메뉴 건너뛰기




Volumn 53, Issue 24, 2010, Pages 8546-8555

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

Author keywords

[No Author keywords available]

Indexed keywords

ACRYLAMIDE DERIVATIVE; BETA ACTIN; CELL DIVISION KINASE 2; CYCLIC AMP DEPENDENT PROTEIN KINASE; EPIDERMAL GROWTH FACTOR RECEPTOR; EPIDERMAL GROWTH FACTOR RECEPTOR 2; HISTONE; HISTONE DEACETYLASE; HISTONE DEACETYLASE INHIBITOR; HISTONE H3; INSULIN RECEPTOR; LAPATINIB; LYSINE; PLATELET DERIVED GROWTH FACTOR BETA RECEPTOR; POLO LIKE KINASE 1; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; UNCLASSIFIED DRUG;

EID: 78650321835     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm100665z     Document Type: Article
Times cited : (99)

References (26)
  • 2
    • 30344477367 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer
    • Minucci, S.; Pelicci, P. G. Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer Nat. Rev. Cancer 2006, 6 (1) 38-51
    • (2006) Nat. Rev. Cancer , vol.6 , Issue.1 , pp. 38-51
    • Minucci, S.1    Pelicci, P.G.2
  • 3
    • 77649171884 scopus 로고    scopus 로고
    • Novel histone deacetylase inhibitors in clinical trials as anti-cancer agents
    • Jiahuai, T.; Cang, S.; Ma, Y.; Petrillo, R. L.; Liu, D. Novel histone deacetylase inhibitors in clinical trials as anti-cancer agents J. Hematol. Onco.l 2010, 3, 5
    • (2010) J. Hematol. Onco.l , vol.3 , pp. 5
    • Jiahuai, T.1    Cang, S.2    Ma, Y.3    Petrillo, R.L.4    Liu, D.5
  • 4
    • 67449127082 scopus 로고    scopus 로고
    • Clinical Studies of Histone Deacetylase Inhibitors
    • Prince, H. M.; Bishton, M. J.; Harrison, S. J. Clinical Studies of Histone Deacetylase Inhibitors Clin. Cancer Res. 2009, 15 (12) 3958-3969
    • (2009) Clin. Cancer Res. , vol.15 , Issue.12 , pp. 3958-3969
    • Prince, H.M.1    Bishton, M.J.2    Harrison, S.J.3
  • 5
    • 67449145358 scopus 로고    scopus 로고
    • Rational Combinations Using HDAC Inhibitors
    • Bots, M.; Johnstone, R. W. Rational Combinations Using HDAC Inhibitors Clin. Cancer Res. 2009, 15 (12) 3970-3977
    • (2009) Clin. Cancer Res. , vol.15 , Issue.12 , pp. 3970-3977
    • Bots, M.1    Johnstone, R.W.2
  • 6
    • 77952853306 scopus 로고    scopus 로고
    • Histone deacetylases and epigenetic therapies of hematological malignancies
    • Mercurio, C.; Minucci, S.; Pelicci, P. G. Histone deacetylases and epigenetic therapies of hematological malignancies Pharm. Res. 2010, 62 (1) 18-34
    • (2010) Pharm. Res. , vol.62 , Issue.1 , pp. 18-34
    • Mercurio, C.1    Minucci, S.2    Pelicci, P.G.3
  • 7
    • 31744448235 scopus 로고    scopus 로고
    • Molecularly targeted therapies in myelodysplastic syndromes and acute myeloid leukemias
    • Morgan, M. A.; Reuter, C. W. Molecularly targeted therapies in myelodysplastic syndromes and acute myeloid leukemias Ann. Hematol. 2006, 85 (3) 139-163
    • (2006) Ann. Hematol. , vol.85 , Issue.3 , pp. 139-163
    • Morgan, M.A.1    Reuter, C.W.2
  • 8
    • 0041347519 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors in cancer therapy: Is transcription the primary target?
    • Johnstone, R. W.; Licht, J. D. Histone deacetylase inhibitors in cancer therapy: is transcription the primary target? Cancer Cell 2003, 4 (1) 13-18
    • (2003) Cancer Cell , vol.4 , Issue.1 , pp. 13-18
    • Johnstone, R.W.1    Licht, J.D.2
  • 9
    • 33745208735 scopus 로고    scopus 로고
    • Epigenetic target as an approach to cancer therapy and chemoprevention
    • Sorbera, L. A. Epigenetic target as an approach to cancer therapy and chemoprevention Drugs Future 2006, 31 (4) 335-344
    • (2006) Drugs Future , vol.31 , Issue.4 , pp. 335-344
    • Sorbera, L.A.1
  • 10
    • 77952240320 scopus 로고    scopus 로고
    • The preclinical activity of the histone deacetylase inhibitor PXD101 (belinostat) in hepatocellular carcinoma cell lines
    • Ma, B. B. Y.; Sung, F.; Tao, Q.; Poon, F. F.; Lui, V. W.; Yeo, W.; Chan, S. L.; Chan, A. T. C. The preclinical activity of the histone deacetylase inhibitor PXD101 (belinostat) in hepatocellular carcinoma cell lines Investigational New Drugs 2010, 28 (2) 107-114
    • (2010) Investigational New Drugs , vol.28 , Issue.2 , pp. 107-114
