Compile Data Set for Download or QSAR

Found 423 hits with Last Name = 'leng' and Initial = 'f'   

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
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541723 (CHEMBL4649122) Show SMILES CCCCCn1c2cn(C)nc2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:21:22:20.19.25:26,THB:21:20:27.22.23:26,23:22:19:25.24.26,23:24:27.22.21:19| Show InChI InChI=1S/C23H32N4O3/c1-3-4-5-6-27-17-13-26(2)25-19(17)20(28)18(22(27)30)21(29)24-23-10-14-7-15(11-23)9-16(8-14)12-23/h13-16,28H,3-12H2,1-2H3,(H,24,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.180	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541729 (CHEMBL4637535) Show SMILES CCCCCN1C2C=NN(C)C2C(O)=C(C(=O)NC23CC4CC(CC(C4)C2)C3)C1=O |c:7,t:14,TLB:21:22:20.19.25:26,THB:21:20:27.22.23:26,23:22:19:25.24.26,23:24:27.22.21:19| Show InChI InChI=1S/C23H34N4O3/c1-3-4-5-6-27-17-13-24-26(2)19(17)20(28)18(22(27)30)21(29)25-23-10-14-7-15(11-23)9-16(8-14)12-23/h13-17,19,28H,3-12H2,1-2H3,(H,25,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.900	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541727 (CHEMBL4647226) Show SMILES CN1N=CC2C1C(O)=C(C(=O)NC13CC4CC(CC(C4)C1)C3)C(=O)N2CCCCF |c:2,t:8,TLB:15:16:14.13.19:20,THB:15:14:21.16.17:20,17:16:13:19.18.20,17:18:21.16.15:13| Show InChI InChI=1S/C22H31FN4O3/c1-26-18-16(12-24-26)27(5-3-2-4-23)21(30)17(19(18)28)20(29)25-22-9-13-6-14(10-22)8-15(7-13)11-22/h12-16,18,28H,2-11H2,1H3,(H,25,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541725 (CHEMBL4635230) Show SMILES CCCCN1C2C=NN(C)C2C(O)=C(C(=O)NC23CC4CC(CC(C4)C2)C3)C1=O |c:6,t:13,TLB:20:21:19.18.24:25,THB:20:19:26.21.22:25,22:21:18:24.23.25,22:23:26.21.20:18| Show InChI InChI=1S/C22H32N4O3/c1-3-4-5-26-16-12-23-25(2)18(16)19(27)17(21(26)29)20(28)24-22-9-13-6-14(10-22)8-15(7-13)11-22/h12-16,18,27H,3-11H2,1-2H3,(H,24,28)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50200170 (5-(4-chloro-3-methyl-phenyl)-1-(4-methyl-benzyl)-1...) Show SMILES Cc1ccc(Cn2nc(cc2-c2ccc(Cl)c(C)c2)C(=O)N[C@H]2[C@@]3(C)CC[C@H](C3)C2(C)C)cc1 |r| Show InChI InChI=1S/C29H34ClN3O/c1-18-6-8-20(9-7-18)17-33-25(21-10-11-23(30)19(2)14-21)15-24(32-33)26(34)31-27-28(3,4)22-12-13-29(27,5)16-22/h6-11,14-15,22,27H,12-13,16-17H2,1-5H3,(H,31,34)/t22-,27-,29+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	1.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Alanine--glyoxylate aminotransferase (Homo sapiens)	BDBM50601014 (CHEMBL5170947) Show SMILES Cl.NCOc1ccc2ccccc2c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c00142 BindingDB Entry DOI: 10.7270/Q25T3QJF
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541721 (CHEMBL4633927) Show SMILES Cn1cc2n(CCCCF)c(=O)c(C(=O)NC34CC5CC(CC(C5)C3)C4)c(O)c2n1 |TLB:19:20:18.17.23:24,THB:19:18:25.20.21:24,21:20:17:23.22.24,21:22:25.20.19:17| Show InChI InChI=1S/C22H29FN4O3/c1-26-12-16-18(25-26)19(28)17(21(30)27(16)5-3-2-4-23)20(29)24-22-9-13-6-14(10-22)8-15(7-13)11-22/h12-15,28H,2-11H2,1H3,(H,24,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541737 (CHEMBL4640659) Show SMILES