Literature DB >> 16188319

Copper complexes of imidazole-2-, pyrrole-2- and indol-3-carbaldehyde thiosemicarbazones: inhibitory activity against fungi and bacteria.

María C Rodríguez-Argüelles1, Estefania C López-Silva, Jesús Sanmartín, P Pelagatti, Franca Zani.   

Abstract

Copper complexes of thiosemicarbazones of imidazole-2-carbaldehyde, pyrrole-2-carbaldehyde and indole-3-carbaldehyde were synthesised and characterised. The antimicrobial properties of the free ligands and their complexes were evaluated against yeasts, moulds and bacteria (Gram-positive and Gram-negative). Some copper chelates exhibited a moderate inhibitory activity, better than that of the corresponding free ligands. In particular, the pyrrole derivative [Cu(HL(2))(2)] proved to be a wide spectrum agent, showing an interesting inhibition of the growth of all Gram-positive bacteria and fungi tested at concentrations of 12-50 microg/mL. In contrast, a selective effect was observed for imidazole and indole chelates against fungi and Gram-positive bacteria, respectively.

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Year:  2005        PMID: 16188319     DOI: 10.1016/j.jinorgbio.2005.07.018

Source DB:  PubMed          Journal:  J Inorg Biochem        ISSN: 0162-0134            Impact factor:   4.155


  16 in total

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Journal:  J Biol Inorg Chem       Date:  2012-12-29       Impact factor: 3.358

2.  Novel palladium (II) complexes with tetradentate thiosemicarbazones. Synthesis, characterization, in vitro cytotoxicity and xanthine oxidase inhibition.

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Journal:  Invest New Drugs       Date:  2019-03-14       Impact factor: 3.850

3.  1H-Indole-3-carbaldehyde thio-semi-carbazone.

Authors:  Razali M Rizal; Hapipah M Ali; Seik Weng Ng
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-04-26

4.  Synthesis and biological evaluation of (acyl)hydrazones and thiosemicarbazones obtained via in situ condensation of iminium salts with nitrogen-containing nucleophiles.

Authors:  Chiara Caneva; Silvana Alfei; Monica De Maria; Cristina Ibba; Ilenia Delogu; Andrea Spallarossa; Roberta Loddo
Journal:  Mol Divers       Date:  2015-06-16       Impact factor: 3.364

5.  Antibacterial, antifungal and in vitro antileukaemia activity of metal complexes with thiosemicarbazones.

Authors:  Elena Pahontu; Felicia Julea; Tudor Rosu; Victor Purcarea; Yurie Chumakov; Petru Petrenco; Aurelian Gulea
Journal:  J Cell Mol Med       Date:  2015-02-24       Impact factor: 5.310

6.  Synthesis, characterization, biological evaluation and molecular docking studies of 2-(1H-benzo[d]imidazol-2-ylthio)-N-(substituted 4-oxothiazolidin-3-yl) acetamides.

Authors:  Snehlata Yadav; Balasubramanian Narasimhan; Siong M Lim; Kalavathy Ramasamy; Mani Vasudevan; Syed Adnan Ali Shah; Manikandan Selvaraj
Journal:  Chem Cent J       Date:  2017-12-22       Impact factor: 4.215

7.  Synthesis and evaluation of antimicrobial, antitubercular and anticancer activities of 2-(1-benzoyl-1H-benzo[d]imidazol-2-ylthio)-N-substituted acetamides.

Authors:  Snehlata Yadav; Siong Meng Lim; Kalavathy Ramasamy; Mani Vasudevan; Syed Adnan Ali Shah; Abhishek Mathur; Balasubramanian Narasimhan
Journal:  Chem Cent J       Date:  2018-05-26       Impact factor: 4.215

8.  N'-[4-[(Substituted imino)methyl]benzylidene]-substituted benzohydrazides: synthesis, antimicrobial, antiviral, and anticancer evaluation, and QSAR studies.

Authors:  Pradeep Kumar; Balasubramanian Narasimhan; Kalavathy Ramasamy; Vasudevan Mani; Rakesh Kumar Mishra; Abu Bakar Abdul Majeed; Erik De Clercq
Journal:  Monatsh Chem       Date:  2012-12-01       Impact factor: 1.451

9.  Antimicrobial activity of a series of thiosemicarbazones and their Zn(II) and Pd(II) complexes.

Authors:  I Kizilcikli; Y D Kurt; B Akkurt; A Y Genel; S Birteksöz; G Otük; B Ulküseven
Journal:  Folia Microbiol (Praha)       Date:  2007       Impact factor: 2.629

10.  Synthesis and evaluation of novel pyrroles and pyrrolopyrimidines as anti-hyperglycemic agents.

Authors:  M S Mohamed; S A Ali; D H A Abdelaziz; Samar S Fathallah
Journal:  Biomed Res Int       Date:  2014-06-26       Impact factor: 3.411

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