BDBM50359368 CHEMBL1929389

SMILES: Cc1cc2ncc(C(=O)NCC(C)(C)NCC(=O)N3CCC[C@H]3C#N)c(n2n1)C(F)(F)F

InChI Key: InChIKey=AYERFFUVGKDBLN-ZDUSSCGKSA-N

Data: 3 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50359368   

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
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50359368 (CHEMBL1929389) Show SMILES Cc1cc2ncc(C(=O)NCC(C)(C)NCC(=O)N3CCC[C@H]3C#N)c(n2n1)C(F)(F)F |r| Show InChI InChI=1S/C20H24F3N7O2/c1-12-7-15-25-9-14(17(20(21,22)23)30(15)28-12)18(32)26-11-19(2,3)27-10-16(31)29-6-4-5-13(29)8-24/h7,9,13,27H,4-6,10-11H2,1-3H3,(H,26,32)/t13-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	32	n/a	n/a	n/a	n/a	n/a	n/a
Sanwa Kagaku Kenkyusho Co. Ltd Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-4 using H-Gly-Pro-AMC as substrate preincubated for 30 mins before substrate addition measured after 20 mins by f...				Bioorg Med Chem 19: 7221-7 (2011) Article DOI: 10.1016/j.bmc.2011.09.043 BindingDB Entry DOI: 10.7270/Q2862GVX
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 9 (Homo sapiens (Human))	BDBM50359368 (CHEMBL1929389) Show SMILES Cc1cc2ncc(C(=O)NCC(C)(C)NCC(=O)N3CCC[C@H]3C#N)c(n2n1)C(F)(F)F |r| Show InChI InChI=1S/C20H24F3N7O2/c1-12-7-15-25-9-14(17(20(21,22)23)30(15)28-12)18(32)26-11-19(2,3)27-10-16(31)29-6-4-5-13(29)8-24/h7,9,13,27H,4-6,10-11H2,1-3H3,(H,26,32)/t13-/m0/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	81	n/a	n/a	n/a	n/a	n/a	n/a
Sanwa Kagaku Kenkyusho Co. Ltd Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-9 expressed in Sf9 cells using H-Gly-Pro-AMC as substrate preincubated for 30 mins before substrate addition meas...				Bioorg Med Chem 19: 7221-7 (2011) Article DOI: 10.1016/j.bmc.2011.09.043 BindingDB Entry DOI: 10.7270/Q2862GVX
					More data for this Ligand-Target Pair
Dipeptidyl peptidase VIII (Homo sapiens (Human))	BDBM50359368 (CHEMBL1929389) Show SMILES Cc1cc2ncc(C(=O)NCC(C)(C)NCC(=O)N3CCC[C@H]3C#N)c(n2n1)C(F)(F)F |r| Show InChI InChI=1S/C20H24F3N7O2/c1-12-7-15-25-9-14(17(20(21,22)23)30(15)28-12)18(32)26-11-19(2,3)27-10-16(31)29-6-4-5-13(29)8-24/h7,9,13,27H,4-6,10-11H2,1-3H3,(H,26,32)/t13-/m0/s1	PDB KEGG UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>100	n/a	n/a	n/a	n/a	n/a	n/a
Sanwa Kagaku Kenkyusho Co. Ltd Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-8 expressed in Sf9 cells using H-Gly-Pro-AMC as substrate preincubated for 30 mins before substrate addition meas...				Bioorg Med Chem 19: 7221-7 (2011) Article DOI: 10.1016/j.bmc.2011.09.043 BindingDB Entry DOI: 10.7270/Q2862GVX
					More data for this Ligand-Target Pair