-
1
-
-
0032170961
-
Sequence-specific DNA minor groove binders. Design and synthesis of netropsin and distamycin analogues
-
Bailly C., Chaires J.B. Sequence-specific DNA minor groove binders. Design and synthesis of netropsin and distamycin analogues. Bioconj. Chem. 9:1998;513-538.
-
(1998)
Bioconj. Chem.
, vol.9
, pp. 513-538
-
-
Bailly, C.1
Chaires, J.B.2
-
3
-
-
0028789119
-
Eukaryotic topoisomerase II cleavage is independent of duplex DNA conformation
-
Choi I.Y., Chung I.K., Muller M.T. Eukaryotic topoisomerase II cleavage is independent of duplex DNA conformation. Biochim. Biophys. Acta. 1264:1995;209-214.
-
(1995)
Biochim. Biophys. Acta
, vol.1264
, pp. 209-214
-
-
Choi, I.Y.1
Chung, I.K.2
Muller, M.T.3
-
4
-
-
0029937080
-
DNA binding specificities of YPF1, a Drosophila homolog to the DNA binding subunit of human DNA-dependent protein kinase, Ku
-
Jacoby D.B., Wensink P.C. DNA binding specificities of YPF1, a Drosophila homolog to the DNA binding subunit of human DNA-dependent protein kinase, Ku. J. Biol. Chem. 271:1996;16827-16832.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 16827-16832
-
-
Jacoby, D.B.1
Wensink, P.C.2
-
5
-
-
0342817540
-
Introduction to DNA sequence-specific agents
-
Palumbo M. Greenwich, CT: JAI Press
-
Palumbo M. Introduction to DNA sequence-specific agents. Palumbo M. Advances in DNA Sequence Specific Agents. 3:1998;1-6 JAI Press, Greenwich, CT.
-
(1998)
Advances in DNA Sequence Specific Agents
, vol.3
, pp. 1-6
-
-
Palumbo, M.1
-
6
-
-
0003776015
-
DNA-protein structural interactions
-
D.M. Lilley. New York: Oxford University Press
-
Lilley D.M. DNA-protein structural interactions. Lilley D.M. Frontiers in Molecular Biology. 1995;Oxford University Press, New York.
-
(1995)
Frontiers in Molecular Biology
-
-
Lilley, D.M.1
-
7
-
-
0029761654
-
Peptidyl anthraquinones as potential antineoplastic drugs: Synthesis, DNA binding, redox cycling, and biological activity
-
Gatto B., Zagotto G., Sissi C., Cera C., Uriarte E., Palu G., Capranico G., Palumbo M. Peptidyl anthraquinones as potential antineoplastic drugs: synthesis, DNA binding, redox cycling, and biological activity. J. Med. Chem. 39:1996;3114-3122.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 3114-3122
-
-
Gatto, B.1
Zagotto, G.2
Sissi, C.3
Cera, C.4
Uriarte, E.5
Palu, G.6
Capranico, G.7
Palumbo, M.8
-
9
-
-
33845552509
-
Use of liquid crystal induced circular dichroism for absolute configurational assignments of beta-amino alcohols
-
Rinaldi P., Wilk M. Use of liquid crystal induced circular dichroism for absolute configurational assignments of beta-amino alcohols. J. Org. Chem. 48:1983;2141-2146.
-
(1983)
J. Org. Chem.
, vol.48
, pp. 2141-2146
-
-
Rinaldi, P.1
Wilk, M.2
-
10
-
-
0025144976
-
Enantioselective synthesis of (S)-amino acids by phenylalanine dehydrogenase from Bacillus sphaericus: Use of natural and recombinant enzymes
-
Asano Y., Yamada A., Kato Y., Yamaguchi K., Hibino Y., Hirai K., Kondo K. Enantioselective synthesis of (S)-amino acids by phenylalanine dehydrogenase from Bacillus sphaericus: use of natural and recombinant enzymes. J. Org. Chem. 55:1990;5567-5571.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 5567-5571
-
-
Asano, Y.1
Yamada, A.2
Kato, Y.3
Yamaguchi, K.4
Hibino, Y.5
Hirai, K.6
Kondo, K.7
-
11
-
-
0025341331
-
New colorimetric cytotoxicity assay for anticancer-drug screening
-
Skehan P., Storeng R., Scudiero D., Monks A., McMahon J., Vistica D., Warren J.T., Bokesch H., Kenney S., Boyd M.R. New colorimetric cytotoxicity assay for anticancer-drug screening. J. Natl. Cancer Inst. 82:1990;1107-1112.
-
(1990)
J. Natl. Cancer Inst.
, vol.82
, pp. 1107-1112
-
-
Skehan, P.1
Storeng, R.2
Scudiero, D.3
Monks, A.4
McMahon, J.5
Vistica, D.6
Warren, J.T.7
Bokesch, H.8
Kenney, S.9
Boyd, M.R.10
-
12
-
-
84855757480
-
-
Chemical Computing Group Inc., 1255 University St, Suite 1600, Montreal, Quebec, Canada, H3B 3X3
-
Molecular Operating Environment (MOE 1998.10), Chemical Computing Group Inc., 1255 University St, Suite 1600, Montreal, Quebec, Canada, H3B 3X3, 1998.
-
(1998)
Molecular Operating Environment (MOE 1998.10)
-
-
-
13
-
-
0037571112
-
Merck molecular force field 1. Basis, form, scope, parameterization, and performance of MMFF94
-
Halgren T.A. Merck molecular force field 1. Basis, form, scope, parameterization, and performance of MMFF94. J. Comput. Chem. 17:1996;490-519.
