Zobrazeno 1 - 10
of 149
pro vyhledávání: '"R Oftebro"'
Autor:
J. M. Dornish, B. Børretzen, Jahn M. Nesland, M. E. H. Juul, Erik O. Pettersen, Einar K. Rofstad, T. E. Aastveit, R. Oftebro, R. O. Larsen
Publikováno v:
British Journal of Cancer
The deuterated benzaldehyde derivative zilascorb(2H), 5,6-O-benzylidene-d-L-ascorbic acid, was administered once daily by i.v. injection in nude mice with grafted tumours of a human malignant melanoma (E.E.) and ovarian carcinoma (OVCAR-3) origins. L
Publikováno v:
ChemInform. 22
Methods are described for the syntheses of chloromethyl propargyl ethers and propargyl halides substituted with a hydroxyalkyl group, and their use in alkylation reactions of 2-pyrimidinones. The N-alkynyl derivatives are reversible inhibitors of mit
Publikováno v:
Anticancer research. 15(5B)
4,6-Benzylidene-D-glucose (BG), is a known antitumour substance with low clinical toxicity. In order to increase the antitumour activity of BG a deuterated compound, 4,6-benzylidene-D-d1-glucose, denoted P-1013, was synthesised. P-1013 induced signif
Publikováno v:
Transplantation proceedings. 26(6)
Publikováno v:
Anticancer research. 12(1)
Zilascorb (2H) (5,6-benzylidene-d1-L-ascorbic acid sodium salt), a derivative of deuterated benzaldehyde inducing reversible protein synthesis inhibition, was tested on human NHIK 3025 cells in combination with the anticancer drug cis-diamminedichlor
Publikováno v:
Anticancer research. 11(3)
Three different benzaldehyde derivatives (viz. beta-cyclodextrin benzaldehyde inclusion compound (CDBA), 4, 6-O-benzylidene-D-glucose (BG) and sodium benzylidene-ascorbate (SBA) have been shown to exert anticancer effects in patients without causing
Autor:
J. de Vries, Kjetill Østgaard, M.J. Peters, Eppo Mulder, Kristen B. Eik-Nes, R. Oftebro, H.J. van der Molen
Publikováno v:
Molecular and Cellular Endocrinology. 11:309-323
Growth of cultured NHIK 3025 cells stemming from a carcinoma of the human uterine cervix can be stimulated by the androgens 4-androstene-3β,17β-diol and testosterone, but is not influenced by oestradiol. In the cytosol fraction of these cells testo
Publikováno v:
British Journal of Cancer
Inactivation of NHIK 3025 cells ny the mitotic inhibitor NY 3170 (1-propargyl-5-chloropyrimidin-2-one) was measured as loss of colony-forming ability. NY 3170 at a concentration of 0.15 nM allowed no formation of colonies after 12 days of continuous
Publikováno v:
Cell Proliferation. 13:163-171
The proliferation kinetics of cells of the line NHIK 1922 grown in vitro and as solid tumours in the athymic mutant nude mouse has been studied. In vitro, growth curves were determined for exponentially growing populations and for populations synchro
Publikováno v:
British Journal of Cancer
Cells from the established cell line NHIK 3025 were synchronized by repeated mitotic selections. Survival of the synchronized cells after treatment with haematoporphyrin and near-UV light was measured by testing the capacity of the cells to form macr