메뉴 건너뛰기




Volumn 4, Issue 8, 2013, Pages 779-783

Development of a chimeric c-Src kinase and HDAC inhibitor

Author keywords

c Src; chimera; combination therapy; HDAC; kinase

Indexed keywords

DASATINIB; HISTONE DEACETYLASE; PANOBINOSTAT; VORINOSTAT;

EID: 84881467331     PISSN: None     EISSN: 19485875     Source Type: Journal    
DOI: 10.1021/ml400175d     Document Type: Article
Times cited : (43)

References (25)
  • 1
    • 0031439247 scopus 로고    scopus 로고
    • Cellular functions regulated by Src family kinases
    • Thomas, S. M.; Brugge, J. S. Cellular functions regulated by Src family kinases Annu. Rev. Cell Dev. Biol. 1997, 13, 513-609
    • (1997) Annu. Rev. Cell Dev. Biol. , vol.13 , pp. 513-609
    • Thomas, S.M.1    Brugge, J.S.2
  • 7
    • 0033652298 scopus 로고    scopus 로고
    • Monotherapy versus combination therapy for bacterial infections
    • Bouza, E.; Muñoz, P. Monotherapy versus combination therapy for bacterial infections Med. Clin. North Am. 2000, 84, 1357-1389
    • (2000) Med. Clin. North Am. , vol.84 , pp. 1357-1389
    • Bouza, E.1    Muñoz, P.2
  • 8
    • 33746622984 scopus 로고    scopus 로고
    • Strategies for optimizing combinations of molecularly targeted anticancer agents
    • Dancey, J. E.; Chen, H. X. Strategies for optimizing combinations of molecularly targeted anticancer agents Nat. Rev. Drug Discovery 2006, 5, 649-659
    • (2006) Nat. Rev. Drug Discovery , vol.5 , pp. 649-659
    • Dancey, J.E.1    Chen, H.X.2
  • 9
    • 40749094921 scopus 로고    scopus 로고
    • Apoptosis of estrogen-receptor negative breast cancer and colon cancer cell lines by PTPα and Src RNAi
    • Zheng, X.; Resnick, R. J.; Shalloway, D. Apoptosis of estrogen-receptor negative breast cancer and colon cancer cell lines by PTPα and Src RNAi Int. J. Cancer 2008, 122, 1999-2007
    • (2008) Int. J. Cancer , vol.122 , pp. 1999-2007
    • Zheng, X.1    Resnick, R.J.2    Shalloway, D.3
  • 10
    • 67349228774 scopus 로고    scopus 로고
    • Development of the pan-HDAC inhibitor panobinostat (LBH589): Successes and challenges
    • Atadja, P. Development of the pan-HDAC inhibitor panobinostat (LBH589): Successes and challenges Cancer Lett. 2009, 280, 233-241
    • (2009) Cancer Lett. , vol.280 , pp. 233-241
    • Atadja, P.1
  • 12
    • 0037068754 scopus 로고    scopus 로고
    • The ubiquitous and tissue specific promoters of the human SRC gene are repressed by inhibitors of tissue deacetylases
    • Kostyniuk, C.; Dehm, S.; Batten, D.; Bonham, K. The ubiquitous and tissue specific promoters of the human SRC gene are repressed by inhibitors of tissue deacetylases Oncogene 2002, 21, 6340-6347
    • (2002) Oncogene , vol.21 , pp. 6340-6347
    • Kostyniuk, C.1    Dehm, S.2    Batten, D.3    Bonham, K.4
  • 13
    • 33846122993 scopus 로고    scopus 로고
    • Dimethyl sulfoxide to vorinostat: Development of this histone deacetylase inhibitor as an anticancer drug
    • Marks, P. A.; Breslow, R. Dimethyl sulfoxide to vorinostat: development of this histone deacetylase inhibitor as an anticancer drug Nat. Biotechnol. 2007, 25, 84-90
    • (2007) Nat. Biotechnol. , vol.25 , pp. 84-90
    • Marks, P.A.1    Breslow, R.2
  • 14
    • 33845762340 scopus 로고    scopus 로고
    • Multi-target therapeutics: When the whole is greater than the sum of the parts
    • Zimmermann, G. R.; Lehár, J.; Keith, C. T. Multi-target therapeutics: When the whole is greater than the sum of the parts Drug Discovery Today 2007, 12, 34-42
    • (2007) Drug Discovery Today , vol.12 , pp. 34-42
    • Zimmermann, G.R.1    Lehár, J.2    Keith, C.T.3
  • 15
    • 84867027478 scopus 로고    scopus 로고
    • The determination and interpretation of the therapeutic index in drug development
    • Muller, Y.; Milton, M. The determination and interpretation of the therapeutic index in drug development Nat. Rev. Drug Discovery 2012, 11, 751-761
    • (2012) Nat. Rev. Drug Discovery , vol.11 , pp. 751-761
    • Muller, Y.1    Milton, M.2
  • 16
    • 77949353758 scopus 로고    scopus 로고
    • Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)- N -hydroxyheptanamide (CUDC-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer
    • Cai, X.; Zhai, H.-X.; Wang, J.; Forrester, J.; Qu, H.; Yin, L.; Lai, C.-J.; Bao, R.; Qian, C. Discovery of 7-(4-(3-ethynylphenylamino)-7- methoxyquinazolin-6-yloxy)- N -hydroxyheptanamide (CUDC-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer J. Med. Chem. 2010, 53, 2000-2009
