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Inhibitor Report for: N-acyl-prolylpyrrolidine-inhibitor-2

General
Type Pyrrolidine, Triazol, Carbamate, tert-Butyloxycarbonyl, tert-Butyl
Chemical_Nomenclature tert-butyl N-[[1-[(3S,5S)-5-[(2S)-2-[(R)-amino(hydroxy)methyl]pyrrolidine-1-carbonyl]-1-(4-phenylbutanoyl)pyrrolidin-3-yl]triazol-4-yl]methyl]carbamate
Canonical SMILES CC(C)(C)OC(=O)NCC1=CN(N=N1)C2CC(N(C2)C(=O)CCCC3=CC=CC=C3)C(=O)N4CCCC4C(N)O
InChI InChI=1S/C28H41N7O5/c1-28(2,3)40-27(39)30-16-20-17-35(32-31-20)21-15-23(26(38)33-14-8-12-22(33)25(29)37)34(18-21)24(36)13-7-11-19-9-5-4-6-10-19/h4-6,9-10,17,21-23,25,37H,7-8,11-16,18,29H2,1-3H3,(H,30,39)/t21-,22-,23-,25+/m0/s1
InChIKey MVZCEONBTBQGTK-KELBGUDLSA-N
Other name(s) JKT
________________________________________________________________________________________________
MW|555.68
Formula|C28H41N7O5
CAS_number|
PubChem|70789753
UniChem|MVZCEONBTBQGTK-KELBGUDLSA-N
IUPHAR|
Wikipedia|

Target
Families | N-acyl-prolylpyrrolidine-inhibitor-2 ligand of proteins in family: S9N_PPCE_Peptidase_S9
Stucture | 1 structure: 4BCC: Prolyl Oligopeptidase from porcine brain with a covalently bound P2-substituted N-acyl-prolylpyrrolidine inhibitor 2
Protein | pig-ppce

References:
Search PubMed for references concerning: N-acyl-prolylpyrrolidine-inhibitor-2
    Title: P2-substituted N-acylprolylpyrrolidine inhibitors of prolyl oligopeptidase: biochemical evaluation, binding mode determination, and assessment in a cellular model of synucleinopathy
    Van der Veken P, Fulop V, Rea D, Gerard M, Van Elzen R, Joossens J, Cheng JD, Baekelandt V, De Meester I and Augustyns K <1 more author(s)>
    Ref: Journal of Medicinal Chemistry, 55:9856, 2012 : PubMed