CCCCn1c2cn(C)nc2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:20:21:19.18.24:25,THB:20:19:26.21.22:25,22:21:18:24.23.25,22:23:26.21.20:18| Show InChI InChI=1S/C22H30N4O3/c1-3-4-5-26-16-12-25(2)24-18(16)19(27)17(21(26)29)20(28)23-22-9-13-6-14(10-22)8-15(7-13)11-22/h12-15,27H,3-11H2,1-2H3,(H,23,28)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541732 (CHEMBL4636524) Show SMILES CCCCCn1c2cn(CCO)nc2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:23:24:22.21.27:28,THB:23:22:29.24.25:28,25:24:21:27.26.28,25:26:29.24.23:21| Show InChI InChI=1S/C24H34N4O4/c1-2-3-4-5-28-18-14-27(6-7-29)26-20(18)21(30)19(23(28)32)22(31)25-24-11-15-8-16(12-24)10-17(9-15)13-24/h14-17,29-30H,2-13H2,1H3,(H,25,31)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	4.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541722 (CHEMBL4641997) Show SMILES Cn1cc2n(CCCCF)c(=O)c(C(=O)NC34CC5CC(CC(O)(C5)C3)C4)c(O)c2n1 |TLB:19:20:18.17.24:25,THB:19:18:26.20.21:25,21:20:17:24.22.25,21:22:26.20.19:17,23:22:26.20.19:17| Show InChI InChI=1S/C22H29FN4O4/c1-26-11-15-17(25-26)18(28)16(20(30)27(15)5-3-2-4-23)19(29)24-21-7-13-6-14(8-21)10-22(31,9-13)12-21/h11,13-14,28,31H,2-10,12H2,1H3,(H,24,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	6.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541720 (CHEMBL4649714) Show SMILES CCCCn1c2cn(C)nc2c(O)c(C(=O)NC23CC4CC(CC(O)(C4)C2)C3)c1=O |TLB:20:21:19.18.25:26,THB:20:19:27.21.22:26,22:21:18:25.23.26,22:23:27.21.20:18,24:23:27.21.20:18| Show InChI InChI=1S/C22H30N4O4/c1-3-4-5-26-15-11-25(2)24-17(15)18(27)16(20(26)29)19(28)23-21-7-13-6-14(8-21)10-22(30,9-13)12-21/h11,13-14,27,30H,3-10,12H2,1-2H3,(H,23,28)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	11	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541735 (CHEMBL4641494) Show SMILES Cn1cc2n(CCCCO)c(=O)c(C(=O)NC34CC5CC(CC(C5)C3)C4)c(O)c2n1 |TLB:19:20:18.17.23:24,THB:19:18:25.20.21:24,21:20:17:23.22.24,21:22:25.20.19:17| Show InChI InChI=1S/C22H30N4O4/c1-25-12-16-18(24-25)19(28)17(21(30)26(16)4-2-3-5-27)20(29)23-22-9-13-6-14(10-22)8-15(7-13)11-22/h12-15,27-28H,2-11H2,1H3,(H,23,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	14	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541724 (CHEMBL4640710) Show SMILES CC(=O)OCCCCn1c2cn(C)nc2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:24:25:23.22.28:29,THB:24:23:30.25.26:29,26:25:22:28.27.29,26:27:30.25.24:22| Show InChI InChI=1S/C24H32N4O5/c1-14(29)33-6-4-3-5-28-18-13-27(2)26-20(18)21(30)19(23(28)32)22(31)25-24-10-15-7-16(11-24)9-17(8-15)12-24/h13,15-17,30H,3-12H2,1-2H3,(H,25,31)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	17	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541731 (CHEMBL4643391) Show SMILES CCCCn1c2cn(CCO)nc2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:22:23:21.20.26:27,THB:22:21:28.23.24:27,24:23:20:26.25.27,24:25:28.23.22:20| Show InChI InChI=1S/C23H32N4O4/c1-2-3-4-27-17-13-26(5-6-28)25-19(17)20(29)18(22(27)31)21(30)24-23-10-14-7-15(11-23)9-16(8-14)12-23/h13-16,28-29H,2-12H2,1H3,(H,24,30)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	18	