ANTIINFLAMMATORY ACTIVITY;
ARTICLE;
CANCER CELL CULTURE;
CONTROLLED STUDY;
CYTOTOXICITY;
DOWN REGULATION;
DRUG MECHANISM;
DRUG POTENCY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME ACTIVATION;
ENZYME INHIBITION;
HUMAN;
HUMAN CELL;
IC 50;
MICROGLIA;
ONE STEP CLAISEN SCHMIDT CONDENSATION;
POLYMERIZATION;
PROTEIN DEGRADATION;
PROTEIN EXPRESSION;
STRUCTURE ACTIVITY RELATION;
The role of apoptosis in therapy and prophylaxis of epithelial tumours by nonsteroidal anti-inflammatory drugs (NSAIDs)
L.F. Fecker, E. Stockfleth, I. Nindl, C. Ulrich, I. Forschner, and J. Eberle The role of apoptosis in therapy and prophylaxis of epithelial tumours by nonsteroidal anti-inflammatory drugs (NSAIDs) Br. J. Dermatol. 156 Suppl 3 2007 25 33
Proinflammatory cytokines in breast cancer: Mechanisms of action and potential targets for therapeutics
J.E. Goldberg, and K.L. Schwertfeger Proinflammatory cytokines in breast cancer: mechanisms of action and potential targets for therapeutics Curr. Drug Targets 11 2010 1133 1146
Influence of the microenvironment on melanoma cell fate determination and phenotype
L.M. Postovit, E.A. Seftor, R.E. Seftor, and M.J. Hendrix Influence of the microenvironment on melanoma cell fate determination and phenotype Cancer Res. 66 2006 7833 7836
Targeting inflammatory pathways for prevention and therapy of cancer: Short-term friend, long-term foe
B.B. Aggarwal, R.V. Vijayalekshmi, and B. Sung Targeting inflammatory pathways for prevention and therapy of cancer: short-term friend, long-term foe Clin. Cancer Res. 15 2009 425 430
Chalcones and their heterocyclic analogs as potential antifungal chemotherapeutic agents
V. Opletalová, and D. Sedivý Chalcones and their heterocyclic analogs as potential antifungal chemotherapeutic agents Ceska Slov. Farm. 48 1999 252 255
Structure-activity relationships of antileishmanial and antimalarial chalcones
M. Liu, P. Wilairat, S.L. Croft, A.L. Tan, and M.L. Go Structure-activity relationships of antileishmanial and antimalarial chalcones Bioorg. Med. Chem. 11 2003 2729 2738
Chalcones and flavonoids as anti-tuberculosis agents
Y.M. Lin, Y. Zhou, M.T. Flavin, L.M. Zhou, W. Nie, and F.C. Chen Chalcones and flavonoids as anti-tuberculosis agents Bioorg. Med. Chem. 10 2002 2795 2802
Emerging role of garcinol, the antioxidant chalcone from Garcinia indica Choisy and its synthetic analogs
S. Padhye, A. Ahmad, N. Oswal, and F.H. Sarkar Emerging role of garcinol, the antioxidant chalcone from Garcinia indica Choisy and its synthetic analogs J. Hematol. Oncol. 2 2009 38
Chalcones (1,3-diarylpropen-1-ones) and their analogs as potential therapeutic agents in cardiovascular system diseases
V. Opletalová, L. Jahodár, D. Jun, and L. Opletal Chalcones (1,3-diarylpropen-1-ones) and their analogs as potential therapeutic agents in cardiovascular system diseases Ceska Slov. Farm 52 2003 12 19
New anticancer agents: In vitro and in vivo evaluation of the antitumor and antimetastatic actions of various compounds isolated from medicinal plants
Y. Kimura New anticancer agents: in vitro and in vivo evaluation of the antitumor and antimetastatic actions of various compounds isolated from medicinal plants In Vivo 19 2005 37 60
The role of chalcones in suppression of NF-κB-mediated inflammation and cancer
V.R. Yadav, S. Prasad, B. Sung, and B.B. Aggarwal The role of chalcones in suppression of NF-κB-mediated inflammation and cancer Int. Immunopharmacol 11 2011 295 309
Synthesis and biological activity of 4-alkoxy chalcones: Potential hydrophobic modulators of P-glycoprotein-mediated multidrug resistance
F. Bois, A. Boumendjel, A. Mariotte, G. Conseil, and A. Di Petro Synthesis and biological activity of 4-alkoxy chalcones: potential hydrophobic modulators of P-glycoprotein-mediated multidrug resistance Bioorg. Med. Chem. 7 1999 2691 2695
A facile synthesis of 3,7-diphenyl-4,6-distyryl-2,8-dioxo-2H,8H-benzo[1, 2-b:5,4-b′]dipyrans and their antifeedant activity
B. Sreenivasulu, and P.N. Sarma A facile synthesis of 3,7-diphenyl-4,6-distyryl-2,8-dioxo-2H,8H-benzo[1,2-b:5,4-b′]dipyrans and their antifeedant activity Syn. Comm. 27 1997 2281 2287
2,4-Bis(substituted cinnamoyl/pyrazol-3-yl)phenoxyacetic acid esters and hydrazides as potential antimicrobial agents
N.K. Sangwan, B.M. Verma, and K.S. Dhindsa 2,4-Bis(substituted cinnamoyl/pyrazol-3-yl)phenoxyacetic acid esters and hydrazides as potential antimicrobial agents Indian J. Chem. 25B 1986 672 674
Reaction of acetic anhydride/zinc chloride reagent with phenols: Improved yields of hydroxyacetophenones
A.S.R. Anjaneyulu, U.V. Mallavadhani, Y. Venkateswaralu, and A.V.R. Prasad Reaction of acetic anhydride/zinc chloride reagent with phenols: improved yields of hydroxyacetophenones Indian J. Chem. Sect. B. 26 1987 823 826
Antitumor Agents. 239. Isolation, structure elucidation, total synthesis, and anti-breast cancer activity of neo-tanshinlactone from Salvia miltiorrhiza
X. Wang, K.F. Bastow, C.M. Sun, Y.L. Lin, H.J. Yu, M.J. Don, T.S. Wu, S. Nakamura, and K.H. Lee Antitumor Agents. 239. Isolation, structure elucidation, total synthesis, and anti-breast cancer activity of neo-tanshinlactone from Salvia miltiorrhiza J. Med. Chem. 47 2004 5816 5819