-
(1996)
J. Comput. Chem.
, vol.17
, pp. 490-519
-
-
Halgren, T.A.1
-
14
-
-
0011134241
-
Merck molecular force field 2. MMFF94 van der Waals and electrostatic parameters for intermolecular interactions
-
Halgren T.A. Merck molecular force field 2. MMFF94 van der Waals and electrostatic parameters for intermolecular interactions. J. Comput. Chem. 17:1996;520-552.
-
(1996)
J. Comput. Chem.
, vol.17
, pp. 520-552
-
-
Halgren, T.A.1
-
15
-
-
0011143599
-
Merck molecular force field 3. Molecular geometries and vibrational frequencies for MMFF94
-
Halgren T.A. Merck molecular force field 3. Molecular geometries and vibrational frequencies for MMFF94. J. Comput. Chem. 17:1996;553-586.
-
(1996)
J. Comput. Chem.
, vol.17
, pp. 553-586
-
-
Halgren, T.A.1
-
16
-
-
0001061464
-
Merck molecular force field 4. Conformational energies and geometries for MMFF94
-
Halgren T.A., Nachbar R.B. Merck molecular force field 4. Conformational energies and geometries for MMFF94. J. Comput. Chem. 17:1996;587-615.
-
(1996)
J. Comput. Chem.
, vol.17
, pp. 587-615
-
-
Halgren, T.A.1
Nachbar, R.B.2
-
17
-
-
5244268272
-
Merck molecular force field 5. Extension of MMFF94 using experimental data, additional computational data, and empirical rules
-
Halgren T.A. Merck molecular force field 5. Extension of MMFF94 using experimental data, additional computational data, and empirical rules. J. Comput. Chem. 17:1996;616-641.
-
(1996)
J. Comput. Chem.
, vol.17
, pp. 616-641
-
-
Halgren, T.A.1
-
18
-
-
0342382573
-
-
Gaussian Inc., Pittsburg PA
-
M.J. Frisch, Gaussian Inc., Pittsburg PA, 1988.
-
(1988)
-
-
Frisch, M.J.1
-
19
-
-
0342817539
-
Chinone
-
J. Houben, Weyl T. Stuttgart: Georg Thieme Verlag
-
Bayer O. Chinone. Houben J., Weyl T. Methoden der Organischen Chemie. VII/3C:1979;Georg Thieme Verlag, Stuttgart.
-
(1979)
Methoden der Organischen Chemie
, vol.73
-
-
Bayer, O.1
-
20
-
-
0030058489
-
Characterization of the major metabolite of the novel topoisomerase I inhibitor NU/ICRF 505
-
Cummings J., Meikle I., Macpherson J.S., Smyth J.F. Characterization of the major metabolite of the novel topoisomerase I inhibitor NU/ICRF 505. Anti Cancer Drug Des. 11:1996;367-382.
-
(1996)
Anti Cancer Drug Des.
, vol.11
, pp. 367-382
-
-
Cummings, J.1
Meikle, I.2
Macpherson, J.S.3
Smyth, J.F.4
-
21
-
-
0030580049
-
Determination of the novel topoisomerase I inhibitor NU/ICRF 505 and its major metabolite in plasma, tissue and tumour by high-performance liquid chromatography
-
Cummings J., Meikle I., Macpherson J.S, Smyth J.F. Determination of the novel topoisomerase I inhibitor NU/ICRF 505 and its major metabolite in plasma, tissue and tumour by high-performance liquid chromatography. J. Chromatogr. B. 685:1996;159-164.
-
(1996)
J. Chromatogr. B
, vol.685
, pp. 159-164
-
-
Cummings, J.1
Meikle, I.2
Macpherson, J.S.3
Smyth, J.F.4
-
22
-
-
0030035729
-
Induction of apoptosis in human cancer cell lines by the novel anthracenyl amino acid topoisomerase I inhibitor NU/ICRF 505
-
Meikle I., Cummings J., Macpherson J.S., Smyth J.F. Induction of apoptosis in human cancer cell lines by the novel anthracenyl amino acid topoisomerase I inhibitor NU/ICRF 505. Br. J. Cancer. 74:1996;374-379.
-
(1996)
Br. J. Cancer
, vol.74
, pp. 374-379
-
-
Meikle, I.1
Cummings, J.2
Macpherson, J.S.3
Smyth, J.F.4
-
23
-
-
0030580063
-
Development of anthracenyl-amino acid conjugates as topoisomerase I and II inhibitors that circumvent drug resistance
-
Meikle I., Cummings J., Macpherson J.S., Smyth J.F. Development of anthracenyl-amino acid conjugates as topoisomerase I and II inhibitors that circumvent drug resistance. Biochem. Pharmacol. 52:1996;979-990.
-
(1996)
Biochem. Pharmacol.
, vol.52
, pp. 979-990
-
-
Meikle, I.1
Cummings, J.2
Macpherson, J.S.3
Smyth, J.F.4
-
24
-
-
0028818643
-
Identification of anthracenyl-dipeptide conjugates as novel topoisomerase I and II inhibitors and their evaluation as potential anticancer drugs
-
Meikle I., Cummings J., Macpherson J.S., Smyth J.F. Identification of anthracenyl-dipeptide conjugates as novel topoisomerase I and II inhibitors and their evaluation as potential anticancer drugs. Anti Cancer Drug Des. 10:1995;515-527.
-
(1995)
Anti Cancer Drug Des.
, vol.10
, pp. 515-527
-
-
Meikle, I.1
Cummings, J.2
Macpherson, J.S.3
Smyth, J.F.4
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