Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

5,6-dimethylchrysene

 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
1999
1999
Both syn and anti dihydrodiol epoxides from 5-methylchrysene (5-MCDE) and 5,6-dimethylchrysene (5,6-DMCDE) were reacted under the… Expand
1998
1998
We compared the tumor-initiating activities toward mouse skin of two structurally related polycyclic aromatic hydrocarbon diol… Expand
1997
1997
The DNA adducts formed from the racemic syn and anti dihydrodiol epoxides of 5,6-dimethylchrysene were characterized through… Expand
1997
1997
Capillary electrochromatography (CEC) was used for the analysis of mixtures of neutral isomeric compounds derived from the… Expand
1995
1995
Dihydrodiol epoxides from 5,6-dimethylchrysene exhibit properties similar to those of fjord region-containing hydrocarbon… Expand
1993
1993
Previous metabolism and DNA-binding studies indicated that 5,6-dimethylchrysene (5,6-diMeC) is metabolically activated in mouse… Expand
1992
1992
In contrast to 5-methylchrysene and 5,9-dimethylchrysene, 5,6-dimethylchrysene and 5,7-dimethylchrysene are weak tumor initiators… Expand
1992
1992
5,6-Dimethylchrysene (5,6-diMeC) is a weaker tumor initiator on mouse skin than 5-methylchrysene (5-MeC). To investigate the… Expand
1991
1991
The polynuclear aromatic hydrocarbon chrysene undergoes a bioalkylation substitution reaction in vitro, in rat liver cytosol… Expand
1984
1984
The presence of a bay-region methyl group in carcinogenic polycyclic aromatic hydrocarbons leads to considerable distortion in… Expand