Compound
L-isoleucyl-L-leucine
A dipeptide zwitterion obtained by transfer of a proton from the carboxy to the amino terminus of Ile-Leu.
Definition from ChEBI (CHEBI:190706), read 2026-09-23. CC BY 4.0.
CHEBI:190706ChEBI
Structure
Loading the model…
- Class
- Organic compound
- Formula
- C12H24N2O3
- Mass
- 244.335 g/mol
- Charge
- 0
- InChIKey
- JWBXCSQZLLIOCI-GUBZILKMSA-N
- SMILES
- CC[C@H](C)[C@H]([NH3+])C(=O)N[C@@H](CC(C)C)C(=O)[O-]
- Look it up
- ChEBIPubChemBy InChIKey
Identity from ChEBI, geometry from PubChem. Not evidence.
Reactions
1 reaction
neurotensin+waterneurotensin(1-11)+L-isoleucyl-L-leucine
Reaction pageLeft to rightBalanced
Rhea RHEA:71475CC BY 4.0Reference data
Other names
5 names
Resolves to: L-isoleucyl-L-leucine
- Also called
- (2S)-2-[(2S,3S)-2-ammonio-3-methylpentanamido]-4-methylpentanoateIL zwitterionL-Ile-L-Leu zwitterionL-isoleucyl-L-leucine zwitterion
- Systematic name
- (2S)-2-{[(2S,3S)-2-azaniumyl-3-methylpentanoyl]amino}-4-methylpentanoate