BIOPEP-UWM: Report
| ID | 15 |
| Name | bitter peptide |
| sequence |
| Function: | |||
| (Rcaf) 0.17 | |||
| Number of residues | 2 |
Activity code | bi |
| Activity : | bitter |
|||
| Chemical mass | 243.3019 | Monoisotopic mass | 243.1578 | |
| EC50 : | 0.00 µM |
|||
| Bibliographic data: | |
| Authors | |
| Ishibashi N., Ono I., Kato K., Shigenaga T., Shinoda I., Okai H., Fukui S. | |
| Title | |
| Role of the hydrophobic amino acid residue in the bitterness of peptides. Agric. Biol. Chem., 52, 91-94, 1988 | |
| Year | Source |
| 1988 | Journal |
| Additional information: |
| BIOPEP-UWM database of sensory peptides and amino acids SMILES: C1C[C@H](NC1)C(=O)N[C@@H](CCCCN)C(=O)O InChI=1S/C11H21N3O3/c12-6-2-1-4-9(11(16)17)14-10(15)8-5-3-7-13-8/h8-9,13H,1-7,12H2,(H,14,15)(H,16,17)/t8-,9-/m0/s1 InChIKey: RVQDZELMXZRSSI-IUCAKERBSA-N Inhibitor of angiotensin-converting enzyme (EC 3.4.15.1) (MEROPS ID: M02-001) according to the AHTPDB database Inhibitor of Dipeptidyl Peptidase IV (EC 3.4.14.5) (MEROPS ID: S09.003) according to the BIOPEP-UWM database of bioactive peptides |
| Database reference: |
| AHTPDB: ID 5443 BIOPEP database of bioactive peptides: ID 8858 BRENDA: Ligand Pro-Lys ChEBI: ID 74792 ChEMBL: ID CHEMBL377325 ChemSpider: ID 7498109 PubChem: ID 9209431 ZINC: ID ZINC08076544 |