ANTINEOPLASTIC ACTIVITY;
ARTICLE;
BREAST CANCER;
CANCER CELL CULTURE;
CANCER GROWTH;
CANCER INHIBITION;
COLON CANCER;
CONTROLLED STUDY;
DRUG INHIBITION;
DRUG SCREENING;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
KIDNEY CANCER;
LEUKEMIA CELL;
LUNG NON SMALL CELL CANCER;
OVARY CANCER;
QUANTITATIVE STRUCTURE ACTIVITY RELATION;
ANTINEOPLASTIC AGENTS;
CELL LINE, TUMOR;
DRUG SCREENING ASSAYS, ANTITUMOR;
HUMANS;
LEUKEMIA;
MAGNETIC RESONANCE SPECTROSCOPY;
QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP;
STATIC ELECTRICITY;
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
Cytotoxic activity of a new paclitaxel formulation, Pacliex, in vitro and in vivo
S. Hassan, S. Dhar, M. Sandstrom, D. Arsenau, M. Budnikova, I. Lokot, N. Lobanov, M.O. Karlsson, R. Larsson, and E. Lindhagen Cytotoxic activity of a new paclitaxel formulation, Pacliex, in vitro and in vivo Cancer Chemother. Pharmacol. 44 2005 47 54
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
Synthesis and bioassay of improved mosquito repellents predicted from chemical structure
A.R. Katritzky, Z. Wang, S. Slavov, M. Tsikolia, D. Dobchev, N.G. Akhmedov, C.D. Hall, U.R. Bernier, G.G. Clark, and K.J. Linthicum Synthesis and bioassay of improved mosquito repellents predicted from chemical structure Proc. Natl. Acad. Sci. 105 2008 7359 7364
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
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
Feasibility of drug screening with panels of human tumor cell lines using a microculture tetrazolium assay
M.C. Alley, D.A. Scudiero, A. Monks, M.L. Hursey, M.J. Czerwinski, D.L. Fine, B.J. Abbott, J.G. Mayo, R.H. Shoemaker, and M.R. Boyd Feasibility of drug screening with panels of human tumor cell lines using a microculture tetrazolium assay Cancer Res. 48 1988 589 601
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
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
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
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.
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ChemDraw Ultra v.11, CambridgeSoft Corporation, Cambridge, MA
Hyperchem, v. 7.5, Hypercube Inc., Gainesville, FL
Hyperchem, v. 7.5, Hypercube Inc., Gainesville, FL. www.hyper.com
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AM1: A new general purpose quantum mechanical molecular model
M.J.S. Dewar, E.G. Zoebisch, E.F. Healy, and J.J.P. Stewart AM1: a new general purpose quantum mechanical molecular model J. Am. Chem. Soc. 107 1985 3902 3909
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
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
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