New N’-(arylidene)-2-[6-(4-bromophenyl)imidazo[2,1-b]thiazol-3-yl]acetohydrazides (3a-i) were synthesized by reacting 2-[6-(4-bromophenyl)imidazo[2,1-b]thiazol-3-yl]acetohydrazide with different aromatic aldehydes. The structures of the title compounds were established by spectral data (IR, 1H NMR, 13C NMR) and elemental analyses. The synthesized compounds were evaluated for in vitro antimycobacterial activity against Mycobacterium tuberculosis H37Rv employing the BACTEC 460 radiometric system. The compounds exhibited varying degrees of inhibition in the in vitro primary screening that was conducted at a concentration of 6.25 mg/ml. Among the synthesized compounds [6-(4-bromophenyl) imidazo[2,1-b]thiazol-3-yl]acetic acid 2,4-dinitrobenzylidenehydrazide (3e) was found to be the most active compound in vitro with MIC of 6.25 mg/ml.
2-[6-(4-Bromofenil)imidazo[2,1-b]tiyazol-3-il]asetohidrazit ile farklı aromatik aldehitlerin
reaksiyonundan yeni N’- (ariliden)-2-[6-(4-bromofenil)imidazo[2,1-b]tiyazol-3-il] asetohidrazitler (3a-i) elde edilmiştir. Elde
edilen bileşiklerin yapıları spektral
veriler (IR, 1H NMR, 13C NMR) ve elementel
analiz ile saptanmıştır. Sentezlenen bileşiklerin Mycobacterium tuberculosis H37Rv’ye karşı
antimikobakteriyel aktiviteleri BACTEC
460 radyometrik sistem kullanılarak tayin edilmiştir. Bileşikler, 6.25 mg/ml konsantrasyonda
gerçekleştirilen in vitro primer tarama
testlerinde değişik derecelerde inhibisyon
göstermişlerdir. Sentezlenen bileşikler arasında [6-(4-bromofenil)imidazo[2,1-b]tiyazol-3-il]asetik
asit 2,4-dinitrobenzilidenhidrazit (3e),
in vitro 6.25 mg/ml MIC değeri ile
aktivitesi en yüksek bileşik olarak bulunmuştur.
Subjects | Health Care Administration |
---|---|
Journal Section | Articles |
Authors | |
Publication Date | September 20, 2016 |
Published in Issue | Year 2017 Volume: 21 Issue: 1 |
.