BDBM50277192 4-(5-(4-(cyclohexylmethyl)thiazol-2-yl)-2-methylphenylsulfonyl)morpholine::CHEMBL474896

SMILES: Cc1ccc(cc1S(=O)(=O)N1CCOCC1)-c1nc(CC2CCCCC2)cs1

InChI Key: InChIKey=OGNXMBCUTKGOQT-UHFFFAOYSA-N

Data: 4 KI  1 EC50

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 = 50277192   

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
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50277192 (4-(5-(4-(cyclohexylmethyl)thiazol-2-yl)-2-methylph...) Show SMILES Cc1ccc(cc1S(=O)(=O)N1CCOCC1)-c1nc(CC2CCCCC2)cs1 Show InChI InChI=1S/C21H28N2O3S2/c1-16-7-8-18(14-20(16)28(24,25)23-9-11-26-12-10-23)21-22-19(15-27-21)13-17-5-3-2-4-6-17/h7-8,14-15,17H,2-6,9-13H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	23	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Adolor Corporation Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from human cloned CB2 receptor by scintillation spectrometry				Bioorg Med Chem Lett 19: 309-13 (2008) Article DOI: 10.1016/j.bmcl.2008.11.091 BindingDB Entry DOI: 10.7270/Q2G73DK3
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50277192 (4-(5-(4-(cyclohexylmethyl)thiazol-2-yl)-2-methylph...) Show SMILES Cc1ccc(cc1S(=O)(=O)N1CCOCC1)-c1nc(CC2CCCCC2)cs1 Show InChI InChI=1S/C21H28N2O3S2/c1-16-7-8-18(14-20(16)28(24,25)23-9-11-26-12-10-23)21-22-19(15-27-21)13-17-5-3-2-4-6-17/h7-8,14-15,17H,2-6,9-13H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	23	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Siena Curated by ChEMBL					Assay Description Displacement of [3H]CP 55940 from human CB2 receptor in cell free system				Eur J Med Chem 46: 547-55 (2011) Article DOI: 10.1016/j.ejmech.2010.11.034 BindingDB Entry DOI: 10.7270/Q2CF9QCJ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50277192 (4-(5-(4-(cyclohexylmethyl)thiazol-2-yl)-2-methylph...) Show SMILES Cc1ccc(cc1S(=O)(=O)N1CCOCC1)-c1nc(CC2CCCCC2)cs1 Show InChI InChI=1S/C21H28N2O3S2/c1-16-7-8-18(14-20(16)28(24,25)23-9-11-26-12-10-23)21-22-19(15-27-21)13-17-5-3-2-4-6-17/h7-8,14-15,17H,2-6,9-13H2,1H3	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	390	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Adolor Corporation Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from human cloned CB1 receptor by scintillation spectrometry				Bioorg Med Chem Lett 19: 309-13 (2008) Article DOI: 10.1016/j.bmcl.2008.11.091 BindingDB Entry DOI: 10.7270/Q2G73DK3
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50277192 (4-(5-(4-(cyclohexylmethyl)thiazol-2-yl)-2-methylph...) Show SMILES Cc1ccc(cc1S(=O)(=O)N1CCOCC1)-c1nc(CC2CCCCC2)cs1 Show InChI InChI=1S/C21H28N2O3S2/c1-16-7-8-18(14-20(16)28(24,25)23-9-11-26-12-10-23)21-22-19(15-27-21)13-17-5-3-2-4-6-17/h7-8,14-15,17H,2-6,9-13H2,1H3	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	390	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Siena Curated by ChEMBL					Assay Description Displacement of [3H]CP 55940 from human CB1 receptor in cell free system				Eur J Med Chem 46: 547-55 (2011) Article DOI: 10.1016/j.ejmech.2010.11.034 BindingDB Entry DOI: 10.7270/Q2CF9QCJ
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50277192 (4-(5-(4-(cyclohexylmethyl)thiazol-2-yl)-2-methylph...) Show SMILES Cc1ccc(cc1S(=O)(=O)N1CCOCC1)-c1nc(CC2CCCCC2)cs1 Show InChI InChI=1S/C21H28N2O3S2/c1-16-7-8-18(14-20(16)28(24,25)23-9-11-26-12-10-23)21-22-19(15-27-21)13-17-5-3-2-4-6-17/h7-8,14-15,17H,2-6,9-13H2,1H3	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	n/a	n/a	120	n/a	n/a	n/a	n/a
Adolor Corporation Curated by ChEMBL					Assay Description Agonist activity at human cloned CB2 receptor assessed as stimulation of [35S]GTPgammaS binding				Bioorg Med Chem Lett 19: 309-13 (2008) Article DOI: 10.1016/j.bmcl.2008.11.091 BindingDB Entry DOI: 10.7270/Q2G73DK3
					More data for this Ligand-Target Pair