Compile Data Set for Download or QSAR

Found 95 hits with Last Name = 'fiasella' and Initial = 'a'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/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))	BDBM50151154 (CHEMBL3770896) Show SMILES CCCCc1ccc(COC(=O)N[C@H]2CNC2=O)cc1 |r| Show InChI InChI=1S/C15H20N2O3/c1-2-3-4-11-5-7-12(8-6-11)10-20-15(19)17-13-9-16-14(13)18/h5-8,13H,2-4,9-10H2,1H3,(H,16,18)(H,17,19)/t13-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	7	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant human NAAA expressed in HEK293 cells after 30 mins by UPLC/MS analysis				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151242 (CHEMBL3770525) Show SMILES O=C(N[C@H]1CNC1=O)OCc1ccc(cc1)C1CCCCC1 |r| Show InChI InChI=1S/C17H22N2O3/c20-16-15(10-18-16)19-17(21)22-11-12-6-8-14(9-7-12)13-4-2-1-3-5-13/h6-9,13,15H,1-5,10-11H2,(H,18,20)(H,19,21)/t15-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	12	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant human NAAA expressed in HEK293 cells after 30 mins by UPLC/MS analysis				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577403 (CHEMBL4878464) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1ccc(COCC)cc1)N2S(=O)(=O)c1c(C)n[nH]c1C |r,TLB:9:7:20:2.3| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	16	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577404 (CHEMBL4864438) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1cnc(CCCC)cn1)N2S(=O)(=O)c1c(C)n[nH]c1C |r,TLB:9:7:20:2.3| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	17	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577396 (CHEMBL4863119) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1ccc(CCCCCC)cc1)N2S(=O)(=O)c1c(C)n[nH]c1C |r,TLB:9:7:22:2.3| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	19	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151055 (CHEMBL3771111) Show SMILES CCc1ccc(COC(=O)N[C@H]2CNC2=O)cc1 |r| Show InChI InChI=1S/C13H16N2O3/c1-2-9-3-5-10(6-4-9)8-18-13(17)15-11-7-14-12(11)16/h3-6,11H,2,7-8H2,1H3,(H,14,16)(H,15,17)/t11-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	22	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant human NAAA expressed in HEK293 cells after 30 mins by UPLC/MS analysis				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151154 (CHEMBL3770896) Show SMILES CCCCc1ccc(COC(=O)N[C@H]2CNC2=O)cc1 |r| Show InChI InChI=1S/C15H20N2O3/c1-2-3-4-11-5-7-12(8-6-11)10-20-15(19)17-13-9-16-14(13)18/h5-8,13H,2-4,9-10H2,1H3,(H,16,18)(H,17,19)/t13-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	23	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577394 (CHEMBL4848541) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1ccc(CCCC)cc1)N2S(=O)(=O)c1c(C)n[nH]c1C |r,TLB:9:7:20:2.3| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	23	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151057 (CHEMBL3770726) Show SMILES O=C(N[C@H]1CNC1=O)OCCCCC1CCCCC1 |r| Show InChI InChI=1S/C14H24N2O3/c17-13-12(10-15-13)16-14(18)19-9-5-4-8-11-6-2-1-3-7-11/h11-12H,1-10H2,(H,15,17)(H,16,18)/t12-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	27	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant human NAAA expressed in HEK293 cells after 30 mins by UPLC/MS analysis				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151155 (CHEMBL3769844) Show SMILES O=C(N[C@H]1CNC1=O)OCCCCC1CCCC1 |r| Show InChI InChI=1S/C13H22N2O3/c16-12-11(9-14-12)15-13(17)18-8-4-3-7-10-5-1-2-6-10/h10-11H,1-9H2,(H,14,16)(H,15,17)/t11-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	33	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577388 (CHEMBL4871884) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1ccc(C)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	36	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151240 (CHEMBL3770558) Show SMILES CCCCCCCCOC(=O)N[C@H]1CNC1=O |r| Show InChI InChI=1S/C12H22N2O3/c1-2-3-4-5-6-7-8-17-12(16)14-10-9-13-11(10)15/h10H,2-9H2,1H3,(H,13,15)(H,14,16)/t10-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	37	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151242 (CHEMBL3770525) Show SMILES O=C(N[C@H]1CNC1=O)OCc1ccc(cc1)C1CCCCC1 |r| Show InChI InChI=1S/C17H22N2O3/c20-16-15(10-18-16)19-17(21)22-11-12-6-8-14(9-7-12)13-4-2-1-3-5-13/h6-9,13,15H,1-5,10-11H2,(H,18,20)(H,19,21)/t15-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	41	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577405 (CHEMBL4875895) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1cnc(COCC)cn1)N2S(=O)(=O)c1c(C)n[nH]c1C |r,TLB:9:7:20:2.3| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	42	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151239 (CHEMBL3769455) Show SMILES O=C(N[C@H]1CNC1=O)OCCCC1CCCCC1 |r| Show InChI InChI=1S/C13H22N2O3/c16-12-11(9-14-12)15-13(17)18-8-4-7-10-5-2-1-3-6-10/h10-11H,1-9H2,(H,14,16)(H,15,17)/t11-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	44	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151096 (CHEMBL3769689) Show SMILES CCCOc1ccc(COC(=O)N[C@H]2CNC2=O)cc1 |r| Show InChI InChI=1S/C14H18N2O4/c1-2-7-19-11-5-3-10(4-6-11)9-20-14(18)16-12-8-15-13(12)17/h3-6,12H,2,7-9H2,1H3,(H,15,17)(H,16,18)/t12-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	48	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant human NAAA expressed in HEK293 cells after 30 mins by UPLC/MS analysis				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151234 (CHEMBL3770490) Show SMILES O=C(N[C@H]1CNC1=O)OCCCCCC1CCCCC1 |r| Show InChI InChI=1S/C15H26N2O3/c18-14-13(11-16-14)17-15(19)20-10-6-2-5-9-12-7-3-1-4-8-12/h12-13H,1-11H2,(H,16,18)(H,17,19)/t13-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	49	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577392 (CHEMBL4875599) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1ccc(CC)cc1)N2S(=O)(=O)c1c(C)n[nH]c1C |r,TLB:9:7:18:2.3| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	51	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151237 (CHEMBL3770240) Show SMILES CCCc1ccc(COC(=O)N[C@H]2CNC2=O)cc1 |r| Show InChI InChI=1S/C14H18N2O3/c1-2-3-10-4-6-11(7-5-10)9-19-14(18)16-12-8-15-13(12)17/h4-7,12H,2-3,8-9H2,1H3,(H,15,17)(H,16,18)/t12-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	52	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151232 (CHEMBL3769763) Show SMILES O=C(N[C@H]1CNC1=O)OCCCCC1CCOCC1 |r| Show InChI InChI=1S/C13H22N2O4/c16-12-11(9-14-12)15-13(17)19-6-2-1-3-10-4-7-18-8-5-10/h10-11H,1-9H2,(H,14,16)(H,15,17)/t11-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	71	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151057 (CHEMBL3770726) Show SMILES O=C(N[C@H]1CNC1=O)OCCCCC1CCCCC1 |r| Show InChI InChI=1S/C14H24N2O3/c17-13-12(10-15-13)16-14(18)19-9-5-4-8-11-6-2-1-3-7-11/h11-12H,1-10H2,(H,15,17)(H,16,18)/t12-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	73	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of GST-tagged human BRD4 bromodomain1 using H4KAc 5/8/12/16 peptide as substrate incubated overnight by HTRF assay				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151149 (CHEMBL3769639) Show SMILES FC(F)(F)c1ccc(CCCCOC(=O)N[C@H]2CNC2=O)cc1 |r| Show InChI InChI=1S/C15H17F3N2O3/c16-15(17,18)11-6-4-10(5-7-11)3-1-2-8-23-14(22)20-12-9-19-13(12)21/h4-7,12H,1-3,8-9H2,(H,19,21)(H,20,22)/t12-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	73	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151220 (CHEMBL3769678) Show SMILES FC1(F)CCC(CCCCOC(=O)N[C@H]2CNC2=O)CC1 |r| Show InChI InChI=1S/C14H22F2N2O3/c15-14(16)6-4-10(5-7-14)3-1-2-8-21-13(20)18-11-9-17-12(11)19/h10-11H,1-9H2,(H,17,19)(H,18,20)/t11-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	76	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant human NAAA expressed in HEK293 cells after 30 mins by UPLC/MS analysis				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151055 (CHEMBL3771111) Show SMILES CCc1ccc(COC(=O)N[C@H]2CNC2=O)cc1 |r| Show InChI InChI=1S/C13H16N2O3/c1-2-9-3-5-10(6-4-9)8-18-13(17)15-11-7-14-12(11)16/h3-6,11H,2,7-8H2,1H3,(H,14,16)(H,15,17)/t11-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	85	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Binding