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Inhibitor Report for: PNPPC

not to be confounded with para-nitrophenylphosphorylcholine (pNPPC)


General
Type pNP, Carbamate
Chemical_Nomenclature (4-nitrophenyl) N-propylcarbamate
Canonical SMILES CCCNC(=O)OC1=CC=C(C=C1)[N+](=O)[O-]
InChI InChI=1S/C10H12N2O4/c1-2-7-11-10(13)16-9-5-3-8(4-6-9)12(14)15/h3-6H,2,7H2,1H3,(H,11,13)
InChIKey FTPSVHHZKHVFNB-UHFFFAOYSA-N
Other name(s) p-nitrophenyl-N-propyl carbamate ; Carbamic acid, propyl-, 4-nitrophenyl ester ; SCHEMBL14617269 ; CTK1I7375 ; Propylcarbamic acid 4-nitrophenyl ester ; OR311785 ; (4-nitrophenyl) N-propylcarbamate ; 4-Nitrophenyl propylcarbamate ; DTXSID50559139
________________________________________________________________________________________________
MW|224.21
Formula|C10H12N2O4
CAS_number|63321-49-3
PubChem|14343338
UniChem|FTPSVHHZKHVFNB-UHFFFAOYSA-N
IUPHAR|
Wikipedia|

Target
Families | PNPPC ligand of proteins in family: ACPH_Peptidase_S9

References:
Search PubMed for references concerning: PNPPC
    Title: Human acylpeptide hydrolase. Studies on its thiol groups and mechanism of action
    Scaloni A, Barra D, Jones WM, Manning JM
    Ref: Journal of Biological Chemistry, 269:15076, 1994 : PubMed