Synthesis, spectroscopic characterization, XRD crystal structure, DFT and antimicrobial study of (2E)-3-(2,6-dichlorophenyl)-1-(4-methoxyphenyl)-prop-2-en-1-one

[1] Rane RA(2010)Synthesis and evaluation of novel chloropyrrole molecules designed by molecular hybridization of common pharmacophores as potential antimicrobial agents Bioorg Med Chem Lett 20 5681-5685

[2] Telekar VN(2004)Antibacterial chalcones—bioisosteric replacement of the 4-hydroxy group Bioorg Med Chem 12 3047-3054

[3] Nielsen SF(2015)Synthesis and antifungal activity of chalcone derivatives Nat Prod Res 29 1804-1810

[4] Bosen T(1993)Antimutagenic effects of flavonoids, chalcones and structurally related compounds on the activity of 2-amino-3-methylinidazo [4,5-ƒ] quinoline (IQ) and other heterocyclic amine mutagens from cooked food Mutat Res 287 261-274

[5] Larsen M(2008)Antimitotic and antiproliferative activities of chalcones: forward structure-activity relationship J Med Chem 51 2307-2310

[6] Schonning K(2010)Synthesis and biological evaluation of indolyl chalcones as antitumor agents Boorg Med Chem Lett 20 3916-3919

[7] Kromann H(2011)Synthesis, antioxidant evaluation, and quantitative structure-activity relationship studies of chalcones Med Chem Res 20 480-492

[8] Zheng Y(2007)A review of anti-infective and anti-inflammatory chalcones Eur J Med Chem 42 125-137

[9] Wang X(2012)Antimalarial activity of newly synthesized chalcone derivatives in vitro Chem Biol Drug Des 80 340-347

[10] Gao S(2003)Structure–activity relationships of antileishmanial and antimalarial chalcones Bioorg Med Chem 11 2729-2738

[1] Rane RA(2010)Synthesis and evaluation of novel chloropyrrole molecules designed by molecular hybridization of common pharmacophores as potential antimicrobial agents Bioorg Med Chem Lett 20 5681-5685

[2] Telekar VN(2004)Antibacterial chalcones—bioisosteric replacement of the 4-hydroxy group Bioorg Med Chem 12 3047-3054

[3] Nielsen SF(2015)Synthesis and antifungal activity of chalcone derivatives Nat Prod Res 29 1804-1810

[4] Bosen T(1993)Antimutagenic effects of flavonoids, chalcones and structurally related compounds on the activity of 2-amino-3-methylinidazo [4,5-ƒ] quinoline (IQ) and other heterocyclic amine mutagens from cooked food Mutat Res 287 261-274

[5] Larsen M(2008)Antimitotic and antiproliferative activities of chalcones: forward structure-activity relationship J Med Chem 51 2307-2310

[6] Schonning K(2010)Synthesis and biological evaluation of indolyl chalcones as antitumor agents Boorg Med Chem Lett 20 3916-3919

[7] Kromann H(2011)Synthesis, antioxidant evaluation, and quantitative structure-activity relationship studies of chalcones Med Chem Res 20 480-492

[8] Zheng Y(2007)A review of anti-infective and anti-inflammatory chalcones Eur J Med Chem 42 125-137

[9] Wang X(2012)Antimalarial activity of newly synthesized chalcone derivatives in vitro Chem Biol Drug Des 80 340-347

[10] Gao S(2003)Structure–activity relationships of antileishmanial and antimalarial chalcones Bioorg Med Chem 11 2729-2738