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541726 (CHEMBL4646331) Show SMILES CCCCN1C2C=NN(C)C2C(O)=C(C(=O)NC23CC4CC(CC(O)(C4)C2)C3)C1=O |c:6,t:13,TLB:20:21:19.18.25:26,THB:20:19:27.21.22:26,22:21:18:25.23.26,22:23:27.21.20:18,24:23:27.21.20:18| Show InChI InChI=1S/C22H32N4O4/c1-3-4-5-26-15-11-23-25(2)17(15)18(27)16(20(26)29)19(28)24-21-7-13-6-14(8-21)10-22(30,9-13)12-21/h11,13-15,17,27,30H,3-10,12H2,1-2H3,(H,24,28)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	19	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541728 (CHEMBL4639191) Show SMILES CN1N=CC2C1C(O)=C(C(=O)NC13CC4CC(CC(O)(C4)C1)C3)C(=O)N2CCCCF |c:2,t:8,TLB:15:16:14.13.20:21,THB:15:14:22.16.17:21,17:16:13:20.18.21,17:18:22.16.15:13,19:18:22.16.15:13| Show InChI InChI=1S/C22H31FN4O4/c1-26-17-15(11-24-26)27(5-3-2-4-23)20(30)16(18(17)28)19(29)25-21-7-13-6-14(8-21)10-22(31,9-13)12-21/h11,13-15,17,28,31H,2-10,12H2,1H3,(H,25,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	19	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541734 (CHEMBL4633168) Show SMILES CCCCn1c2cnn(CCO)c2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:22:23:21.20.26:27,THB:22:21:28.23.24:27,24:23:20:26.25.27,24:25:28.23.22:20| Show InChI InChI=1S/C23H32N4O4/c1-2-3-4-26-17-13-24-27(5-6-28)19(17)20(29)18(22(26)31)21(30)25-23-10-14-7-15(11-23)9-16(8-14)12-23/h13-16,28-29H,2-12H2,1H3,(H,25,30)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	27	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Alanine--glyoxylate aminotransferase (Homo sapiens)	BDBM50601018 (CHEMBL5207596) Show SMILES NOCc1cccc(c1)-c1ccccc1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	27	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c00142 BindingDB Entry DOI: 10.7270/Q25T3QJF
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541723 (CHEMBL4649122) Show SMILES CCCCCn1c2cn(C)nc2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:21:22:20.19.25:26,THB:21:20:27.22.23:26,23:22:19:25.24.26,23:24:27.22.21:19| Show InChI InChI=1S/C23H32N4O3/c1-3-4-5-6-27-17-13-26(2)25-19(17)20(28)18(22(27)30)21(29)24-23-10-14-7-15(11-23)9-16(8-14)12-23/h13-16,28H,3-12H2,1-2H3,(H,24,29)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	34	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541727 (CHEMBL4647226) Show SMILES CN1N=CC2C1C(O)=C(C(=O)NC13CC4CC(CC(C4)C1)C3)C(=O)N2CCCCF |c:2,t:8,TLB:15:16:14.13.19:20,THB:15:14:21.16.17:20,17:16:13:19.18.20,17:18:21.16.15:13| Show InChI InChI=1S/C22H31FN4O3/c1-26-18-16(12-24-26)27(5-3-2-4-23)21(30)17(19(18)28)20(29)25-22-9-13-6-14(10-22)8-15(7-13)11-22/h12-16,18,28H,2-11H2,1H3,(H,25,29)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	39	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Alanine--glyoxylate aminotransferase (Homo sapiens)	BDBM50146549 (CHEMBL3764222) Show SMILES Cl.COc1cccc(CON)c1 Show InChI InChI=1S/C8H11NO2.ClH/c1-10-8-4-2-3-7(5-8)6-11-9;/h2-5H,6,9H2,1H3;1H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c00142 BindingDB Entry DOI: 10.7270/Q25T3QJF
					More data for this Ligand-Target Pair
