BIOPEP-UWM: Report

ID 480
Name Bitter peptide
sequence
DY

Function:
Bitter taste
 
Number of residues
2
Activity code
bi
Activity :
bitter
Chemical mass 296.2753 Monoisotopic mass 296.1004
EC50 :
0.00 µM



Bibliographic data:
Authors
Miyashita Y., Takahashi Y., Takayama C., Sumi K., Nakatsuka. K., Ohkubo T., Abe H., Sasaki S.
Title
Structure-taste correlation of L-aspartyl dipeptides using SIMCA method. J. Med. Chem., 29, 906-912, 1986
Year Source
1986 Journal



Additional information:
BIOPEP-UWM database of bioactive peptides


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

InChI=1S/C13H16N2O6/c14-9(6-11(17)18)12(19)15-10(13(20)21)5-7-1-3-8(16)4-2-7/h1-4,9-10,16H,5-6,14H2,(H,15,19)(H,17,18)(H,20,21)/t9-,10-/m0/s1

InChIKey: NALWOULWGHTVDA-UWVGGRQHSA-N


Inhibitor of Angiotensin-Converting Enzyme (ACE) (EC 3.4.15.1) (MEROPS ID: M02-001) according to the AHTPDB database, the BindingDB database; the BioPepDB database; the BIOPEP-UWM database of bioactive peptides (ID 9072); the ChEMBL database; the PubChem database
Inhibitor of tripeptidyl peptidase 2 (EC 3.4.14.10) (MEROPS ID: S08.090) according to the ChEMBL database; the PubChem database
Ion flow regulating peptide according to the BIOPEP-UWM database of bioactive peptides (ID 2749); the EROP-Moscow database



Database reference:
ACToR: ID 22840-03-5

AHTPDB: ID 1350, 4215, 4954

BindingDB: ID 50049712

BioPepDB: ID biopep00157

BIOPEP-UWM database of bioactive peptides: ID 2749, 9072

Brenda: Ligand Asp-Tyr

ChEBI: ID 73455

ChEMBL: ID CHEMBL171132

ChemSpider: ID 134366

EPA CompTox: ID DTXSID20177389

EPA DSSTox: ID DTXCID3099880

EROP-Moscow: ID E01600

J-GLOBAL: ID 200907055017390758

Metabolights: ID MTBLC73455

Nikkaji: ID J861.377J

PubChem: CID 152455

SATPdb: ID satpdb22485

SureChEMBL: ID SCHEMBL7935661

ZINC: ID ZINC000002391137