|
Volumn 16, Issue 8, 2008, Pages 4222-4232
|
Synthesis of 1-substituted 3-pyridinylmethylidenylindolin-2-ones and 1-substituted 3-quinolinylmethylidenylindolin-2-ones as the enhancers of ATRA-induced differentiation in HL-60 cells
|
Author keywords
ATRA; Differentiation; HL 60; Indolinone; Leukemia; Pyridinylidenylindolinone; Quinolinylidenylindolinone
|
Indexed keywords
1 (1 NAPHTHYLMETHYL) 3 (4 PYRIDINYLMETHYLIDENYL)INDOLIN 2 ONE;
1 (1 PHENYLETHYL) 3 (2 PYRIDINYLMETHYLIDENYL)INDOLIN 2 ONE;
1 (1 PHENYLETHYL) 3 (2 QUINOLINYLMETHYLIDENYL)INDOLIN 2 ONE;
1 (1 PHENYLETHYL) 3 (3 PYRIDINYLMETHYLIDENYL)INDOLIN 2 ONE;
1 (1 PHENYLETHYL) 3 (3 QUINOLINYLMETHYLIDENYL)INDOLIN 2 ONE;
1 (1 PHENYLETHYL) 3 (4 PYRIDINYLMETHYLIDENYL)INDOLIN 2 ONE;
1 (1 PHENYLETHYL) 3 (4 QUINOLINYLMETHYLIDENYL)INDOLIN 2 ONE;
1 (2 NAPHTHYLMETHYL) 3 (4 PYRIDINYLMETHYLIDENYL)INDOLIN 2 ONE;
1 BENZYL 3 (2 PYRIDINYLMETHYLIDENYL)INDOLIN 2 ONE;
1 BENZYL 3 (2 QUINOLINYLMETHYLIDENYL)INDOLIN 2 ONE;
1 BENZYL 3 (3 PYRIDINYLMETHYLIDENYL)INDOLIN 2 ONE;
1 BENZYL 3 (3 QUINOLINYLMETHYLIDENYL)INDOLIN 2 ONE;
1 BENZYL 3 (4 PYRIDINYLMETHYLIDENYL)INDOLIN 2 ONE;
1 BENZYL 3 (4 QUINOLINYLMETHYLIDENYL)INDOLIN 2 ONE;
1 BENZYL 3 [4 (N OXY PYRIDINYLMETHYLIDENYL)]INDOLIN 2 ONE;
INDOLE DERIVATIVE;
RETINOIC ACID;
UNCLASSIFIED DRUG;
ARTICLE;
CELL CYCLE ARREST;
CELL CYCLE G1 PHASE;
CELL DIFFERENTIATION;
CELL PROLIFERATION;
CELL STRAIN HL 60;
CELL STRUCTURE;
CONTROLLED STUDY;
CYTOTOXICITY;
DRUG ACTIVITY;
DRUG EFFECT;
DRUG POTENTIATION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
ISOMERISM;
NUCLEAR OVERHAUSER EFFECT;
PROTON NUCLEAR MAGNETIC RESONANCE;
THIN LAYER CHROMATOGRAPHY;
CELL DIFFERENTIATION;
CELL PROLIFERATION;
CELL SHAPE;
HL-60 CELLS;
HUMANS;
MAGNETIC RESONANCE SPECTROSCOPY;
METHYLATION;
MOLECULAR STRUCTURE;
PYRIMIDINES;
QUINOLINES;
STRUCTURE-ACTIVITY RELATIONSHIP;
TRETINOIN;
|
EID: 42149182035
PISSN: 09680896
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmc.2008.02.093 Document Type: Article |
Times cited : (14)
|
References (13)
|