Alanine--glyoxylate aminotransferase (Homo sapiens)	BDBM50146407 (CHEMBL3763469) Show SMILES Cl.NOCc1cccc(Br)c1 Show InChI InChI=1S/C7H8BrNO.ClH/c8-7-3-1-2-6(4-7)5-10-9;/h1-4H,5,9H2;1H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	50	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c00142 BindingDB Entry DOI: 10.7270/Q25T3QJF
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541729 (CHEMBL4637535) Show SMILES CCCCCN1C2C=NN(C)C2C(O)=C(C(=O)NC23CC4CC(CC(C4)C2)C3)C1=O |c:7,t:14,TLB:21:22:20.19.25:26,THB:21:20:27.22.23:26,23:22:19:25.24.26,23:24:27.22.21:19| Show InChI InChI=1S/C23H34N4O3/c1-3-4-5-6-27-17-13-24-26(2)19(17)20(28)18(22(27)30)21(29)25-23-10-14-7-15(11-23)9-16(8-14)12-23/h13-17,19,28H,3-12H2,1-2H3,(H,25,29)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	56	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541733 (CHEMBL4641147) Show SMILES CCCCCn1c2cn(CCO)nc2c(O)c(C(=O)NC23CC4CC(CC(O)(C4)C2)C3)c1=O |TLB:23:24:22.21.28:29,THB:23:22:30.24.25:29,25:24:21:28.26.29,25:26:30.24.23:21,27:26:30.24.23:21| Show InChI InChI=1S/C24H34N4O5/c1-2-3-4-5-28-17-13-27(6-7-29)26-19(17)20(30)18(22(28)32)21(31)25-23-9-15-8-16(10-23)12-24(33,11-15)14-23/h13,15-16,29-30,33H,2-12,14H2,1H3,(H,25,31)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	57	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541725 (CHEMBL4635230) Show SMILES CCCCN1C2C=NN(C)C2C(O)=C(C(=O)NC23CC4CC(CC(C4)C2)C3)C1=O |c:6,t:13,TLB:20:21:19.18.24:25,THB:20:19:26.21.22:25,22:21:18:24.23.25,22:23:26.21.20:18| Show InChI InChI=1S/C22H32N4O3/c1-3-4-5-26-16-12-23-25(2)18(16)19(27)17(21(26)29)20(28)24-22-9-13-6-14(10-22)8-15(7-13)11-22/h12-16,18,27H,3-11H2,1-2H3,(H,24,28)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	69	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Alanine--glyoxylate aminotransferase (Homo sapiens)	BDBM50146448 (CHEMBL3764351) Show SMILES Cl.COc1ccc(CON)cc1 Show InChI InChI=1S/C8H11NO2.ClH/c1-10-8-4-2-7(3-5-8)6-11-9;/h2-5H,6,9H2,1H3;1H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c00142 BindingDB Entry DOI: 10.7270/Q25T3QJF
					More data for this Ligand-Target Pair
Alanine--glyoxylate aminotransferase (Homo sapiens)	BDBM50146526 (CHEMBL3765396) Show SMILES Cl.NOCc1ccc(F)cc1 Show InChI InChI=1S/C7H8FNO.ClH/c8-7-3-1-6(2-4-7)5-10-9;/h1-4H,5,9H2;1H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	86	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c00142 BindingDB Entry DOI: 10.7270/Q25T3QJF
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541726 (CHEMBL4646331) Show SMILES CCCCN1C2C=NN(C)C2C(O)=C(C(=O)NC23CC4CC(CC(O)(C4)C2)C3)C1=O |c:6,t:13,TLB:20:21:19.18.25:26,THB:20:19:27.21.22:26,22:21:18:25.23.26,22:23:27.21.20:18,24:23:27.21.20:18| Show InChI InChI=1S/C22H32N4O4/c1-3-4-5-26-15-11-23-25(2)17(15)18(27)16(20(26)29)19(28)24-21-7-13-6-14(8-21)10-22(30,9-13)12-21/h11,13-15,17,27,30H,3-10,12H2,1-2H3,(H,24,28)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	87	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541732 (CHEMBL4636524) Show SMILES CCCCCn1c2cn(CCO)nc2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:23:24:22.21.27:28,THB:23:22:29.24.25:28,25:24:21:27.26.28,25:26:29.24.23:21| Show