Indexed keywords
1 (3 BROMOPHENYL) 3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL]PROP 2 EN 1 ONE;
1 (3 CHLOROPHENYL) 3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL]PROP 2 EN 1 ONE;
1 (3,4 DICHLOROPHENYL) 3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL]PROP 2 EN 1 ONE;
1 (4 AMINOPHENYL) 3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL]PROP 2 EN 1 ONE;
1 (4 BROMOPHENYL) 3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL]PROP 2 EN 1 ONE;
1 (4 BUTOXYPHENYL) 3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL]PROP 2 EN 1 ONE;
1 (4 CHLOROPHENYL) 3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL]PROP 2 EN 1 ONE;
1 [(1,1' BIPHENYL) 4 YL] 3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL]PROP 2 EN 1 ONE;
1 [4 (DIETHYLAMINO)PHENYL] 3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL]PROP 2 EN 1 ONE;
3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL] 1 (2,4 DIMETHYLPHENYL)PROP 2 EN 1 ONE;
3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL] 1 (3 METHOXYPHENYL)PROP 2 EN 1 ONE;
3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL] 1 (3,4 DIMETHYLPHENYL)PROP 2 EN 1 ONE;
3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL] 1 (4 ETHOXYPHENYL)PROP 2 EN 1 ONE;
3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL] 1 (4 FLUOROPHENYL)PROP 2 EN 1 ONE;
3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL] 1 (4 METHOXYPHENYL)PROP 2 EN 1 ONE;
3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL] 1 (4 MORPHOLINOPHENYL)PROP 2 EN 1 ONE;
3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL] 1 (4 TOLYL)PROP 2 EN 1 ONE;
3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL] 1 (O TOLYL)PROP 2 EN 1 ONE;
3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL] 1 [4 (DODECYLOXY)PHENYL]PROP 2 EN 1 ONE;
3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL] 1 [4 (HEXYLOXY)PHENYL]PROP 2 EN 1 ONE;
3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL] 1 [4 (PENTAN 2 YLOXY)PHENYL]PROP 2 EN 1 ONE;
3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL] 1 [4 (TRIFLUOROMETHYL)PHENYL]PROP 2 EN 1 ONE;
3 [2,4 DIMETHOXY 6 (4 METHOXYSTYRYL)PHENYL] 1 PHENYLPROP 2 EN 1 ONE;
CHALCONE;
COLCHICINE;
RESVERATROL;
TUBULIN;
TUBULIN MODULATOR;
UNCLASSIFIED DRUG;
ARTICLE;
CELL CYCLE ARREST;
CELL PROLIFERATION;
CELL STRAIN HEPG2;
CONTROLLED STUDY;
DRUG BINDING SITE;
DRUG POTENCY;
DRUG PROTEIN BINDING;
DRUG STRUCTURE;
DRUG SYNTHESIS;
GROWTH INHIBITION;
HUMAN;
HUMAN CELL;
HYDROGEN BOND;
HYDROPHOBICITY;
IC 50;
MELANOMA CELL;
MICROTUBULE ASSEMBLY;
MOLECULAR DOCKING;
MOLECULAR MODEL;
NONHUMAN;
BINDING SITES;
CELL LINE, TUMOR;
CHALCONE;
DOSE-RESPONSE RELATIONSHIP, DRUG;
HUMANS;
PROTEIN BINDING;
STILBENES;
STRUCTURE-ACTIVITY RELATIONSHIP;
TUBULIN MODULATORS;
1
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