Compile Data Set for Download or QSAR

Found 1485 hits with Last Name = 'kocer' and Initial = 'b'   

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))	BDBM597927 (US11608347, Example 55 | [(7R,9aR)-7-(3-chloro-4- ...) Show SMILES COc1cccc(C(=O)N2CCN3C[C@H](CC[C@@H]3C2)c2ccc(F)c(Cl)c2)c1Cl |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	0.200	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description In one embodiment, the present invention provides compounds of formula (Ie) and their pharmaceutically acceptable salts as described herein, wherein ...				Citation and Details BindingDB Entry DOI: 10.7270/Q2HX1HKS
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Monoglyceride lipase (Homo sapiens (Human))	BDBM50569654 (CHEMBL4875383 | US11802133, Example 239) Show SMILES [H][C@@]12CN(CC[C@]1([H])OCC(=O)N2)C(=O)N1CC(C1)OCc1ccc(Cl)cc1Oc1ccccc1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM50569652 (CHEMBL4874643 | US11802133, Example 221) Show SMILES [H][C@@]12CN(CC[C@]1([H])OCC(=O)N2)C(=O)N1CC(CCc2ccc(cc2Br)C(F)(F)F)C1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	0.700	n/a	n/a	n/a	n/a	n/a	n/a
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					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50569653 (CHEMBL4865707 | US11802133, Example 229) Show SMILES [H][C@@]12CN(CC[C@]1([H])OCC(=O)N2)C(=O)N1CC(OCc2ccc(C)c(c2)C(F)(F)F)C1C |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	0.900	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM50569655 (CHEMBL4869836 | US11802133, Example 279) Show SMILES [H][C@@]12CN(CC[C@]1([H])OCC(=O)N2)C(=O)N1CC(CCc2ccc(cc2F)C(F)(F)F)C1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM50569651 (CHEMBL4871897 | US11802133, Example 108) Show SMILES [H][C@@]12CN(CC[C@]1([H])OCC(=O)N2)C(=O)N1CC(C1)OCc1ccc(c(Cl)c1)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631222 ((4aR,8aS)-6-(4-((2-chloro-4-fluorophenoxy)methyl)-...) Show SMILES CC1(COc2ccc(F)cc2Cl)CCN(CC1)C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
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Monoglyceride lipase (Homo sapiens (Human))	BDBM50569650 (CHEMBL4848022 | US11802133, Example 54) Show SMILES [H][C@@]12CN(CC[C@]1([H])OCC(=O)N2)C(=O)N1CCC(COc2ccc(cc2Cl)C(F)(F)F)CC1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631296 (US11802133, Example 233 | US11802133, Example 236 ...) Show SMILES CC1C(CN1C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1)OCc1ccc(cc1F)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631282 (US11802133, Example 219) Show SMILES Cc1ccc(CCC2CN(C2)C(=O)N2CC[C@@H]3OCC(=O)N[C@@H]3C2)c(c1)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631297 (US11802133, Example 234) Show SMILES FC(F)(F)c1cnc(COC2CN(C2)C(=O)N2CC[C@@H]3OCC(=O)N[C@@H]3C2)cc1C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631260 (US11802133, Example 139) Show SMILES Fc1cccc(c1CCC1CN(C1)C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
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Tyrosine-protein kinase BTK (Homo sapiens (Human))	BDBM50039982 (CHEMBL3358345) Show SMILES CCN1CCN(CC1)c1ccc(Nc2cc(cn(C)c2=O)-c2cccc(c2CO)-n2ncc3cc(cc(F)c3c2=O)C(C)(C)C)nc1 Show InChI InChI=1S/C36H40FN7O3/c1-6-42-12-14-43(15-13-42)26-10-11-32(38-20-26)40-30-17-24(21-41(5)34(30)46)27-8-7-9-31(28(27)22-45)44-35(47)33-23(19-39-44)16-25(18-29(33)37)36(2,3)4/h7-11,16-21,45H,6,12-15,22H2,1-5H3,(H,38,40)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
Hoffmann-La Roche Inc. Curated by ChEMBL					Assay Description Inhibition of BTK in human whole blood assessed as decrease in CD69 positive cells				Bioorg Med Chem Lett 25: 367-71 (2014) Article DOI: 10.1016/j.bmcl.2014.11.030 BindingDB Entry DOI: 10.7270/Q2BZ67N2
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM631219 (US11802133, Example 75) Show SMILES FC(F)(F)c1ccc(COC2CN(C2)C(=O)N2CC[C@@H]3OCC(=O)N[C@@H]3C2)c(Cl)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM597939 ((4-chlorothieno[2,3- b]pyridin-5-yl)-[rac- (7R,9aR...) Show SMILES Fc1ccc(cc1Cl)[C@H]1CC[C@@H]2CN(CCN2C1)C(=O)c1cnc2sccc2c1Cl |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	2.40	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description In one embodiment, the present invention provides compounds of formula (Ie) and their pharmaceutically acceptable salts as described herein, wherein ...				Citation and Details BindingDB Entry DOI: 10.7270/Q2HX1HKS
