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Results: 1-7 |
Results: 7
Inhibition of the action of the topoisomerase II poison amsacrine by simple aniline derivatives: Evidence for drug-protein interactions
Authors: Finlay, GJ Atwell, GJ Baguley, BC
Citation: Gj. Finlay et al., Inhibition of the action of the topoisomerase II poison amsacrine by simple aniline derivatives: Evidence for drug-protein interactions, ONCOL RES, 11(6), 1999, pp. 249-254
Dimeric analogues of non-cationic tricyclic aromatic carboxamides are a new class of cytotoxic agents
Authors: Spicer, JA Gamage, SA Atwell, GJ Finlay, GJ Baguley, BC Denny, WA
Citation: Ja. Spicer et al., Dimeric analogues of non-cationic tricyclic aromatic carboxamides are a new class of cytotoxic agents, ANTI-CAN DR, 14(3), 1999, pp. 281-289
Synthesis of 1-substituted 3-(chloromethyl)-6-aminoindoline (6-amino-seco-CI) DNA minor groove alkylating agents and structure-activity relationshipsfor their cytotoxicity
Authors: Milbank, JBJ Tercel, M Atwell, GJ Wilson, WR Hogg, A Denny, WA
Citation: Jbj. Milbank et al., Synthesis of 1-substituted 3-(chloromethyl)-6-aminoindoline (6-amino-seco-CI) DNA minor groove alkylating agents and structure-activity relationshipsfor their cytotoxicity, J MED CHEM, 42(4), 1999, pp. 649-658
N-substituted 2-(2,6-dinitrophenylamino)propanamides: Novel prodrugs that release a primary amine via nitroreduction and intramolecular cyclization
Authors: Sykes, BM Atwell, GJ Hogg, A Wilson, WR O'Connor, CJ Denny, WA
Citation: Bm. Sykes et al., N-substituted 2-(2,6-dinitrophenylamino)propanamides: Novel prodrugs that release a primary amine via nitroreduction and intramolecular cyclization, J MED CHEM, 42(3), 1999, pp. 346-355
5-amino-1-(chloromethyl)-1,2 dihydro-3H-benz [e]indoles: Relationships between structure and cytotoxicity for analogues bearing different DNA minor groove binding subunits
Authors: Atwell, GJ Milbank, JJB Wilson, WR Hogg, A Denny, WA
Citation: Gj. Atwell et al., 5-amino-1-(chloromethyl)-1,2 dihydro-3H-benz [e]indoles: Relationships between structure and cytotoxicity for analogues bearing different DNA minor groove binding subunits, J MED CHEM, 42(17), 1999, pp. 3400-3411
Structure-activity relationships for substituted bis(acridine-4-calrboxamides): A new class of anticancer agents
Authors: Gamage, SA Spicer, JA Atwell, GJ Finlay, GJ Baguley, BC Denny, WA
Citation: Sa. Gamage et al., Structure-activity relationships for substituted bis(acridine-4-calrboxamides): A new class of anticancer agents, J MED CHEM, 42(13), 1999, pp. 2383-2393
Synthesis and cytotoxicity of 5-amino-1-(chloromethyl)-3-[(5,6,7-trimethoxyindol-2-yl)carbonyl]-1,2-dihydro-3H-benz[e]indole (amino-seco-CBI-TMI) andrelated 5-alkylamino analogues: New DNA minor groove alkylating agents
Authors: Atwell, GJ Tercel, M Boyd, M Wilson, WR Denny, WA
Citation: Gj. Atwell et al., Synthesis and cytotoxicity of 5-amino-1-(chloromethyl)-3-[(5,6,7-trimethoxyindol-2-yl)carbonyl]-1,2-dihydro-3H-benz[e]indole (amino-seco-CBI-TMI) andrelated 5-alkylamino analogues: New DNA minor groove alkylating agents, J ORG CHEM, 63(25), 1998, pp. 9414-9420
Risultati: 1-7 |