SCOPUS 정보 검색 플랫폼

Volumn 46, Issue 6, 2011, Pages 2586-2595

Anticancer effects of the metabolic products of the resveratrol analogue, DMU-212: Structural requirements for potency

(6) Androutsopoulos, Vasilis P a Ruparelia, Ketan C b Papakyriakou, Athanasios c Filippakis, Harilaos a Tsatsakis, Aristeidis M a Spandidos, Demetrios A a

a UNIVERSITY OF CRETE (Greece)

b DE MONTFORT UNIVERSITY (United Kingdom)

c Institute of Physical Chemistry (Greece)

Author keywords

Tubulin; Antiproliferation; Apoptosis; Cell cycle inhibition; DMU 212; Docking; HepG2 cells; MCF 7 cells; Molecular modeling; Paclitaxel binding site; Resveratrol

Indexed keywords

3 HYDROXY 4,5,4' TRIMETHOXYSTILBENE; 3' HYDROXY 3,4,5,4' TETRAMETHOXYSTILBENE; 3,4,5,4' TETRAMETHOXYSTILBENE; 4 HYDROXY 3,5,4' TRIMETHOXYSTILBENE; 4' HYDROXY 3,4,5 TRIMETHOXYSTILBENE; ANTINEOPLASTIC AGENT; BETA ACTIN; BETA TUBULIN; CYCLIN D1; DMU 212; DMU 214; DMU 281; DMU 291; DMU 807; MESSENGER RNA; PROTEIN BAX; PROTEIN BCL XL; PROTEIN P53; RESVERATROL; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; APOPTOSIS; ARTICLE; BREAST ADENOCARCINOMA; CELL CYCLE; CELL CYCLE ARREST; CELL CYCLE G2 PHASE; CELL CYCLE M PHASE; CELL NUCLEUS; CELL PROLIFERATION; CELL VIABILITY; CONCENTRATION RESPONSE; CONTROLLED STUDY; DOWN REGULATION; DRUG CYTOTOXICITY; DRUG EFFECT; DRUG POTENCY; DRUG STRUCTURE; HEPATOMA CELL; HUMAN; HUMAN CELL; IMMUNOHISTOCHEMISTRY; INCUBATION TIME; MITOSIS INHIBITION; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; SUBSTITUTION REACTION; UPREGULATION; WESTERN BLOTTING;

ANTINEOPLASTIC AGENTS; CELL CYCLE; CELL PROLIFERATION; COMPUTATIONAL BIOLOGY; COMPUTER SIMULATION; CRYSTALLOGRAPHY, X-RAY; DOSE-RESPONSE RELATIONSHIP, DRUG; DRUG SCREENING ASSAYS, ANTITUMOR; HEP G2 CELLS; HUMANS; MODELS, MOLECULAR; MOLECULAR STRUCTURE; STEREOISOMERISM; STILBENES; STRUCTURE-ACTIVITY RELATIONSHIP; TUMOR CELLS, CULTURED;

EID: 79955589531 PISSN: 02235234 EISSN: 17683254 Source Type: Journal
DOI: 10.1016/j.ejmech.2011.03.049 Document Type: Article

Times cited : (62)

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