Literature DB >> 10665475

Tyrosine kinase inhibitors in preclinical development.

M L Levitt1, P P Koty.   

Abstract

Due to the limited efficacy of cytotoxic chemotherapy in the treatment of advanced malignancy and its excessive toxicity precluding its use in chemoprevention, new therapeutic and preventive strategies have been sought. One of the most interesting of these new approaches is the manipulation of signal transduction pathways. Among the approaches being considered to eventuate such a strategy is the inhibition of autophosphorylation, a critical first step in the signal transduction pathways of many cell surface receptor tyrosine kinases, as well as of non-receptor tyrosine kinases. This article is intended to review those tyrosine kinase inhibitors that are currently in preclinical development, for which there are data to support consideration for their use in chemoprevention or cancer treatment. We will focus upon those agents that have received attention in the past several years.

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Year:  1999        PMID: 10665475     DOI: 10.1023/a:1006372102543

Source DB:  PubMed          Journal:  Invest New Drugs        ISSN: 0167-6997            Impact factor:   3.850


  118 in total

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Journal:  Science       Date:  1995-04-14       Impact factor: 47.728

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Journal:  J Med Chem       Date:  1989-10       Impact factor: 7.446

6.  Dysregulation of epidermal growth factor receptor expression in premalignant lesions during head and neck tumorigenesis.

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Journal:  Cancer Res       Date:  1994-06-15       Impact factor: 12.701

7.  Synthesis and biochemical evaluation of a series of aminoflavones as potential inhibitors of protein-tyrosine kinases p56lck, EGFr, and p60v-src.

Authors:  M Cushman; H Zhu; R L Geahlen; A J Kraker
Journal:  J Med Chem       Date:  1994-09-30       Impact factor: 7.446

8.  Increase in activity and level of pp60c-src in progressive stages of human colorectal cancer.

Authors:  M S Talamonti; M S Roh; S A Curley; G E Gallick
Journal:  J Clin Invest       Date:  1993-01       Impact factor: 14.808

9.  Tyrphostins. 3. Structure-activity relationship studies of alpha-substituted benzylidenemalononitrile 5-S-aryltyrphostins.

Authors:  A Gazit; N Osherov; I Posner; A Bar-Sinai; C Gilon; A Levitzki
Journal:  J Med Chem       Date:  1993-11-12       Impact factor: 7.446

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Authors:  J N Ihle
Journal:  Nature       Date:  1995-10-19       Impact factor: 49.962

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Review 2.  Epidermal growth factor receptor tyrosine kinase inhibitors as anticancer agents.

Authors:  F Ciardiello
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3.  Synthesis and anti-breast cancer activities of substituted quinolines.

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Journal:  Bioorg Med Chem Lett       Date:  2008-04-13       Impact factor: 2.823

4.  Development and Evaluation of 18F-IRS for Molecular Imaging Mutant EGF Receptors in NSCLC.

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5.  Tumoricidal activity of lauryl gallate towards chemically induced skin tumours in mice.

Authors:  E Ortega; M C Sadaba; A I Ortiz; C Cespon; A Rocamora; J M Escolano; G Roy; L M Villar; P Gonzalez-Porque
Journal:  Br J Cancer       Date:  2003-03-24       Impact factor: 7.640

  5 in total

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