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Volumn 16, Issue 7-9, 2007, Pages 449-460

QSAR study on aminophenylbenzamides and acrylamides as histone deacetylase inhibitors: An insight into the structural basis of antiproliferative activity

Author keywords

Aminophenylacrylamides; Aminophenylbenzamides; Drug design; Histone deacetylases; QSAR; Tool for Structure Activity Relationships (TSAR)

Indexed keywords

ACRYLAMIDE; AMINOPHENYLBENZAMIDE; HISTONE DEACETYLASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 51749087688     PISSN: 10542523     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00044-007-9085-9     Document Type: Article
Times cited : (16)

References (31)
  • 1
    • 0018976157 scopus 로고
    • Changing rates of histone mRNA synthesis and turnover in Drosophila embryos
    • KV Anderson JA Lengyel 1980 Changing rates of histone mRNA synthesis and turnover in Drosophila embryos Cell 21 717 727
    • (1980) Cell , vol.21 , pp. 717-727
    • Anderson, K.V.1    Lengyel, J.A.2
  • 3
    • 33745920222 scopus 로고    scopus 로고
    • Histone Deacetylase Inhibitors: Gathering Pace
    • N Carey BN Thangue 2006 Histone Deacetylase Inhibitors: Gathering Pace Curr opin Pharmacol 6 369 375
    • (2006) Curr Opin Pharmacol , vol.6 , pp. 369-375
    • Carey, N.1    Thangue, B.N.2
  • 5
    • 0141988610 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: The Abbott experience
    • M Curtin K Glaser 2003 Histone deacetylase inhibitors: the Abbott experience Curr Med Chem 10 2373 2392
    • (2003) Curr Med Chem , vol.10 , pp. 2373-2392
    • Curtin, M.1    Glaser, K.2
  • 6
    • 33846554894 scopus 로고    scopus 로고
    • Quantitative structure-activity relationship (QSAR) for neuroprotective activity of terpenoids
    • HJ Chang HJ Kim HS Chun 2007 Quantitative structure-activity relationship (QSAR) for neuroprotective activity of terpenoids Life Sci 80 835 841
    • (2007) Life Sci , vol.80 , pp. 835-841
    • Chang, H.J.1    Kim, H.J.2    Chun, H.S.3
  • 7
    • 34250339309 scopus 로고    scopus 로고
    • 3D-QSAR and molecular docking study on bisarylmaleimide series as glycogen synthase kinase 3, cyclin dependent kinase 2 and cyclin dependent kinase 4 inhibitors: An insight into the criteria for selectivity
    • N Dessalew PV Bharatam 2007 3D-QSAR and molecular docking study on bisarylmaleimide series as glycogen synthase kinase 3, cyclin dependent kinase 2 and cyclin dependent kinase 4 inhibitors: An insight into the criteria for selectivity Eur J Med Chem 42 1014 1027
    • (2007) Eur J Med Chem , vol.42 , pp. 1014-1027
    • Dessalew, N.1    Bharatam, P.V.2
  • 8
    • 33846786989 scopus 로고    scopus 로고
    • 3D-QSAR and molecular docking studies on pyrazolopyrimidine derivatives as glycogen synthase kinase-3b inhibitors
    • N Dessalew DS Patel PV Bharatam 2007 3D-QSAR and molecular docking studies on pyrazolopyrimidine derivatives as glycogen synthase kinase-3b inhibitors J Mol Graph Mod 25 885 895
    • (2007) J Mol Graph Mod , vol.25 , pp. 885-895
    • Dessalew, N.1    Patel, D.S.2    Bharatam, P.V.3
  • 9
    • 33846796243 scopus 로고    scopus 로고
    • 3D-QSAR CoMFA Study on aminothiazole derivatives as cyclin-dependent kinase 2 inhibitors
    • N Dessalew PV Bharatam SK Singh 2007 3D-QSAR CoMFA Study on aminothiazole derivatives as cyclin-dependent kinase 2 inhibitors QSAR Comb Sci 26 85 91
    • (2007) QSAR Comb Sci , vol.26 , pp. 85-91
    • Dessalew, N.1    Bharatam, P.V.2    Singh, S.K.3
  • 10
    • 4544323749 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors; Understanding a new wave of anticancer agents
    • VA Garea M Esteller 2004 Histone deacetylase inhibitors; understanding a new wave of anticancer agents Int J Cancer 112 171 178
    • (2004) Int J Cancer , vol.112 , pp. 171-178
    • Garea, V.A.1    Esteller, M.2
  • 11
    • 5344281161 scopus 로고    scopus 로고
    • Novel histone deacetylase inhibitory activity of cyclic tetrapeptide with trifluoromethyl and pentafluoro ethyl ketones
    • B Jose Y Oniki T Kato N Nishino Y Sumida M Yoshida 2004 Novel histone deacetylase inhibitory activity of cyclic tetrapeptide with trifluoromethyl and pentafluoro ethyl ketones Bioorg Med Chem Lett 14 5343 5346
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 5343-5346
    • Jose, B.1    Oniki, Y.2    Kato, T.3    Nishino, N.4    Sumida, Y.5    Yoshida, M.6
  • 13
    • 0033813236 scopus 로고    scopus 로고
    • A QSAR study investigating the effect of L-alanine ester variation on the anti-HIV activity of some phosphoramidate derivatives of d4T
    • MH Knaggs C McGuigan SA Harris P Heshmati D Cahard IH Gilberta J Balzarini 2000 A QSAR study investigating the effect of L-alanine ester variation on the anti-HIV activity of some phosphoramidate derivatives of d4T Bioorg Med Chem Lett 10 2075 2078
