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SMILES: CN1CC[C@@H](C1)N(Cc1ccccn1)c1ccc(C#N)c(Cl)c1

InChI Key: InChIKey=DSQRFKXGBMHWQO-KRWDZBQOSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50298042   

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
Progesterone receptor (Homo sapiens (Human))	BDBM50298042 ((S)-2-chloro-4-((1-methylpyrrolidin-3-yl)(pyridin-...) Show SMILES CN1CC[C@@H](C1)N(Cc1ccccn1)c1ccc(C#N)c(Cl)c1 |r| Show InChI InChI=1S/C18H19ClN4/c1-22-9-7-17(13-22)23(12-15-4-2-3-8-21-15)16-6-5-14(11-20)18(19)10-16/h2-6,8,10,17H,7,9,12-13H2,1H3/t17-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a
GlaxoSmithKline Pharmaceuticals Curated by ChEMBL					Assay Description Agonist activity at PR expressed in african green monkey CV-1 cells by luciferase reporter assay				Bioorg Med Chem Lett 19: 4777-80 (2009) Article DOI: 10.1016/j.bmcl.2009.06.055 BindingDB Entry DOI: 10.7270/Q2TB16XG
					More data for this Ligand-Target Pair
Progesterone receptor (Homo sapiens (Human))	BDBM50298042 ((S)-2-chloro-4-((1-methylpyrrolidin-3-yl)(pyridin-...) Show SMILES CN1CC[C@@H](C1)N(Cc1ccccn1)c1ccc(C#N)c(Cl)c1 |r| Show InChI InChI=1S/C18H19ClN4/c1-22-9-7-17(13-22)23(12-15-4-2-3-8-21-15)16-6-5-14(11-20)18(19)10-16/h2-6,8,10,17H,7,9,12-13H2,1H3/t17-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Pharmaceuticals Curated by ChEMBL					Assay Description Binding affinity to PR by fluorescence polarization based competition binding assay				Bioorg Med Chem Lett 19: 4777-80 (2009) Article DOI: 10.1016/j.bmcl.2009.06.055 BindingDB Entry DOI: 10.7270/Q2TB16XG
					More data for this Ligand-Target Pair