Compile Data Set for Download or QSAR

Found 38 hits Enz. Inhib. hit(s) with all data for entry = 50013219   

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
Monoglyceride lipase (Homo sapiens (Human))	BDBM50065646 (CHEMBL3087181) Show SMILES O=C(N1CCC(CC1)C(c1ccc2OCOc2c1)c1ccc2OCOc2c1)n1cncn1 Show InChI InChI=1S/C23H22N4O5/c28-23(27-12-24-11-25-27)26-7-5-15(6-8-26)22(16-1-3-18-20(9-16)31-13-29-18)17-2-4-19-21(10-17)32-14-30-19/h1-4,9-12,15,22H,5-8,13-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	<0.400	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50242634 (5-((biphenyl-4-yl)methyl)-N,N-dimethyl-2H-tetrazol...) Show SMILES CN(C)C(=O)n1nnc(Cc2ccc(cc2)-c2ccccc2)n1 Show InChI InChI=1S/C17H17N5O/c1-21(2)17(23)22-19-16(18-20-22)12-13-8-10-15(11-9-13)14-6-4-3-5-7-14/h3-11H,12H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.900	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of MAGL (unknown origin)				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM179929 (US9133148, 1a) Show SMILES OC(C1CCN(CC1)C(=O)OC(C(F)(F)F)C(F)(F)F)(c1ccc2OCOc2c1)c1ccc2OCOc2c1 Show InChI InChI=1S/C24H21F6NO7/c25-23(26,27)20(24(28,29)30)38-21(32)31-7-5-13(6-8-31)22(33,14-1-3-16-18(9-14)36-11-34-16)15-2-4-17-19(10-15)37-12-35-17/h1-4,9-10,13,20,33H,5-8,11-12H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.90	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL transfected in human HEK293T cells assessed as reduction in ABPP binding by competitive binding assay				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM60622 (BDBM50300355 | US11753371, Compound JZL-184 | US91...) Show SMILES OC(C1CCN(CC1)C(=O)Oc1ccc(cc1)[N+]([O-])=O)(c1ccc2OCOc2c1)c1ccc2OCOc2c1 Show InChI InChI=1S/C27H24N2O9/c30-26(38-21-5-3-20(4-6-21)29(32)33)28-11-9-17(10-12-28)27(31,18-1-7-22-24(13-18)36-15-34-22)19-2-8-23-25(14-19)37-16-35-23/h1-8,13-14,17,31H,9-12,15-16H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of MAGL (unknown origin)				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563791 (CHEMBL4778803) Show SMILES Fc1ccc(NCC(=O)Nc2ccc(cc2)-c2nc3ccccc3s2)cc1Cl Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563792 (CHEMBL4788586) Show SMILES Clc1cccc(Cl)c1NCC(=O)Nc1ccc(cc1)-c1nc2ccccc2s1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563794 (CHEMBL4793668) Show SMILES Fc1ccc(NCC(=O)Nc2ccc(cc2)-c2nc3ccccc3s2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563793 (CHEMBL4793997) Show SMILES Clc1ccc(NCC(=O)Nc2ccc(cc2)-c2nc3ccccc3s2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	9	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563790 (CHEMBL4780294) Show SMILES Brc1ccc(NCC(=O)Nc2ccc(cc2)-c2nc3ccccc3s2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	9	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563801 (CHEMBL4779678) Show SMILES Cc1cc(C)n(CC(=O)Nc2ccc(cc2)-c2nc3ccccc3s2)n1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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 human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563802 (CHEMBL4793265) Show SMILES O=C(Cn1cncn1)Nc1ccc(cc1)-c1nc2ccccc2s1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD 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 human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50414921 (CHEMBL570812) Show SMILES COc1nn(-c2ccc(NC(=O)OCc3ccccc3)c(C)c2)c(=O)o1 Show InChI InChI=1S/C18H17N3O5/c1-12-10-14(21-18(23)26-17(20-21)24-2)8-9-15(12)19-16(22)25-11-13-6-4-3-5-7-13/h3-10H,11H2,1-2H3,(H,19,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem	Article PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of MAGL (unknown origin)				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563803 (CHEMBL4797565) Show SMILES O=C(Cn1ccnc1)Nc1ccc(cc1)-c1nc2ccccc2s1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	22	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563795 (CHEMBL4786239) Show SMILES O=C(CNc1ccccc1)Nc1ccc(cc1)-c1nc2ccccc2s1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	68	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563785 (CHEMBL4792393) Show SMILES NS(=O)(=O)c1ccc(NCC(=O)Nc2ccc(cc2)-c2nc3ccccc3s2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	74	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50432829 (CHEMBL2171700) Show SMILES COc1nn(-c2ccc(Oc3ccccc3)cc2)c(=O)o1 Show InChI InChI=1S/C15H12N2O4/c1-19-14-16-17(15(18)21-14)11-7-9-13(10-8-11)20-12-5-3-2-4-6-12/h2-10H,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	