Search Results - "Lukash, L.L."

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  1. 1

    Design, synthesis and biological evaluation of N-phenylthieno[2,3-d]pyrimidin-4-amines as inhibitors of FGFR1 by Gryshchenko, A.A., Bdzhola, V.G., Balanda, A.O., Briukhovetska, N.V., Kotey, I.M., Golub, A.G., Ruban, T.P., Lukash, L.L., Yarmoluk, S.M.

    Published in Bioorganic & medicinal chemistry (01-05-2015)
    “…Protein kinase FGFR1 inhibitors: We report a series of N-phenylthieno[2,3-d]pyrimidin-4-amines as a novel class of nanomolar-range FGFR1 inhibitors. These new…”
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    Journal Article
  2. 2

    Design, synthesis and biological evaluation of 5-amino-4-(1H-benzoimidazol-2-yl)-phenyl-1,2-dihydro-pyrrol-3-ones as inhibitors of protein kinase FGFR1 by Gryshchenko, A.A., Tarnavskiy, S.S., Levchenko, K.V., Bdzhola, V.G., Volynets, G.P., Golub, A.G., Ruban, T.P., Vygranenko, K.V., Lukash, L.L., Yarmoluk, S.M.

    Published in Bioorganic & medicinal chemistry (01-05-2016)
    “…[Display omitted] Fibroblast growth factor receptor 1 (FGFR1) plays an important role in tumorigenesis and is therefore an attractive target for anticancer…”
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    The action of the tumour promoter, TPA, on mutagenesis induced by different agents (UV light, chemical and viral mutagens) by Manuilova, E S, Lukash, L L, Shapiro, N I

    Published in Mutation research (01-08-1987)
    “…The present paper deals with effects of 12-O-tetradecanoylphorbol-13-acetate (TPA) on the frequency of induced mutations to 6-mercaptopurine (6MP) and ouabain…”
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