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Volumn 15, Issue 10, 2016, Pages 2378-2387

Irreversible inhibition of EGFR: Modeling the combined pharmacokinetic-pharmacodynamic relationship of osimertinib and its active metabolite AZ5104

Author keywords

[No Author keywords available]

Indexed keywords

AZ 5104; EPIDERMAL GROWTH FACTOR RECEPTOR KINASE INHIBITOR; OSIMERTINIB; UNCLASSIFIED DRUG; ANTINEOPLASTIC AGENT; EPIDERMAL GROWTH FACTOR RECEPTOR; PIPERAZINE DERIVATIVE; PROTEIN KINASE INHIBITOR;

EID: 84990985638     PISSN: 15357163     EISSN: 15388514     Source Type: Journal    
DOI: 10.1158/1535-7163.MCT-16-0142     Document Type: Article
Times cited : (27)

References (10)
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  • 4
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    • Discovery of a potent and selective EGFR inhibitor (AZD9291) of both sensitizing and T790M resistance mutations that spares the wild type form of the receptor
    • Finlay MRV, Anderton M, Ashton S, Ballard P, Bethel PA, Box MR, et al. Discovery of a potent and selective EGFR inhibitor (AZD9291) of both sensitizing and T790M resistance mutations that spares the wild type form of the receptor. J Med Chem 2014;57:8249-67.
    • (2014) J Med Chem , vol.57 , pp. 8249-8267
    • Finlay, M.R.V.1    Anderton, M.2    Ashton, S.3    Ballard, P.4    Bethel, P.A.5    Box, M.R.6
  • 5
    • 84904898065 scopus 로고    scopus 로고
    • AZD9291, an irreversible EGFR TKI, overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer
    • Cross DAE, Ashton SE, Ghiorghiu S, Eberlein C, Nebhan CA, Spitzler PJ, et al. AZD9291, an irreversible EGFR TKI, overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer. Cancer Discov 2014;4:1046-61.
    • (2014) Cancer Discov , vol.4 , pp. 1046-1061
    • Cross, D.A.E.1    Ashton, S.E.2    Ghiorghiu, S.3    Eberlein, C.4    Nebhan, C.A.5    Spitzler, P.J.6
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    • The design and analysis of parallel experiments to produce structurally identifiable models
    • Cheung SYA, Yates JWT, Aarons L. The design and analysis of parallel experiments to produce structurally identifiable models. J Pharmacokinet Pharmacodyn 2013;40:93-100.
    • (2013) J Pharmacokinet Pharmacodyn , vol.40 , pp. 93-100
    • Cheung, S.Y.A.1    Yates, J.W.T.2    Aarons, L.3
  • 7
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    • Covalent EGFR inhibitor analysis reveals importance of reversible interactions to potency and mechanism of drug resistance
    • Schwartz PA, Kuzmic P, Solowiej J, Bergqvist S, Bolanos B, Almaden C, et al. Covalent EGFR inhibitor analysis reveals importance of reversible interactions to potency and mechanism of drug resistance. Proc Natl Acad Sci U S A 2014;111:173-8.
    • (2014) Proc Natl Acad Sci U S A , vol.111 , pp. 173-178
    • Schwartz, P.A.1    Kuzmic, P.2    Solowiej, J.3    Bergqvist, S.4    Bolanos, B.5    Almaden, C.6
  • 8
    • 84884162850 scopus 로고    scopus 로고
    • Computational modeling of ERBB2-amplified breast cancer identifies combined ErbB2/3 blockade as superior to combination of MEK and AKT inhibitors
    • Kirouac DC, Du JY, Lahdenranta J, Overland R, Yarar D, Paragas V, et al. Computational modeling of ERBB2-amplified breast cancer identifies combined ErbB2/3 blockade as superior to combination of MEK and AKT inhibitors. Sci Signal 2013;6:ra68.
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    • Modelling of tumor growth and cytotoxic effect of docetaxel in xenografts
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.