rdf:type |
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lifeskim:mentions |
umls-concept:C0028197,
umls-concept:C0030054,
umls-concept:C0068234,
umls-concept:C0332120,
umls-concept:C0439596,
umls-concept:C0441587,
umls-concept:C1314939,
umls-concept:C1521991,
umls-concept:C1522492,
umls-concept:C1710236,
umls-concept:C1979928
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pubmed:issue |
1-2
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pubmed:dateCreated |
1984-7-9
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pubmed:abstractText |
The formation of the products of microsomal metabolism of the cyclic nitrosamine, nitrosohexamethyleneimine (NO-HEX) were studied. Information on the origins of the oxygen atoms in four major metabolites of NO-HEX was obtained by metabolizing this compound in an 18O2 atmosphere using microsomes and cytosol, beta- and gamma-Hydroxy-NO-HEX are formed as a result of the insertion of a hydroxyl group derived from molecular oxygen into NO-HEX. All of the oxygen atoms in epsilon-aminocaproate (EAC) were derived from water. Approximately half of the molecules of epsilon- hydroxycaproate ( EHC ) contain an 18O atom; thus, half of the alpha-hydroxy-NO-HEX formed incorporates a hydroxyl group derived from molecular oxygen with the remainder of the hydroxyls being from water. To account for the above data and the related metabolic origins of EAC and EHC ( Hecker and McClusky , Cancer Res., 42 (1982) 59; Hecker et al., Teratogen. Carcinogen. Mutagen (1982) in press), we have proposed a mechanism for the formation of these compounds from cyclic nitrosamines catalyzed by microsomal and cytosolic enzymes.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/6-Aminocaproic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/6-hydroxyhexanoic acid,
http://linkedlifedata.com/resource/pubmed/chemical/Aminocaproic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Caproates,
http://linkedlifedata.com/resource/pubmed/chemical/Carcinogens,
http://linkedlifedata.com/resource/pubmed/chemical/Hexanoic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Mixed Function Oxygenases,
http://linkedlifedata.com/resource/pubmed/chemical/N-nitrosoperhydroazepine,
http://linkedlifedata.com/resource/pubmed/chemical/Nitrosamines,
http://linkedlifedata.com/resource/pubmed/chemical/Oxygen,
http://linkedlifedata.com/resource/pubmed/chemical/Water
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0009-2797
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
235-48
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:6722936-6-Aminocaproic Acid,
pubmed-meshheading:6722936-Aminocaproic Acids,
pubmed-meshheading:6722936-Animals,
pubmed-meshheading:6722936-Caproates,
pubmed-meshheading:6722936-Carcinogens,
pubmed-meshheading:6722936-Chemical Phenomena,
pubmed-meshheading:6722936-Chemistry,
pubmed-meshheading:6722936-Cytosol,
pubmed-meshheading:6722936-Hexanoic Acids,
pubmed-meshheading:6722936-Male,
pubmed-meshheading:6722936-Mass Spectrometry,
pubmed-meshheading:6722936-Microsomes, Liver,
pubmed-meshheading:6722936-Mixed Function Oxygenases,
pubmed-meshheading:6722936-Nitrosamines,
pubmed-meshheading:6722936-Oxygen,
pubmed-meshheading:6722936-Rats,
pubmed-meshheading:6722936-Water
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pubmed:year |
1984
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pubmed:articleTitle |
Formation of epsilon-hydroxycaproate and epsilon-aminocaproate from N-nitrosohexamethyleneimine: evidence that microsomal alpha-hydroxylation of cyclic nitrosamines may not always involve the insertion of molecular oxygen into the substrate.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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