BDBM50364104 CHEMBL1950930
SMILES: CC(=O)N1CCC(Cn2c(nc3cc(ccc23)S(=O)(=O)CCCO)C(C)(C)C)CC1
InChI Key: InChIKey=ZXNXVLWQTMVGIP-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 50364104 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)) | BDBM50364104
(CHEMBL1950930)Show SMILES CC(=O)N1CCC(Cn2c(nc3cc(ccc23)S(=O)(=O)CCCO)C(C)(C)C)CC1 Show InChI InChI=1S/C22H33N3O4S/c1-16(27)24-10-8-17(9-11-24)15-25-20-7-6-18(30(28,29)13-5-12-26)14-19(20)23-21(25)22(2,3)4/h6-7,14,17,26H,5,8-13,15H2,1-4H3 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 145 | n/a | n/a | n/a | n/a |
Janssen Research& Development
Curated by ChEMBL
| Assay Description Agonist activity at human CB2 receptor |
Bioorg Med Chem Lett 22: 547-52 (2011)
Article DOI: 10.1016/j.bmcl.2011.10.091 BindingDB Entry DOI: 10.7270/Q2JW8FBF |
More data for this Ligand-Target Pair | |
Cannabinoid receptor 1
(Homo sapiens (Human)) | BDBM50364104
(CHEMBL1950930)Show SMILES CC(=O)N1CCC(Cn2c(nc3cc(ccc23)S(=O)(=O)CCCO)C(C)(C)C)CC1 Show InChI InChI=1S/C22H33N3O4S/c1-16(27)24-10-8-17(9-11-24)15-25-20-7-6-18(30(28,29)13-5-12-26)14-19(20)23-21(25)22(2,3)4/h6-7,14,17,26H,5,8-13,15H2,1-4H3 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
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 |
Janssen Research& Development
Curated by ChEMBL
| Assay Description Agonist activity at human CB1 receptor |
Bioorg Med Chem Lett 22: 547-52 (2011)
Article DOI: 10.1016/j.bmcl.2011.10.091 BindingDB Entry DOI: 10.7270/Q2JW8FBF |
More data for this Ligand-Target Pair | |