BDBM50338475 CHEMBL1683109::trans-N-(4-((R)-1-amino-2-(2,5-difluorophenyl)ethyl)cyclohexyl)-N,1-dimethyl-1H-pyrazole-3-carboxamide

SMILES: CN([C@H]1CC[C@@H](CC1)[C@H](N)Cc1cc(F)ccc1F)C(=O)c1ccn(C)n1

InChI Key: InChIKey=GKRYDWZPJSMUJG-MZMPZRCHSA-N

Data: 5 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 5 hits for monomerid = 50338475   

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
Fibroblast activation protein alpha (Homo sapiens (Human))	BDBM50338475 (CHEMBL1683109 | trans-N-(4-((R)-1-amino-2-(2,5-dif...) Show SMILES CN([C@H]1CC[C@@H](CC1)[C@H](N)Cc1cc(F)ccc1F)C(=O)c1ccn(C)n1 |r,wU:8.9,2.1,wD:5.5,(50.48,-32.21,;50.48,-30.67,;49.15,-29.9,;47.81,-30.67,;46.49,-29.9,;46.49,-28.36,;47.82,-27.58,;49.15,-28.36,;45.16,-27.59,;45.15,-26.05,;43.82,-28.37,;42.49,-27.6,;42.48,-26.05,;41.15,-25.28,;41.14,-23.74,;39.82,-26.06,;39.82,-27.6,;41.15,-28.37,;41.15,-29.91,;51.82,-29.91,;51.82,-28.37,;53.15,-30.68,;53.31,-32.21,;54.82,-32.53,;55.59,-31.2,;57.12,-31.04,;54.56,-30.05,)| Show InChI InChI=1S/C20H26F2N4O/c1-25-10-9-19(24-25)20(27)26(2)16-6-3-13(4-7-16)18(23)12-14-11-15(21)5-8-17(14)22/h5,8-11,13,16,18H,3-4,6-7,12,23H2,1-2H3/t13-,16-,18-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>3.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibition of FAP				Bioorg Med Chem Lett 21: 1880-6 (2011) Article DOI: 10.1016/j.bmcl.2010.12.060 BindingDB Entry DOI: 10.7270/Q2SX6DJG
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 9 (Homo sapiens (Human))	BDBM50338475 (CHEMBL1683109 | trans-N-(4-((R)-1-amino-2-(2,5-dif...) Show SMILES CN([C@H]1CC[C@@H](CC1)[C@H](N)Cc1cc(F)ccc1F)C(=O)c1ccn(C)n1 |r,wU:8.9,2.1,wD:5.5,(50.48,-32.21,;50.48,-30.67,;49.15,-29.9,;47.81,-30.67,;46.49,-29.9,;46.49,-28.36,;47.82,-27.58,;49.15,-28.36,;45.16,-27.59,;45.15,-26.05,;43.82,-28.37,;42.49,-27.6,;42.48,-26.05,;41.15,-25.28,;41.14,-23.74,;39.82,-26.06,;39.82,-27.6,;41.15,-28.37,;41.15,-29.91,;51.82,-29.91,;51.82,-28.37,;53.15,-30.68,;53.31,-32.21,;54.82,-32.53,;55.59,-31.2,;57.12,-31.04,;54.56,-30.05,)| Show InChI InChI=1S/C20H26F2N4O/c1-25-10-9-19(24-25)20(27)26(2)16-6-3-13(4-7-16)18(23)12-14-11-15(21)5-8-17(14)22/h5,8-11,13,16,18H,3-4,6-7,12,23H2,1-2H3/t13-,16-,18-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibition of DPP9				Bioorg Med Chem Lett 21: 1880-6 (2011) Article DOI: 10.1016/j.bmcl.2010.12.060 BindingDB Entry DOI: 10.7270/Q2SX6DJG
