Reaction Details Report a problem with these data
Target
Glutaminyl-peptide cyclotransferase-like protein
Ligand
BDBM50299852
Substrate
n/a
Meas. Tech.
Fluorometric Assay
pH
8±n/a
IC50
8790±n/a nM
Comments
extracted
Citation
Buchholz, M; Heiser, U; Hamann, A Inhibitors of glutaminyl cyclase US Patent US8772508 Publication Date 7/8/2014
More Info.:
Target
Name:
Glutaminyl-peptide cyclotransferase-like protein
Synonyms:
Glutaminyl Cyclase | Glutaminyl-peptide cyclotransferase-like protein (QC) | QPCTL | QPCTL_HUMAN
Type:
Protein
Mol. Mass.:
42941.16
Organism:
Homo sapiens (Human)
Description:
Q9NXS2
Residue:
382
Sequence:
MRSGGRGRPRLRLGERGLMEPLLPPKRRLLPRVRLLPLLLALAVGSAFYTIWSGWHRRTEELPLGRELRVPLIGSLPEARLRRVVGQLDPQRLWSTYLRPLLVVRTPGSPGNLQVRKFLEATLRSLTAGWHVELDPFTASTPLGPVDFGNVVATLDPRAARHLTLACHYDSKLFPPGSTPFVGATDSAVPCALLLELAQALDLELSRAKKQAAPVTLQLLFLDGEEALKEWGPKDSLYGSRHLAQLMESIPHSPGPTRIQAIELFMLLDLLGAPNPTFYSHFPRTVRWFHRLRSIEKRLHRLNLLQSHPQEVMYFQPGEPFGSVEDDHIPFLRRGVPVLHLISTPFPAVWHTPADTEVNLHPPTVHNLCRILAVFLAEYLGL
Inhibitor
Name:
BDBM50299852
Synonyms:
CHEMBL568073 | N-(1-(3-(4-Methyl-1H-imidazol-1-yl)propylamino)-2-nitrovinyl)-2,3-dihydrobenzo[b][1,4]-dioxin-6-amine | US8772508, 13
Type:
Small organic molecule
Emp. Form.:
C17H21N5O4
Mol. Mass.:
359.3797
SMILES:
Cc1cn(CCCNC(C[N+]([O-])=O)=Nc2ccc3OCCOc3c2)cn1 |w:13.13|