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benzo(a)pyrene-3,6-quinol

Known as: 3,6-dihydroxybenzo(a)pyrene, BP-3,6-quinol 
 
National Institutes of Health

Papers overview

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Review
2004
Review
2004
Abstract(1)The role of conjugating enzymes is best understood by looking at the interaction between phase I (mostly cytochromes P… Expand
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1995
1995
Glucuronidation of quinols of polycyclic aromatic hydrocarbons (PAHs) represents an important detoxication pathway preventing… Expand
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1994
1994
Indirect evidence has suggested that multiple subunits of microsomal UDP-glucuronosyltransferases (UGTs) are involved in… Expand
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1992
1992
Mono- and diphenols of chrysene and benzo(a)pyrene are suspected substrates of a 3-methylcholanthrene (MC)-inducible phenol UDP… Expand
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1991
1991
P450-dependent mono-oxygenase and conjugating enzyme activities were studied in rat liver epithelial cells (RLEs) and compared to… Expand
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1987
1987
(1) UDP-glucuronosyltransferase (UDP-GT) activities and their inducibility were investigated in human liver microsomes from a… Expand
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1986
1986
The effect of dicoumarol on glucuronidation of 3-OH-benzo(a)pyrene (BP) appears to be due to inhibition of… Expand
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1986
1986
Glucuronidation of various substrates in hepatic, intestinal and renal microsomes of control, phenobarbital (PB), 3… Expand
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1985
1985
  • Christina Lind
  • Archives of biochemistry and biophysics
  • 1985
  • Corpus ID: 23978609
The formation of benzo[a]pyrene (BP)-3,6 quinol glucuronides in liver microsomes in the presence of UDP-glucuronic acid and NAD(P… Expand
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1985
1985
Cytotoxic effects of quinones are thought to be mediated by redox cycles between quinones and quinols whereby reactive oxygen… Expand
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