ANTINEOPLASTIC ACTIVITY;
ARTICLE;
BREAST CANCER;
DRUG CYTOTOXICITY;
DRUG POTENCY;
DRUG SCREENING;
DRUG SELECTIVITY;
DRUG SYNTHESIS;
HOLLOW FIBER;
HUMAN;
HUMAN CELL;
IN VITRO STUDY;
IN VIVO STUDY;
LEUKEMIA;
PROSTATE CANCER;
STRUCTURE ACTIVITY RELATION;
TECHNIQUE;
TUMOR CELL LINE;
A review of the chemistry of the antitumor benzo[c]phenanthridine alkaloids nitidine and fagaronine and of the related antitumor alkaloid coralyne
Phillips, S. D.; Castle, R. N. A review of the chemistry of the antitumor benzo[c]phenanthridine alkaloids nitidine and fagaronine and of the related antitumor alkaloid coralyne. J. Heterocycl. Chem. 1981, 18, 223-232.
Preparation and antileukemic activity of some alkoxybenzo[c] phenanthridinium salts and corresponding dihydro derivatives
Zee-Cheng, R. K.-Y.; Cheng, C. C. Preparation and antileukemic activity of some alkoxybenzo[c]phenanthridinium salts and corresponding dihydro derivatives. J. Med. Chem. 1975, 18, 66-71.
Synthesis and evaluation of new 6-amino-substituted benzo[c] phenanthridine derivatives
Janin, Y. L.; Croisy, A.; Riou, J.-F.; Bisagni, E. Synthesis and evaluation of new 6-amino-substituted benzo[c]phenanthridine derivatives. J. Med. Chem. 1993, 36, 3686-3692.
A formal new access to the benzo[c]phenanthridine alkaloids, synthesis of nitidine and O-methylfagaronine analogues
Janin, Y. L.; Bisagni, E. A formal new access to the benzo[c] phenanthridine alkaloids, synthesis of nitidine and O-methylfagaronine analogues. Tetrahedron 1993, 49, 10305-10316.
Phenanthridinderivate und ihre Herstellung, dt. Patentanmeldung. 195 38 088.6-44, PCT/DE 96/ 01958; EP 0873315; US 006030981; 1995
Clement, B., Weide, M. Phenanthridinderivate und ihre Herstellung, dt. Patentanmeldung. 195 38 088.6-44, PCT/DE 96/ 01958; EP 0873315; US 006030981; 1995.
A two-step synthesis of cytostatically active benzo[c]phenanthridine derivatives
Clement, B., Weide, M., Wolschendorf, U., Kock, I. A two-step synthesis of cytostatically active benzo[c]phenanthridine derivatives. Angew. Chem., Int. Ed. 2005, 44, 635-638.
A convenient synthesis of substituted stilbenes by condensation of o- or p-tolunitrile with p-substituted benzaldehydes
Takahashi, K.; Okamoto, T.; Yamada, K.; Iida, H. A convenient synthesis of substituted stilbenes by condensation of o- or p-tolunitrile with p-substituted benzaldehydes. Synthesis 1977, 58-59.
Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines
Monks, A.; Scudiero, D.; Skehan, P.; Shoemaker, R.; Paull, K.; Vistica, D.; Hose, C.; Langley, J.; Cronise, P.; Vaigro-Wolff, A.; Gray-Goodrich, M.; Campbell, H.; Mayo, J.; Boyd, M. Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines. J. Natl. Cancer Inst. 1991, 83, 757-766.
Some practical considerations and applications of the National Cancer Institute in vitro anticancer drug discovery screen
Boyd, M. R.; Paull, K. D. Some practical considerations and applications of the National Cancer Institute in vitro anticancer drug discovery screen. Drug Dev. Res. 1995, 34, 91-109.
An information-intensive approach to the molecular pharmacology of cancer
Weinstein, J. N.; Myers, T. G.; O'Connor, P. M.; Friend, S. H.; Fornace, A. J., Jr.; Kohn, K. W.; Fojo, T.; Bates, S. E.; Rubinstein, L. V.; Anderson, N. L.; Buolamwini, J. K.; van Osdol, W. W.; Monks, A. P.; Scudiero, D. A.; Sausville, E. A.; Zaharevitz, D. W.; Bunow, B.; Viswanadhan, V. N.; Johnson, G. S.; Wittes, R. E.; Paull, K. D. An information-intensive approach to the molecular pharmacology of cancer. Science 1997, 275, 343-349.
Data concerning the NCI screening methods in detail are accessible from the NCI via the Internet from following addresses: http://dtp.nci.nih.gov/ branches/btb/ivclsp.html; http:// dtp.nci.nih.gov/branches/btb/hfa.html.
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Data concerning test results for established antitumor agents are accessible from the NCI via the Internet from the following address: http://dtp.nci.nih.gov/docs/cancer/searches/ standard_mechanism_list.html.
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0024312538
Display and analysis of patterns of differential activity of drugs against human tumor cell lines: Development of mean graph and COMPARE algorithm
Paull, K. D.; Shoemaker, R. H.; Hodes, L.; Monks, A.; Scudiero, D. A.; Rubinstein, L.; Plowman, J.; Boyd, M. R. Display and analysis of patterns of differential activity of drugs against human tumor cell lines: Development of mean graph and COMPARE algorithm. J. Natl. Cancer Inst. 1989, 81, 1088-1092.
Identification of novel antimitotic agents acting at the tubulin level by computer-assisted evaluation of differential cytotoxicity data
Paull, K. D.; Lin, C. M.; Malspeis, L.; Hamel, E. Identification of novel antimitotic agents acting at the tubulin level by computer-assisted evaluation of differential cytotoxicity data. Cancer Res. 1992, 52, 3892-3900.
In vivo cultivation of tumor cells in hollow fibers
Hollingshead, M. G.; Alley, M. C.; Camalier, R. F.; Abbott, B. J.; Mayo, J. G.; Malspeis, L.; Grever, M. R. In vivo cultivation of tumor cells in hollow fibers. Life Sci. 1895, 57, 131-141.