null

SMILES: C[C@H]1CC[C@H](CC1)NC(=O)c1cc2cccnc2n(CCCCF)c1=O

InChI Key:

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50600941   

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))	BDBM50600941 (CHEMBL5173890) Show SMILES C[C@H]1CC[C@H](CC1)NC(=O)c1cc2cccnc2n(CCCCF)c1=O |r,wD:4.7,1.0,(6.66,5.77,;5.33,5,;4,5.77,;2.66,5,;2.66,3.46,;4,2.69,;5.33,3.46,;1.33,2.69,;-0,3.46,;-0,5,;-1.33,2.69,;-2.67,3.46,;-4,2.7,;-5.33,3.47,;-6.66,2.7,;-6.66,1.15,;-5.33,.39,;-4,1.16,;-2.66,.39,;-2.66,-1.15,;-4,-1.92,;-4,-3.46,;-5.33,-4.23,;-5.33,-5.77,;-1.33,1.16,;-0,.39,)| Show InChI	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c00256 BindingDB Entry DOI: 10.7270/Q2Z89HGZ
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50600941 (CHEMBL5173890) Show SMILES C[C@H]1CC[C@H](CC1)NC(=O)c1cc2cccnc2n(CCCCF)c1=O |r,wD:4.7,1.0,(6.66,5.77,;5.33,5,;4,5.77,;2.66,5,;2.66,3.46,;4,2.69,;5.33,3.46,;1.33,2.69,;-0,3.46,;-0,5,;-1.33,2.69,;-2.67,3.46,;-4,2.7,;-5.33,3.47,;-6.66,2.7,;-6.66,1.15,;-5.33,.39,;-4,1.16,;-2.66,.39,;-2.66,-1.15,;-4,-1.92,;-4,-3.46,;-5.33,-4.23,;-5.33,-5.77,;-1.33,1.16,;-0,.39,)| Show InChI	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c00256 BindingDB Entry DOI: 10.7270/Q2Z89HGZ
					More data for this Ligand-Target Pair