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Results: 1-13 |
Results: 13
DESIGN, SYNTHESIS, AND EVALUATION OF POTENTIAL GAR AND AICAR TRANSFORMYLASE INHIBITORS
Authors: BOGER DL KOCHANNY MJ CAI H WYATT D KITOS PA WARREN MS RAMCHARAN J GOOLJARSINGH LT BENKOVIC SJ
Citation: Dl. Boger et al., DESIGN, SYNTHESIS, AND EVALUATION OF POTENTIAL GAR AND AICAR TRANSFORMYLASE INHIBITORS, Bioorganic & medicinal chemistry, 6(6), 1998, pp. 643-659
ANTIBODY TRANSPORT IN CULTURED TUMOR-CELL LAYERS
Authors: TOPP EM KITOS PA VIJAYKUMAR V DESILVA BS HENDRICKSON TL
Citation: Em. Topp et al., ANTIBODY TRANSPORT IN CULTURED TUMOR-CELL LAYERS, Journal of controlled release, 53(1-3), 1998, pp. 15-23
10-FORMYL-5,8,10-TRIDEAZAFOLIC ACID (10-FORMYL-TDAF) - A POTENT INHIBITOR OF GLYCINAMIDE RIBONUCLEOTIDE TRANSFORMYLASE
Authors: BOGER DL HAYNES NE KITOS PA WARREN MS RAMCHARAN J MAROLEWSKI AE BENKOVIC SJ
Citation: Dl. Boger et al., 10-FORMYL-5,8,10-TRIDEAZAFOLIC ACID (10-FORMYL-TDAF) - A POTENT INHIBITOR OF GLYCINAMIDE RIBONUCLEOTIDE TRANSFORMYLASE, Bioorganic & medicinal chemistry, 5(9), 1997, pp. 1817-1830
FUNCTIONALIZED ANALOGS OF 5,8,10-TRIDEAZAFOLATE AS POTENTIAL INHIBITORS OF GAR TFASE OR AICAR TFASE
Authors: BOGER DL HAYNES NE WARREN MS GOOLJARSINGH LT RAMCHARAN J KITOS PA BENKOVIC SJ
Citation: Dl. Boger et al., FUNCTIONALIZED ANALOGS OF 5,8,10-TRIDEAZAFOLATE AS POTENTIAL INHIBITORS OF GAR TFASE OR AICAR TFASE, Bioorganic & medicinal chemistry, 5(9), 1997, pp. 1831-1838
FUNCTIONALIZED ANALOGS OF 5,8,10-TRIDEAZAFOLATE - DEVELOPMENT OF AN ENZYME-ASSEMBLED TIGHT-BINDING INHIBITOR OF GAR TFASE AND A POTENTIAL IRREVERSIBLE INHIBITOR OF AICAR TFASE
Authors: BOGER DL HAYNES NE WARREN MS RAMCHARAN J KITOS PA BENKOVIC SJ
Citation: Dl. Boger et al., FUNCTIONALIZED ANALOGS OF 5,8,10-TRIDEAZAFOLATE - DEVELOPMENT OF AN ENZYME-ASSEMBLED TIGHT-BINDING INHIBITOR OF GAR TFASE AND A POTENTIAL IRREVERSIBLE INHIBITOR OF AICAR TFASE, Bioorganic & medicinal chemistry, 5(9), 1997, pp. 1839-1846
ABENZYL 10-FORMYL-TRIDEAZAFOLIC ACID (ABENZYL 10-FORMYL-TDAF) - AN EFFECTIVE INHIBITOR OF GLYCINAMIDE RIBONUCLEOTIDE TRANSFORMYLASE
Authors: BOGER DL HAYNES NE WARREN MS RAMCHARAN J MAROLEWSKI AE KITOS PA BENKOVIC SJ
Citation: Dl. Boger et al., ABENZYL 10-FORMYL-TRIDEAZAFOLIC ACID (ABENZYL 10-FORMYL-TDAF) - AN EFFECTIVE INHIBITOR OF GLYCINAMIDE RIBONUCLEOTIDE TRANSFORMYLASE, Bioorganic & medicinal chemistry, 5(9), 1997, pp. 1847-1852
MULTISUBSTRATE ANALOG BASED ON 5,8,10-TRIDEAZAFOLATE
Authors: BOGER DL HAYNES NE WARREN MS RAMCHARAN J KITOS PA BENKOVIC SJ
Citation: Dl. Boger et al., MULTISUBSTRATE ANALOG BASED ON 5,8,10-TRIDEAZAFOLATE, Bioorganic & medicinal chemistry, 5(9), 1997, pp. 1853-1857
