Antimicrobial activity of a series of thiosemicarbazones and their ZnII and PdII complexes
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[1] K. Waisser,et al. New antimycobacterial 2,3-dihydro-1-alkylindole-2-thiones , 2008, Folia Microbiologica.
[2] R. Doležal,et al. 1-Aryl-5-benzylsulfanyltetrazoles, a new group of antimycobacterial compounds against potentially pathogenic strains , 2008, Folia Microbiologica.
[3] P. Pelagatti,et al. Copper complexes of imidazole-2-, pyrrole-2- and indol-3-carbaldehyde thiosemicarbazones: inhibitory activity against fungi and bacteria. , 2005, Journal of inorganic biochemistry.
[4] P. Yogeeswari,et al. Synthesis and evaluation of anti-HIV activity of isatin β-thiosemicarbazone derivatives , 2005 .
[5] V. Onnis,et al. In vitro antimycobacterial activity of newly synthesised S-alkylisothiosemicarbazone derivatives and synergistic interactions in combination with rifamycins against Mycobacterium avium. , 2005, International journal of antimicrobial agents.
[6] C. Supuran,et al. Organometallic-based antibacterial and antifungal compounds: transition metal complexes of 1,1′-diacetylferrocene-derived thiocarbohydrazone, carbohydrazone, thiosemicarbazone and semicarbazone , 2005, Journal of enzyme inhibition and medicinal chemistry.
[7] K. Waisser,et al. New antimycobacterial S-alkylisothiosemicarbazones. , 2005, Folia microbiologica.
[8] T. Varadinova,et al. Toxic effects of bis(thiosemicarbazone) compounds and its palladium(II) complexes on herpes simplex virus growth. , 2004, Toxicology and applied pharmacology.
[9] B. Akkurt,et al. Zn(II) and Pd(II) Complexes of Thiosemicarbazone‐S‐alkyl Esters Derived from 2/3‐Formylpyridine , 2004 .
[10] D. Richardson,et al. Novel aroylhydrazone and thiosemicarbazone iron chelators with anti-malarial activity against chloroquine-resistant and -sensitive parasites. , 2004, The international journal of biochemistry & cell biology.
[11] R. Butcher,et al. Spectroscopic, structural and antibacterial properties of copper(II) complexes with bio-relevant 5-methyl-3-formylpyrazole N(4)-benzyl-N(4)-methylthiosemicarbazone , 2003, Molecular and Cellular Biochemistry.
[12] B. Ülküseven,et al. POTENTIOMETRIC INVESTIGATION OF Fe(IlI),Ni(II) AND Cu(II) COMPLEXES OF SOME ISATIN AND THIOPHENE ISOTHIOSEMICARBAZONES , 2004 .
[13] Shailendra,et al. New palladium(II) complexes of 5-nitrothiophene-2-carboxaldehyde thiosemicarbazones. synthesis, spectral studies and in vitro anti-amoebic activity. , 2003, Bioorganic & medicinal chemistry.
[14] E. De Clercq,et al. Anti‐HIV Activity of Thiosemicarbazone and Semicarbazone Derivatives of (±)‐3‐Menthone , 2002, Archiv der Pharmazie.
[15] V. Onnis,et al. Synthesis and antimycobacterial activity of new S-alkylisothiosemicarbazone derivatives. , 2002, Bioorganic & medicinal chemistry.
[16] T. Varadinova,et al. Antiviral activity of platinum (II) and palladium (II) complexes of pyridine-2-carbaldehyde thiosemicarbazone. , 2001, Acta virologica.
[17] N. C. Kasuga,et al. Synthesis, structural characterization and antimicrobial activities of 4- and 6-coordinate nickel(II) complexes with three thiosemicarbazones and semicarbazone ligands. , 2001, Journal of inorganic biochemistry.
[18] E. Maccioni,et al. Synthesis and antimicrobial activity of novel arylideneisothiosemicarbazones. , 2000, Farmaco.
[19] Mary Jane Ferraro,et al. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically : approved standard , 2000 .
[20] W. Denny,et al. Nitrogen, sulfur and oxygen donor adducts with copper(II) complexes of antitumor 2-formylpyridinethiosemicarbazone analogs: physicochemical and cytotoxic studies. , 1998, Journal of inorganic biochemistry.
[21] Paul D. Bloom,et al. Structures and spectral properties of palladium(II) complexes of 2-acetylpyridine N(4)-dimethylthiosemicarbazone , 1996 .
[22] C. Carlberg,et al. Thiazolidine Diones, Specific Ligands of the Nuclear Receptor Retinoid Z Receptor/Retinoid Acid Receptor-related Orphan Receptor α with Potent Antiarthritic Activity* , 1996, The Journal of Biological Chemistry.
[23] B. Ülküseven. Studies of the S-Ethylthiosemicarbazones with Cu(I), Zn(II), Cd(II), Hg(II) Chloride Salts , 1995 .
[24] S. Martelli,et al. Antibacterial activity of metal complexes of benzil and benzoin thiosemicarbazones. , 1994, Farmaco.
[25] S. Martelli,et al. Synthesis, antibacterial and antifungal activity of metal (II) complexes of 2-acetylpyridine thiosemicarbazones. , 1993, Farmaco.
[26] A. De Logu,et al. Antimicrobial activity of some isothiosemicarbazones. , 1990, Farmaco.
[27] S. Smith,et al. Thiosemicarbazones of 2-acetylpyridine, 2-acetylquinoline, 1-acetylisoquinoline, and related compounds as inhibitors of herpes simplex virus in vitro and in a cutaneous herpes guinea pig model. , 1986, Antiviral research.
[28] G. Kauffman,et al. Transition metal complexes of semicarbazones and thiosemicarbazones , 1985 .
[29] R. Amlacher. Route-dependent different relations between acute and subacute toxicity of the potential antiviral agent benzoxazolyl-2-formyl-S-ethyl-isothiosemicarbazone in mice. , 1985, Die Pharmazie.
[30] J. Raynaud,et al. Présence de (6″-O-acétyl)glucosyl-3-quercétine chez Doronicum grandiflorum Lam. (Compositae) , 1985 .
[31] A. Omar,et al. SYNTHESES OF SOME SUBSTITUTED ISATIN β-THIOSEMICARBAZONES AND ISATIN β-HYDRAZONOTHIAZOLINE DERIVATIVES AS POTENTIAL ANTIVIRAL AND ANTIMICROBIAL AGENTS , 1984 .
[32] D. Tresselt,et al. [Complex formation of antiviral isatin-3-isothiosemicarbazones and thiocarbonylhydrazones using transition-group metals]. , 1977, Die Pharmazie.
[33] M. Campbell. Transition metal complexes of thiosemicarbazide and thiosemicarbazones , 1975 .
[34] C. Yamazaki. The Structure of Isothiosemicarbazones , 1975 .
[35] F. Gialdi,et al. [Antibacterial activity of quinoline derivatives. V. Preparation and in vitro antibacterial activity of 6-6-diquinolylsulfone and various thiosemicarbazones of quinoline aldehydes]. , 1951, Il Farmaco, scienza e tecnica.