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5-hydroxy-3-methylindole

Known as: 3-methyl-1H-indol-5-ol 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
  • M. Gray, E. Squires
  • The Journal of Steroid Biochemistry and Molecular…
  • 2013
  • Corpus ID: 45036306
The accumulation of the testicular steroid androstenone (AND) and tryptophan degradation product skatole (3MI) in fat results in… Expand
2012
2012
Boar taint is the unfavourable odour and taste from pork fat, which results in part from the accumulation of skatole (3… Expand
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2012
2012
Bazedoxifene is a selective estrogen receptor modulator (SERM) that has been developed for use in post-menopausal osteoporosis… Expand
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2007
2007
Metabolism and bioactivation of 3-methylindole (3MI) were investigated in human liver microsomes. The metabolism of two deuterium… Expand
2003
2003
  • G. Diaz, E. Squires
  • Xenobiotica; the fate of foreign compounds in…
  • 2003
  • Corpus ID: 20384039
1. The Phase II in vitro metabolism of 3-methylindole (3MI) metabolites was investigated in pigs to determine the possible… Expand
1978
1978
Electron capture gas chromatography was used to estimate the urinary 5-hydroxy-3-methylindole in epileptic patients and normal… Expand
1972
1972
1970
1970