Antimicrobial activity of a series of thiosemicarbazones and their ZnII and PdII complexes

[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.