Zobrazeno 1 - 10
of 26
pro vyhledávání: '"D S, Duch"'
Publikováno v:
Analytical Letters. 25:219-230
Two different analytical methods were used to estimate reduced folates from the same cultured hepatoma cell preparation. A method based on HPLC separation of reduced folate pools in cells prelabelled with [3H]-folic acid was compared to a method base
Publikováno v:
Seminars in oncology. 23(2 Suppl 5)
Vinorelbine (Navelbine; Burroughs Wellcome Co, Research Triangle Park, NC; Pierre Fabre Medicament, Paris, France), a semisynthetic vinca alkaloid that is a potent inhibitor of mitotic microtubule polymerization, was recently approved for the treatme
Publikováno v:
Seminars in oncology. 23(2 Suppl 5)
Publikováno v:
Cancer research. 55(24)
The purpose of this investigation was to determine whether antitumor selectivity of the third generation thymidylate synthase inhibitor 1843U89 could be enhanced by a combination of the drug with folic acid. The effects of folic acid on toxicity of 1
Publikováno v:
Molecular pharmacology. 48(1)
The voltage- and frequency-dependent interactions of pentobarbital with voltage-gated sodium channels were examined in whole-cell patch-clamp recordings. Using rat brain IIA and rat muscle rSkM1 sodium channels expressed in stably transfected Chinese
Publikováno v:
European journal of anaesthesiology. 12(1)
In order to begin separating the roles of membrane protein structure and membrane protein milieu in anaesthetic interactions a new planar lipid bilayer technology is being used. Membrane proteins such as sodium channels from diverse tissue sources ar
Autor:
M, Jansen, M, Dykstra, J I, Lee, J, Stables, P, Topley, V C, Knick, R J, Mullin, D S, Duch, G K, Smith
Publikováno v:
Biochemical pharmacology. 47(6)
Clinical responses for anticancer agents are based upon tumor regression. We have investigated the potential of glycineamide ribonucleotide transformylase (GAR TFase) inhibitors to produce regressions in multiple preclinical models of colon carcinoma
Autor:
D S, Duch, S, Banks, I K, Dev, S H, Dickerson, R, Ferone, L S, Heath, J, Humphreys, V, Knick, W, Pendergast, S, Singer
Publikováno v:
Cancer research. 53(4)
Studies on a series of benzoquinazoline folate analogues as inhibitors of human thymidylate synthase led to the selection of 1843U89 for further evaluation. This compound had a Ki of 90 pM versus human thymidylate synthase and was noncompetitive with
Publikováno v:
Cancer research. 52(18)
Metabolic effects and mode of cytotoxicity of 5-deazaacyclotetrahydrofolate (5-DACTHF, BW543U76), a glycineamide ribonucleotide transformylase inhibitor, were studied in MOLT-4 cells, a human T-cell leukemia line. 5-DACTHF inhibits purine synthesis w
Publikováno v:
The Journal of biological chemistry. 267(8)
N-Acetylserotonin (compound 1) and N-acetyldopamine (compound 7) inhibit bovine adrenal medullary sepiapterin reductase in a manner competitive with the pterin substrate and have Ki values of 0.12 and 0.4 microM, respectively. Molecular modeling sugg