null

SMILES: CCCCCn1cc(cc1-c1ccccc1F)C(=O)c1cccc2ccccc12

InChI Key: InChIKey=WYNZPDDTQGVCLZ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50192607   

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))	BDBM50192607 ((5-(2-fluorophenyl)-1-pentyl-1H-pyrrol-3-yl)(napht...) Show SMILES CCCCCn1cc(cc1-c1ccccc1F)C(=O)c1cccc2ccccc12 Show InChI InChI=1S/C26H24FNO/c1-2-3-8-16-28-18-20(17-25(28)23-13-6-7-15-24(23)27)26(29)22-14-9-11-19-10-4-5-12-21(19)22/h4-7,9-15,17-18H,2-3,8,16H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Clemson University Curated by ChEMBL					Assay Description Displacement of [3H]CP 55940 from human cloned CB2 receptor				Bioorg Med Chem Lett 16: 5432-5 (2006) Article DOI: 10.1016/j.bmcl.2006.07.051 BindingDB Entry DOI: 10.7270/Q2610ZXH
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50192607 ((5-(2-fluorophenyl)-1-pentyl-1H-pyrrol-3-yl)(napht...) Show SMILES CCCCCn1cc(cc1-c1ccccc1F)C(=O)c1cccc2ccccc12 Show InChI InChI=1S/C26H24FNO/c1-2-3-8-16-28-18-20(17-25(28)23-13-6-7-15-24(23)27)26(29)22-14-9-11-19-10-4-5-12-21(19)22/h4-7,9-15,17-18H,2-3,8,16H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Clemson University Curated by ChEMBL					Assay Description Displacement of [3H]CP 55940 from CB1 receptor in rat brain				Bioorg Med Chem Lett 16: 5432-5 (2006) Article DOI: 10.1016/j.bmcl.2006.07.051 BindingDB Entry DOI: 10.7270/Q2610ZXH
					More data for this Ligand-Target Pair