BDBM50419412 CHEMBL1915013

SMILES: Cc1cc(nn1Cc1cc(Cl)cc2cc(oc12)C1CC1)C(O)=O

InChI Key: InChIKey=IELJQUDZLQUQEX-UHFFFAOYSA-N

Data: 1 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 1 hit for monomerid = 50419412   

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
Prostaglandin E2 receptor EP1 subtype (EP1) (Homo sapiens (Human))	BDBM50419412 (CHEMBL1915013) Show SMILES Cc1cc(nn1Cc1cc(Cl)cc2cc(oc12)C1CC1)C(O)=O Show InChI InChI=1S/C17H15ClN2O3/c1-9-4-14(17(21)22)19-20(9)8-12-6-13(18)5-11-7-15(10-2-3-10)23-16(11)12/h4-7,10H,2-3,8H2,1H3,(H,21,22)	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	50.1	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Displacement of [3H]GW875240X from human prostanoid EP1 receptor expressed in CHO-K1 cells after 45 mins by topcount liquid scintillation counting				Bioorg Med Chem Lett 21: 4343-8 (2011) Article DOI: 10.1016/j.bmcl.2011.05.047 BindingDB Entry DOI: 10.7270/Q2RN394N
					More data for this Ligand-Target Pair