    • (2010) J. Med. Chem. , vol.53 , pp. 2000-2009
    • Cai, X.1    Zhai, H.-X.2    Wang, J.3    Forrester, J.4    Qu, H.5    Yin, L.6    Lai, C.-J.7    Bao, R.8    Qian, C.9
  • 17
    • 65249135408 scopus 로고    scopus 로고
    • Design of chimeric histone deacetylase- and tyrosine kinase-inhibitors: A series of imatinib hybrides as potent inhibitors of wild-type and mutant BCR-ABL, PDGFRβ, and histone deacetylases
    • Mahboobi, S.; Dove, S.; Sellmer, A.; Winkler, M.; Eichhorn, E.; Pongratz, H.; Ciossek, T.; Baer, T.; Maier, T.; Beckers, T. Design of chimeric histone deacetylase- and tyrosine kinase-inhibitors: A series of imatinib hybrides as potent inhibitors of wild-type and mutant BCR-ABL, PDGFRβ, and histone deacetylases J. Med. Chem. 2009, 52, 2265-2344
    • (2009) J. Med. Chem. , vol.52 , pp. 2265-2344
    • Mahboobi, S.1    Dove, S.2    Sellmer, A.3    Winkler, M.4    Eichhorn, E.5    Pongratz, H.6    Ciossek, T.7    Baer, T.8    Maier, T.9    Beckers, T.10
  • 18
    • 78650321835 scopus 로고    scopus 로고
    • Novel chimeric histone deacetylase inhibitors: A series of lapatinib hybrides as potent inhibitors of epidermal growth factor receptor (EGFR), human epidermal growth factor receptor 2 (HER2), and histone deacetylase activity
    • Mahboobi, S.; Dove, S.; Sellmer, A.; Winkler, M.; Eichhorn, E.; Pongratz, H.; Ciossek, T.; Baer, T.; Maier, T.; Beckers, T. Novel chimeric histone deacetylase inhibitors: a series of lapatinib hybrides as potent inhibitors of epidermal growth factor receptor (EGFR), human epidermal growth factor receptor 2 (HER2), and histone deacetylase activity J. Med. Chem. 2010, 53, 8546-8601
    • (2010) J. Med. Chem. , vol.53 , pp. 8546-8601
    • Mahboobi, S.1    Dove, S.2    Sellmer, A.3    Winkler, M.4    Eichhorn, E.5    Pongratz, H.6    Ciossek, T.7    Baer, T.8    Maier, T.9    Beckers, T.10
  • 19
    • 41149089267 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: From bench to clinic
    • Paris, M.; Porcelloni, M.; Binaschi, M.; Fattori, D. Histone deacetylase inhibitors: From bench to clinic J. Med. Chem. 2008, 51, 1505-1534
    • (2008) J. Med. Chem. , vol.51 , pp. 1505-1534
    • Paris, M.1    Porcelloni, M.2    Binaschi, M.3    Fattori, D.4
  • 20
    • 0000096835 scopus 로고    scopus 로고
    • Click chemistry: Diverse chemical function from a few good reactions
    • Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Click chemistry: Diverse chemical function from a few good reactions Angew. Chem., Int. Ed. 2001, 40, 2004-2021
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 21
    • 43049104161 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationship of histone deacetylase (HDAC) inhibitors with triazole-linked cap group
    • Chen, P.; Patil, V.; Guerrant, W.; Green, P.; Oyelere, A. Synthesis and structure-activity relationship of histone deacetylase (HDAC) inhibitors with triazole-linked cap group Bioorg. Med. Chem. 2008, 16, 4839-4892
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 4839-4892
    • Chen, P.1    Patil, V.2    Guerrant, W.3    Green, P.4    Oyelere, A.5
  • 23
    • 33244458905 scopus 로고    scopus 로고
    • Self-reporting fluorescent substrates of protein tyrosine kinases
    • Wang, Q.; Cahill, S. M.; Blumenstein, M.; Lawrence, D. S. Self-reporting fluorescent substrates of protein tyrosine kinases J. Am. Chem. Soc. 2006, 128, 1808-1809
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 1808-1809
    • Wang, Q.1    Cahill, S.M.2    Blumenstein, M.3    Lawrence, D.S.4
  • 24
    • 4644295841 scopus 로고    scopus 로고
    • Kinetics and comparative reactivity of human class i and IIb histone deacetylases
    • Shultz, B. E.; Misialek, S.; Wu, J.; Tang, J.; Conn, M. T.; Tahilramani, R.; Wong, L. Kinetics and comparative reactivity of human class I and IIb histone deacetylases Biochemistry 2004, 43, 11083-11091
    • (2004) Biochemistry , vol.43 , pp. 11083-11091
    • Shultz, B.E.1    Misialek, S.2    Wu, J.3    Tang, J.4    Conn, M.T.5    Tahilramani, R.6    Wong, L.7
  • 25
    • 33749011163 scopus 로고    scopus 로고
    • The NCI60 human tumour cell line anticancer drug screen
    • Shoemaker, R. H. The NCI60 human tumour cell line anticancer drug screen Nat. Rev. Cancer 2006, 6, 813-823
    • (2006) Nat. Rev. Cancer , vol.6 , pp. 813-823
    • Shoemaker, R.H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.