null

SMILES: NC(=O)CC[C@@H]1NC(=O)\C=C/C(=O)NNCCCCC(NCCCCNC(=O)[C@@H](Cc2ccc(cc2)C(=O)c2ccccc2)NC(=O)[C@H](CC2CCCCC2)NC1=O)C(=O)COCCOCCOCCCNC(=O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@H]12

InChI Key: InChIKey=VSZVBZAJQSQQHJ-LXFUHHPCSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 209048   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Insulin-degrading enzyme (Homo sapiens (Human))	BDBM209048 (US9243038, 28) Show SMILES NC(=O)CC[C@@H]1NC(=O)\C=C/C(=O)NNCCCCC(NCCCCNC(=O)[C@@H](Cc2ccc(cc2)C(=O)c2ccccc2)NC(=O)[C@H](CC2CCCCC2)NC1=O)C(=O)COCCOCCOCCCNC(=O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@H]12 |r,c:9| Show InChI InChI=1S/C62H91N11O13S/c63-53(75)26-25-47-60(81)70-49(38-42-14-3-1-4-15-42)61(82)69-48(39-43-21-23-45(24-22-43)58(79)44-16-5-2-6-17-44)59(80)66-30-12-11-29-64-46(18-9-10-32-67-73-56(78)28-27-55(77)68-47)51(74)40-86-37-36-85-35-34-84-33-13-31-65-54(76)20-8-7-19-52-57-50(41-87-52)71-62(83)72-57/h2,5-6,16-17,21-24,27-28,42,46-50,52,57,64,67H,1,3-4,7-15,18-20,25-26,29-41H2,(H2,63,75)(H,65,76)(H,66,80)(H,68,77)(H,69,82)(H,70,81)(H,73,78)(H2,71,72,83)/b28-27-/t46?,47-,48+,49-,50-,52-,57-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	80	n/a	n/a	n/a	n/a	n/a	n/a
President and Fellows of Harvard College US Patent					Assay Description Macrocycles were assayed for IDE inhibition by monitoring cleavage of a substrate peptide containing a fluorophore-quencher pair such that cleavage o...				US Patent US9243038 (2016) BindingDB Entry DOI: 10.7270/Q2MW2FZV
					More data for this Ligand-Target Pair