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Volumn 20, Issue 12, 2010, Pages 3526-3529
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5-Ureidobenzofuranone indoles as potent and efficacious inhibitors of PI3 kinase-α and mTOR for the treatment of breast cancer
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Author keywords
mTOR inhibitor; PI3K inhibitor
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Indexed keywords
4 METHYLPIPERAZIN 1 YL;
4 MORPHOLINYL;
[2 (DIMETHYLAMINO)ETHYL]METHYLAMINO;
ANTINEOPLASTIC AGENT;
BINEDALINE;
INDOLE DERIVATIVE;
MAMMALIAN TARGET OF RAPAMYCIN INHIBITOR;
PHOSPHATIDYLINOSITOL 3 KINASE;
PHOSPHATIDYLINOSITOL 3 KINASE ALPHA;
PHOSPHATIDYLINOSITOL 3 KINASE INHIBITOR;
UNCLASSIFIED DRUG;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ANTINEOPLASTIC ACTIVITY;
ARTICLE;
BREAST CANCER;
CANCER CELL CULTURE;
CANCER MODEL;
DRUG EFFICACY;
DRUG INHIBITION;
DRUG POTENCY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
IN VIVO STUDY;
MOUSE;
NONHUMAN;
PROTEIN PHOSPHORYLATION;
RAT;
TUMOR VOLUME;
1-PHOSPHATIDYLINOSITOL 3-KINASE;
ANIMALS;
BENZOFURANS;
BREAST NEOPLASMS;
CELL LINE, TUMOR;
DISEASE MODELS, ANIMAL;
FEMALE;
HUMANS;
INDOLES;
INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS;
MICE;
MICE, NUDE;
MICROSOMES;
PROTEIN-SERINE-THREONINE KINASES;
RATS;
STRUCTURE-ACTIVITY RELATIONSHIP;
TUMOR BURDEN;
UREA;
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EID: 77954213226
PISSN: 0960894X
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmcl.2010.04.139 Document Type: Article |
Times cited : (33)
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References (12)
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