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Bioorganic and Medicinal Chemistry

Volumn 22, Issue 13, 2014, Pages 3386-3392

Anti-proliferative effect of chalcone derivatives through inactivation of NF-κB in human cancer cells

(5) Venkateswararao, Eeda a Sharma, Vinay K a Yun, Jieun b Kim, Youngsoo c Jung, Sang Hun a

a Chungnam National University (South Korea)

b Korea Research Institute of Bioscience and Biotechnology (KRIBB) (South Korea)

c Chungbuk National University (South Korea)

Author keywords

Anti proliferative activity; Chalcones; Inactivation of NF B

Indexed keywords

1 (2 BUTOXY 6 HYDROXYPHENYL) 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 1 (2 HYDROXY 6 ISOBUTOXYPHENYL) 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 1 (6 CYCLOHEXYLMETHOXY 2 HYDROXYPHENYL) 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 1 [2 (2 CYCLOHEXYLETHOXY) 6 HYDROXYPHENYL] 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 1 [2 (2 CYCLOPENTYLETHOXY) 6 HYDROXYPHENYL] 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 1 [2 (2 ETHYLBUTOXY) 6 HYDROXYPHENYL] 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 1 [2 (3,3 DIMETHYLBUTOXY) 6 HYDROXYPHENYL] 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 1 [2 (3,3 DIMETHYLBUTOXY) 6 METHOXYPHENYL] 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 1 [2 (ADAMANTYLMETHOXY) 6 HYDROXYPHENYL] 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 1 [2 (BENZYLOXY) 6 HYDROXYPHENYL] 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 1 [2 (CYCLOPENTYLMETHOXY) 6 HYDROXYPHENYL] 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 1 [2 (HEXYLOXY) 6 HYDROXYPHENYL] 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 1 [2 HYDROXY 6 (3 METHYLBUT 2 ENYLOXY)PHENYL] 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 1 [2 HYDROXY 6 (3,3 DIMETHYLBUTOXY)PHENYL] 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 1 [2 HYDROXY 6 (4 METHYLPENTYLOXY)PHENYL] 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 1 [2 HYDROXY 6(ISOPENTYLOXY)PHENYL] 3 (4 HYDROXYPHENYL)PROP 2 EN 1 ONE; 4 [3 [2 (3,3 DIMETHYLBUTOXY) 6 HYDROXYPHENYL] 3 OXOPROP 1 ENYL]BENZENESULFONAMIDE; 4 [3 [2 HYDROXY 6 (3,3 DIMETHYLBUTOXY)PHENYL] 3 OXOPROP 1 ENYL]BENZENESULFONAMIDE; 4 [3 [2 HYDROXY 6 (3,3 DIMETHYLBUTOXY)PHENYL] 3 OXOPROP 1 ENYL]BENZOIC ACID; CHALCONE DERIVATIVE; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; UNCLASSIFIED DRUG; CHALCONE;

ACHN CELL LINE; ANTIPROLIFERATIVE ACTIVITY; ARTICLE; CANCER CELL; CANCER CELL LINE; CONTROLLED STUDY; HCT 15 CELL LINE; HUMAN; HUMAN CELL; IC 50; IN VITRO STUDY; INHIBITION KINETICS; MDA MB 231 CELL LINE; NCI H23 CELL LINE; NUGC 3 CELL LINE; PC 3 CELL LINE; STRUCTURE ACTIVITY RELATION; ANTAGONISTS AND INHIBITORS; CELL PROLIFERATION; CHEMICAL STRUCTURE; CHEMISTRY; DOSE RESPONSE; DRUG EFFECTS; DRUG SCREENING; METABOLISM; SYNTHESIS; TUMOR CELL LINE;

CELL LINE, TUMOR; CELL PROLIFERATION; CHALCONE; DOSE-RESPONSE RELATIONSHIP, DRUG; DRUG SCREENING ASSAYS, ANTITUMOR; HUMANS; MOLECULAR STRUCTURE; NF-KAPPA B; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84901923000 PISSN: 09680896 EISSN: 14643391 Source Type: Journal
DOI: 10.1016/j.bmc.2014.04.045 Document Type: Article

Times cited : (18)

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