Compile Data Set for Download or QSAR

Found 17 hits with Last Name = 'battistello' and Initial = 'v'   

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))	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	9	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Irreversible inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate preincubated for 60 mins followed by substrate addition				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					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	26	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Irreversible inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate preincubated for 30 mins followed by substrate addition				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					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	144	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate after 30 mins				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					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	146	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Irreversible inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50021981 (CHEMBL3297865) Show SMILES COc1ccc(cc1)C(=O)N1CCC(CC1)C(=O)c1ccc(Cl)cc1 Show InChI InChI=1S/C20H20ClNO3/c1-25-18-8-4-16(5-9-18)20(24)22-12-10-15(11-13-22)19(23)14-2-6-17(21)7-3-14/h2-9,15H,10-13H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	8.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate by Michaelis-Menten equation analysis				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50021981 (CHEMBL3297865) Show SMILES COc1ccc(cc1)C(=O)N1CCC(CC1)C(=O)c1ccc(Cl)cc1 Show InChI InChI=1S/C20H20ClNO3/c1-25-18-8-4-16(5-9-18)20(24)22-12-10-15(11-13-22)19(23)14-2-6-17(21)7-3-14/h2-9,15H,10-13H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	1.17E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate after 30 mins				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50021981 (CHEMBL3297865) Show SMILES COc1ccc(cc1)C(=O)N1CCC(CC1)C(=O)c1ccc(Cl)cc1 Show InChI InChI=1S/C20H20ClNO3/c1-25-18-8-4-16(5-9-18)20(24)22-12-10-15(11-13-22)19(23)14-2-6-17(21)7-3-14/h2-9,15H,10-13H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Irreversible inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50021981 (CHEMBL3297865) Show SMILES COc1ccc(cc1)C(=O)N1CCC(CC1)C(=O)c1ccc(Cl)cc1 Show InChI InChI=1S/C20H20ClNO3/c1-25-18-8-4-16(5-9-18)20(24)22-12-10-15(11-13-22)19(23)14-2-6-17(21)7-3-14/h2-9,15H,10-13H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	1.22E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Irreversible inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate preincubated for 60 mins followed by substrate addition				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50021981 (CHEMBL3297865) Show SMILES COc1ccc(cc1)C(=O)N1CCC(CC1)C(=O)c1ccc(Cl)cc1 Show InChI InChI=1S/C20H20ClNO3/c1-25-18-8-4-16(5-9-18)20(24)22-12-10-15(11-13-22)19(23)14-2-6-17(21)7-3-14/h2-9,15H,10-13H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	1.27E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Irreversible inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate preincubated for 30 mins followed by substrate addition				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50021982 (CHEMBL3297868) Show SMILES Cc1nc2cc(ccc2n1-c1ccccc1)C(=O)N1CCC(Cc2ccccc2)CC1 Show InChI InChI=1S/C27H27N3O/c1-20-28-25-19-23(12-13-26(25)30(20)24-10-6-3-7-11-24)27(31)29-16-14-22(15-17-29)18-21-8-4-2-5-9-21/h2-13,19,22H,14-18H2,1H3	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	2.43E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate after 30 mins				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50021984 (CHEMBL3297867) Show SMILES COc1ccc(CNC(=O)c2ccc3nc(-c4ccoc4)c(nc3c2)-c2ccoc2)cc1 Show InChI InChI=1S/C25H19N3O4/c1-30-20-5-2-16(3-6-20)13-26-25(29)17-4-7-21-22(12-17)28-24(19-9-11-32-15-19)23(27-21)18-8-10-31-14-18/h2-12,14-15H,13H2,1H3,(H,26,29)	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	>5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate after 30 mins				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50021983 (CHEMBL3297866) Show SMILES O=C(Cn1nnc(n1)-c1ccc(cc1)N1CCOCC1)N1CCN(CC1)c1ccccc1 Show InChI InChI=1S/C23H27N7O2/c31-22(29-12-10-27(11-13-29)20-4-2-1-3-5-20)18-30-25-23(24-26-30)19-6-8-21(9-7-19)28-14-16-32-17-15-28/h1-9H,10-18H2	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	>5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate after 30 mins				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50021980 (CHEMBL1458886) Show SMILES COc1ccc(cc1)-c1nnn(CC(=O)N2CCN(CC2)c2ccc(F)cc2)n1 Show InChI InChI=1S/C20H21FN6O2/c1-29-18-8-2-15(3-9-18)20-22-24-27(23-20)14-19(28)26-12-10-25(11-13-26)17-6-4-16(21)5-7-17/h2-9H,10-14H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate after 30 mins				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50021979 (CHEMBL1499740) Show SMILES Fc1ccc(cc1)N1CCN(CC1)C(=O)C1CCN(CC1)C(=O)Cc1ccccc1 Show InChI InChI=1S/C24H28FN3O2/c25-21-6-8-22(9-7-21)26-14-16-28(17-15-26)24(30)20-10-12-27(13-11-20)23(29)18-19-4-2-1-3-5-19/h1-9,20H,10-18H2	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	>5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate after 30 mins				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50021978 (CHEMBL3297864) Show SMILES [O-][N+](=O)c1ccc(cc1)C(=O)c1ccc2C(=O)N(C(=O)c2c1)c1cccnc1 Show InChI InChI=1S/C20H11N3O5/c24-18(12-3-6-14(7-4-12)23(27)28)13-5-8-16-17(10-13)20(26)22(19(16)25)15-2-1-9-21-11-15/h1-11H	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	>5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate after 30 mins				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50021977 (CHEMBL3297863) Show SMILES COc1ccc(cc1)N1CCN(CC1)C(=O)CSc1nnc(o1)-c1ccc(OC)cc1 Show InChI InChI=1S/C22H24N4O4S/c1-28-18-7-3-16(4-8-18)21-23-24-22(30-21)31-15-20(27)26-13-11-25(12-14-26)17-5-9-19(29-2)10-6-17/h3-10H,11-15H2,1-2H3	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	>5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate after 30 mins				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50021976 (CHEMBL3297862) Show SMILES CCOc1ccc(cc1)N1CC(CC1=O)C(=O)Nc1ccc(cc1)C(C)=O Show InChI InChI=1S/C21H22N2O4/c1-3-27-19-10-8-18(9-11-19)23-13-16(12-20(23)25)21(26)22-17-6-4-15(5-7-17)14(2)24/h4-11,16H,3,12-13H2,1-2H3,(H,22,26)	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	>5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Pisa Curated by ChEMBL					Assay Description Inhibition of human recombinant MAGL using 4-nitrophenylacetate as substrate after 30 mins				Bioorg Med Chem 22: 3285-91 (2014) Article DOI: 10.1016/j.bmc.2014.04.057 BindingDB Entry DOI: 10.7270/Q2P84DGB
					More data for this Ligand-Target Pair