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50338475 (CHEMBL1683109 | trans-N-(4-((R)-1-amino-2-(2,5-dif...) Show SMILES CN([C@H]1CC[C@@H](CC1)[C@H](N)Cc1cc(F)ccc1F)C(=O)c1ccn(C)n1 |r,wU:8.9,2.1,wD:5.5,(50.48,-32.21,;50.48,-30.67,;49.15,-29.9,;47.81,-30.67,;46.49,-29.9,;46.49,-28.36,;47.82,-27.58,;49.15,-28.36,;45.16,-27.59,;45.15,-26.05,;43.82,-28.37,;42.49,-27.6,;42.48,-26.05,;41.15,-25.28,;41.14,-23.74,;39.82,-26.06,;39.82,-27.6,;41.15,-28.37,;41.15,-29.91,;51.82,-29.91,;51.82,-28.37,;53.15,-30.68,;53.31,-32.21,;54.82,-32.53,;55.59,-31.2,;57.12,-31.04,;54.56,-30.05,)| Show InChI InChI=1S/C20H26F2N4O/c1-25-10-9-19(24-25)20(27)26(2)16-6-3-13(4-7-16)18(23)12-14-11-15(21)5-8-17(14)22/h5,8-11,13,16,18H,3-4,6-7,12,23H2,1-2H3/t13-,16-,18-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	140	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibition of DPP4				Bioorg Med Chem Lett 21: 1880-6 (2011) Article DOI: 10.1016/j.bmcl.2010.12.060 BindingDB Entry DOI: 10.7270/Q2SX6DJG
					More data for this Ligand-Target Pair
Dipeptidyl peptidase VIII (Homo sapiens (Human))	BDBM50338475 (CHEMBL1683109 | trans-N-(4-((R)-1-amino-2-(2,5-dif...) Show SMILES CN([C@H]1CC[C@@H](CC1)[C@H](N)Cc1cc(F)ccc1F)C(=O)c1ccn(C)n1 |r,wU:8.9,2.1,wD:5.5,(50.48,-32.21,;50.48,-30.67,;49.15,-29.9,;47.81,-30.67,;46.49,-29.9,;46.49,-28.36,;47.82,-27.58,;49.15,-28.36,;45.16,-27.59,;45.15,-26.05,;43.82,-28.37,;42.49,-27.6,;42.48,-26.05,;41.15,-25.28,;41.14,-23.74,;39.82,-26.06,;39.82,-27.6,;41.15,-28.37,;41.15,-29.91,;51.82,-29.91,;51.82,-28.37,;53.15,-30.68,;53.31,-32.21,;54.82,-32.53,;55.59,-31.2,;57.12,-31.04,;54.56,-30.05,)| Show InChI InChI=1S/C20H26F2N4O/c1-25-10-9-19(24-25)20(27)26(2)16-6-3-13(4-7-16)18(23)12-14-11-15(21)5-8-17(14)22/h5,8-11,13,16,18H,3-4,6-7,12,23H2,1-2H3/t13-,16-,18-/m1/s1	PDB KEGG UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibition of DPP8				Bioorg Med Chem Lett 21: 1880-6 (2011) Article DOI: 10.1016/j.bmcl.2010.12.060 BindingDB Entry DOI: 10.7270/Q2SX6DJG
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 2 (DPP II) (Homo sapiens (Human))	BDBM50338475 (CHEMBL1683109 | trans-N-(4-((R)-1-amino-2-(2,5-dif...) Show SMILES CN([C@H]1CC[C@@H](CC1)[C@H](N)Cc1cc(F)ccc1F)C(=O)c1ccn(C)n1 |r,wU:8.9,2.1,wD:5.5,(50.48,-32.21,;50.48,-30.67,;49.15,-29.9,;47.81,-30.67,;46.49,-29.9,;46.49,-28.36,;47.82,-27.58,;49.15,-28.36,;45.16,-27.59,;45.15,-26.05,;43.82,-28.37,;42.49,-27.6,;42.48,-26.05,;41.15,-25.28,;41.14,-23.74,;39.82,-26.06,;39.82,-27.6,;41.15,-28.37,;41.15,-29.91,;51.82,-29.91,;51.82,-28.37,;53.15,-30.68,;53.31,-32.21,;54.82,-32.53,;55.59,-31.2,;57.12,-31.04,;54.56,-30.05,)| Show InChI InChI=1S/C20H26F2N4O/c1-25-10-9-19(24-25)20(27)26(2)16-6-3-13(4-7-16)18(23)12-14-11-15(21)5-8-17(14)22/h5,8-11,13,16,18H,3-4,6-7,12,23H2,1-2H3/t13-,16-,18-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibition of QPP				Bioorg Med Chem Lett 21: 1880-6 (2011) Article DOI: 10.1016/j.bmcl.2010.12.060 BindingDB Entry DOI: 10.7270/Q2SX6DJG
					More data for this Ligand-Target Pair