Compile Data Set for Download or QSAR

Found 2 hits of ic50 for monomerid = 50253527   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50253527 (5-(5-(Cyclohexylethynyl)thiophen-2-yl)-1-(2,4-dich...) Show SMILES Cc1c(nn(c1-c1ccc(s1)C#CC1CCCCC1)-c1ccc(Cl)cc1Cl)C(=O)NN1CCCCC1 Show InChI InChI=1S/C28H30Cl2N4OS/c1-19-26(28(35)32-33-16-6-3-7-17-33)31-34(24-14-11-21(29)18-23(24)30)27(19)25-15-13-22(36-25)12-10-20-8-4-2-5-9-20/h11,13-15,18,20H,2-9,16-17H2,1H3,(H,32,35)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.30	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from human CB1 receptor expressed in HEK293 cells				J Med Chem 51: 5397-412 (2008) Article DOI: 10.1021/jm800066v BindingDB Entry DOI: 10.7270/Q24M94BM
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50253527 (5-(5-(Cyclohexylethynyl)thiophen-2-yl)-1-(2,4-dich...) Show SMILES Cc1c(nn(c1-c1ccc(s1)C#CC1CCCCC1)-c1ccc(Cl)cc1Cl)C(=O)NN1CCCCC1 Show InChI InChI=1S/C28H30Cl2N4OS/c1-19-26(28(35)32-33-16-6-3-7-17-33)31-34(24-14-11-21(29)18-23(24)30)27(19)25-15-13-22(36-25)12-10-20-8-4-2-5-9-20/h11,13-15,18,20H,2-9,16-17H2,1H3,(H,32,35)	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.58E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from human CB2 receptor expressed in HEK293 cells				J Med Chem 51: 5397-412 (2008) Article DOI: 10.1021/jm800066v BindingDB Entry DOI: 10.7270/Q24M94BM
					More data for this Ligand-Target Pair