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Volumn 44, Issue 4, 2009, Pages 1427-1436
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New acyclic nucleosides analogues as potential analgesic, anti-inflammatory, anti-oxidant and anti-microbial derived from pyrimido[4,5-b]quinolines
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Author keywords
2 Thioxopyrimido 4,5 b quinoline; Analgesic; Anti inflammatory activities; Anti oxidant; Glycosidopyrimido 4,5 b quinolines; Microwave
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Indexed keywords
2 (1',2',3',4' TETRA O ACETYLARABINOSYLHYDRAZON) N3 ACETYL 5 (4 CHLOROPHENYL) 9 (4 CHLOROPHENYLMETHYLENE) 6,7,8,9 TETRAHYDRO 1H PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
2 (1',2',3',4' TETRA O ACETYLRIBOSYLHYDRAZON) N3 ACETYL 5 (4 CHLOROPHENYL) 9 (4 CHLOROPHENYLMETHYLENE) 6,7,8,9 TETRAHYDRO 1H PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
2 (1',2',3',4' TETRA O ACETYLXYLOSYLHYDRAZON) N3 ACETYL 5 (4 CHLOROPHENYL) 9 (4 CHLOROPHENYLMETHYLENE) 6,7,8,9 TETRAHYDRO 1H PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
2 (ARABINOSYLHYDRAZON) 5 (4 CHLOROPHENYL) 9 (4 CHLOROPHENYLMETHYLENE) 3,6,7,8,9 PENTAHYDRO 1H PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
2 (GALACTOSYLHYDRAZON) 5 (4 CHLOROPHENYL) 9 (4 CHLOROPHENYLMETHYLENE) 3,6,7,8,9 PENTAHYDRO 1H PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
2 (GLUCOSYLHYDRAZON) 5 (4 CHLOROPHENYL) 9 (4 CHLOROPHENYLMETHYLENE) 3,6,7,8,9 PENTAHYDRO 1H PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
2 (MANNOSYLHYDRAZON) 5 (4 CHLOROPHENYL) 9 (4 CHLOROPHENYLMETHYLENE) 3,6,7,8,9 PENTAHYDRO 1H PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
2 (RIBOSYLHYDRAZON) 5 (4 CHLOROPHENYL) 9 (4 CHLOROPHENYLMETHYLENE) 3,6,7,8,9 PENTAHYDRO 1H PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
2 (XYLOSYLHYDRAZON) 5 (4 CHLOROPHENYL) 9 (4 CHLOROPHENYLMETHYLENE) 3,6,7,8,9 PENTAHYDRO 1H PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
3 (1',2',3',4','5' PENTA O ACETYLGALACTOSYL) 6 (4 CHLOROPHENYL) 10 (4 CHLOROPHENYLMETHYLENE) 7,8,9,10 TETRAHYDRO[1,2,4]TRIAZOLO[4',3':1,2] PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
3 (1',2',3',4',5' PENTA O ACETYLGLUCOSYL) 6 (4 CHLOROPHENYL) 10 (4 CHLOROPHENYLMETHYLENE) 7,8,9,10 TETRAHYDRO[1,2,4]TRIAZOLO[4',3':1,2] PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
3 (1',2',3',4',5' PENTA O ACETYLMANNOSYL) 6 (4 CHLOROPHENYL) 10 (4 CHLOROPHENYLMETHYLENE) 7,8,9,10 TETRAHYDRO[1,2,4]TRIAZOLO[4',3':1,2]PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
3 (ARABINOSYL) 6 (4 CHLOROPHENYL) 10 (4 CHLOROPHENYLMETHYLENE) 7,8,9,10 TETRAHYDRO[1,2,4]TRIAZOLO[4',3':1,2]PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
3 (GALACTOSYL) 6 (4 CHLOROPHENYL) 10 (4 CHLOROPHENYLMETHYLENE) 7,8,9,10 TETRAHYDRO[1,2,4]TRIAZOLO[4',3':1,2]PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
3 (GLUCOSYL) 6 (4 CHLOROPHENYL) 10 (4 CHLOROPHENYLMETHYLENE) 7,8,9,10 TETRAHYDRO [1,2,4]TRIAZOLO[4',3':1,2]PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
3 (MANNOSYL) 6 (4 CHLOROPHENYL) 10 (4 CHLOROPHENYLMETHYLENE) 7,8,9,10 TETRAHYDRO [1,2,4]TRIAZOLO[4',3':1,2]PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
5 (4 CHLOROPHENYL) 9 (4 CHLOROPHENYLMETHYLENE) 2 HYDRAZINO 3,6,7,8,9 PENTAHYDRO 1H PYRIMIDO[4,5 B]QUINOLIN 4(4H) ONE;
9 (4 CHLOROPHENYLMETHYLENE) 5 (4 CHLOROPHENYL) 2 THIOXO 2,3,6,7,8,9 HEXAHYDRO PYRIMIDO[4,5 B]QUINOLIN 4 ONE;
9 (4 METHOXYPHENYMETHYLENE) 5 (4 METHOXYPHENYL) 2 THIOXO 2,3,6,7,8,9 HEXAHYDROPYRIMIDO[4,5 B]QUINOLIN 4 ONE;
9 PHENYLMETHYLENE 5 PHENYL 2 THIOXO 2,3,6,7,8,9 HEXAHYDROPYRIMIDO[4,5 B]QUINO LIN 4 ONE;
ACYCLIC NUCLEOSIDE;
ANALGESIC AGENT;
ANTIINFECTIVE AGENT;
ANTIINFLAMMATORY AGENT;
ANTIOXIDANT;
ASCORBIC ACID;
NUCLEOSIDE DERIVATIVE;
PYRIMIDINONE DERIVATIVE;
QUINOLINE DERIVATIVE;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
ANALGESIC ACTIVITY;
ANTIINFLAMMATORY ACTIVITY;
ANTIMICROBIAL ACTIVITY;
ANTIOXIDANT ACTIVITY;
ARTICLE;
ASPERGILLUS FUMIGATUS;
BACILLUS SUBTILIS;
CANDIDA ALBICANS;
CARBON NUCLEAR MAGNETIC RESONANCE;
CONTROLLED STUDY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ESCHERICHIA COLI;
GRAM NEGATIVE BACTERIUM;
GRAM POSITIVE BACTERIUM;
HEMOLYSIS;
INFRARED SPECTROSCOPY;
MASS SPECTROMETRY;
MICROWAVE OVEN;
MINIMUM INHIBITORY CONCENTRATION;
NONHUMAN;
PROTON NUCLEAR MAGNETIC RESONANCE;
PSEUDOMONAS AERUGINOSA;
STAPHYLOCOCCUS AUREUS;
ANALGESICS;
ANIMALS;
ANTI-INFECTIVE AGENTS;
ANTI-INFLAMMATORY AGENTS;
ANTIOXIDANTS;
BACTERIA;
CARRAGEENAN;
DRUG DISCOVERY;
EDEMA;
FEMALE;
LIPID PEROXIDATION;
MALE;
MICE;
MICROWAVES;
NUCLEOSIDES;
QUINOLINES;
RATS;
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EID: 61449168879
PISSN: 02235234
EISSN: 17683254
Source Type: Journal
DOI: 10.1016/j.ejmech.2008.09.030 Document Type: Article |
Times cited : (124)
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References (29)
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