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Inhibitor Report for: R-Pro-(decarboxy-Pro)-X98

General
Type Pyrrolidine, Quinoxaline
Chemical_Nomenclature 1-[3-oxo-3-[(2S)-2-(pyrrolidine-1-carbonyl)pyrrolidin-1-yl]propyl]-3-phenylquinoxalin-2-one
Canonical SMILES C1CCN(C1)C(=O)C2CCCN2C(=O)CCN3C4=CC=CC=C4N=C(C3=O)C5=CC=CC=C5
InChI InChI=1S/C26H28N4O3/c31-23(29-17-8-13-22(29)25(32)28-15-6-7-16-28)14-18-30-21-12-5-4-11-20(21)27-24(26(30)33)19-9-2-1-3-10-19/h1-5,9-12,22H,6-8,13-18H2/t22-/m0/s1
InChIKey KWCKZIJGKMCYCI-QFIPXVFZSA-N
Other name(s) CHEMBL459149 ; BDBM50274985 ; DB08738 ; 1-{3-Oxo-3-[(2S)-2-(pyrrolidinocarbonyl)pyrrolidin-1-yl]propyl}-3-phenylquinoxalin-2(1H)-one ; 3eq8 ; X98
________________________________________________________________________________________________
MW|444.53
Formula|C26H28N4O3
CAS_number|
PubChem|25155578
UniChem|KWCKZIJGKMCYCI-QFIPXVFZSA-N
IUPHAR|
Wikipedia|

Target
Families | R-Pro-(decarboxy-Pro)-X98 ligand of proteins in family: S9N_PPCE_Peptidase_S9
Stucture | 1 structure: 3EQ8: Prolyl oligopeptidase complexed with R-Pro-(decarboxy-Pro)-Type inhibitors 2
Protein | pig-ppce

References:
Search PubMed for references concerning: R-Pro-(decarboxy-Pro)-X98
    Title: Prolyl oligopeptidase inhibition by N-acyl-pro-pyrrolidine-type molecules
    Kannai K, Aranyi P, Bocskei Z, Ferenczy G, Harmat V, Simon K, Batori S, Naray-Szabo G, Hermecz I
    Ref: Journal of Medicinal Chemistry, 51:7514, 2008 : PubMed