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Volumn 45, Issue 11, 2010, Pages 5183-5199

QSAR modeling, synthesis and bioassay of diverse leukemia RPMI-8226 cell line active agents

Author keywords

Anti tumor agents; Bis(oxy)bis urea derivatives; Bis(sulfanediyl)bis urea derivatives; CODESSA PRO; Leukemia RPMI 8226 cell line; QSAR

Indexed keywords

1,1' [2,2' [BUTANE 1,4 DIYLBIS(SULFANEDIYL)]BIS(2,1 PHENYLENE)]BIS[3 (4 CHLOROPHENYL)UREA]; 1,1' [2,2' [BUTANE 1,4 DIYLBIS(SULFANEDIYL)]BIS(2,1 PHENYLENE)]BIS[3 (4 METHOXYPHENYL)UREA]; 1,1' [2,2' [PROPANE 1,3 DIYLBIS(OXY)]BIS(2,1 PHENYLENE)]BIS[3 (4 METHOXYPHENYL)UREA]; 1,1' [4,4' [PROPANE 1,3 DIYLBIS(OXY)]BIS(4,1 PHENYLENE)]BIS[3 (4 CHLOROPHENYL)UREA]; 1,1' [4,4' [PROPANE 1,3 DIYLBIS(OXY)]BIS(4,1 PHENYLENE)]BIS[3 (4 METHOXYPHENYL)UREA]; 2,2' [1,4 BUTANEDIYLBIS(THIO)]BISBENZENAMINE; 4,4' [PROPANE 1,3 DIYLBIS(OXY)]DIANILINE; ANTINEOPLASTIC AGENT; N,N' [2,2' [PROPANE 1,3 DIYL(OXY)]BIS(2,1 PHENYLENE)]DIACETAMIDE; N,N' [4,4' [PROPANE 1,3 DIYL(OXY)]BIS(4,1 PHENYLENE)]DIACETAMIDE; UNCLASSIFIED DRUG; UREA DERIVATIVE;

EID: 77957824684     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2010.08.033     Document Type: Article
Times cited : (24)

