4-methylquinoline

 
National Institutes of Health

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2014
2014
BACKGROUND Synthetic preservatives have been consistently used to maintain the quality of food products. However, the degree of… Expand
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2014
2014
The acaricidal and insecticidal potential of the active constituent isolated from Citrullus colocynthis fruits and its… Expand
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2009
2009
A series of Thiazole Orange (TO) derivatives were synthesized and modified by introducing different substitutional groups on… Expand
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2008
2008
N-heterocyclic compounds are known pollutants at tar oil contaminated sites. Here we report the degradation of methyl-, and… Expand
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2000
2000
We have previously shown that fluorine-substitution at position 3 of quinoline deprived this molecule of mutagenicity, possibly… Expand
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1999
1999
Strain Lep1, isolated from a bacterial consortium capable of aerobic degradation of 4-methylquinoline (4-MQ), was chosen for… Expand
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1996
1996
Methylquinolines and related N-heterocyclic aromatic compounds are common contaminants associated with the use of hydrocarbons in… Expand
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1996
1996
4-Methylquinoline (4-MeQ) showed an extraordinarily potent mutagenicity when compared to quinoline and isomeric methylquinolines… Expand
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1988
1988
The relative tumorigenic activity of quinoline, 4-methylquinoline, 8-methylquinoline, and all three isomeric benzoquinolines was… Expand
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1984
1984
Quinoline and all 7 positional isomers of methylquinoline were assayed for tumor-initiating activity on the skin of SENCAR female… Expand
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