Antifungal activity and studies on mode of action of novel xanthoxyline-derived chalcones
P. Boeck, P.C. Leal, R.A. Yunes, V. Cechinel-Filho, S. Lopez, M. Sortino, A. Escalante, R.L.E. Furlan, and S. Zacchino Antifungal activity and studies on mode of action of novel xanthoxyline-derived chalcones Arch. Pharm. 338 2005 87 95
Chalcones and flavonoids as anti-tuberculosis agents
Y.M. Lin, Y. Zhou, M.T. Flavin, L.M. Zhow, W. Nie, and F.C. Chen Chalcones and flavonoids as anti-tuberculosis agents Bioorg. Med. Chem. 10 2002 2795 2802
Antimalarial alkoxylated and hydroxylated chalcones: Structure-activity relationship analysis
M. Liu, P. Wilairat, and M.L. Go Antimalarial alkoxylated and hydroxylated chalcones: structure-activity relationship analysis J. Med. Chem. 44 2001 4443 4452
S.E. Nielsen, S.B. Christensen, G. Cruciani, A. Kharazmi, and T. Liljefors Antileishmanial chalcones: statistical design, synthesis, and three-dimensional quantitative structure-activity relationship analysis J. Med. Chem. 41 1998 4819 4832
Antinociceptive properties of chalcones, structure-activity relationships
R. Correra, M.A.S. Pereira, D. Buffon, L. dos Santos, V. Cechinel-Filho, A.R.S. Santos, and R. Nunes Antinociceptive properties of chalcones, structure-activity relationships Archiv der Pharmazie 334 2001 332 334
Synthesis and pharmacological activity of chalcones derived from 2,4,6-trimethoxyacetophenone in RAW 264.7 cells stimulated by LPS: Quantitative structure-activity relationships
L.D. Chiaradia, S. Rodrigo, C.E. Vitor, A.A. Vieira, P.C. Leal, R.J. Nunes, J.B. Calixto, and R.A. Yunes Synthesis and pharmacological activity of chalcones derived from 2,4,6-trimethoxyacetophenone in RAW 264.7 cells stimulated by LPS: quantitative structure-activity relationships Bioorg. Med. Chem. 16 2008 658 667
Cytotoxic 2′,5′-dihydroxychalcones with unexpected antiangiogenic activity
N.H. Nam, Y. Kim, Y.J. You, D.H. Hong, H.M. Kim, and B.Z. Ahn Cytotoxic 2′,5′-dihydroxychalcones with unexpected antiangiogenic activity Eur. J. Med. Chem. 38 2003 179 187
Synthesis and cytotoxic, anti-inflammatory, and anti-oxidant activities of 2′,5′-dialkoxylchalcones as cancer chemopreventive agents
J.H. Cheng, C.F. Hung, S.C. Yang, J.P. Wang, S.J. Won, and C.N. Lin Synthesis and cytotoxic, anti-inflammatory, and anti-oxidant activities of 2′,5′-dialkoxylchalcones as cancer chemopreventive agents Bioorg. Med. Chem. 16 2008 7270 7276
Antimitotic and antiproliferative activities of chalcones: Forward structure-activity relationship
Boumendjel, J. Boccard, P.A. Carrupt, E. Nicolle, M. Blanc, A. Geze, L. Choisnard, D. Wouessidjewe, E.L. Matera, and C. Dumontet Antimitotic and antiproliferative activities of chalcones: forward structure-activity relationship J. Med. Chem. 51 2008 2307 2310
Synthetic chalcones, flavanones, and flavones as antitumoral agents: Biological evaluation and structure-activity relationships
M. Cabrera, M. Simoens, G. Falchi, M.L. Lavaggi, O.E. Piro, E.E. Castellano, A. Vidal, A. Azqueta, A. Monge, A. Lopez de Cerian, G. Sagrera, G. Seoane, H. Cerecetto, and M. Gonzalez Synthetic chalcones, flavanones, and flavones as antitumoral agents: biological evaluation and structure-activity relationships Bioorg. Med. Chem. 15 2007 3356 3367
Effects of alpha-substitutions on structure and biological activity of anticancer chalcones
N.J. Lawrence, R.P. Patterson, L.L. Ooi, D. Cook, and S. Ducki Effects of alpha-substitutions on structure and biological activity of anticancer chalcones Bioorg. Med. Chem. Lett. 16 2006 5844 5848