References (29)
  • 1
    • 3142697244 scopus 로고    scopus 로고
    • Canadian Cancer Society - National Cancer Institute of Canada Toronto, Canada
    • Canadian Cancer Statistics 2005 2005 Canadian Cancer Society - National Cancer Institute of Canada Toronto, Canada
    • (2005) Canadian Cancer Statistics 2005
  • 2
    • 0003575143 scopus 로고    scopus 로고
    • National Cancer Institute of Canada Toronto, Canada
    • Canadian Cancer Statistics 2002 2002 National Cancer Institute of Canada Toronto, Canada
    • (2002) Canadian Cancer Statistics 2002
  • 3
    • 0014215657 scopus 로고
    • A statistical survey of leukemia in Ontario and at the Ontario cancer foundation clinics, 1938-1958
    • E.N. MacKay, and A.H. Sellers A statistical survey of leukemia in Ontario and at the Ontario cancer foundation clinics, 1938-1958 Can. Med. Assoc. J. 96 1967 1626 1635
    • (1967) Can. Med. Assoc. J. , vol.96 , pp. 1626-1635
    • MacKay, E.N.1    Sellers, A.H.2
  • 4
    • 17644427902 scopus 로고    scopus 로고
    • American Cancer Society American Cancer Society Atlanta
    • American Cancer Society Cancer Facts and Figures 2006 2006 American Cancer Society Atlanta
    • (2006) Cancer Facts and Figures 2006
  • 5
    • 0242331085 scopus 로고    scopus 로고
    • Multidrug resistance reversal agents
    • J. Robert, and C. Jarry Multidrug resistance reversal agents J. Med. Chem. 46 2003 4805 4817
    • (2003) J. Med. Chem. , vol.46 , pp. 4805-4817
    • Robert, J.1    Jarry, C.2
  • 7
    • 27644491739 scopus 로고    scopus 로고
    • University of Florida
    • CODESSA PRO Software 2002 University of Florida www.codessa-pro.com
    • (2002) CODESSA PRO Software
  • 8
    • 47349120200 scopus 로고    scopus 로고
    • QSAR modeling of the antifungal activity against Candida albicans for a diverse set of organic compounds
    • A.R. Katritzky, S.H. Slavov, D.A. Dobchev, and M. Karelson QSAR modeling of the antifungal activity against Candida albicans for a diverse set of organic compounds Bioorg. Med. Chem. 16 2008 7055 7069
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 7055-7069
    • Katritzky, A.R.1    Slavov, S.H.2    Dobchev, D.A.3    Karelson, M.4
  • 10
    • 18044378153 scopus 로고    scopus 로고
    • Prediction of partitioning properties for environmental pollutants using mathematical structural descriptors
    • S.C. Basak, and D. Mills Prediction of partitioning properties for environmental pollutants using mathematical structural descriptors Arkivoc ii 2005 60 76
    • (2005) Arkivoc , vol.2 , pp. 60-76
    • Basak, S.C.1    Mills, D.2
  • 11
    • 23744516503 scopus 로고    scopus 로고
    • QSAR study on benzenesulfonamide dissociation constant pKa: Physicochemical approach using surface tension
    • A. Thakur QSAR study on benzenesulfonamide dissociation constant pKa: physicochemical approach using surface tension Arkivoc xiv 2005 49 58
    • (2005) Arkivoc , vol.14 , pp. 49-58
    • Thakur, A.1
  • 12
    • 33646560008 scopus 로고    scopus 로고
    • Novel synthesis of nicotinamide derivatives of cytotoxic properties
    • A.S. Girgis, H.M. Hosni, and F.F. Barsoum Novel synthesis of nicotinamide derivatives of cytotoxic properties Bioorg. Med. Chem. 14 2006 4466 4476
    • (2006) Bioorg. Med. Chem. , vol.14 , pp. 4466-4476
    • Girgis, A.S.1    Hosni, H.M.2    Barsoum, F.F.3
  • 13
    • 57949106458 scopus 로고    scopus 로고
    • Regioselective synthesis of dispiro[1H-indene-2,3′-pyrrolidine- 2″,3″-[3H]indole-1,2″ (1″H)-diones of potential anti-tumor properties
    • A.S. Girgis Regioselective synthesis of dispiro[1H-indene-2,3′- pyrrolidine-2″,3″-[3H]indole-1,2″ (1″H)-diones of potential anti-tumor properties Eur. J. Med. Chem. 44 2009 91 100
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 91-100
    • Girgis, A.S.1
  • 14
    • 60549090802 scopus 로고    scopus 로고
    • Regioselective synthesis and stereochemical structure of anti-tumor active dispiro[3H-indole-3,2′pyrrolidine-3′,3″-piperidine]- 2(1H),4″-diones
    • A.S. Girgis Regioselective synthesis and stereochemical structure of anti-tumor active dispiro[3H-indole-3,2′pyrrolidine-3′,3″- piperidine]-2(1H),4″-diones Eur. J. Med. Chem. 44 2009 1257 1264
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 1257-1264
    • Girgis, A.S.1
  • 16
    • 0026676380 scopus 로고
    • The National Cancer Institute: Cancer drug discovery and development program
