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New pathway for the biodegradation of indole in Aspergillus nigerExpansion of substrate specificity of cytochrome P450 2A6 by random and site-directed mutagenesis.Cytochrome P450 BM-3 evolved by random and saturation mutagenesis as an effective indole-hydroxylating catalyst.What makes P450s work? Searches for answers with known and new P450s.Colonic contribution to uremic solutes.Gastrointestinal and hepatotoxicity assessment of an anticancer extract from muricid molluscs.Possible roles of excess tryptophan metabolites in cancer.Peroxide oxidation of indole to oxindole by chloroperoxidase catalysis.A history of drug metabolism in the United Kingdom.Indoxyl sulfate, a uremic toxin in chronic kidney disease, suppresses both bone formation and bone resorption.The arthritogenic effect of indole, skatole and other tryptophan metabolites in rabbits.5-hydroxyindole causes convulsions and increases transmitter release in the CA1 region of the rat hippocampus.The metabolism of some 1-hydroxylated indoles in the rat.Dose-dependent effect of an oral adsorbent, AST-120, in patients with early chronic renal failure.Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 24 (FGE.24): Pyridine, pyrrole, indole and quinoline derivatives from chemical group 28...Pyridine, pyrrole, indole and quinoline derivatives from chemical group 28 Flavouring Group Evaluation 24, Revision 1 - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)Scientific opinion on Flavouring Group Evaluation 24, Revision 2 (FGE.24Rev2): Pyridine, pyrrole, indole and quinoline derivatives from chemical group 28Safety and efficacy of pyridine and pyrrole derivatives belonging to chemical group 28 when used as flavourings for all animal speciesPlasma and brain levels of oxindole in experimental chronic hepatic encephalopathy: effects of systemic ammonium acetate and L-tryptophan.Synthesis of (2-mercaptoacetyl)-L-[2-14 C]tryptophan as a selective metallo-β-lactamase inhibitor via [2-14 C]indole based on chiral pool strategy.Formation of the indigo precursor indican in genetically engineered tobacco plants and cell cultures.Simultaneous identification and quantitation of diphenhydramine and methaqualone.Indole
P2860
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P2860
description
1966 nî lūn-bûn
@nan
1966年の論文
@ja
1966年論文
@yue
1966年論文
@zh-hant
1966年論文
@zh-hk
1966年論文
@zh-mo
1966年論文
@zh-tw
1966年论文
@wuu
1966年论文
@zh
1966年论文
@zh-cn
name
The metabolism of [2-14C] indole in the rat
@en
The metabolism of [2-14C] indole in the rat
@nl
type
label
The metabolism of [2-14C] indole in the rat
@en
The metabolism of [2-14C] indole in the rat
@nl
prefLabel
The metabolism of [2-14C] indole in the rat
@en
The metabolism of [2-14C] indole in the rat
@nl
P2093
P2860
P356
P1433
P1476
The metabolism of [2-14C] indole in the rat
@en
P2093
P2860
P304
P356
10.1042/BJ0980266
P407
P577
1966-01-01T00:00:00Z