affinity to his-tagged human BRD4 bromodomain1 by isothermal titration calorimetric analysis				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577386 (CHEMBL4861341) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1ccccc1)N2S(=O)(=O)c1c(C)n[nH]c1C |r,TLB:9:7:16:2.3| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	93	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577397 (CHEMBL4877336) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1ccc(CCC(C)C)cc1)N2S(=O)(=O)c1c(C)n[nH]c1C |r,TLB:9:7:21:2.3| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	114	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151127 (CHEMBL3770640) Show SMILES CCCCCCCOC(=O)N[C@H]1CNC1=O |r| Show InChI InChI=1S/C11H20N2O3/c1-2-3-4-5-6-7-16-11(15)13-9-8-12-10(9)14/h9H,2-8H2,1H3,(H,12,14)(H,13,15)/t9-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	122	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151148 (CHEMBL3769700) Show SMILES O=C(N[C@H]1CNC1=O)OCc1ccc2CCCc2c1 |r| Show InChI InChI=1S/C14H16N2O3/c17-13-12(7-15-13)16-14(18)19-8-9-4-5-10-2-1-3-11(10)6-9/h4-6,12H,1-3,7-8H2,(H,15,17)(H,16,18)/t12-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	130	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151152 (CHEMBL3771196) Show SMILES O=C(N[C@H]1CNC1=O)OCc1ccc2CCCCc2c1 |r| Show InChI InChI=1S/C15H18N2O3/c18-14-13(8-16-14)17-15(19)20-9-10-5-6-11-3-1-2-4-12(11)7-10/h5-7,13H,1-4,8-9H2,(H,16,18)(H,17,19)/t13-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	140	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151055 (CHEMBL3771111) Show SMILES CCc1ccc(COC(=O)N[C@H]2CNC2=O)cc1 |r| Show InChI InChI=1S/C13H16N2O3/c1-2-9-3-5-10(6-4-9)8-18-13(17)15-11-7-14-12(11)16/h3-6,11H,2,7-8H2,1H3,(H,14,16)(H,15,17)/t11-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	160	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577385 (CHEMBL4861841) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1ccccn1)N2S(=O)(=O)c1c(C)n[nH]c1C |r,TLB:9:7:16:2.3| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	162	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577399 (CHEMBL4879033) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1ccc(OC)cc1)N2S(=O)(=O)c1c(C)n[nH]c1C |r,TLB:9:7:18:2.3| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	175	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577398 (CHEMBL4857016) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1ccc(cc1)C(F)(F)F)N2S(=O)(=O)c1c(C)n[nH]c1C |r,TLB:9:7:20:2.3| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	212	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577380 (CHEMBL4848387) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1cnccn1)N2S(=O)(=O)c1c(C)n[nH]c1C |r,TLB:9:7:16:2.3| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	230	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151151 (CHEMBL3770354) Show SMILES CCc1ccc(CCCCOC(=O)N[C@H]2CNC2=O)cc1 |r| Show InChI InChI=1S/C16H22N2O3/c1-2-12-6-8-13(9-7-12)5-3-4-10-21-16(20)18-14-11-17-15(14)19/h6-9,14H,2-5,10-11H2,1H3,(H,17,19)(H,18,20)/t14-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	230	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151236 (CHEMBL3770695) Show SMILES C[C@@H]1NC(=O)[C@H]1NC(=O)OCCCCC1CCCCC1 |r| Show InChI InChI=1S/C15H26N2O3/c1-11-13(14(18)16-11)17-15(19)20-10-6-5-9-12-7-3-2-4-8-12/h11-13H,2-10H2,1H3,(H,16,18)(H,17,19)/t11-,13-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	240	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151096 (CHEMBL3769689) Show SMILES CCCOc1ccc(COC(=O)N[C@H]2CNC2=O)cc1 |r| Show InChI InChI=1S/C14H18N2O4/c1-2-7-19-11-5-3-10(4-6-11)9-20-14(18)16-12-8-15-13(12)17/h3-6,12H,2,7-9H2,1H3,(H,15,17)(H,16,18)/t12-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	250	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of GST-tagged human BRD4 bromodomain2 using H4KAc 5/8/12/16 peptide as substrate incubated overnight by HTRF assay				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577391 (CHEMBL4869873) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1ccccc1C)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	