DESIGN, SYNTHESIS AND EVALUATION OF BOUVARDIN, DEOXYBOUVARDIN AND RA-I-XIV PHARMACOPHORE ANALOGS (VOL 2, PG 85, 1994)
Authors: BOGER DL PATANE MA JIN Q KITOS PA
Citation: Dl. Boger et al., DESIGN, SYNTHESIS AND EVALUATION OF BOUVARDIN, DEOXYBOUVARDIN AND RA-I-XIV PHARMACOPHORE ANALOGS (VOL 2, PG 85, 1994), Bioorganic & medicinal chemistry, 5(7), 1997, pp. 1453-1453
REVERSED AND SANDWICHED ANALOGS OF DUOCARMYCIN SA - ESTABLISHMENT OF THE ORIGIN OF THE SEQUENCE-SELECTIVE ALKYLATION OF DNA AND NEW INSIGHTS INTO THE SOURCE OF CATALYSIS
Authors: BOGER DL BOLLINGER B HERTZOG DL JOHNSON DS CAI H MESINI P GARBACCIO RM JIN Q KITOS PA
Citation: Dl. Boger et al., REVERSED AND SANDWICHED ANALOGS OF DUOCARMYCIN SA - ESTABLISHMENT OF THE ORIGIN OF THE SEQUENCE-SELECTIVE ALKYLATION OF DNA AND NEW INSIGHTS INTO THE SOURCE OF CATALYSIS, Journal of the American Chemical Society, 119(21), 1997, pp. 4987-4998
HIGH-DENSITY CULTURE OF MAMMALIAN-CELLS IN A NONWOVEN POLYESTER MATRIX
Authors: VIJAYKUMAR V KITOS PA TOPP EM
Citation: V. Vijaykumar et al., HIGH-DENSITY CULTURE OF MAMMALIAN-CELLS IN A NONWOVEN POLYESTER MATRIX, In vitro cellular & developmental biology. Animal, 32(8), 1996, pp. 465-468
A HAMMETT CORRELATION FOR CC-1065 AND DUOCARMYCIN ANALOGS - MAGNITUDEOF SUBSTITUENT ELECTRONIC EFFECTS ON FUNCTIONAL REACTIVITY
Authors: BOGER DL MCKIE JA HAN NH TARBY CM RIGGS HQW KITOS PA
Citation: Dl. Boger et al., A HAMMETT CORRELATION FOR CC-1065 AND DUOCARMYCIN ANALOGS - MAGNITUDEOF SUBSTITUENT ELECTRONIC EFFECTS ON FUNCTIONAL REACTIVITY, Bioorganic & medicinal chemistry letters, 6(6), 1996, pp. 659-664
SYNTHESIS, CHEMICAL-PROPERTIES, AND PRELIMINARY EVALUATION OF SUBSTITUTED CBI ANALOGS OF CC-1065 AND THE DUOCARMYCINS INCORPORATING THE 1,2,9,9A-TETRAHYDROCYCLOPROPA[C]BENZ[E]INDOL-4-ONE ALKYLATION SUBUNIT - HAMMETT QUANTITATION OF THE MAGNITUDE OF ELECTRONIC EFFECTS ON FUNCTIONAL REACTIVITY
Authors: BOGER DL HAN NH TARBY CM BOYCE CW CAI H JIN Q KITOS PA
Citation: Dl. Boger et al., SYNTHESIS, CHEMICAL-PROPERTIES, AND PRELIMINARY EVALUATION OF SUBSTITUTED CBI ANALOGS OF CC-1065 AND THE DUOCARMYCINS INCORPORATING THE 1,2,9,9A-TETRAHYDROCYCLOPROPA[C]BENZ[E]INDOL-4-ONE ALKYLATION SUBUNIT - HAMMETT QUANTITATION OF THE MAGNITUDE OF ELECTRONIC EFFECTS ON FUNCTIONAL REACTIVITY, Journal of organic chemistry, 61(15), 1996, pp. 4894-4912
TOTAL SYNTHESIS AND PRELIMINARY EVALUATION OF (-DUOCARMYCIN AND ENT-(-)-DUOCARMYCIN SA())
Authors: BOGER DL MACHIYA K HERTZOG DL KITOS PA HOLMES D
Citation: Dl. Boger et al., TOTAL SYNTHESIS AND PRELIMINARY EVALUATION OF (-DUOCARMYCIN AND ENT-(-)-DUOCARMYCIN SA()), Journal of the American Chemical Society, 115(20), 1993, pp. 9025-9036
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