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抗肿瘤药Voreloxin 被引量:3

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出处 《药学进展》 CAS 2010年第2期89-91,共3页 Progress in Pharmaceutical Sciences
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同被引文献13

  • 1谭耀红,杨纯正,齐静,王金宏,王彩云,彭辉.3-取代芳基氧化吲哚(PHII-7)对肿瘤细胞周期的影响[J].药学学报,2003,38(11):805-808. 被引量:3
  • 2Marc J E , Darin A , Josh C Y , et al . Metabolism of(+)- 1,4-Dihydro-7-(trans-3-methoxy-4-methylamino- l-pyrrolidinyl)-4-oxo- 1 -(2-thiazolyl)-1,8-naphthyridine-3-carboxytic Acid (Voreloxin; Formerly SNS- 595), a Novel Replication-Dependent DNA-Damaging Agent[J]. The American Society for Pharmacology and Experimental Therapeutics, 2009, 37(3): 594-601. 被引量:1
  • 3Mariyana A , Sonia I , Boris G . QSAR analysis ofl , 4-dihydro-4-oxo-1-(2-thiazolyl)-1, 8-naphthyridines with anticancer activity [J]. European Journal of Medicinal Chemistry, 2007, 42.- 1184-1192. 被引量:1
  • 4Moualla H, Mills D A, Hromas R, et al. Voreloxin[J]. Drugs of the Future, 2009, 34(5): 363-374. 被引量:1
  • 5Yasunori T, Kyoji T, Yuji S, et al. Synthesis and structure activity relationships of 3-substituted 1,4-dihydro-4-oxo- 1-(2-thiazolyl)- 1,8-naphthyri dines as novel antitumor agents[J]. Bioorganic & Medicinal Chemistry Letters, 2004, 14: 3189-3193. 被引量:1
  • 6Kyoji T, Yasunori T, Kohichiro S, et at. Synthesis and Structure-Activity Relationships of Novel 7-Substituted 1,4-Dihydro-4-oxo-1-(2-thiazolyl)-1,8- naphthyridine-3-carboxytic Acids as Antitumor Agents. Part l[J]. Journal of Medicinal Chemistry, 2002, 45: 5564-5575. 被引量:1
  • 7Kyoji T, Katsumi C, Shigeki K, et al. Compounds, processes for the preparation thereof and antitumoragents[P]. 1998-10-06. US: 5817669. 被引量:1
  • 8Yasunori T, Kyoji T, Kohichiro S, et al. Synthesis and Structure-Activity Relationships of Novel 7-Substituted 1,4-Dihydro-4-oxo-1-(2-thiazolyl)-1,8- naphthyridine-3-carboxylic Acids as Antitumor Agents. Part 2[J]. Journal of Medicinal Chemistry, 2004, 47: 2097-2109. 被引量:1
  • 9陈淑芹,金敬顺,陈霞.肿瘤的综合治疗方法[J].医学信息(中旬刊),2011,24(2):562-563. 被引量:5
  • 10谷晓辉,姜标.新型海洋双吲哚类生物碱的研究进展[J].有机化学,2000,20(2):168-177. 被引量:4

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