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Akademický článek
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Autor:
Shigehiro Tohyama, Masayuki Igarashi, Kazuaki Matoba, Ryuichi Sawa, Hiroyuki Inoue, Hideyuki Muramatsu, Manabu Kawada, Masaki Hatano
Publikováno v:
The Journal of Antibiotics. 74:743-751
Specific inhibitors of protein phosphatase 2A (PP2A) mediate anticancer effects by augmenting the tumor-killing activity of natural killer (NK) cells. In this study, new PP2A inhibitors, aminocytostatins A-E, were isolated from Kitasatospora sp. MJ65
Autor:
Anne-Frédérique Salit, Christophe Meyer, Benedicte Delouvrie, Janine Cossy, Laurent Francois Andre Hennequin
Publikováno v:
Tetrahedron. 64:6684-6697
Synthetic approaches toward the natural product cytostatin, an inhibitor of protein phosphatase 2A possessing cytotoxic and antimetastatic activities, have been investigated. A formal synthesis of cytostatin has been achieved according to a strategy
Publikováno v:
Synlett. 2007:0934-0938
A formal synthesis of cytostatin, an antitumor agent, has been achieved according to a convergent approach involving the coupling of a functionalized organolithium (C1-C8 subunit) with an aldehyde (C9-C13 subunit).
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 65:874-887
Fostriecin (CI-920), isolated from Streptomyces pulveraceus, shows in vitro antitumor activity against leukemia, lung breast and ovarian cancer, and in vivo against L 1210 and P 388 leukemia. Its analogous compounds, such as leustroducsins, phoslacto
Autor:
Laurent Bialy, Herbert Waldmann
Publikováno v:
Angewandte Chemie International Edition. 41:1748-1751
Autor:
Laurent Bialy, Herbert Waldmann
Publikováno v:
Angewandte Chemie. 114:1819-1822
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1452(2):209-217
Cytostatin, which is isolated from a microbial cultured broth as a low molecular weight inhibitor of cell adhesion to extracellular matrix (ECM), has anti-metastatic activity against B16 melanoma cells in vivo. In this study, we examined a target of
Autor:
Keith C. Ellis, James A. Marshall
Publikováno v:
Tetrahedron Letters. 45:1351-1353
A 12-step synthesis of a C3–C13 precursor of the protein phosphatase inhibitor cytostatin is described. Key stereocenters were introduced by a chiral allenylzinc addition and Noyori asymmetric-transfer hydrogenation.