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Volumn 22, Issue 1, 2014, Pages 366-373
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Design, synthesis and evaluation of novel indole derivatives as AKT inhibitors
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Author keywords
AKT inhibitors; GSK3 ; Inhibition rate; Tetra substituted indoles
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Indexed keywords
1 (1H INDOL 3 YL) 3 [[7 METHOXY 1 METHYL 2 (3 METHYL 1,2,4 OXADIAZOL 5 YL) 1H INDOL 4 YL]OXY]PROPAN 2 AMINE;
1 [[7 METHOXY 1 METHYL 2 (3 METHYL 1,2,4 OXADIAZOL 5 YL) 1H INDOL 4 YL]OXY] 3 PHENYLPROPAN 2 AMINE;
1 [[7 METHOXY 1 METHYL 2 (3 METHYL 1,2,4 OXADIAZOL 5 YL) 1H INDOL 4 YL]OXY] 4 (METHYLTHIO)BUTAN 2 AMINE;
1 [[7 METHOXY 1 METHYL 2 (3 METHYL 1,2,4 OXAOXADIAZOL 5 YL) 1H INDOL 4 YL]OXY] 3 PHENYLPROPAN 2 AMINE;
1,2,4,7 TETRA SUBSTITUTED INDOLE DERIVATIVE;
METHYL 4 (2 AMINO 3 PHENYLPROPOXY) 7 BROMO 1 METHYL 1H INDOLE 2 CARBOXYLIC ACID;
METHYL 4 (2 AMINO 3 PHENYLPROPOXY) 7 CHLORO 1 METHYL 1H INDOLE 2 CARBOXYLIC ACID;
METHYL 4 (2 AMINO 3 PHENYLPROPOXY) 7 METHOXY 1 METHYL 1H INDOLE 2 CARBOXYLIC ACID;
METHYL 4 [(2 AMINO 4 METHYLPENTYL)OXY] 7 METHOXY 1 METHYL 1H INDOLE 2 CARBOXYLIC ACID;
METHYL 4 [2 AMINO 3 (1H INDOL 3 YL)PROPOXY] 7 BROMO 1 METHYL 1H INDOLE 2 CARBOXYLIC ACID;
METHYL 4 [2 AMINO 3 (1H INDOL 3 YL)PROPOXY] 7 CHLORO 1 METHYL 1H INDOLE 2 CARBOXYLIC ACID;
METHYL 4 [2 AMINO 4 (METHYLTHIO)BUTOXY] 7 METHOXY 1 METHYL 1H INDOLE 2 CARBOXYLIC ACID;
METHYL 4 HYDROXY 7 METHOXY 1 METHYL 1H INDOLE 2 CARBOXYLIC ACID;
METHYL 4[(2 AMINO 3 METHYLPENTYL)OXY] 7 METHOXY 1 METHYL 1H INDOLE 2 CARBOXYLIC ACID;
METHYL 7 BROMO 4 HYDROXY 1 METHYL 1H INDOLE 2 CARBOXYLIC ACID;
METHYL 7 CHLORO 4 HYDROXY 1 METHYL 1H INDOLE 2 CARBOXYLIC ACID;
PROTEIN KINASE B INHIBITOR;
TERT BUTYL (1 HYDROXY 3 METHYLPENTAN 2 YL)CARBAMIC ACID;
TERT BUTYL (1 HYDROXY 3 PHENYLPROPAN 2 YL)CARBAMIC ACID;
TERT BUTYL (1 HYDROXY 4 METHYLPENTAN 2 YL)CARBAMIC ACID;
TERT BUTYL [1 HYDROXY 3 (1H INDOL 3 YL)PROPAN 2 YL]CARBAMIC ACID;
TERT BUTYL [1 HYDROXY 4 (METHYLTHIO)BUTAN 2 YL]CARBAMIC ACID;
UNCLASSIFIED DRUG;
ANTIPROLIFERATIVE ACTIVITY;
ARTICLE;
CANCER CELL;
CELL LINE;
CONTROLLED STUDY;
DRUG DESIGN;
DRUG POTENCY;
DRUG SCREENING;
DRUG SYNTHESIS;
ENZYME ACTIVITY;
ENZYME INHIBITION;
HUMAN;
HUMAN CELL;
IN VITRO STUDY;
MOLECULAR DOCKING;
PC 3 CELL;
PROSTATE CANCER;
PROTEIN PHOSPHORYLATION;
STRUCTURE ACTIVITY RELATION;
WESTERN BLOTTING;
TETRA;
AKT INHIBITORS;
GSK3Β;
INHIBITION RATE;
TETRA-SUBSTITUTED INDOLES;
GLYCOGEN SYNTHASE KINASE 3;
HUMANS;
INDOLES;
PHOSPHORYLATION;
PROTO-ONCOGENE PROTEINS C-AKT;
SIGNAL TRANSDUCTION;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 84891491552
PISSN: 09680896
EISSN: 14643391
Source Type: Journal
DOI: 10.1016/j.bmc.2013.11.022 Document Type: Article |
Times cited : (18)
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References (26)
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