Inhibition of rat liver glutathione S-transferases by glutathione conjugates and corresponding l-cysteines and mercapturic acids

1986 ◽  
Vol 35 (4) ◽  
pp. 651-654 ◽  
Author(s):  
Lay Khoon Ong ◽  
Alan G. Clark
1983 ◽  
Vol 258 (18) ◽  
pp. 11321-11325 ◽  
Author(s):  
A B Frey ◽  
T Friedberg ◽  
F Oesch ◽  
G Kreibich

1971 ◽  
Vol 125 (1) ◽  
pp. 159-168 ◽  
Author(s):  
P. Sims

The syntheses of 10,11-dihydrobenz[a]anthracene 8,9-oxide, benz[a]anthracene 8,9-oxide and 9-hydroxybenz[a]anthracene are described, together with those of a number of related compounds. The epoxides react both chemically and enzymically with water to yield the corresponding dihydrodiols and with reduced glutathione to form glutathione conjugates, and they react chemically with N-acetylcysteine to yield the corresponding mercapturic acids. 8,9-Dihydro-8,9-dihydroxybenz[a]anthracene, formed enzymically from benz[a]anthracene 8,9-oxide, was identical with a dihydrodiol formed when benz[a]anthracene was metabolized by rat liver homogenates. Similarly 10,11-dihydrobenz[a]anthracene 8,9-oxide yielded a dihydrodiol identical with the product formed when 10,11-dihydrobenz[a]anthracene was metabolized.


1982 ◽  
Vol 108 (2) ◽  
pp. 461-467 ◽  
Author(s):  
Chen-Pei D. Tu ◽  
Mitchell J. Weiss ◽  
C. Channa Reddy

1985 ◽  
Vol 34 (15) ◽  
pp. 2695-2704 ◽  
Author(s):  
Michael K. Bach ◽  
John R. Brashler ◽  
Mark A. Johnson

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