358655-92-2Relevant academic research and scientific papers
Synthesis, molecular docking and anti-inflammatory screening of novel quinoline incorporated pyrazole derivatives using the Pfitzinger reaction II
El-Feky, Said A. H.,Abd El-Samii, Zakaria K.,Osman, Nermine A.,Lashine, Jasmine,Kamel, Mohamed A.,Thabet, Hamdy Kh.
, p. 104 - 116 (2015/02/19)
In continuation of our study of novel quinolines with anti-inflammatory activity using the Pfitzinger reaction, several new quinoline derivatives were synthesized and tested for their anti-inflammatory and ulcerogenic effect. A docking study on the COX-2
Synthesis, spectral investigation and biological interphase of drug-based cytotoxic square pyramidal coordination compounds
Patel, Mohan N.,Bhatt, Bhupesh S.,Dosi, Promise A.,Amaravady, Narasimhacharya V. R. L.,Movaliya, Hetal V.
scheme or table, p. 217 - 224 (2012/07/13)
We have synthesized ciprofloxacin-based metal complexes of bipyridine derivatives [Cu(CFL)(An)Cl].2H2O (where CFL=ciprofloxacin and A=bipyridines e.g. A1=4-(4-fluorophenyl)-6-p-tolyl-2,2′- bipyridine, A6=4-(4-(b
Design, synthesis and preliminary antiviral screening of new N-phenylpyrazole and dihydroisoxazole derivatives
Rashad, Adel A.,El-Sabbagh, Osama I.,Baraka, Mohamed M.,Ibrahim, Samy M.,Pannecouque, Christophe,Andrei, Graciela,Snoeck, Robert,Balzarini, Jan,Mostafa, Ahmed
experimental part, p. 1025 - 1035 (2011/10/12)
A new series of N-phenylpyrazoles and dihydroisoxazles was synthesized starting from α,β-unsaturated ketones in basic media using phenyl hydrazine and hydroxylamine HCl, respectively. Antiviral evaluation of the target compounds revealed that the dihydroi
Synthesis and antiviral activity of new pyrazole and thiazole derivatives
El-Sabbagh, Osama I.,Baraka, Mohamed M.,Ibrahim, Samy M.,Pannecouque, Christophe,Andrei, Graciela,Snoeck, Robert,Balzarini, Jan,Rashad, Adel A.
body text, p. 3746 - 3753 (2009/12/04)
New N-acetyl (5-8) and N-thiocarbamoyl (9-12) derivatives of 4,5-dihydropyrazole were synthesized starting from α,β-unsaturated ketones under the effect of hydrazine hydrate and thiosemicarbazide, respectively. N-Thiocarbamoylpyrazole derivatives (9-12) w