    • (2000) Bioorg Med Chem Lett , vol.10 , pp. 2075-2078
    • Knaggs, M.H.1    McGuigan, C.2    Harris, S.A.3    Heshmati, P.4    Cahard, D.5    Gilberta, I.H.6    Balzarini, J.7
  • 15
    • 0030771347 scopus 로고    scopus 로고
    • QSAR and 3D-QSAR in drug design Part 1: Methodology
    • H Kubinyi 1997 QSAR and 3D-QSAR in drug design Part 1: methodology Drug Discovery Today 2 457 467
    • (1997) Drug Discovery Today , vol.2 , pp. 457-467
    • Kubinyi, H.1
  • 16
    • 33746758901 scopus 로고    scopus 로고
    • 3D QSAR studies of N-4-arylacryloylpiperazin-1-yl-phenyloxazolidinones: A novel class of antibacterial agentsq
    • BB Lohray N Gandhi KB Srivastava VB Lohray 2006 3D QSAR studies of N-4-arylacryloylpiperazin-1-yl-phenyloxazolidinones: A novel class of antibacterial agentsq Bioorg Med Chem Lett 16 3817 3823
    • (2006) Bioorg Med Chem Lett , vol.16 , pp. 3817-3823
    • Lohray, B.B.1    Gandhi, N.2    Srivastava, K.B.3    Lohray, V.B.4
  • 18
    • 0042933857 scopus 로고    scopus 로고
    • The cell cycle, chromatin and cancer: Mechanism based therapeutics come of age
    • F McLaughlin P Finn NB La Thangue 2003 The cell cycle, chromatin and cancer: mechanism based therapeutics come of age Drug Disc Today 8 793 802
    • (2003) Drug Disc Today , vol.8 , pp. 793-802
    • McLaughlin, F.1    Finn, P.2    La Thangue, N.B.3
  • 19
    • 4143140016 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors open new doors in cancer therapy
    • F McLaughlin NB La Thangue 2004 Histone deacetylase inhibitors open new doors in cancer therapy Biochem Pharmacol 68 1139 1144
    • (2004) Biochem Pharmacol , vol.68 , pp. 1139-1144
    • McLaughlin, F.1    La Thangue, N.B.2
  • 21
    • 11844278521 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors
    • C Monneret 2005 Histone deacetylase inhibitors Eur J Med Chem 40 1 13
    • (2005) Eur J Med Chem , vol.40 , pp. 1-13
    • Monneret, C.1
  • 23
    • 0035962636 scopus 로고    scopus 로고
    • Transcription therapy for cancer
    • PP Pandolfi 2001 Transcription therapy for cancer Oncogene 20 3116 3127
    • (2001) Oncogene , vol.20 , pp. 3116-3127
    • Pandolfi, P.P.1
  • 24
    • 33644872992 scopus 로고    scopus 로고
    • Keynote review: Chromatin control and cancer-drug discovery: Realizing the promise
    • AG Inche NB La Thangue 2006 Keynote review: Chromatin control and cancer-drug discovery: realizing the promise Drug Discovery Today 11 97 109
    • (2006) Drug Discovery Today , vol.11 , pp. 97-109
    • Inche, A.G.1    La Thangue, N.B.2
  • 25
    • 3242765335 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors- a new tool to treat cancer
    • R Somech S Izraeli JA Simon 2004 histone deacetylase inhibitors- a new tool to treat cancer Cancer Treatm Rev 30 401 472
    • (2004) Cancer Treatm Rev , vol.30 , pp. 401-472
    • Somech, R.1    Izraeli, S.2    Simon, J.A.3
  • 27
    • 0037140821 scopus 로고    scopus 로고
    • Novel histone deacetylase inhibitors: N-hydroxycarboxamides possessing a terminal bicyclic aryl group
    • S Uesato M Kitagawa Y Nagaoka T Maeda H Kuwajima T Yamori 2002 Novel histone deacetylase inhibitors: N-hydroxycarboxamides possessing a terminal bicyclic aryl group Bioorg Med Chem Lett 12 1347 1349
    • (2002) Bioorg Med Chem Lett , vol.12 , pp. 1347-1349
    • Uesato, S.1    Kitagawa, M.2    Nagaoka, Y.3    Maeda, T.4    Kuwajima, H.5    Yamori, T.6
  • 28
    • 0000910008 scopus 로고
    • Development and application of new steric substituent parameters in drug design
    • Ariens EJ (ed.), New York: Academic
    • Verloop A, Tipker HW (1976a) Development and application of new steric substituent parameters in drug design. In: Ariens EJ (ed.), Drug design 7, 165-207. New York: Academic
    • (1976) Drug Design , vol.7 , pp. 165-207
    • Verloop, A.1    Tipker, H.W.2
  • 29
    • 84981604834 scopus 로고
    • Use of linear free energy related and other parameters in the study of fungicidal selectivity
    • A Verloop J Tipker 1976 Use of linear free energy related and other parameters in the study of fungicidal selectivity Pestic Sci 7 379 390
    • (1976) Pestic Sci , vol.7 , pp. 379-390
    • Verloop, A.1    Tipker, J.2
  • 31
    • 33748509517 scopus 로고    scopus 로고
    • Recent advances in medicinal chemistry of histone deacetylase inhibitors
    • H Weinmann E Ottow 2004 recent advances in medicinal chemistry of histone deacetylase inhibitors Ann Rep Med Chem 39 185 196
    • (2004) Ann Rep Med Chem , vol.39 , pp. 185-196
    • Weinmann, H.1    Ottow, E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.