rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
1
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pubmed:dateCreated |
1983-9-9
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pubmed:abstractText |
A nitrogen-centered free radical was spin-trapped from superoxide-catalyzed oxidation of indolic compounds, using the spin-trap phenyl-t-butyl-nitrone. The hyperfine splitting constants observed were aN = 13.9 G, a beta N = 3.6 G and a beta H = 2.3 G. Incubation of various indolic compounds with goat lung microsomes showed that only 3-methylindole was able to generate a free radical in the NADPH-dependent microsomal system, as tested by spin-trapping. The splitting constants were the same as those seen with superoxide incubations with 3-methylindole. The study demonstrates the generality of formation of a nitrogen-centered free radical from various indolic compounds. Enzymatic radical formation from 3-methylindole suggests a microsomal-activated free radical mechanism for the specificity of 3-methylindole-induced pulmonary toxicity.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
|
pubmed:status |
MEDLINE
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pubmed:month |
Jul
|
pubmed:issn |
0006-291X
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:day |
18
|
pubmed:volume |
114
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
168-74
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:6309164-Animals,
pubmed-meshheading:6309164-Biotransformation,
pubmed-meshheading:6309164-Chemical Phenomena,
pubmed-meshheading:6309164-Chemistry,
pubmed-meshheading:6309164-Cyclic N-Oxides,
pubmed-meshheading:6309164-Electron Spin Resonance Spectroscopy,
pubmed-meshheading:6309164-Free Radicals,
pubmed-meshheading:6309164-Goats,
pubmed-meshheading:6309164-Indoles,
pubmed-meshheading:6309164-Lung,
pubmed-meshheading:6309164-Microsomes,
pubmed-meshheading:6309164-Microsomes, Liver,
pubmed-meshheading:6309164-Nitrogen Oxides,
pubmed-meshheading:6309164-Spin Labels,
pubmed-meshheading:6309164-Structure-Activity Relationship
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pubmed:year |
1983
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pubmed:articleTitle |
The spin-trapping of enzymatically and chemically catalyzed free radicals from indolic compounds.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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