Authors:
BEALL HD
HUDNOTT AR
WINSKI S
SIEGEL D
SWANN E
ROSS D
MOODY CJ
Citation: Hd. Beall et al., INDOLEQUINONE ANTITUMOR AGENTS - RELATIONSHIP BETWEEN QUINONE STRUCTURE AND RATE OF METABOLISM BY RECOMBINANT HUMAN NQO1, Bioorganic & medicinal chemistry letters, 8(5), 1998, pp. 545-548
Authors:
SLOAN KB
BEALL HD
TAYLOR HE
GETZ JJ
VILLANEUVA R
NIPPER R
SMITH K
Citation: Kb. Sloan et al., TRANSDERMAL DELIVERY OF THEOPHYLLINE FROM ALCOHOL VEHICLES, International journal of pharmaceutics, 171(2), 1998, pp. 185-193
Authors:
BEALL HD
WINSKI S
SWANN E
HUDNOTT AR
COTTERILL AS
OSULLIVAN N
GREEN SJ
BIEN R
SIEGEL D
ROSS D
MOODY CJ
Citation: Hd. Beall et al., INDOLEQUINONE ANTITUMOR AGENTS - CORRELATION BETWEEN QUINONE STRUCTURE, RATE OF METABOLISM BY RECOMBINANT HUMAN NAD(P)H-QUINONE OXIDOREDUCTASE, AND IN-VITRO CYTOTOXICITY, Journal of medicinal chemistry, 41(24), 1998, pp. 4755-4766
Citation: Dn. Fish et al., STABILITY OF SUMATRIPTAN SUCCINATE IN EXTEMPORANEOUSLY PREPARED ORAL LIQUIDS, American journal of health-system pharmacy, 54(14), 1997, pp. 1619-1622
Citation: Ai. Patrick et al., EFFECT OF VEHICLES ON TOPICAL DELIVERY OF 5-FLUOROURACIL (5FU) BY 1-ACYL-5FU PRODRUGS, International journal of pharmaceutics, 154(1), 1997, pp. 39-48
Citation: Hd. Beall et al., 1,3-BISALKYLCARBONYL-5-FLUOROURACIL AND 3-ALKYLCARBONYL-5-FLUOROURACIL PRODRUGS - SYNTHESES, THERMAL, AND HYDROLYTIC STABILITY, Drug development and industrial pharmacy, 23(6), 1997, pp. 517-525
Authors:
TRAVER RD
SIEGEL D
BEALL HD
PHILLIPS RM
GIBSON NW
FRANKLIN WA
ROSS D
Citation: Rd. Traver et al., CHARACTERIZATION OF A POLYMORPHISM IN NAD(P)H - QUINONE OXIDOREDUCTASE (DT-DIAPHORASE), British Journal of Cancer, 75(1), 1997, pp. 69-75
Citation: Hd. Beall et Kb. Sloan, TRANSDERMAL DELIVERY OF 5-FLUOROURACIL (5-FU) BY 1-ALKYLCARBONYL-5-FUPRODRUGS, International journal of pharmaceutics, 129(1-2), 1996, pp. 203-210
Citation: Hd. Beall et al., 1-ALKYLCARBONYL-5-FLUOROURACIL PRODRUGS - SYNTHESIS, THERMAL AND HYDROLYTIC STABILITY, Drug development and industrial pharmacy, 22(2), 1996, pp. 85-90
Authors:
GUSTAFSON DL
BEALL HD
BOLTON EM
ROSS D
WALDREN CA
Citation: Dl. Gustafson et al., EXPRESSION OF HUMAN NAD(P)H-QUINONE OXIDOREDUCTASE (DT-DIAPHORASE) INCHINESE-HAMSTER OVARY CELLS - EFFECT ON THE TOXICITY OF ANTITUMOR QUINONES, Molecular pharmacology, 50(4), 1996, pp. 728-735
Authors:
BEALL HD
LIU YF
SIEGEL D
BOLTON EM
GIBSON NW
ROSS D
Citation: Hd. Beall et al., ROLE OF NAD(P)H-QUINONE OXIDOREDUCTASE (DT-DIAPHORASE) IN CYTOTOXICITY AND INDUCTION OF DNA-DAMAGE BY STREPTONIGRIN, Biochemical pharmacology, 51(5), 1996, pp. 645-652
Citation: Dm. Peterson et al., NONCOVALENT BINDING OF A MITOMYCIN-C METABOLITE, 2,7-DIAMINOMITOSENE,TO DUPLEX DNA, Cancer letters, 90(2), 1995, pp. 133-138
Authors:
BEALL HD
MURPHY AM
SIEGEL D
HARGREAVES RHJ
BUTLER J
ROSS D
Citation: Hd. Beall et al., NICOTINAMIDE ADENINE-DINUCLEOTIDE (PHOSPHATE)QUINONE OXIDOREDUCTASE (DT-DIAPHORASE) AS A TARGET FOR BIOREDUCTIVE ANTITUMOR QUINONES - QUINONE CYTOTOXICITY AND SELECTIVITY IN HUMAN LUNG AND BREAST-CANCER CELL-LINES, Molecular pharmacology, 48(3), 1995, pp. 499-504
Authors:
BEALL HD
MULCAHY RT
SIEGEL D
TRAVER RD
GIBSON NW
ROSS D
Citation: Hd. Beall et al., METABOLISM OF BIOREDUCTIVE ANTITUMOR COMPOUNDS BY PURIFIED RAT AND HUMAN DT-DIAPHORASES, Cancer research, 54(12), 1994, pp. 3196-3201
Citation: Hd. Beall et al., STRUCTURE OF 3-ACETYL-5-FLUOROURACIL (5-FU) - IMPLICATION FOR ITS REARRANGEMENTS DURING HYDROLYSIS AND UPON HEATING, Pharmaceutical research, 10(6), 1993, pp. 905-912
Citation: Kb. Sloan et al., TRANSDERMAL DELIVERY OF 5-FLUOROURACIL (5-FU) THROUGH HAIRLESS MOUSE SKIN BY 1-ALKYLAMINOCARBONYL-5-FU PRODRUGS - PHYSICOCHEMICAL CHARACTERIZATION OF PRODRUGS AND CORRELATIONS WITH TRANSDERMAL DELIVERY, International journal of pharmaceutics, 93(1-3), 1993, pp. 27-36
Citation: Hd. Beall et al., THE ESTIMATION OF RELATIVE WATER SOLUBILITY FOR PRODRUGS THAT ARE UNSTABLE IN WATER, International journal of pharmaceutics, 93(1-3), 1993, pp. 37-47