Structure
Loading the model…
- Class
- Organic compound
- Formula
- C10H16N4O3
- Mass
- 240.263 g/mol
- Charge
- 0
- InChIKey
- MYYIAHXIVFADCU-QMMMGPOBSA-N
- SMILES
- Cn1cncc1C[C@H](NC(=O)CC[NH3+])C(=O)[O-]
- Look it up
- ChEBIPubChemBy InChIKey
Identity from ChEBI, geometry from PubChem. Not evidence.
What the reference databases state
Statements
2 statements
2 statements · 1 reference database · Subject: anserine · Sources: Rhea
- carnosine is converted to anserineCompoundRhea RHEA:14205Inferred only
- anserine is a substrate of CNDP1ProteinRhea RHEA:59576Inferred only
Reactions
2 reactions
carnosine+S-adenosyl-L-methionineanserine+S-adenosyl-L-homocysteine+hydron
Catalysed by CARNMT1
Reaction pageLeft to rightBalanced
Rhea RHEA:14205CC BY 4.0Reference data
anserine+waterN(pros)-methyl-L-histidine+beta-alanine
Catalysed by CNDP1
Reaction pageLeft to rightBalanced
Rhea RHEA:59576CC BY 4.0Reference data
On the label
Labelled products
1 product
Source: NIH DSLD · Ingredient: anserine · 1 product · Declared amount per serving: Not stated
0 labels state an amount1 does not
- VPXPower Shock Lime SplashAnserine Note: beta-alanyl-1-methylhistidineamount not statedper 13.5 gDSLD:2015
Label record: NIH Office of Dietary Supplements · CC0
Other names
1 name
Resolves to: anserine
- Systematic name
- (2S)-2-[(3-ammoniopropanoyl)amino]-3-(1-methyl-1H-imidazol-5-yl)propanoate