D-glycero-D-ido-hexitol and 2, 4:5,6-Di-O-isopropylidene-1-C-phenyl-D-glycero-D-gulo-hexitol [J]. J Chem Soc Perkin Trans,1992,887-893.
  • 7Brimacombe JS, Tucker LCN. Reaction of D-gulo-heptono-γ-lactone with acetone [J].Carbohydrate Res. 1996, 2: 341.
  • 8陈若芸,于德泉,马林,吴丰,宋万志.海南哥纳香抗癌有效成分研究[J].药学学报,1998,33(6):453-456. 被引量:9
  • 9何剑华,叶玉梅,徐承熊.从海南哥纳香中分离的一种新化合物──海南哥纳香醇甲的抗肿瘤作用[J].药学学报,1998,33(7):493-497. 被引量:6
  • 10何剑华,徐承熊.海南哥纳香醇甲(GHM-10)对L1210细胞生物大分子合成的抑制作用[J].药学学报,1998,33(12):886-890. 被引量:1

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