2017
DOI: 10.1039/c7ra04819j
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Synthesis of novel 1,2,4-triazole derivatives containing the quinazolinylpiperidinyl moiety and N-(substituted phenyl)acetamide group as efficient bactericides against the phytopathogenic bacterium Xanthomonas oryzae pv. oryzae

Abstract: Some 1,2,4-triazole derivatives containing the quinazolinylpiperidinyl moiety andN-(substituted phenyl)acetamide group were developed as efficient bactericides against pathogenic bacteriumXoo.

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Cited by 42 publications
(37 citation statements)
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“…Antibacterial activities of target compounds 7a – 7r against three pathogenic bacteria ( Xoo , Rs , and Xac ) were firstly evaluated at 200 and 100 μg/mL in vitro , based on the turbidimetric method . At the same time, commercial agrobactericides Bismerthiazol (BMT) and Thiodiazole‐copper (TDC) were chosen as positive control agents.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Antibacterial activities of target compounds 7a – 7r against three pathogenic bacteria ( Xoo , Rs , and Xac ) were firstly evaluated at 200 and 100 μg/mL in vitro , based on the turbidimetric method . At the same time, commercial agrobactericides Bismerthiazol (BMT) and Thiodiazole‐copper (TDC) were chosen as positive control agents.…”
Section: Resultsmentioning
confidence: 99%
“…The synthesized compounds were evaluated for antibacterial activity against Xoo and Xcc in vitro by the turbidimeter test . Commercial agricultural antibacterial Bismerthiazol was used as control.…”
Section: Antimicrobial Bioassaymentioning
confidence: 99%
“…Yang and Bao synthesized 1,2,4-triazole derivatives 50 bearing quinazolinylpiperidinyl moiety and N -(substituted phenyl)acetamide unit ( Fig. 8 ) and evaluated them for their antimicrobial activities [ 66 ]. Compounds 50e , 50g , 50i , 50l and 50n (EC 50 : 34.5–47.5 μ g/mL) had better bactericidal activity than control bismerthiazol (85.6 μ g/mL) against phytopathogenic bacterium X. oryzae pv.…”
Section: Biological Activities Of 124-triazole Derivativesmentioning
confidence: 99%
“…By considering the diverse range of activities of quinazoline and triazole scaffolds, Yang et al designed hybrid analogues by linking these motifs together. 109 Molecules were designed with the following rationale: (a) 1,2,4-triazole-based analogues are well reported with anti-bacterial activities, 105,110,111 with Triadimefon, Triadimenol, Diniconazole, Flusilazole, and Difenoconazole, which are clinically used agrofungicides. (b) The quinazoline moiety is found in many pesticidal drugs such as Fluquinconazole and Pyriuquinazon.…”
Section: Anti-tubercular Hybridsmentioning
confidence: 99%