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Volumn 23, Issue 11, 2013, Pages 3314-3319
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Preparation of S14161 and its analogues and the discovery of 6-bromo-8-ethoxy-3-nitro-2H-chromene as a more potent antitumor agent in vitro
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Author keywords
3 kinase pathway (PI3K); 3 Nitro 2H chromene; Akt phosphorylation; Antiproliferative; Antitumor; Apoptosis; inhibitors; Oxa Michael Henry reaction; Phosphoinositide
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Indexed keywords
6 BROMO 8 ETHOXY 3 NITRO 2H CHROMENE;
ANTINEOPLASTIC AGENT;
CASPASE 3;
CHROMENE DERIVATIVE;
PROTEIN KINASE B;
S 14161;
UNCLASSIFIED DRUG;
ANTIANGIOGENIC ACTIVITY;
ANTINEOPLASTIC ACTIVITY;
ANTIPROLIFERATIVE ACTIVITY;
APOPTOSIS;
ARTICLE;
BREAST CANCER;
CANCER CELL CULTURE;
CELL MIGRATION;
CELL PROLIFERATION;
DNA REPAIR;
DRUG DESIGN;
DRUG STRUCTURE;
HELA CELL;
HIGH THROUGHPUT SCREENING;
HINGE REGION;
HUMAN;
HUMAN CELL;
HYDROGEN BOND;
IN VITRO STUDY;
LUNG CANCER;
OVARY CANCER;
PROSTATE CANCER;
PROTEIN PHOSPHORYLATION;
UTERINE CERVIX CANCER;
ANTINEOPLASTIC AGENTS;
BENZOPYRANS;
BINDING SITES;
CATALYSIS;
CELL LINE, TUMOR;
CELL MOVEMENT;
CELL PROLIFERATION;
DRUG EVALUATION, PRECLINICAL;
DRUG SCREENING ASSAYS, ANTITUMOR;
HUMAN UMBILICAL VEIN ENDOTHELIAL CELLS;
HUMANS;
MOLECULAR DOCKING SIMULATION;
NEOVASCULARIZATION, PHYSIOLOGIC;
PHOSPHATIDYLINOSITOL 3-KINASES;
PHOSPHORYLATION;
PIPERAZINES;
PROLINE;
PROTEIN STRUCTURE, TERTIARY;
PROTO-ONCOGENE PROTEINS C-AKT;
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EID: 84877582940
PISSN: 0960894X
EISSN: 14643405
Source Type: Journal
DOI: 10.1016/j.bmcl.2013.03.097 Document Type: Article |
Times cited : (46)
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References (23)
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