null

SMILES: [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1ccc(F)cc1)N2S(=O)(=O)c1c(C)n[nH]c1C

InChI Key:

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50577401   

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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577401 (CHEMBL4873115) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1ccc(F)cc1)N2S(=O)(=O)c1c(C)n[nH]c1C |r,TLB:9:7:17:2.3| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	143	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human NAAA expressed in HEK293 cells using PAMCA as fluorogenic substrate preincubated for 30 mins followed by substrate ad...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00575 BindingDB Entry DOI: 10.7270/Q2P272ZJ
					More data for this Ligand-Target Pair