Literature DB >> 19939519

Synthesis and antimicrobial activity evaluation of new 1,2,4-triazoles and 1,3,4-thiadiazoles bearing imidazo[2,1-b]thiazole moiety.

Nuray Ulusoy Güzeldemirci1, Omer Küçükbasmaci.   

Abstract

A series of 4-alkyl/aryl-2,4-dihydro-5-((6-(4-bromophenyl)imidazo[2,1-b]thiazol-3-yl)methyl)-3H-1,2,4-triazole-3-thiones (3a-i) and 2-alkyl/arylamino-5-((6-(4-bromophenyl)imidazo[2,1-b]thiazol-3-yl)methyl)-1,3,4-thiadiazoles (4a-c) were synthesized starting from 6-(4-bromophenyl)imidazo[2,1-b]thiazole-3-acetic acid hydrazide. The newly synthesized compounds were characterized by IR, (1)H NMR, mass and elemental analysis. All compounds were tested for antibacterial and antifungal activities. The antimicrobial activities of the compounds were assessed by the microbroth dilution technique. The compounds were also evaluated for antituberculosis activity against Mycobacterium tuberculosis H37Rv (ATCC 27294). The preliminary results revealed that some of the compounds exhibited promising antimicrobial activities. Copyright 2009 Elsevier Masson SAS. All rights reserved.

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Year:  2009        PMID: 19939519     DOI: 10.1016/j.ejmech.2009.09.024

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


  16 in total

Review 1.  Isocyanide-Based Multicomponent Reactions in Water: Advanced Green Tools for the Synthesis of Heterocyclic Compounds.

Authors:  Siamak Javanbakht; Mohammad Taghi Nazeri; Hassan Farhid; Tahereh Nasiriani; Vida Khodkari; Ahmad Shaabani
Journal:  Top Curr Chem (Cham)       Date:  2022-09-22

2.  A structure-activity relationship study on multi-heterocyclic molecules: two linked thiazoles are required for cytotoxic activity.

Authors:  Seong Jong Kim; Chun Chieh Lin; Chung-Mao Pan; Dimple P Rananaware; Deborah M Ramsey; Shelli R McAlpine
Journal:  Medchemcomm       Date:  2012-11-29       Impact factor: 3.597

3.  Microwave-assisted Hantzsch thiazole synthesis of N-phenyl-4-(6-phenylimidazo[2,1-b]thiazol-5-yl)thiazol-2-amines from the reaction of 2-chloro-1-(6-phenylimidazo[2,1-b]thiazol-5-yl)ethanones and thioureas.

Authors:  Sukanta Kamila; Kimberly Mendoza; Edward R Biehl
Journal:  Tetrahedron Lett       Date:  2012-07-03       Impact factor: 2.415

4.  Antibacterial, Antitubercular and Antiviral Activity Evaluations of Some Arylidenehydrazide Derivatives Bearing Imidazo[2,1-b]thiazole Moiety.

Authors:  Nuray Ulusoy Güzeldemirci; Berin Karaman; Ömer Küçükbasmaci
Journal:  Turk J Pharm Sci       Date:  2017-08-15

5.  2-[6-(4-Chloro-phen-yl)imidazo[2,1-b][1,3]thia-zol-2-yl]-N'-[(E)-4-meth-oxy-benzyl-idene]acetohydrazide.

Authors:  Mehmet Akkurt; Nuray Ulusoy Güzeldemirci; Berin Karaman; Orhan Büyükgüngör
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-12-18

6.  1-(4-Chloro-phen-yl)-3-{5-[(E)-2-phenyl-ethen-yl]-1,3,4-thia-diazol-2-yl}urea.

Authors:  Xiu-Huan Zhan; Zi-Yun Wang
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-01-29

7.  2-[6-(4-Bromo-phen-yl)imidazo[2,1-b][1,3]thia-zol-3-yl]-N-[8-(4-hy-droxy-phen-yl)-2-methyl-3-oxo-1-thia-4-aza-spiro-[4.5]decan-4-yl]acetamide ethanol disolvate.

Authors:  Mehmet Akkurt; Elif Gürsoy; Nuray Ulusoy Güzeldemirci; Sevim Türktekin-Çelikesir; Muhammad Nawaz Tahir
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-04-21

8.  6-(4-Chloro-phen-yl)-3-methyl-imidazo[2,1-b]thia-zole.

Authors:  Alexander S Bunev; Elena V Sukhonosova; Vladimir E Statsyuk; Gennady I Ostapenko; Victor N Khrustalev
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-10-26

Review 9.  2-Amino-1,3,4-thiadiazole as a potential scaffold for promising antimicrobial agents.

Authors:  Georgeta Serban; Oana Stanasel; Sanda Bota; Eugenia Serban
Journal:  Drug Des Devel Ther       Date:  2018-05-31       Impact factor: 4.162

10.  Antimicrobial Activity of Some Novel Armed Thiophene Derivatives and Petra/Osiris/Molinspiration (POM) Analyses.

Authors:  Yahia Nasser Mabkhot; Fatima Alatibi; Nahed Nasser E El-Sayed; Salim Al-Showiman; Nabila Abdelshafy Kheder; Abdul Wadood; Abdur Rauf; Saud Bawazeer; Taibi Ben Hadda
Journal:  Molecules       Date:  2016-02-17       Impact factor: 4.411

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