BIOPEP-UWM: Report

ID 478
Name Bitter peptide
sequence
FY
Function:
Bitter taste
 
Number of residues
2
Activity code
bi
Activity :
bitter
Chemical mass 328.3616 Monoisotopic mass 328.1418
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 sensory peptides and amino acids


SMILES: N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)O

InChI: InChI=1S/C18H20N2O4/c19-15(10-12-4-2-1-3-5-12)17(22)20-16(18(23)24)11-13-6-8-14(21)9-7-13/h1-9,15-16,21H,10-11,19H2,(H,20,22)(H,23,24)/t15-,16-/m0/s1

InChIKey: FSXRLASFHBWESK-HOTGVXAUSA-N


Inhibitor of Angiotensin-Converting Enzyme (ACE) (EC 3.4.15.1) (MEROPS ID: M02-001) according to the AHTPDB database; the BIOPEP-UWM database of bioactive peptides; the CHEMBL database; the PubChem database


Database reference:
AHTPDB: ID 1136; 1413; 1442; 1446; 1457; 1472; 1810; 1817; 1857; 2654; 2672; 2685; 2775; 2883; 3880; 3913; 4254; 4258; 4731; 4950; 5148; 5587; 5741; 5774; 5808; 6260; 6270; 6469; 6876

BIOPEP-UWM database of bioactive peptides: ID 3556

BRENDA: Ligand Phe-Tyr

ChEBI: ID 73637

ChEMBL: ID CHEMBL54572

ChemSpider: ID 449878

EPA DSSTox: ID DTXCID40284746

EROP-Moscow: ID E00283

NIAID: ID 192291

ParaPep: ID 1532; 1560

PubChem: CID 515709

SATPdb: ID satpdb15002

ZINC: ID ZINC02384778