Skip to search formSkip to main contentSkip to account menu

1-methylhistidine

Known as: 1-MeHis, 2-Amino-3-(1-Methyl-1H-Imidazol-4-Yl)Propanoic Acid, Pi-Methylhistidine 
A histidine derivative that has a methyl group bound to the nitrogen at position 1 and results from the metabolism of the dipeptide anserine. Urinary… 
National Institutes of Health

Related topics

Related topics

2 relations
1-Methylhistidine:SCnc:Pt:Urine:Qn

Broader (1)

Methylhistidines

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2002
2002
Modeling Non-Ideal Inductors in SPICE
The non-ideal inductor exhibits both resonance and non-linear current characteristics. These effects can be modelled in SPICE by… 
1992
1992
Gas chromatographic/mass spectrometric analysis of stable isotopes of 3-methylhistidine in biological fluids: application to plasma kinetics in vivo.
A simple and rapid method for measuring 3-methylhistidine (3MH) in plasma and urine is described. Internal standard, 1… 
Highly Cited
1988
Highly Cited
1988
Detection, characterisation, and quantification of carnosine and other histidyl derivatives in cardiac and skeletal muscle.
Highly Cited
1985
Highly Cited
1985
Purification and properties of a pyridoxal 5'-phosphate-dependent histidine decarboxylase from Morganella morganii AM-15.
1984
1984
Triple-column ion-exchange physiological amino acid analysis with fluorescent detection: baseline characterization of human cerebrospinal fluid.
1980
1980
Biosynthesis and degradation of carnosine and turnover rate of its constituent amino acids in rats.
The biosynthesis and destruction of anserine and carnosine in the rat were investigated in vivo using radioactive β-alanine… 
1979
1979
An automatic method for determination of urinary 3-methylhistidine: normal values.
1971
1971
Enzymatic methylation of skeletal muscle contractile proteins.
1960
1960
The metabolism of anserine and carnosine in normal and vitamin E-deficient rabbits.
Highly Cited
1957
Highly Cited
1957
The metabolism of methylhistidine compounds in animals.
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)