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM631352 (US11802133, Example 289) Show SMILES Fc1cccc(c1\C=C\C1CN(C1)C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM561384 (US11390610, Example 213) Show SMILES CCC1(CC)CCN(C1)c1ccc(cc1)C(=O)N1CCN(CC1)c1nc2ccccc2c(=O)[nH]1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds of the present invention are MAGL inhibitors. Thus, in one aspect, the present invention provides the use of compounds of Formula (I) or a ...				Citation and Details BindingDB Entry DOI: 10.7270/Q2W0994M
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM597917 (US11608347, Example 46 | [(7R,9aR)-7-(3,4- dichlor...) Show SMILES COc1cccc(C(=O)N2CCN3C[C@H](CC[C@@H]3C2)c2ccc(Cl)c(Cl)c2)c1Br |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description In one embodiment, the present invention provides compounds of formula (Ie) and their pharmaceutically acceptable salts as described herein, wherein ...				Citation and Details BindingDB Entry DOI: 10.7270/Q2HX1HKS
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM631281 (US11802133, Example 218) Show SMILES COc1cccc(c1CCC1CN(C1)C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631271 (US11802133, Example 208) Show SMILES FC(F)(F)c1ccc(OC2CCN(CC2)C(=O)N2CC[C@@H]3OCC(=O)N[C@@H]3C2)cc1C1CC1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631275 (US11802133, Example 212) Show SMILES Fc1c(OC2CCN(CC2)C(=O)N2CC[C@@H]3OCC(=O)N[C@@H]3C2)ccc(Cl)c1-c1ccc(Cl)cc1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM631250 (US11802133, Example 115) Show SMILES COc1cc(ccc1COC1CN(C1)C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631283 (US11802133, Example 220) Show SMILES CC(=O)c1cc(ccc1CCC1CN(C1)C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631287 (US11802133, Example 224) Show SMILES Clc1ccc(COC2CN(C2)C(=O)N2CC[C@@H]3OCC(=O)N[C@@H]3C2)cc1Cl |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Tyrosine-protein kinase BTK (Homo sapiens (Human))	BDBM50039983 (CHEMBL3358346) Show SMILES CN1CCN(CC1)c1ccc(Nc2cc(cn(C)c2=O)-c2cccc(c2CO)-n2ncc3cc(cc(F)c3c2=O)C(C)(C)C)nc1 Show InChI InChI=1S/C35H38FN7O3/c1-35(2,3)24-15-22-18-38-43(34(46)32(22)28(36)17-24)30-8-6-7-26(27(30)21-44)23-16-29(33(45)41(5)20-23)39-31-10-9-25(19-37-31)42-13-11-40(4)12-14-42/h6-10,15-20,44H,11-14,21H2,1-5H3,(H,37,39)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Hoffmann-La Roche Inc. Curated by ChEMBL					Assay Description Inhibition of BTK in human whole blood assessed as decrease in CD69 positive cells				Bioorg Med Chem Lett 25: 367-71 (2014) Article DOI: 10.1016/j.bmcl.2014.11.030 BindingDB Entry DOI: 10.7270/Q2BZ67N2
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM631208 (US11802133, Example 58) Show SMILES FC(F)(F)c1ccc(CC2CCN(CC2)C(=O)N2CC[C@@H]3OCC(=O)N[C@@H]3C2)c(c1)C1CCCC1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631218 (US11802133, Example 74) Show SMILES C[C@H]1CN(CC[C@H]1COc1ccc(F)cc1Cl)C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
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Monoglyceride lipase (Homo sapiens (Human))	BDBM597939 ((4-chlorothieno[2,3- b]pyridin-5-yl)-[rac- (7R,9aR...) Show SMILES Fc1ccc(cc1Cl)[C@H]1CC[C@@H]2CN(CCN2C1)C(=O)c1cnc2sccc2c1Cl |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	3.20	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description In one embodiment, the present invention provides compounds of formula (Ie) and their pharmaceutically acceptable salts as described herein, wherein ...				Citation and Details BindingDB Entry DOI: 10.7270/Q2HX1HKS
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM631184 (US11802133, Example 33) Show SMILES Fc1cc(CC2CCN(CC2)C(=O)N2CC[C@@H]3OCC(=O)N[C@@H]3C2)ccc1Cl |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631158 (US11802133, Example 24 | US11802133, Example 7) Show SMILES Fc1ccc(OCC2CCN(CC2)C(=O)N2CC[C@@H]3OCC(=O)N[C@@H]3C2)c(Cl)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631251 (US11802133, Example 116) Show SMILES FC(F)(F)c1cc(Cl)ccc1COC1CN(C1)C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Tyrosine-protein kinase BTK (Homo sapiens (Human))	BDBM50039978 (CHEMBL3352876) Show SMILES CCN1CCN(CC1)c1ccc(Nc2cc(cn(C)c2=O)-c2cccc(c2CO)-n2ccc3cc(cc(F)c3c2=O)C2CC2)nc1 Show InChI InChI=1S/C36H37FN6O3/c1-3-41-13-15-42(16-14-41)27-9-10-33(38-20-27)39-31-19-26(21-40(2)35(31)45)28-5-4-6-32(29(28)22-44)43-12-11-24-17-25(23-7-8-23)18-30(37)34(24)36(43)46/h4-6,9-12,17-21,23,44H,3,7-8,13-16,22H2,1-2H3,(H,38,39)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	PDB Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
