Location Of Unified Power Flow Controller For Congesition Management

Kumar, J. Sunil; Immanuel, A.; Reddy, V. Usha; Kanth, V. Rajani; Marutheswar, G.V. Venkata

doi:10.26634/jee.5.1.1563

Cited by 2 publications

(2 citation statements)

References 5 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…The results of antioxidant activity showed that few synthesized compounds exhibit considerable antioxidant activity. Chloro substitution 9d at the para position of phenyl ring increases the antioxidant activity, which is also supported by Kumar et al [21]. Substitution of bulky group like naphthol (9h and 7f) also increases the activity, which is also favored by Bhalghat et al [22].…”

Section: Free Radical Scavenging Activitymentioning

confidence: 78%

Synthesis and biological evaluation of thiazolo and imidazo N-(4-nitrophenyl)-7-methyl-5-aryl-pyrimidine-6 carboxamide derivatives

et al. 2015

View full text Add to dashboard Cite

Two new series of thiazolo and imidazo N-(4-nitrophenyl)-7-methyl-5-aryl-pyrimidine-6 carboxamide derivatives were synthesized. All the synthesized compounds were evaluated for their antimicrobial activity against Gram-positive bacteria: Staphylococcus aureus MTCC 3160, Bacillus subtilis MTCC 441, Gramnegative bacterium: Escherichia coli MTCC 443 and antifungal activity against Candida albicans MTCC 227 and Aspergillus niger MTCC 281 and free radical scavenging activity. Compound 7e was found the most active antimicrobial comparable to standards taken. Compounds 7a, 7c, 9a, and 9d also showed significant antibacterial and antifungal activity. Further, compounds 7f, 9d, and 9h showed significant antioxidant activity with IC 50 comparable with the standard compound. The synthesized compounds were confirmed for their structure by means of various spectrometric techniques like IR, 1 H NMR, mass, and elemental analysis.

show abstract

Section: Free Radical Scavenging Activitymentioning

confidence: 78%

Synthesis and biological evaluation of thiazolo and imidazo N-(4-nitrophenyl)-7-methyl-5-aryl-pyrimidine-6 carboxamide derivatives

et al. 2015

View full text Add to dashboard Cite

show abstract

“…[6]. Bignelli reaction, a threecomponent cyclocondensation reaction, is one of the methods described to synthesize dihydropyrimidine derivatives [7]. Further, the dihydropyrimidine moiety has been considered as an important class of heterocyclic compounds exhibiting a variety of potent biological activities such as antiviral [8], antimicrobial [9], antioxidant [10], anti-inflammatory [11], anti-allergic [12], anticancer [13], calcium channel blockers [14], and antidiabetic, etc.…”

Section: Introductionmentioning

confidence: 99%

Design, synthesis, and biological evaluation of thiourea and guanidine derivatives of pyrimidine-6-carboxylate

et al. 2014

View full text Add to dashboard Cite

Two new series of methyl 7-methyl-5-(substituted-phenyl)-3,5-dihydro-2H-substituted [3,2-a]pyrimidine-6-carboxylate derivatives of thiourea and guanidine were synthesized. These compounds were characterized and evaluated for their antibacterial activity against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and antifungal Aspergillus niger and Candida albicans and free radical scavenging activity using DPPH reagent method. Compound 7f was found to be the most active antibacterial and antifungal agent comparable to the standard drugs ciprofloxacin and fluconazole. Further, the compounds 5e, 7g, and 7h were also found to have significant antimicrobial activity. Compound 5a was found to be the most active antioxidant among all the targeted compounds, while compounds 5b, 5g, 7b, and 7f also had significant antioxidant activity compared to standard ascorbic acid.

show abstract

Location Of Unified Power Flow Controller For Congesition Management

Cited by 2 publications

References 5 publications

Synthesis and biological evaluation of thiazolo and imidazo N-(4-nitrophenyl)-7-methyl-5-aryl-pyrimidine-6 carboxamide derivatives

Synthesis and biological evaluation of thiazolo and imidazo N-(4-nitrophenyl)-7-methyl-5-aryl-pyrimidine-6 carboxamide derivatives

Design, synthesis, and biological evaluation of thiourea and guanidine derivatives of pyrimidine-6-carboxylate

Contact Info

Product

Resources

About