Reinvestigation of structure-activity relationship of methoxylated chalcones as antimalarials: Synthesis and evaluation of 2,4,5-trimethoxy substituted patterns as lead candidates derived from abundantly available natural β-asarone
R. Kumar, D. Mohanakrishnan, A. Sharma, N.K. Kaushik, K. Kalia, A.K. Sinha, and D. Sahal Reinvestigation of structure-activity relationship of methoxylated chalcones as antimalarials: synthesis and evaluation of 2,4,5-trimethoxy substituted patterns as lead candidates derived from abundantly available natural β-asarone Eur. J. Med. Chem. 45 2010 5292 5301
Comparative study on the MDR reversal effects of selected chalcones
A.B. Ivanova, D.I. Batovaska, I.T. Todarova, B.A.J. Serly, and J. Molnar Comparative study on the MDR reversal effects of selected chalcones Int. J. Med. Chem. 2011 2011 1 7
Synthesis and biological evaluation of 3′,4′,5′- trimethoxychalcone analogues as inhibitors of nitric oxide production and tumor cell proliferation
Y.K. Rao, S.H. Fang, and Y.M. Tzeng Synthesis and biological evaluation of 3′,4′,5′-trimethoxychalcone analogues as inhibitors of nitric oxide production and tumor cell proliferation Bioorg. Med. Chem. 17 2009 7909 7914
Investigation of chalcones and benzochalcones as inhibitors of breast cancer resistance protein
K. Juvale, V.F.S. Pape, and M. Wiese Investigation of chalcones and benzochalcones as inhibitors of breast cancer resistance protein Bioorg. Med. Chem. 20 2012 346 355
Solid-phase synthesis of 2′-hydroxychalcones. Effects on cell growth inhibition, cell cycle and apoptosis of human tumor cell lines
M.P. Neves, S. Cravo, R.T. Lima, M.H. Vasconcelos, M.S.J. Nascimento, A.M.S. Silva, M. Pinto, H. Cidade, and A.G. Correra Solid-phase synthesis of 2′-hydroxychalcones. Effects on cell growth inhibition, cell cycle and apoptosis of human tumor cell lines Bioorg. Med. Chem. 20 2012 25 33
The synthesis and effect of fluorinated chalcone derivatives on nitric oxide production
J. Rojas, M. Paya, J.N. Dominguez, and M.L. Ferrandiz The synthesis and effect of fluorinated chalcone derivatives on nitric oxide production Bioorg. Med. Chem. Lett. 12 2002 1951 1954
Stilbene-chalcone hybrids: Design, synthesis, and evaluation as a new class of antimalarial scaffolds that trigger cell death through stage specific apoptosis
N. Sharma, D. Mohanakrishnan, A. Shard, A. Sharma, Saima, A.K. Sinha, and D. Sahal Stilbene-chalcone hybrids: design, synthesis, and evaluation as a new class of antimalarial scaffolds that trigger cell death through stage specific apoptosis J. Med. Chem. 55 2012 297 311
The antioxidant activity of phloretin: The disclosure of a new antioxidant pharmacophore in flavonoids
B.M. Rezk, G.R.M. Haenen, W.F.F. Nan der Vijgh, and A. Bast The antioxidant activity of phloretin: the disclosure of a new antioxidant pharmacophore in flavonoids Biochem. Biophys. Res. Commun. 295 2002 9 13
A unique water soluble formulation of β-asarone from sweet flag (Acorus calamus L.) and its in vitro activity against some fungal plant pathogens
S. Shenvi, Vinod, R. Hegde, A. Kush, and G.C. Reddy A unique water soluble formulation of β-asarone from sweet flag (Acorus calamus L.) and its in vitro activity against some fungal plant pathogens J. Med. Plant Res. 5 2011 5132 5137
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
T. Mossman Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays J. Immunol. Methods 65 1983 55 63
Inhibitory effect of the flavonoid silymarin on the erythrocyte hemolysis induced by phenylhydrazine
Valenzuela, T. Barria, R. Guerra, and a. Garrido Inhibitory effect of the flavonoid silymarin on the erythrocyte hemolysis induced by phenylhydrazine Biochem. Biophy. Res. Commun. 126 1985 712 718