Hoffmann-La Roche Inc. Curated by ChEMBL					Assay Description Inhibition of BTK in human whole blood assessed as decrease in CD69 positive cells				Bioorg Med Chem Lett 25: 367-71 (2014) Article DOI: 10.1016/j.bmcl.2014.11.030 BindingDB Entry DOI: 10.7270/Q2BZ67N2
					More data for this Ligand-Target Pair				3D Structure (crystal)
Monoglyceride lipase (Homo sapiens (Human))	BDBM561025 (US11390610, Example 67) Show SMILES CC(C)(C)Cc1nc(no1)-c1ccc(cc1)C(=O)N1CCN(CC1)c1nc2ccccc2c(=O)[nH]1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	4.40	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds of the present invention are MAGL inhibitors. Thus, in one aspect, the present invention provides the use of compounds of Formula (I) or a ...				Citation and Details BindingDB Entry DOI: 10.7270/Q2W0994M
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM631355 (US11802133, Example 292) Show SMILES Cc1cc(ccc1COC1CN(C1)C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631249 (US11802133, Example 114) Show SMILES Fc1cc(COC2CN(C2)C(=O)N2CC[C@@H]3OCC(=O)N[C@@H]3C2)ccc1C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM561355 (US11390610, Example 184) Show SMILES Clc1cccc(OCc2ccc(cc2Cl)C(=O)N2CCN(CC2)c2nc3ccccc3c(=O)[nH]2)c1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds of the present invention are MAGL inhibitors. Thus, in one aspect, the present invention provides the use of compounds of Formula (I) or a ...				Citation and Details BindingDB Entry DOI: 10.7270/Q2W0994M
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631312 (US11802133, Example 249) Show SMILES FC(F)(F)c1ccc(COC2CN(C2)C(=O)N2CC[C@@H]3OCC(=O)N[C@@H]3C2)c(c1)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631314 (US11802133, Example 251) Show SMILES Cc1cc(OC(F)(F)F)ccc1COC1CN(C1)C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631315 (US11802133, Example 252) Show SMILES CC1C(CN1C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1)OCc1ccc(OC(F)(F)F)cc1C |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM561217 (US11390610, Example 116) Show SMILES Clc1ccc(cc1Cl)-c1nc2ccc(cc2o1)C(=O)N1CCN(CC1)c1nc2ccccc2c(=O)[nH]1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds of the present invention are MAGL inhibitors. Thus, in one aspect, the present invention provides the use of compounds of Formula (I) or a ...				Citation and Details BindingDB Entry DOI: 10.7270/Q2W0994M
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631278 (US11802133, Example 215) Show SMILES Cc1ccc(CCC2CN(C2)C(=O)N2CC[C@@H]3OCC(=O)N[C@@H]3C2)c(F)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631294 (US11802133, Example 231) Show SMILES C[C@H]1CN(CC[C@H]1COc1cnc(c(C)c1)C(F)(F)F)C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631178 (US11802133, Example 27 | US11802133, Example 29) Show SMILES Fc1cc(ccc1COC1CN(C1)C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631196 (US11802133, Example 46) Show SMILES FC(F)(F)Oc1ccc(OCC2CCN(CC2)C(=O)N2CC[C@@H]3OCC(=O)N[C@@H]3C2)c(Cl)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631197 (US11802133, Example 47) Show SMILES Fc1cc(ccc1OCC1CN(C1)C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631225 (US11802133, Example 88) Show SMILES COc1cc(COC2CN(C2)C(=O)N2CC[C@@H]3OCC(=O)N[C@@H]3C2)ccc1C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631240 (US11802133, Example 103 | US11802133, Example 104 ...) Show SMILES CC1C(CN1C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1)OCc1ccc(cc1)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM631248 (US11802133, Example 113) Show SMILES Fc1ccc(cc1COC1CN(C1)C(=O)N1CC[C@@H]2OCC(=O)N[C@@H]2C1)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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Monoglyceride lipase (Homo sapiens (Human))	BDBM597977 ((2-chloro-3- methoxyphenyl)-[rac- (7R,9aS)-7-(4-ch...) Show SMILES COc1cccc(C(=O)N2CCN3C[C@](F)(CC[C@@H]3C2)c2ccc(Cl)cc2)c1Cl |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.70	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description In one embodiment, the present invention provides compounds of formula (Ie) and their pharmaceutically acceptable salts as described herein, wherein ...				Citation and Details BindingDB Entry DOI: 10.7270/Q2HX1HKS
					More data for this Ligand-Target Pair
Monoglyceride lipase (Homo sapiens (Human))	BDBM631328 ((+)-(4aR,8aS)-6-[3-[3-(2-Azaspiro[3.3]heptan-2-yl)...) Show SMILES FC(F)(F)c1ccc(OC2CN(C2)C(=O)N2CC[C@@H]3OCC(=O)N[C@@H]3C2)cc1N1CC2(CCC2)C1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	6	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
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