H-Pro-Lys-OH

Chemical Information
Pro-Lys is a dipeptide formed from L-proline and L-lysine residues. It has a role as a metabolite.
| CAS Number | 71227-70-8 |
| PubChem CID | 9209431 |
| IUPAC Name | (2S)-6-amino-2-[[(2S)-pyrrolidine-2-carbonyl]amino]hexanoic acid |
| Molecular Formula | C11H21N3O3 |
| Molecular Weight | 243.30 |
| XLogP | -4 |
| Topological Polar Surface Area | 104 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 7 |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 271 |
| Property | Value |
|---|---|
| Molecular Weight | 243.30 |
| XLogP3 | -4 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 7 |
| Exact Mass | 243.15829154 |
| Monoisotopic Mass | 243.15829154 |
| Topological Polar Surface Area | 104 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 271 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
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