Compound
L-histidyl-L-leucine
A dipeptide zwitterion obtained by transfer of a proton from the carboxy to the amino terminus of His-Leu. Major species at pH 7.3.
Definition from ChEBI (CHEBI:147392), read 2026-09-23. CC BY 4.0.
CHEBI:147392ChEBI
Structure
No depiction stored
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- Class
- Organic compound
- Formula
- C12H20N4O3
- Mass
- 268.317 g/mol
- Charge
- 0
- InChIKey
- MMFKFJORZBJVNF-UWVGGRQHSA-N
- SMILES
- CC(C)C[C@H](NC(=O)[C@@H]([NH3+])Cc1cncn1)C(=O)[O-]
- Look it up
- ChEBIPubChemBy InChIKey
Identity from ChEBI, geometry from PubChem. Not evidence.
Reactions
1 reaction
angiotensin I+waterL-histidyl-L-leucine+angiotensin II
Catalysed by ACE
Reaction pageLeft to rightBalanced
Rhea RHEA:63560CC BY 4.0Reference data
Other names
4 names
Resolves to: L-histidyl-L-leucine
- Also called
- H-L zwitterionhistidylleucine zwitterionL-His-L-Leu zwitterion
- Systematic name
- (2S)-2-{[(2S)-2-azaniumyl-3-(1H-imidazol-4-yl)propanoyl]amino}-4-methylpentanoate