    • Ma, B.B.Y.1    Sung, F.2    Tao, Q.3    Poon, F.F.4    Lui, V.W.5    Yeo, W.6    Chan, S.L.7    Chan, A.T.C.8
  • 18
    • 0141743694 scopus 로고    scopus 로고
    • Stereoselective Synthesis of Novel Dipeptide β-Turn Mimetics Targeting Melanocortin Peptide Receptors
    • Zhang, J.; Xiong, C.; Ying, J.; Wang, W.; Hruby, V. J. Stereoselective Synthesis of Novel Dipeptide β-Turn Mimetics Targeting Melanocortin Peptide Receptors Org. Lett. 2003, 5 (17) 3115-3118
    • (2003) Org. Lett. , vol.5 , Issue.17 , pp. 3115-3118
    • Zhang, J.1    Xiong, C.2    Ying, J.3    Wang, W.4    Hruby, V.J.5
  • 19
    • 49549139072 scopus 로고
    • Peptide coupling reagents. IV. N-[Oxytris(dimethylamino)phosphonium] benzotriazole hexafluorophosphate
    • Castro, B.; Dormoy, J. R.; Evin, G.; Selve, C. Peptide coupling reagents. IV. N-[Oxytris(dimethylamino)phosphonium]benzotriazole hexafluorophosphate Tetrahedron Lett. 1975, 14, 1219-1222
    • (1975) Tetrahedron Lett. , vol.14 , pp. 1219-1222
    • Castro, B.1    Dormoy, J.R.2    Evin, G.3    Selve, C.4
  • 20
    • 0034598022 scopus 로고    scopus 로고
    • Synthesis of piperazinones and benzopiperazinones from 1,2-diamines and organoboronic acids
    • Petasis, N. A.; Patel, Z. D. Synthesis of piperazinones and benzopiperazinones from 1,2-diamines and organoboronic acids Tetrahedron Lett. 2000, 41, 9607-9611
    • (2000) Tetrahedron Lett. , vol.41 , pp. 9607-9611
    • Petasis, N.A.1    Patel, Z.D.2
  • 21
    • 65249135408 scopus 로고    scopus 로고
    • Novel designed chimeric HDAC- and tyrosine kinase inhibitors: A series of Imatinib hybrides as potent inhibitors of wild-type and mutant BCR-ABL, PDGF-Rβ and histone deacetylases
    • Mahboobi, S.; Sellmer, A.; Winkler, M.; Eichhorn, E.; Pongratz, H.; Ciossek, T.; Baer, T.; T., M.; Beckers, T. Novel designed chimeric HDAC- and tyrosine kinase inhibitors: A series of Imatinib hybrides as potent inhibitors of wild-type and mutant BCR-ABL, PDGF-Rβ and histone deacetylases J. Med. Chem. 2009, 52 (8) 2265-2279
    • (2009) J. Med. Chem. , vol.52 , Issue.8 , pp. 2265-2279
    • Mahboobi, S.1    Sellmer, A.2    Winkler, M.3    Eichhorn, E.4    Pongratz, H.5    Ciossek, T.6    Baer, T.7    Beckers, T.8
  • 22
    • 34547094822 scopus 로고    scopus 로고
    • Distinct pharmacological properties of 2nd generation HDAC inhibitors with the benzamide or hydroxamate head group
    • Beckers, T.; Burkhardt, C.; Wieland, H.; Gimmnich, P.; Ciossek, T.; Maier, T.; Sanders, K. Distinct pharmacological properties of 2nd generation HDAC inhibitors with the benzamide or hydroxamate head group Int. J. Cancer 2007, 121, 1138-1148
    • (2007) Int. J. Cancer , vol.121 , pp. 1138-1148
    • Beckers, T.1    Burkhardt, C.2    Wieland, H.3    Gimmnich, P.4    Ciossek, T.5    Maier, T.6    Sanders, K.7
  • 23
    • 0037253808 scopus 로고    scopus 로고
    • A fluorogenic histone deacetylase assay well suited for high-throughput activity screening
    • Wegener, D.; Wirsching, F.; Riester, D.; Schwienhorst, A. A fluorogenic histone deacetylase assay well suited for high-throughput activity screening Chem. Biol. 2003, 10 (1) 61-68
    • (2003) Chem. Biol. , vol.10 , Issue.1 , pp. 61-68
    • Wegener, D.1    Wirsching, F.2    Riester, D.3    Schwienhorst, A.4
  • 25
    • 0033856957 scopus 로고    scopus 로고
    • Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell toxicity
    • O'Brian, J.; Wilson, I.; Orton, T.; Pognan, F. Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell toxicity Eur. J. Biochem. 2000, 267 (17) 5421-5426
    • (2000) Eur. J. Biochem. , vol.267 , Issue.17 , pp. 5421-5426
    • O'Brian, J.1    Wilson, I.2    Orton, T.3    Pognan, F.4
  • 26
    • 0037169881 scopus 로고    scopus 로고
    • Use of lithium N,O-dimethylhydroxylamide as an efficient in situ protecting agent for aromatic aldehydes
    • Roschangar, F.; Brown, J. C.; Cooley, B. E.; Sharp, M. J.; Matsuoka, R. T. Use of lithium N,O-dimethylhydroxylamide as an efficient in situ protecting agent for aromatic aldehydes Tetrahedron 2002, 58 (9) 1657-1666
    • (2002) Tetrahedron , vol.58 , Issue.9 , pp. 1657-1666
    • Roschangar, F.1    Brown, J.C.2    Cooley, B.E.3    Sharp, M.J.4    Matsuoka, R.T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.