    • M.R. Grever, S.A. Schepartz, and B.A. Chabner The National Cancer Institute: cancer drug discovery and development program Semin. Oncol. 19 1992 622 638
    • (1992) Semin. Oncol. , vol.19 , pp. 622-638
    • Grever, M.R.1    Schepartz, S.A.2    Chabner, B.A.3
  • 17
    • 0028906786 scopus 로고
    • Some practical considerations and applications of the national cancer institute in vitro anticancer drug discovery screen
    • M.R. Boyd, and K.D. Paull Some practical considerations and applications of the national cancer institute in vitro anticancer drug discovery screen Drug Dev. Res. 34 1995 91 109
    • (1995) Drug Dev. Res. , vol.34 , pp. 91-109
    • Boyd, M.R.1    Paull, K.D.2
  • 18
    • 0038778278 scopus 로고    scopus 로고
    • Discovery of substituted N-phenyl nicotinamides as potent inducers of apoptosis using a cell- and caspase-based high throughput screening assay
    • S.X. Cai, B. Nguyen, S. Jia, J. Herich, J. Guastella, S. Reddy, B. Tseng, J. Drewe, and S. Kasibhatla Discovery of substituted N-phenyl nicotinamides as potent inducers of apoptosis using a cell- and caspase-based high throughput screening assay J. Med. Chem. 46 2003 2474 2481
    • (2003) J. Med. Chem. , vol.46 , pp. 2474-2481
    • Cai, S.X.1    Nguyen, B.2    Jia, S.3    Herich, J.4    Guastella, J.5    Reddy, S.6    Tseng, B.7    Drewe, J.8    Kasibhatla, S.9
  • 19
    • 77957830584 scopus 로고    scopus 로고
    • Unpublished data, Anti-tumor activity of these compounds screened through the Developmental Therapeutics Program of National Cancer Institute, Bethesda, USA and observed anti-tumor activity properties of these 24 compounds are given Table 1
    • Unpublished data, Anti-tumor activity of these compounds screened through the Developmental Therapeutics Program of National Cancer Institute, Bethesda, USA and observed anti-tumor activity properties of these 24 compounds are given Table 1.
  • 20
    • 77957838829 scopus 로고    scopus 로고
    • ChemDraw Ultra v.11, CambridgeSoft Corporation, Cambridge, MA
    • ChemDraw Ultra v.11, CambridgeSoft Corporation, Cambridge, MA. www.cambridgesoft.com
  • 21
    • 77957830103 scopus 로고    scopus 로고
    • Hyperchem, v. 7.5, Hypercube Inc., Gainesville, FL
    • Hyperchem, v. 7.5, Hypercube Inc., Gainesville, FL. www.hyper.com
  • 24
    • 1642306443 scopus 로고    scopus 로고
    • Quantitative structure-pharmacokinetic relationship modelling: Apparent volume of distribution
    • T. Ghafourian, M. Barzegar-Jalali, N. Hakimiha, and M.T.D. Cronin Quantitative structure-pharmacokinetic relationship modelling: apparent volume of distribution J. Pharm. Pharmacol. 56 2004 339 350
    • (2004) J. Pharm. Pharmacol. , vol.56 , pp. 339-350
    • Ghafourian, T.1    Barzegar-Jalali, M.2    Hakimiha, N.3    Cronin, M.T.D.4
  • 25
    • 0043132440 scopus 로고    scopus 로고
    • Methods for reliability and uncertainty assessment and for applicability evaluations of classification- and regression-based QSARs
    • L. Eriksson, J. Jaworska, A.P. Worth, M.T.D. Cronin, R.M. McDowell, and P. Gramatica Methods for reliability and uncertainty assessment and for applicability evaluations of classification- and regression-based QSARs Environ. Health Perspect. 111 2003 1361 1375
    • (2003) Environ. Health Perspect. , vol.111 , pp. 1361-1375
    • Eriksson, L.1    Jaworska, J.2    Worth, A.P.3    Cronin, M.T.D.4    McDowell, R.M.5    Gramatica, P.6
  • 27
    • 0345314306 scopus 로고
    • On nitro- and aminophenoxyacetic acids
    • W.A. Jacobs, and M. Heidelberger On nitro- and aminophenoxyacetic acids J. Am. Chem. Soc. 39 1917 2188 2224
    • (1917) J. Am. Chem. Soc. , vol.39 , pp. 2188-2224
    • Jacobs, W.A.1    Heidelberger, M.2
  • 28
    • 37049065866 scopus 로고
    • The chemotherapy of schistosomiasis, Part I. Derivatives and Analogues of αω-Di-(p-aminophenoxy)alkanes
    • J.N. Ashley, R.F. Collins, M. Davis, and N.E. Sirett The chemotherapy of schistosomiasis, Part I. Derivatives and Analogues of αω-Di-(p- aminophenoxy)alkanes J. Chem. Soc. 1958 3298 3313
    • (1958) J. Chem. Soc. , pp. 3298-3313
    • Ashley, J.N.1    Collins, R.F.2    Davis, M.3    Sirett, N.E.4
  • 29
    • 34248160923 scopus 로고    scopus 로고
    • A convenient synthesis of thiamacrocyclic dilactams
    • A.A. Abbas, and A.S. Girgis A convenient synthesis of thiamacrocyclic dilactams Heteroatom. Chem. 18 2007 249 254
    • (2007) Heteroatom. Chem. , vol.18 , pp. 249-254
    • Abbas, A.A.1    Girgis, A.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.