Synthesis and anticonvulsant activity of 1-substituted-7-benzyloxy-4,5- dihydro-[1,2,4]triazolo[4,3-a]quinoline

Biological and Pharmaceutical Bulletin

Volumn 28, Issue 7, 2005, Pages 1216-1220

  Cui, Li Jing ^a   Xie, Zhi Feng ^a   Piao, Hu Ri ^a   Li, Gao ^a   Chai, Kyu Yun ^b   Quan, Zhe Shan ^a  

^a YANBIAN UNIVERSITY   (China)

^b Wonkwang University   (South Korea)

Author keywords

1,2,4 triazolo 4,3 a quinoline; Anticonvulsant; Maximal electroshock test; Neurotoxicity; Pentylenetetrazole

Indexed keywords

1 BENZYL 7 BENZYLOXY 4,5 DIHYDRO[1,2,4]TRIAZOLO[4,3 A]QUINOLINE; 7 BENZYLOXY 1 (2,5 DICHLOROPHENYL) 4,5 DIHYDRO[1,2,4]TRIAZOLO[4,3 A]QUINOLINE; 7 BENZYLOXY 1 (3 CHLOROPHENYL) 4,5 DIHYDRO[1,2,4]TRIAZOLO[4,3 A]QUINOLINE; 7 BENZYLOXY 1 (3 METHOXYPHENYL) 4,5 DIHYDRO[1,2,4]TRIAZOLO[4,3 A]QUINOLINE; 7 BENZYLOXY 1 (4 CHLOROBENZYL) 4,5 DIHYDRO[1,2,4]TRIAZOLO[4,3 A]QUINOLINE; 7 BENZYLOXY 1 (4 CHLOROPHENOXYMETHYL) 4,5 DIHYDRO[1,2,4]TRIAZOLO[4,3 A]QUINOLINE; 7 BENZYLOXY 1 3 TOLYL 4,5 DIHYDRO[1,2,4]TRIAZOLO[4,3 A]QUINOLINE; 7 BENZYLOXY 1 METHYL 4,5 DIHYDRO[1,2,4]TRIAZOLO[4,3 A]QUINOLINE; 7 BENZYLOXY 1 PENTYL 4,5 DIHYDRO[1,2,4]TRIAZOLO[4,3 A]QUINOLINE; 7 BENZYLOXY 1 PHENOXYMETHYL 4,5 DIHYDRO[1,2,4]TRIAZOLO[4,3 A]QUINOLINE; 7 BENZYLOXY 1 PHENYL 4,5 DIHYDRO[1,2,4]TRIAZOLO[4,3 A]QUINOLINE; 7 BENZYLOXY 1 PROPYL 4,5 DIHYDRO[1,2,4]TRIAZOLO[4,3 A]QUINOLINE; 7 BENZYLOXY 1 PYRIDIN 4 YL 4,5 DIHYDRO[1,2,4]TRIAZOLO[4,3 A]QUINOLINE; 7 BENZYLOXY 4,5 DIHYDRO[1,2,4]TRIAZOLO[4,3 A]QUINOLINE; PENTETRAZOLE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANTICONVULSANT ACTIVITY; ARTICLE; CONTROLLED STUDY; DRUG ACTIVITY; DRUG EFFICACY; DRUG SCREENING; DRUG STRUCTURE; DRUG SYNTHESIS; ELECTRIC SHOCK; INFRARED SPECTROSCOPY; MASS SPECTROMETRY; MOUSE; NEUROTOXICITY; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; SEIZURE; STRUCTURE ACTIVITY RELATION; SUBSTITUTION REACTION;

ANIMALS; ANTICONVULSANTS; MAGNETIC RESONANCE SPECTROSCOPY; MASS SPECTROMETRY; MICE; MICE, INBRED C57BL; QUINOLONES; SPECTROPHOTOMETRY, INFRARED;

EID: 24944482063     PISSN: 09186158     EISSN: None     Source Type: Journal    
DOI: 10.1248/bpb.28.1216     Document Type: Article

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