BDBM50164436 5,5-Bis-(4-bromo-phenyl)-3-butyl-imidazolidine-2,4-dione::5,5-bis(4-bromophenyl)-3-butylimidazolidine-2,4-dione::CHEMBL190411
SMILES: CCCCN1C(=O)NC(C1=O)(c1ccc(Br)cc1)c1ccc(Br)cc1
InChI Key: InChIKey=KMJDATHIDYYGSK-UHFFFAOYSA-N
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 1 (Homo sapiens (Human)) | BDBM50164436 (5,5-Bis-(4-bromo-phenyl)-3-butyl-imidazolidine-2,4...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 5.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Université catholique de Louvain Curated by ChEMBL | Assay Description Inhibition of [3H]-SR-141,716A binding to human CB1 receptor expressed in CHO cells | J Med Chem 48: 2509-17 (2005) Article DOI: 10.1021/jm049263k BindingDB Entry DOI: 10.7270/Q2Q23ZRD | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Fatty-acid amide hydrolase 1 (aa 30-579) (Rattus norvegicus (rat)) | BDBM50164436 (5,5-Bis-(4-bromo-phenyl)-3-butyl-imidazolidine-2,4...) | PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.95E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ catholique de Louvain Curated by ChEMBL | Assay Description Inhibitory activity against FAAH in Wistar rat brain homogenate | J Med Chem 49: 417-25 (2006) Article DOI: 10.1021/jm050977k BindingDB Entry DOI: 10.7270/Q2FB545W | |||||||||||
More data for this Ligand-Target Pair |