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Inhibitors of farnesyltransferase: a rational approach to cancer chemotherapy?

作者信息

Bell Ian M

机构信息

Merck Research Laboratories, WP14-2, P.O. Box 4, Sumneytown Pike, West Point, PA 19486, USA.

出版信息

J Med Chem. 2004 Apr 8;47(8):1869-78. doi: 10.1021/jm0305467.

DOI:10.1021/jm0305467
PMID:15055985
Abstract
摘要

相似文献

1
Inhibitors of farnesyltransferase: a rational approach to cancer chemotherapy?法尼基转移酶抑制剂:癌症化疗的合理方法?
J Med Chem. 2004 Apr 8;47(8):1869-78. doi: 10.1021/jm0305467.
2
Farnesyltransferase inhibitors: an overview of the results of preclinical and clinical investigations.法尼基转移酶抑制剂:临床前和临床研究结果概述
Cancer Res. 2003 Sep 15;63(18):5656-68.
3
Farnesyltransferase inhibitors.法尼基转移酶抑制剂
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4
Farnesyltransferase inhibitors.法尼基转移酶抑制剂
Cancer Chemother Biol Response Modif. 2002;20:151-67.
5
Farnesyltransferase inhibitors: targeting the molecular basis of cancer.法尼基转移酶抑制剂:针对癌症的分子基础
Biochim Biophys Acta. 1999 May 31;1423(3):C19-30. doi: 10.1016/s0304-419x(99)00007-4.
6
Farnesyltransferase inhibitors as anticancer agents: current status.法尼基转移酶抑制剂作为抗癌剂:现状
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7
Effects of statins and farnesyltransferase inhibitors on the development and progression of cancer.他汀类药物和法尼基转移酶抑制剂对癌症发生发展的影响。
Cancer Treat Rev. 2004 Nov;30(7):609-41. doi: 10.1016/j.ctrv.2004.06.010.
8
Ras farnesyltransferase inhibition: a novel and safe approach for cancer chemotherapy.Ras法尼基转移酶抑制:一种用于癌症化疗的新型安全方法。
Acta Pharmacol Sin. 2000 May;21(5):396-404.
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Farnesyltransferase inhibitors: antineoplastic properties, mechanisms of action, and clinical prospects.法尼基转移酶抑制剂:抗肿瘤特性、作用机制及临床前景。
Semin Cancer Biol. 2000 Dec;10(6):443-52. doi: 10.1006/scbi.2000.0335.
10
Farnesyltransferase inhibitors as anticancer agents: critical crossroads.法尼基转移酶抑制剂作为抗癌药物:关键转折点。
Curr Opin Drug Discov Devel. 2004 Jul;7(4):478-86.

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Discovery of an Anion-Dependent Farnesyltransferase Inhibitor from a Phenotypic Screen.通过表型筛选发现一种阴离子依赖性法尼基转移酶抑制剂。
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Novel route to chaetomellic acid A and analogues: serendipitous discovery of a more competent FTase inhibitor.
新型 chaetomellic 酸 A 及其类似物的合成途径:法尼基转移酶抑制剂的意外发现。
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Structure-based design and synthesis of potent, ethylenediamine-based, mammalian farnesyltransferase inhibitors as anticancer agents.基于结构的设计与合成强效、乙二胺基的哺乳动物法尼基转移酶抑制剂作为抗癌药物。
J Med Chem. 2010 Oct 14;53(19):6867-88. doi: 10.1021/jm1001748.
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Working together: Farnesyl transferase inhibitors and statins block protein prenylation.协同作用:法尼基转移酶抑制剂和他汀类药物可阻断蛋白质异戊二烯化。
Mol Cell Pharmacol. 2009 Jan 1;1(1):1-6. doi: 10.4255/mcpharmacol.09.01.
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Synthesis and anticancer activity of new hydroxamic acid containing 1,4-benzodiazepines.新型含异羟肟酸的1,4-苯二氮䓬类化合物的合成及其抗癌活性
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Potent, Plasmodium-selective farnesyltransferase inhibitors that arrest the growth of malaria parasites: structure-activity relationships of ethylenediamine-analogue scaffolds and homology model validation.强效、疟原虫选择性法尼基转移酶抑制剂可阻止疟原虫生长:乙二胺类似物支架的构效关系及同源模型验证
J Med Chem. 2008 Sep 11;51(17):5176-97. doi: 10.1021/jm800113p. Epub 2008 Aug 8.