BIOPEP-UWM: Report

ID 10755
Name Inhibitor of tripeptidyl peptidase II
sequence
{Nle}{Nle}{~!C1}
Function:
Inhibitor of tripeptidyl peptidase II (EC 3.4.14.10) (MEROPS ID: S08.090)
 
Number of residues
3
Activity code
tpp2
Activity :
inhibitor of tripeptidyl peptidase II
Chemical mass 257.3713 Monoisotopic mass 257.2097
IC50 :
0.00 µM


Bibliographic data:
Authors
Ganellin C. R., Bishop P. B., Bambal R. B., Chan S. M., Law J. K., Marabout B., Luthra P. M., Moore A. N., Peschard O., Bourgeat P., Rose C., Vargas F.
Title
Inhibitors of tripeptidyl peptidase II. 2. Generation of the first novel lead inhibitor of cholecystokinin-8-inactivating peptidase: a strategy for the design of peptidase inhibitors. J. Med. Chem., 43, 664-674, 2000
Year Source
2000 Journal


Additional information:
BIOPEP-UWM database of bioactive peptides


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

InChI=1S/2C13H27N3O2/c2*1-4-6-8-10(14)12(17)16-11(9-7-5-2)13(18)15-3/h2*10-11H,4-9,14H2,1-3H3,(H,15,18)(H,16,17)/t2*10-,11-/m00/s1

InChIKey=JJXHJMGOHJSIHA-SGUUPRDWSA-N


{~!C1} - C-terminal aminomethane (ID 131 in the BIOPEP-UWM repository of amino acids and modifications)
{Nle} - Norleucine (ID 231 in the BIOPEP-UWM repository of amino acids and modifications)



Databases PubChem (CID 10563118), BRENDA (Ligand Nle-Nle-NHCH3) and ChemSpider (ID 8738506) annotate isomer of this peptide)

Idntifiers of isomer according to the PubChem database:

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

InChI=1S/C13H27N3O2/c1-4-6-8-10(14)12(17)16-11(9-7-5-2)13(18)15-3/h10-11H,4-9,14H2,1-3H3,(H,15,18)(H,16,17)/t10-,11-/m0/s1

InChIKey=HDZRQFPHMAOEHQ-QWRGUYRKSA-N


Database reference: