Synthesis of novel pyrano[3,2-f]quinoline, phenanthroline derivatives and studies of their interactions with proteins: An application in mammalian cell imaging

European Journal of Medicinal Chemistry

Volumn 71, Issue , 2014, Pages 306-315

  Majumdar, K C ^a   Ponra, Sudipta ^a   Ghosh, Tapas ^a   Sadhukhan, Ratan ^a   Ghosh, Utpal ^a  

^a UNIVERSITY OF KALYANI   (India)

Author keywords

Fluorophore; HeLa cell; Phenanthroline; Protein binding; Pyrano 3,2 f quinoline

Indexed keywords

1 ETHY 6 (ETHYLAMINO) 5 (3 HYDROXY 3 METHYLBUT 1 YNYL)QUINOLIN 2(1H) ONE; 1 ETHYL 5 (3 HYDROXY 3 METHYLBUT 1 YNYL) 6 (METHYLAMINO)QUINOLIN 2(1H) ONE; 3,3,4,7 TETRAMETHYL 3,4 DIHYDRO 4,7 PHENANTHROLINE 1,8(2H,7H) DIONE; 3,3,7 TRIMETHYL 3,4 DIHYDRO 4,7 PHENANTHROLINE 1,8(2H,7H) DIONE; 4 ETHYL 3,3,7 TRIMETHYL 3,4 DIHYDRO 4,7 PHENANTHROLINE 1,8(2H,7H) DIONE; 4,7 DIETHYL 3,3 DIMETHYL 3,4 DIHYDRO 4,7 PHENANTHROLINE 1,8(2H,7H) DIONE; 5 (3 HYDROXY 3 METHYLBUT 1 YNYL) 1 METHYL 6 (METHYLAMINO)QUINOLIN 2(1H) ONE; 5 (3 HYDROXY 3 METHYLBUT 1 YNYL) 6 (METHYLAMINO) 2H CHROMEN 2 ONE; 6 (ETHYLAMINO) 5 (3 HYDROXY 3 METHYLBUT 1 YNYL) 1 METHYLQUINOLIN 2(1H) ONE; 6 (ETHYLAMINO) 5 (3 HYDROXY 3 METHYLBUT 1 YNYL) 2H CHROMEN 2 ONE; 6 AMINO 1 ETHYL 5 (3 HYDROXY 3 METHYLBUT 1 YNYL)QUINOLIN 2(1H) ONE; 6 AMINO 5 (3 HYDROXY 3 METHYLBUT 1 YNYL) 1 METHYLQUINOLIN 2(1H) ONE; 6 AMINO 5 (3 HYDROXY 3 METHYLBUT 1 YNYL) 2H CHROMEN 2 ONE:; 7 ETHYL 3,3 DIMETHYL 3,4 DIHYDRO 4,7 PHENANTHROLINE 1,8(2H,7H) DIONE; 7 ETHYL 3,3 TRIMETHYL 3,3,4 DIHYDRO 4,7 PHENANTHROLINE 1,8(2H,7H) DIONE; 7 ETHYL 8,8 DIMETHYL 8,9 DIHYDRO 3H PYRANO[3,2 F]QUINOLINE 3,10(7H) DIONE; 7,8,8 TRIMETHYL 8,9 DIHYDRO 3H PYRANO[3,2 F]QUINOLINE 3,10(7H) DIONE; 8,8 DIMETHYL 8,9 DIHYDRO 3H PYRANO[3,2 F]QUINOLINE 3,10(7H) DIONE; N [1 ETHYL 5 (3 HYDROXY 3 METHYLBUT 1 YNYL) 2 OXO 1,2 DIHYDROQUINOLIN 6 YL]ACETAMIDE; N [5 (3 HYDROXY 3 METHYLBUT 1 YNYL) 2 OXO 2H CHROMEN 6 YL]ACETAMIDE; PHENANTHROLINE DERIVATIVE; PYRANO[3,2 F]PHENANTHROLINE DERIVATIVE; PYRANO[3,2 F]QUINOLINE DERIVATIVE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG; 3,3,4,7 TETRAMETHYL 3,4 DIHYDRO 4,7 PHENANTHROLINE 1,8(2H,7H)DIONE; 3,3,7 TRIMETHYL 3,4 DIHYDRO 4,7 PHENANTHROLINE 1,8(2H,7H)DIONE; 4 ETHYL 3,3,7 TRIMETHYL 3,4 DIHYDRO 4,7 PHENANTHROLINE 1,8(2H,7H)DIONE; 4,7 DIETHYL 3,3 DIMETHYL 3,4 DIHYDRO 4,7 PHENANTHROLINE 1,8(2H,7H)DIONE; 7 ETHYL 3,3 DIMETHYL 3,4 DIHYDRO 4,7 PHENANTHROLINE 1,8(2H,7H)DIONE; 7 ETHYL 3,3,4 TRIMETHYL 3,4 DIHYDRO 4,7 PHENANTHROLINE 1,8(2H,7H)DIONE; 7 ETHYL 8,8 DIMETHYL 8,9 DIHYDRO 3H PYRANO [3,2 F]QUINOLINE 3,10(7H)DIONE; 7,8,8 TRIMETHYL 8,9 DIHYDRO 3H PYRANO [3,2 F]QUINOLINE 3,10(7H)DIONE; 8,8 DIMETHYL 8,9 DIHYDRO 3H PYRANO [3,2 F]QUINOLINE 3,10(7H)DIONE;

ARTICLE; BINDING AFFINITY; CARBON NUCLEAR MAGNETIC RESONANCE; CELL CULTURE; CYCLIZATION; DEACETYLATION; DISSOCIATION CONSTANT; DRUG SYNTHESIS; HELA CELL; HUMAN; HUMAN CELL; MELTING POINT; MICROWAVE COOKING; MICROWAVE IRRADIATION; ONE POT SYNTHESIS; PROTEIN BINDING; PROTEIN INTERACTION; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION TIME; SONOGASHIRA REACTION; STAINING; ULTRAVIOLET RADIATION; CHROMATOGRAPHY; DRUG PROTEIN BINDING; EMBRYO; FEMALE; HELA CELL LINE; MAMMAL CELL; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; RING CLOSING METATHESIS;

FLUOROPHORE; HELA CELL; PHENANTHROLINE; PROTEIN BINDING; PYRANO[3,2-F]QUINOLINE;

HELA CELLS; HUMANS; MICROSCOPY, FLUORESCENCE; OPTICAL IMAGING; PHENANTHROLINES; PROTEINS; PYRANS; QUINOLINES; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84889003832     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2013.10.067     Document Type: Article

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