نتایج جستجو برای: thiosemicarbazones

تعداد نتایج: 522  

2016
Brian J. Anderson Jerry P. Jasinski Michael B. Freedman Sean P. Millikan Kelly A. O’Rourke Victoria A. Smolenski

The crystal and molecular structures of three new thiosemicarbazones, 2-[1-(2-hydroxy-5-methoxyphenyl)ethylidene]-N-methyl-hydrazinecarbothioamide monohydrate (1), 2-[1-(2-hydroxy-5-methoxyphenyl)ethylidene]-N-ethyl-hydrazinecarbothioamide (2) and 2-[1-(2-hydroxy-4-methoxyphenyl)ethylidene]-N-ethyl-hydrazinecarbothioamide acetonitrile solvate (3), are reported and confirmed by single crystal X-...

Journal: :Cancer research 1971
E C Moore B A Booth A C Sartorelli

inhibited mammalian ribonucleoside diphosphate reductase in vitro. The inhibition was partially reversed by increasing the concentration of the dithiol substrate, but not of ferrous ion, magnesium ion, nucleotide substrate, or allosteric activator. Increasing the concentration of ferrous ion resulted in greater enzymic inhibition, a finding that is consistent with a model in which either the ac...

Journal: :Molecules 2012
Maciej Serda Anna Mrozek-Wilczkiewicz Josef Jampilek Matus Pesko Katarina Kralova Marcela Vejsova Robert Musiol Alicja Ratuszna Jaroslaw Polanski

Two series of thiosemicarbazone-based iron chelators (twenty-seven compounds) were designed and synthesized using a microwave-assisted approach. Quinoline and halogenated phenyl were selected as parent scaffolds on the basis of a similarity search. The lipophilicity of the synthesized compounds was measured using HPLC and then calculated. Primary in vitro screening of the synthesized compounds ...

Journal: :Metal-Based Drugs 1997
Iris H. Hall Merrill C. Miller Douglas X. West

Nickel(II) complexes of thiosemicarbazons were observed to be potent cytotoxic agents in human and rodent tissue cultured tumor cells. Each compound demonstrated a slightly different profile in the various histological types of tumors. The nickel complex of Appip demonstrated the most potent in vivo activity in the Ehrlich ascites carcinoma. This agent selectively inhibited L1210 DNA and purine...

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