2008
DOI: 10.1016/j.bmcl.2008.04.033
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Synthesis and anti-Helicobacter pylori activity of 5-(nitroaryl)-1,3,4-thiadiazoles with certain sulfur containing alkyl side chain

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Cited by 40 publications
(22 citation statements)
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“…Nowadays, for developing new potential anti-H. pylori candidates, scientists in the medicinal chemistry field are also equally concerned with the creation of new synthetic drug compounds (Foroumadi et al, 2008a(Foroumadi et al, ,b, 2009aLetafat et al, 2008;Mohammadhosseini et al, 2008Mohammadhosseini et al, , 2009Moshafi et al, 2011;Tafti et al, 2011). Complementary and alternative modes of treatment, particularly non-toxic, natural, and inexpensive products are attractive.…”
Section: Introductionmentioning
confidence: 99%
“…Nowadays, for developing new potential anti-H. pylori candidates, scientists in the medicinal chemistry field are also equally concerned with the creation of new synthetic drug compounds (Foroumadi et al, 2008a(Foroumadi et al, ,b, 2009aLetafat et al, 2008;Mohammadhosseini et al, 2008Mohammadhosseini et al, , 2009Moshafi et al, 2011;Tafti et al, 2011). Complementary and alternative modes of treatment, particularly non-toxic, natural, and inexpensive products are attractive.…”
Section: Introductionmentioning
confidence: 99%
“…Ponadto większość pochodnych pozostaje aktywna również przy mniejszych stężeniach, tj. 2-4 µg na płytkę (strefa zahamowania wzrostu > 20 mm) w prze-ciwieństwie do MTZ, który w takich dawkach ma niewielką aktywność przeciwbakteryjną [41,42].…”
Section: Nowe Substancjeunclassified
“…As illustrated in Figure 1, the key intermediate compounds, 4a-c were synthesised according to the general methods previously described by us [20]. The purity of the synthesised compounds was confirmed by thin layer chromatography (TLC) using various solvents of different polarities.…”
Section: Chemistrymentioning
confidence: 99%
“…The oxidative cyclisation of 1a-c in the presence of NH 4 Fe(SO 4 ) 2 caused the formation of 2-amino-1,3,4-thiadiazoles 2a-c. The diazotation and the subsequent chlorination of 2a-c in hydrochloric acid in the presence of NaNO 2 and copper powder afforded 3a-c, which then reacted with an equivalent amount of thiourea in refluxing EtOH to produce 4a-c [20]. The reaction of compound 4a-c with appropriate phenacyl bromide in stirring KOH/EtOH gave the target compounds 5-13; while the treatment of 4a,b with 3-chloro-1-phenylpropan-1-one, 2-chloro-1-phenylpropan-1-one or (1-chloroethyl)benzene in stirring KOH/EtOH afforded target compounds 14-19.…”
Section: Chemistrymentioning
confidence: 99%