BIOPEP-UWM: Report

ID 491
Name Bitter peptide
sequence
PY
Function:
 
Number of residues
2
Activity code
bi
Activity :
bitter
Chemical mass 278.3030 Monoisotopic mass 278.1262
EC50 :
0.00 µM


Bibliographic data:
Authors
Asao M., Iwamura H., Akamatsu M., Fujita T.
Title
Quantitative structure-activity relationships of the bitter thresholds of amino acids, peptides, and their derivatives. J. Med. Chem., 30, 1873-1879, 1987
Year Source
1987 Journal


Additional information:
BIOPEP-UWM database of bioactive peptides

SMILES: [H][C@@](CC1=CC=C(O)C=C1)(NC(=O)[C@]1([H])CCCN1)C(O)=O

InChI=1S/C14H18N2O4/c17-10-5-3-9(4-6-10)8-12(14(19)20)16-13(18)11-2-1-7-15-11/h3-6,11-12,15,17H,1-2,7-8H2,(H,16,18)(H,19,20)/t11-,12-/m0/s1

InChIKey=OIDKVWTWGDWMHY-RYUDHWBXSA-N


Another reference concerning bitterness:
Collantes E. R., Dunn W. J., 1995, Amino acid side chain descriptors for quantitative structure-activity relationship studies of peptide analogues. J. Med. Chem., 38, 2705-2713


Insecticidal peptide according to the ChEMBL database
Antinociceptive peptide according to the ChEMBL database
Ligand of neurotensin receptor according to the ChEMBL database
Inhibitor of Dipeptidyl Peptidase IV (EC 3.4.14.5) (MEROPS ID: S09.003) according to the BIOPEP-UWM database of bioactive peptides (ID 8866)
Anti-inflammatory peptide according to the BIOPEP-UWM database of bioactive peptides (ID 9856); the EROP-Moscow database


Database reference:
ACToR: ID 19786-36-8

AHTPDB: ID ahtpdb_3874

BioPepDB: ID biopep01129

BIOPEP-UWM database of bioactive peptides: ID 8866; 9856

BRENDA: Ligand Pro-Tyr

ChEBI: ID 74799

ChEMBL: ID CHEMBL298979

ChemIplus: ID 19786-36-8

ChemSpider: ID 134207

CTD: ID 19786-36-8

eChemPortal: ID 19786-36-8

EPA CompTox: ID DTXSID30173493

EPA DSSTox: ID DTXCID8095984

EROP-Moscow: ID E23771

FeptideDB: ID 8866

J-GLOBAL: ID 200907072092938094

Metabolights: ID MTBLC74799

Nikkaji: ID J151.291I

PubChem: CID 152264

SATPdb: ID satpdb26503

SureChEMBL: ID SCHEMBL6367397

ZINC: ID ZINC000004899447