2000
DOI: 10.1515/hc.2000.6.5.421
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Synthesis and Antibacterial Activity of some Heterocyclic β-Enamino Ester Derivatives with 1,2,3-triazole

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Cited by 81 publications
(32 citation statements)
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“…Compounds (26a-c) and (27) inhibited the growth of H 37 Rv strain at concentrations of 8 lg/mL. These compounds (26,27) found even active in the concentrations 32-64 lg/ mL. From SAR, the 2-mercaptobenzothiazoles conjugated to 1,2,3-triazole ring were more active when compared to the aromatic/aliphatic/cyclic secondary amines attached through an amide linkage.…”
Section: 23-triazole Derivatives For Treatment Of Tuberculosismentioning
confidence: 95%
“…Compounds (26a-c) and (27) inhibited the growth of H 37 Rv strain at concentrations of 8 lg/mL. These compounds (26,27) found even active in the concentrations 32-64 lg/ mL. From SAR, the 2-mercaptobenzothiazoles conjugated to 1,2,3-triazole ring were more active when compared to the aromatic/aliphatic/cyclic secondary amines attached through an amide linkage.…”
Section: 23-triazole Derivatives For Treatment Of Tuberculosismentioning
confidence: 95%
“…Gill et al reported some novel [1,2,3] triazoles clubbed with fluorine benzimidazole (5) series of H37Rv strain inhibitors which were found to be potentially active against Mycobacterium tuberculosis on the basis of promising results of preliminary antimicrobial study. Some of the derivatives under further evaluation are showing improved activity compared to rifampin [31].…”
Section: Pharmacological Significance Of Triazole Scaffoldmentioning
confidence: 99%
“…It follows from the literature that the triazole derivatives possess a wide range of pharmacological activities such as antimicrobial [3,4], analgesic [5], anti-inflammatory, local anaesthetic [6], anticonvulsant [7], antineoplastic [8], antimalarial [9], antiviral [10], antiproliferative [11], and anticancer activities [12]. Many triazole-based derivatives are available as medicines [13].…”
Section: Introductionmentioning
confidence: 99%
“…On the other hand, 1,2,3-triazoles and their derivatives have emerged as powerful pharmacophores [23], gaining interest for their various biological activities [24e26] as chemotherapeutic agents [27,28], potent antimicrobial [29], anti-inflammatory [30,31], local anaesthetic [32], anticonvulsant [33], antineoplastic [34], antimalarial [35] and antiviral activity [36]. Considering such a biological importance of 1,2,3-triazoles, a new series of the diarylhetherocycles having the aryl groups positioned on N 1 and C 4 of the triazole nucleus was projected to explore further productive and selective interactions with COXs active site.…”
Section: Designmentioning
confidence: 99%