2011
DOI: 10.3109/14756366.2011.631536
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Synthesis, antibacterial, antielastase, antiurease and antioxidant activities of new methoxy substitued bis-1,2,4-triazole derivatives

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Cited by 16 publications
(9 citation statements)
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“…17 Moreover, it has been indicated in several reports that bisheterocyclic compounds displayed much better antibacterial activity than mono-heterocyclic compounds. [18][19][20][21] In view of these observations, and also in continuation of our previous work on the synthesis of bis-heterocyclic compounds, [22][23][24][25] we now report the synthesis of some novel pyridine bis-1,2,4-triazoles and bis-1,3,4-thiadiazoles.…”
mentioning
confidence: 54%
“…17 Moreover, it has been indicated in several reports that bisheterocyclic compounds displayed much better antibacterial activity than mono-heterocyclic compounds. [18][19][20][21] In view of these observations, and also in continuation of our previous work on the synthesis of bis-heterocyclic compounds, [22][23][24][25] we now report the synthesis of some novel pyridine bis-1,2,4-triazoles and bis-1,3,4-thiadiazoles.…”
mentioning
confidence: 54%
“…In addition, Rodis and Digenis [68] reported that low molecular weight thiocarbamate compounds also have inhibitory effect on leukocyte elastase activity. Sokmen et al showed that triazole compounds which include halogen, carboxylate, heterocyclic sulfide, sulfone, and/or methoxy groups in their structure inhibit elastase enzyme [42]. In our study, it can be assumed that compounds which have halogen and sulfoxide groups in their structure inhibit elastase enzyme, yet, not in high ratio.…”
Section: Enzyme Inhibitionmentioning
confidence: 75%
“…Elastase (EC: 3.4.21.37) is a serine protease of the chymotrypsin family that hydrolytically degrades extracellular matrix components such as elastin, fibronectin, collagen, proteoglycans, laminin, and some matrix metalloproteinases [42]. This enzyme is particularly abundant in the skin, arteries, lungs, and ligaments.…”
Section: Introductionmentioning
confidence: 99%
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“…The inhibition was increased with increasing dihydroxy coumarin concentration ( 44 . Previous studies have shown that the attachment of various leaving groups (halogen, carboxylate, heterocyclic sulfide, sulfone, methoxy) to the triazole compound yields highly potent inhibitors of human leukocyte elastase 45 . We have demonstrated the potency of the dihydroxy coumarin derivatives to inhibit elastase.…”
Section: ' -( Et H a N E -1 2 -D I Y L B I S ( P H E N Y L A Z A mentioning
confidence: 99%