2016
DOI: 10.1016/j.bmcl.2016.04.038
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Synthesis of novel triazole/isoxazole functionalized 7-(trifluoromethyl)pyrido[2,3- d ]pyrimidine derivatives as promising anticancer and antibacterial agents

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Cited by 83 publications
(19 citation statements)
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“…Kumar et al . prepared a series of novel pyrido[2,3d]pyrimidine derivatives with a long carbon chain and screened for their antibacterial activity.…”
Section: Othersmentioning
confidence: 99%
“…Kumar et al . prepared a series of novel pyrido[2,3d]pyrimidine derivatives with a long carbon chain and screened for their antibacterial activity.…”
Section: Othersmentioning
confidence: 99%
“…Compounds b29 and b30 showed highest activity against PANC-1 (pancreatic cancer) and A549 (lung cancer) cell lines respectively (Table 26 , Fig. 7 ) [ 34 ].…”
Section: Biological Significance Of Pyrimidine Scaffoldsmentioning
confidence: 99%
“…Many of the fused pyridine compounds have been proven as valuable candidates possessing anti-bacterial (Elagamey, Sattar, El-Taweel, & Said, 2015), anti-fungal (Hanafy, 2011), anti-microbial (Paresh & Yogesh, 2015), antioxidant (Farghaly, Abass, Abdalla, & Mahgoub, 2011;Flefel et al, 2014), anti-cancer (Bladt, Frisvad, Knudsen, & Larsen, | 465 LAVANYA et AL. 2013;Naresh Kumar et al, 2016), anti-psychotic (Swain et al, 1992), anti-inflammatory (Hend, At-Allah, A-Rahman, & El-Gazza, 2008;Piero & Lucio, 2012), anti-leishmanial (Samai, Nandi, Chowdhury, & Singh, 2011), anti-viral (Tai et al, 2014, anti-hypersensitive (Smith et al, 1989), anticonvulsants (Kaminski, Obniska, Zagorska, & Maciag, 2006), anti-malarial (Davoll, Clarke, & Elslage, 1972), potassium channel openers (Gadwood et al, 1993), anti-diabetic (Sarges, Bordner, Dominy, Peterson, & Whipple, 1985) and anti-tumour activities (Mohamed & Giuseppe, 2016). A few of previously reported bio-active fused compounds (A-D) were represented in Figure 1.…”
Section: Introductionmentioning
confidence: 99%
“…Among the heterocyclic compounds, pyridine and their analogues are the most prevalent structural units due to their wide spectrum of applications (Song, Huang, Yi, & Zhang, ), in natural products (Michael, ), pharmaceutical (Baumann & Baxendale, ; Vitaku, Smith, & Njardarson, ), agrochemical (Guan, Liu, Sun, & Xie, ) and material science (Desimoni, Faita, & Quadrelli, ; Gillissen et al., ). Many of the fused pyridine compounds have been proven as valuable candidates possessing anti‐bacterial (Elagamey, Sattar, El‐Taweel, & Said, ), anti‐fungal (Hanafy, ), anti‐microbial (Paresh & Yogesh, ), anti‐oxidant (Farghaly, Abass, Abdalla, & Mahgoub, ; Flefel et al., ), anti‐cancer (Bladt, Frisvad, Knudsen, & Larsen, ; Naresh Kumar et al., ), anti‐psychotic (Swain et al., ), anti‐inflammatory (Hend, At‐Allah, A‐Rahman, & El‐Gazza, ; Piero & Lucio, ), anti‐leishmanial (Samai, Nandi, Chowdhury, & Singh, ), anti‐viral (Tai et al., ), anti‐hypersensitive (Smith et al., ), anti‐convulsants (Kaminski, Obniska, Zagorska, & Maciag, ), anti‐malarial (Davoll, Clarke, & Elslage, ), potassium channel openers (Gadwood et al., ), anti‐diabetic (Sarges, Bordner, Dominy, Peterson, & Whipple, ) and anti‐tumour activities (Mohamed & Giuseppe, ). A few of previously reported bio‐active fused compounds ( A–D ) were represented in Figure .…”
Section: Introductionmentioning
confidence: 99%