Literature DB >> 17239490

Clubbed triazoles: a novel approach to antitubercular drugs.

Mahendra Shiradkar1, Gorentla Venkata Suresh Kumar, Varaprasad Dasari, Suresh Tatikonda, Kalyan Chakravarthy Akula, Rachit Shah.   

Abstract

In last few decades, though significant progress has been made in the treatment and control strategies of tubercular infections by introducing new diagnostic and monitoring tools and combination therapy, it still continues to be a severe problem. Thus with the aim of developing novel molecules with improved potency for treating Mycobacterium tuberculosis H37Rv strain infections and with decreased probability of developing drug resistance, herein we report the synthesis of thiazolyl triazole derivatives, starting from ethyl acetoacetate, by microwave organic reaction enhancement method (MORE) and results of investigations of their antimycobacterial and antimicrobial activities. Many compounds have shown promising activity while others were inactive.

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Year:  2006        PMID: 17239490     DOI: 10.1016/j.ejmech.2006.12.001

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  9 in total

1.  Evaluation of the anti-Schistosoma mansoni activity of thiosemicarbazones and thiazoles.

Authors:  Edna de Farias Santiago; Sheilla Andrade de Oliveira; Gevânio Bezerra de Oliveira Filho; Diogo Rodrigo Magalhaes Moreira; Paulo André Teixeira Gomes; Anekécia Lauro da Silva; Andréia Ferreira de Barros; Aline Caroline da Silva; Thiago André Ramos Dos Santos; Valéria Rêgo Alves Pereira; Gabriel Gazzoni Araújo Gonçalves; Fábio André Brayner; Luiz Carlos Alves; Almir Gonçalves Wanderley; Ana Cristina Lima Leite
Journal:  Antimicrob Agents Chemother       Date:  2013-10-28       Impact factor: 5.191

2.  Methyl (Z)-3-({5-[(E)-(tert-butyl-amino)-methyl-idene]-4-oxo-4,5-dihydro-1,3-thia-zol-2-yl}sulfan-yl)prop-2-enoate.

Authors:  Robabeh Baharfar; Nasim Porahmad; S Mohammad Vahdat
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-08-18

3.  Anti-inflammatory and antinociceptive evaluation of newly synthesized 4-(substituted ethanoyl) amino-3-mercapto-5-(4-methoxy) phenyl-1,2,4-triazoles.

Authors:  Neeraj Upmanyu; Jeetendra Kumar Gupta; Kamal Shah; Pradeep Mishra
Journal:  J Pharm Bioallied Sci       Date:  2011-04

4.  2-Anilino-3-(2-hy-droxy-prop-yl)-4-methyl-1,3-thia-zol-3-ium chloride.

Authors:  Shaaban K Mohamed; Mehmet Akkurt; Muhammad N Tahir; Antar A Abdelhamid; Ali N Khalilov
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-05-26

5.  A facile access and evaluation of some novel thiazole and 1,3,4-thiadiazole derivatives incorporating thiazole moiety as potent anticancer agents.

Authors:  Sobhi M Gomha; Mohamad R Abdelaziz; Nabila A Kheder; Hassan M Abdel-Aziz; Seham Alterary; Yahia N Mabkhot
Journal:  Chem Cent J       Date:  2017-10-16       Impact factor: 4.215

6.  Synthesis, docking study and biological evaluation of some new thiourea derivatives bearing benzenesulfonamide moiety.

Authors:  Mostafa M Ghorab; Mohamed S A El-Gaby; Aiten M Soliman; Mansour S Alsaid; Marwa M Abdel-Aziz; Mahmoud M Elaasser
Journal:  Chem Cent J       Date:  2017-05-19       Impact factor: 4.215

7.  A facile synthesis and anticancer activity of some novel thiazoles carrying 1,3,4-thiadiazole moiety.

Authors:  Sobhi M Gomha; Nabila A Kheder; Mohamad R Abdelaziz; Yahia N Mabkhot; Ahmad M Alhajoj
Journal:  Chem Cent J       Date:  2017-03-21       Impact factor: 4.215

8.  Synthesis and Characterization of Some New Bis-Pyrazolyl-Thiazoles Incorporating the Thiophene Moiety as Potent Anti-Tumor Agents.

Authors:  Sobhi M Gomha; Mastoura M Edrees; Farag M A Altalbawy
Journal:  Int J Mol Sci       Date:  2016-09-07       Impact factor: 5.923

9.  Synthesis, Characterization and Molecular Docking of Novel Bioactive Thiazolyl-Thiazole Derivatives as Promising Cytotoxic Antitumor Drug.

Authors:  Sobhi M Gomha; Taher A Salaheldin; Huwaida M E Hassaneen; Hassan M Abdel-Aziz; Mohammed A Khedr
Journal:  Molecules       Date:  2015-12-22       Impact factor: 4.411

  9 in total

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