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Volumn 26, Issue 7, 2008, Pages 1169-1178

3D-QSAR CoMFA analysis of C5 substituted pyrrolotriazines as HER2 (ErbB2) inhibitors

Author keywords

CoMFA; EGFR; Human epidermal growth factor receptor; Receptor tyrosine kinase

Indexed keywords

CRYSTAL STRUCTURE; MATHEMATICAL MODELS; ONCOLOGY; PROTEINS; SUBSTITUTION REACTIONS;

EID: 40649119472     PISSN: 10933263     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jmgm.2007.10.008     Document Type: Article
Times cited : (17)

References (15)
  • 2
    • 33847359176 scopus 로고    scopus 로고
    • Pharmacogenomics of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors
    • A. Jimeno M. Hidalgo Pharmacogenomics of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors Biochim. Biophys. Acta (BBA)-Rev. Cancer 1766 2006 217 229
    • (2006) Biochim. Biophys. Acta (BBA)-Rev. Cancer , vol.1766 , pp. 217-229
    • Jimeno, A.1    Hidalgo, M.2
  • 3
    • 0033605560 scopus 로고    scopus 로고
    • ErbB-2 amplification inhibits down-regulation and induces constitutive activation of both ErbB-2 and epidermal growth factor receptors
    • R. Worthylake L.K. Opresko H.S. Wiley ErbB-2 amplification inhibits down-regulation and induces constitutive activation of both ErbB-2 and epidermal growth factor receptors J. Biol. Chem. 274 1999 8865 8874
    • (1999) J. Biol. Chem. , vol.274 , pp. 8865-8874
    • Worthylake, R.1    Opresko, L.K.2    Wiley, H.S.3
  • 4
    • 85120104620 scopus 로고    scopus 로고
    • Genetic alterations in intraductal and invasive breast cancer
    • M. Van de Vijver Genetic alterations in intraductal and invasive breast cancer Eur. J. Cancer 37 2001 12 112
    • (2001) Eur. J. Cancer , vol.37 , pp. 12-112
    • Van de Vijver, M.1
  • 7
    • 33846651190 scopus 로고    scopus 로고
    • QSAR analysis of tyrosine kinase inhibitor using modified ant colony optimization and multiple linear regression
    • W.-m. Shi Q. Shen W. Kong B.-x. Ye QSAR analysis of tyrosine kinase inhibitor using modified ant colony optimization and multiple linear regression Eur. J. Med. Chem. 42 2007 81 86
    • (2007) Eur. J. Med. Chem. , vol.42 , pp. 81-86
    • Shi, W.-m.1    Shen, Q.2    Kong, W.3    Ye, B.-x.4
  • 8
    • 0142124197 scopus 로고    scopus 로고
    • Receptor-guided alignment-based comparative 3D-QSAR studies of benzylidene malonitrile tyrphostins as EGFR and HER-2 kinase inhibitors
    • S. Kamath J.K. Buolamwini Receptor-guided alignment-based comparative 3D-QSAR studies of benzylidene malonitrile tyrphostins as EGFR and HER-2 kinase inhibitors J. Med. Chem. 46 2003 4657 4668
    • (2003) J. Med. Chem. , vol.46 , pp. 4657-4668
    • Kamath, S.1    Buolamwini, J.K.2
  • 10
    • 0023751431 scopus 로고
    • Effect of shape on binding of steroids to carrier proteins
    • R.D. Cramer III D.E. Patterson J.D. Bunce Effect of shape on binding of steroids to carrier proteins J. Am. Chem. Soc. 110 1988 5959 5967
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 5959-5967
    • Cramer, R.D.1    Patterson, D.E.2    Bunce, J.D.3
  • 11
    • 85120141790 scopus 로고    scopus 로고
    • SYBYL7.1, Tripos Inc., St. Louis, MO 63144, USA.
  • 12
    • 0002309097 scopus 로고
    • PLS-partial least square projection to latent structures
    • S. Wold A. Johansson M. Cochi PLS-partial least square projection to latent structures H. Kubinyi 3D-QSAR in Drug Design: Theory, Methods and Applications 1993 ESCOM Leiden 523 550
    • (1993) , pp. 523-550
    • Wold, S.1    Johansson, A.2    Cochi, M.3
  • 13
    • 84987100711 scopus 로고
    • Cross-validation, boot-strapping and partial least squares compared with multiple regression in conventional QSAR studies
    • R.D. Cramer III J.D. Bunce D.E. Paterson I.E. Frank Cross-validation, boot-strapping and partial least squares compared with multiple regression in conventional QSAR studies Quant. Struct. -Act. Relat. 7 1988 18 25
    • (1988) Quant. Struct. -Act. Relat. , vol.7 , pp. 18-25
    • Cramer, R.D.1    Bunce, J.D.2    Paterson, D.E.3    Frank, I.E.4
  • 15
    • 0030893008 scopus 로고    scopus 로고
    • Structure-based design of a potent, selective and irreversible inhibitors of the catalytic domain of erbB receptor subfamily of protein tyrosine kinases
    • J. Singh E.M. Dobrusin D.W. Fry T. Haske A. Whitty D.J. McNamara Structure-based design of a potent, selective and irreversible inhibitors of the catalytic domain of erbB receptor subfamily of protein tyrosine kinases J. Med. Chem. 40 1997 1130 1135
    • (1997) J. Med. Chem. , vol.40 , pp. 1130-1135
    • Singh, J.1    Dobrusin, E.M.2    Fry, D.W.3    Haske, T.4    Whitty, A.5    McNamara, D.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.