Leu-Pro
Basic information
- CAS
6403-35-6- Standard SMILES
CC(C)C[C@H](N)C(=O)N1CCC[C@H]1C(=O)O- InChIKey
VTJUNIYRYIAIHF-IUCAKERBSA-N- Molecular formula
- C11H20N2O3
- Average molar mass
- 228.29 g/mol
- Monoisotopic mass
- 228.1473925
Overview
Leu-Pro is a dipeptide formed from L-leucine and L-proline residues. It has a role as a metabolite. It is functionally related to a L-leucine and a L-proline. It is a tautomer of a Leu-Pro zwitterion.
Names & identifiers
- Preferred name
- Leu-Pro
- IUPAC
- (2S)-1-[(2S)-2-amino-4-methylpentanoyl]pyrrolidine-2-carboxylic acid
- English name
- leucylproline
- Molecular formula
- C11H20N2O3
- Molecular weight
- 228.29
Names & synonyms
Leu-proCHEBI:73580RefChem:1088421Leucylprolinel-leucyl-l-proline6403-35-6(2S)-1-[(2S)-2-amino-4-methylpentanoyl]pyrrolidine-2-carboxylic acidCHEMBL189210leucyl-prolineH-Leu-Pro-OHL-Leu-L-Prostarbld0035034
Show more names
L-Proline, L-leucyl-
L-Proline, 1-L-leucyl-orb1985873SCHEMBL3052903DTXSID30214012VTJUNIYRYIAIHF-IUCAKERBSA-NLPBDBM50169151AKOS010419273
Database identifiers
- CAS
6403-35-6- PubChem CID
- 80817
- DTXSID
DTXSID30214012- ChEMBL
CHEMBL189210- ChEBI
CHEBI:73580- Nikkaji
- J151.043F
Properties
Computed structural properties
- XLogP
- -1.8
- Topological polar surface area
- 83.6 Ų
- Hydrogen bond donors
- 2
- Hydrogen bond acceptors
- 4
- Rotatable bonds
- 4
- Heavy atoms
- 16
- Formal charge
- 0
- Complexity
- 278
Experimental & physicochemical properties
Physical DescriptionSolid
Collision Cross Section149.5 Ų [M+H-H2O]+ [CCS Type: DT; Method: single field calibrated with Agilent tune mix (Agilent)]
Chemistry & industry
Applications
UsesLeucylproline, a dipeptide, plays important roles in the medium-dependent regulation of proteinase activity[1].
Additional notes
DefinitionChEBI: A dipeptide formed from L-leucine and L-proline residues.
Related reactions
1 records
Compound notes
Loading…