291	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151241 (CHEMBL3770549) Show SMILES O=C(N[C@H]1CNC1=O)OCCCCCc1ccccc1 |r| Show InChI InChI=1S/C15H20N2O3/c18-14-13(11-16-14)17-15(19)20-10-6-2-5-9-12-7-3-1-4-8-12/h1,3-4,7-8,13H,2,5-6,9-11H2,(H,16,18)(H,17,19)/t13-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	298	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151153 (CHEMBL3769597) Show SMILES CC(C)(C)c1ccc(COC(=O)N[C@H]2CNC2=O)cc1 |r| Show InChI InChI=1S/C15H20N2O3/c1-15(2,3)11-6-4-10(5-7-11)9-20-14(19)17-12-8-16-13(12)18/h4-7,12H,8-9H2,1-3H3,(H,16,18)(H,17,19)/t12-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	310	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151222 (CHEMBL3770519) Show SMILES CCCCC1CCC(CC1)OC(=O)N[C@H]1CNC1=O |r,wU:14.14,(-6.41,.92,;-5.34,1.53,;-4,.77,;-2.67,1.54,;-1.33,.77,;,1.54,;1.33,.77,;1.33,-.77,;,-1.54,;-1.33,-.77,;2.67,-1.54,;2.66,-3.08,;1.6,-3.7,;4,-3.86,;4,-5.4,;5.08,-6.44,;3.99,-7.52,;2.9,-6.43,;1.67,-6.41,)| Show InChI InChI=1S/C14H24N2O3/c1-2-3-4-10-5-7-11(8-6-10)19-14(18)16-12-9-15-13(12)17/h10-12H,2-9H2,1H3,(H,15,17)(H,16,18)/t10?,11?,12-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	323	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577376 (CHEMBL4866583) Show SMILES CCCc1n[nH]c(C)c1S(=O)(=O)N1CCC(CC1)Oc1cnccn1 Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	330	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151220 (CHEMBL3769678) Show SMILES FC1(F)CCC(CCCCOC(=O)N[C@H]2CNC2=O)CC1 |r| Show InChI InChI=1S/C14H22F2N2O3/c15-14(16)6-4-10(5-7-14)3-1-2-8-21-13(20)18-11-9-17-12(11)19/h10-11H,1-9H2,(H,17,19)(H,18,20)/t11-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	330	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human BRD3 bromodomain2 using H4KAc 5/8/12/16 peptide as substrate incubated overnight by HTRF assay				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151053 (CHEMBL3770509) Show SMILES CCCCCCCCC(=O)N[C@H]1CNC1=O |r| Show InChI InChI=1S/C12H22N2O2/c1-2-3-4-5-6-7-8-11(15)14-10-9-13-12(10)16/h10H,2-9H2,1H3,(H,13,16)(H,14,15)/t10-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	340	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577381 (CHEMBL4865423) Show SMILES [H][C@]12CCC[C@]([H])(C[C@@H](C1)Oc1cnccn1)N2S(=O)(=O)c1c(C)n[nH]c1C |r,TLB:18:17:2.3.4:7.8.9,10:8:2.3.4:17| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	370	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
Acid ceramidase (Homo sapiens (Human))	BDBM50151154 (CHEMBL3770896) Show SMILES CCCCc1ccc(COC(=O)N[C@H]2CNC2=O)cc1 |r| Show InChI InChI=1S/C15H20N2O3/c1-2-3-4-11-5-7-12(8-6-11)10-20-15(19)17-13-9-16-14(13)18/h5-8,13H,2-4,9-10H2,1H3,(H,16,18)(H,17,19)/t13-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	390	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human acid ceramidase by UPLC/MS analysis				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50577402 (CHEMBL4869850) Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](C1)Oc1ccc(OCCC)cc1)N2S(=O)(=O)c1c(C)n[nH]c1C |r,TLB:9:7:20:2.3| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	450	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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151238 (CHEMBL3770031) Show SMILES O=C(N[C@H]1CNC1=O)OCc1ccc(cc1)-c1ccccc1 |r| Show InChI InChI=1S/C17H16N2O3/c20-16-15(10-18-16)19-17(21)22-11-12-6-8-14(9-7-12)13-4-2-1-3-5-13/h1-9,15H,10-11H2,(H,18,20)(H,19,21)/t15-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	513	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151147 (CHEMBL3770722) Show SMILES COc1ccc(CCCCOC(=O)N[C@H]2CNC2=O)cc1 |r| Show InChI InChI=1S/C12H14N2O3/c1-8-2-4-9(5-3-8)7-17-12(16)14-10-6-13-11(10)15/h2-5,10H,6-7H2,1H3,(H,13,15)(H,14,16)/t10-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	520	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) Article DOI: 10.1016/j.ejmech.2016.01.046 BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair

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