Synthesis, crystal structure and antidiabetic activity of substituted (E)-3-(Benzo [d]thiazol-2-ylamino) phenylprop-2-en-1-one

European Journal of Medicinal Chemistry

Volumn 59, Issue , 2013, Pages 304-309

  Patil, Vijay S ^a,b   Nandre, Kamalakar P ^b   Ghosh, Sougata ^c   Rao, Vaidya Jayathirtha ^b   Chopade, Balu A ^c   Sridhar, Balasubramanian ^b   Bhosale, Sheshanath V ^d   Bhosale, Sidhanath V ^a,b  

^a NORTH MAHARASHTRA UNIVERSITY   (India)

^b INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

^c UNIVERSITY OF PUNE   (India)

^d RMIT UNIVERSITY   (Australia)

Author keywords

Aroylketene dithioacetals; 2 Aminobenzothiazole; Antidiabetic

Indexed keywords

1 (4 BROMOPHENYL) 3 (5,6 DIMETHYLBENZO[D]THIAZOL 2 YLAMINO) 3 (METHYLTHIO)PROP 2 EN 1 ONE; 1 (4 BROMOPHENYL) 3 (6 ETHOXYBENZO[D]THIAZOL 2 YLAMINO) 3 (METHYLTHIO)PROP 2 EN 1 ONE; 1 (4 CHLOROPHENYL) 3 (6 ETHOXYBENZO[D]THIAZOL 2 YLAMINO) 3 (METHYLTHIO)PROP 2 EN 1 ONE; 3 (6 ETHOXYBENZO [D]THIAZOL 2 YLAMINO) 3 (METHYLTHIO) 1 4 TOLYLPROP 2 EN 1 ONE; 3 (6 ETHOXYBENZO[D]THIAZOL 2 YLAMINO) 1 (4 FLUOROPHENYL) 3 (METHYLTHIO)PROP 2 EN 1 ONE; 3 (6 ETHOXYBENZO[D]THIAZOL 2 YLAMINO) 1 (4 METHOXYPHENYL) 3 (METHYLTHIO)PROP 2 EN 1 ONE; 3 (6 ETHOXYBENZO[D]THIAZOL 2 YLAMINO) 3 (METHYLTHIO) 1 PHENYLPROP 2 EN 1 ON; 3 (BENZO [D]THIAZOL 2 YLAMINO) 1 (4 BROMOPHENYL) 3 (METHYLTHIO)PROP 2 EN 1 ONE; 3 (BENZO [D]THIAZOL 2 YLAMINO) 1 (4 CHLOROPHENYL) 3 (METHYLTHIO)PROP 2 EN 1; 3 (BENZO [D]THIAZOL 2 YLAMINO) 1 (4 FLUOROPHENYL) 3 (METHYLTHIO)PROP 2 EN 1 ONE; 3 (BENZO [D]THIAZOL 2 YLAMINO) 3 (METHYLTHIO) 1 4 TOLYLPROP 2 EN 1 ONE; ANTIDIABETIC AGENT; UNCLASSIFIED DRUG;

ANTIDIABETIC ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CRYSTAL STRUCTURE; DRUG STRUCTURE; DRUG SYNTHESIS; INFRARED SPECTROSCOPY; MASS SPECTROMETRY; PROTON NUCLEAR MAGNETIC RESONANCE;

AMYLASES; ANIMALS; BENZOTHIAZOLES; CRYSTALLOGRAPHY, X-RAY; ENZYME ACTIVATION; GLUCOSIDASES; HYPOGLYCEMIC AGENTS; INHIBITORY CONCENTRATION 50; MAGNETIC RESONANCE SPECTROSCOPY; MICE; MOLECULAR STRUCTURE; PROPIOPHENONES; SWINE;

EID: 84871150692     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2012.11.020     Document Type: Article

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