78	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of MAGL (unknown origin)				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563809 (CHEMBL4794817) Show SMILES O=C(Cn1cnc2ccccc12)Nc1ccc(cc1)-c1nc2ccccc2s1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	117	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563797 (CHEMBL4777523) Show SMILES O=C(CNC1CCCCC1)Nc1ccc(cc1)-c1nc2ccccc2s1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	151	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563808 (CHEMBL4793077) Show SMILES O=C(Cn1ccc2ccccc12)Nc1ccc(cc1)-c1nc2ccccc2s1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	196	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563796 (CHEMBL4780477) Show SMILES O=C(CNCc1ccccc1)Nc1ccc(cc1)-c1nc2ccccc2s1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	242	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563800 (CHEMBL4776276) Show SMILES O=C(CN1CCCCC1)Nc1ccc(cc1)-c1nc2ccccc2s1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	282	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50414921 (CHEMBL570812) Show SMILES COc1nn(-c2ccc(NC(=O)OCc3ccccc3)c(C)c2)c(=O)o1 Show InChI InChI=1S/C18H17N3O5/c1-12-10-14(21-18(23)26-17(20-21)24-2)8-9-15(12)19-16(22)25-11-13-6-4-3-5-7-13/h3-10H,11H2,1-2H3,(H,19,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem	Article PubMed	n/a	n/a	424	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563799 (CHEMBL4785038) Show SMILES O=C(CN1CCOCC1)Nc1ccc(cc1)-c1nc2ccccc2s1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	780	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563798 (CHEMBL4800406) Show SMILES CN1CCN(CC(=O)Nc2ccc(cc2)-c2nc3ccccc3s2)CC1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	815	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563788 (CHEMBL4798413) Show SMILES Cc1ccc(NCC(=O)Nc2ccc(cc2)-c2nc3ccccc3s2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563787 (CHEMBL4788417) Show SMILES COc1ccc(NCC(=O)Nc2ccc(cc2)-c2nc3ccccc3s2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563786 (CHEMBL4783652) Show SMILES Oc1ccc(NCC(=O)Nc2ccc(cc2)-c2nc3ccccc3s2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563782 (CHEMBL4786879) Show SMILES Cc1cc(NCC(=O)Nc2ccc(cc2)-c2nc3ccccc3s2)no1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50128581 (Biphenyl-3-yl-carbamic acid cyclohexyl ester | CHE...) Show SMILES O=C(Nc1cccc(c1)-c1ccccc1)OC1CCCCC1 Show InChI InChI=1S/C19H21NO2/c21-19(22-18-12-5-2-6-13-18)20-17-11-7-10-16(14-17)15-8-3-1-4-9-15/h1,3-4,7-11,14,18H,2,5-6,12-13H2,(H,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of MAGL (unknown origin)				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50274981 (4-(4,5-dihydrothiazol-2-yl)phenyl butylcarbamate |...) Show SMILES CCCCNC(=O)Oc1ccc(cc1)C1=NCCS1 |t:15| Show InChI InChI=1S/C14H18N2O2S/c1-2-3-8-16-14(17)18-12-6-4-11(5-7-12)13-15-9-10-19-13/h4-7H,2-3,8-10H2,1H3,(H,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of MAGL (unknown origin)				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563781 (CHEMBL4800077) Show SMILES O=C(CNc1nc2ccccc2s1)Nc1ccc(cc1)-c1nc2ccccc2s1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563784 (CHEMBL4796478) Show SMILES Clc1ccc(cc1)-c1csc(NCC(=O)Nc2ccc(cc2)-c2nc3ccccc3s2)n1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563783 (CHEMBL4777889) Show SMILES Clc1ccc(cc1)-c1nnc(NCC(=O)Nc2ccc(cc2)-c2nc3ccccc3s2)o1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563807 (CHEMBL4777402) Show SMILES O=C(CN1C(=O)C(=O)c2ccccc12)Nc1ccc(cc1)-c1nc2ccccc2s1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563806 (CHEMBL4783153) Show SMILES O=C(CN(c1ccccc1)c1ccccc1)Nc1ccc(cc1)-c1nc2ccccc2s1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563804 (CHEMBL4800531) Show SMILES O=C(CN1C2CCCCC2c2ccccc12)Nc1ccc(cc1)-c1nc2ccccc2s1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563789 (CHEMBL4799435) Show SMILES [O-][N+](=O)c1ccc(NCC(=O)Nc2ccc(cc2)-c2nc3ccccc3s2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50563805 (CHEMBL4784727) Show SMILES O=C(Cn1c2ccccc2c2ccccc12)Nc1ccc(cc1)-c1nc2ccccc2s1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human MAGL using 4-Nitrophenylacetate as substrate				Citation and Details Article DOI: 10.1016/j.ejmech.2016.05.038 BindingDB Entry DOI: 10.7270/Q28056BZ
					More data for this Ligand-Target Pair