BIOPEP-UWM: Report

ID 16
Name bitter peptide
sequence
GR

Function:
(Rcaf) 0.01
 
Number of residues
2
Activity code
bi
Activity :
bitter
Chemical mass 231.2516 Monoisotopic mass 231.1328
EC50 :
0.00 µM



Bibliographic data:
Authors
Otagiri K., Nosho Y., Shinoda I., Fukui H., Okai H.
Title
Studies on a model bitter peptides including arginine, proline and phenylalanine residues. I. Bitter taste of di- and tripeptides and bitterness increase of the model peptides by extension of the peptide chain. Agric. Biol. Chem., 49, 1019-1026, 1985
Year Source
1985 Journal



Additional information:

BIOPEP-UWM database of sensory peptides and amino acids


SMILES: C(C[C@@H](C(=O)O)NC(=O)CN)CNC(=N)N

InChI=1S/C8H17N5O3/c9-4-6(14)13-5(7(15)16)2-1-3-12-8(10)11/h5H,1-4,9H2,(H,13,14)(H,15,16)(H4,10,11,12)/t5-/m0/s1

InChIKey: JLXVRFDTDUGQEE-YFKPBYRVSA-N


Inhibitor of angiotensin-converting enzyme (EC 3.4.15.1) (MEROPS ID: M02-001) according to the AHTPDB database; the BindingDB database; the BIOPEP-UWM database of bioactive peptides, the ChEMBL database, the EROP-Moscow database; the PubChem database



Database reference:


ACToR: ID 18635-55-7

AHTPDB: ID 1427; 3000; 3042; 3085; 3114; 3236; 3491; 3807; 3933; 4416; 4513; 4668; 5152; 5421; 5434; 6109; 6589

BindingDB: ID 50407457

BioPepDB: ID biopep00409

BIOPEP-UWM database of bioactive peptides: ID 7603

BRENDA: Ligand Gly-Arg

ChEBI: ID 73860

ChEMBL: ID CHEMBL96806

ChemSpider: ID 4932140

EROP-Moscow: ID E10383

J-GLOBAL: ID 200907022189681376

Metabolights: ID MTBLC73860

Nikkaji: ID J1.481.855C

PubChem: CID 6426706

SATPdb: ID satpdb16592

SureChEMBL: ID SCHEMBL187696

ZINC: ID ZINC01576211