InChI InChI=1S/C24H34N4O4/c1-2-3-4-5-28-18-14-27(6-7-29)26-20(18)21(30)19(23(28)32)22(31)25-24-11-15-8-16(12-24)10-17(9-15)13-24/h14-17,29-30H,2-13H2,1H3,(H,25,31)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	108	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Alanine--glyoxylate aminotransferase (Homo sapiens)	BDBM50601022 (CHEMBL5181500) Show SMILES NOCc1cc2ccccc2s1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	110	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c00142 BindingDB Entry DOI: 10.7270/Q25T3QJF
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50200170 (5-(4-chloro-3-methyl-phenyl)-1-(4-methyl-benzyl)-1...) Show SMILES Cc1ccc(Cn2nc(cc2-c2ccc(Cl)c(C)c2)C(=O)N[C@H]2[C@@]3(C)CC[C@H](C3)C2(C)C)cc1 |r| Show InChI InChI=1S/C29H34ClN3O/c1-18-6-8-20(9-7-18)17-33-25(21-10-11-23(30)19(2)14-21)15-24(32-33)26(34)31-27-28(3,4)22-12-13-29(27,5)16-22/h6-11,14-15,22,27H,12-13,16-17H2,1-5H3,(H,31,34)/t22-,27-,29+/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	116	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541730 (CHEMBL4641784) Show SMILES CCCn1c2cn(CCO)nc2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:21:22:20.19.25:26,THB:21:20:27.22.23:26,23:22:19:25.24.26,23:24:27.22.21:19| Show InChI InChI=1S/C22H30N4O4/c1-2-3-26-16-12-25(4-5-27)24-18(16)19(28)17(21(26)30)20(29)23-22-9-13-6-14(10-22)8-15(7-13)11-22/h12-15,27-28H,2-11H2,1H3,(H,23,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	159	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541728 (CHEMBL4639191) Show SMILES CN1N=CC2C1C(O)=C(C(=O)NC13CC4CC(CC(O)(C4)C1)C3)C(=O)N2CCCCF |c:2,t:8,TLB:15:16:14.13.20:21,THB:15:14:22.16.17:21,17:16:13:20.18.21,17:18:22.16.15:13,19:18:22.16.15:13| Show InChI InChI=1S/C22H31FN4O4/c1-26-17-15(11-24-26)27(5-3-2-4-23)20(30)16(18(17)28)19(29)25-21-7-13-6-14(8-21)10-22(31,9-13)12-21/h11,13-15,17,28,31H,2-10,12H2,1H3,(H,25,29)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	161	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50541736 (CHEMBL4636552) Show SMILES CCCn1c2cn(CCOC(C)=O)nc2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:24:25:23.22.28:29,THB:24:23:30.25.26:29,26:25:22:28.27.29,26:27:30.25.24:22| Show InChI InChI=1S/C24H32N4O5/c1-3-4-28-18-13-27(5-6-33-14(2)29)26-20(18)21(30)19(23(28)32)22(31)25-24-10-15-7-16(11-24)9-17(8-15)12-24/h13,15-17,30H,3-12H2,1-2H3,(H,25,31)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	186	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541737 (CHEMBL4640659) Show SMILES CCCCn1c2cn(C)nc2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:20:21:19.18.24:25,THB:20:19:26.21.22:25,22:21:18:24.23.25,22:23:26.21.20:18| Show InChI InChI=1S/C22H30N4O3/c1-3-4-5-26-16-12-25(2)24-18(16)19(27)17(21(26)29)20(28)23-22-9-13-6-14(10-22)8-15(7-13)11-22/h12-15,27H,3-11H2,1-2H3,(H,23,28)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	231	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Alanine--glyoxylate aminotransferase (Homo sapiens)	BDBM50601016 (CHEMBL5204588) Show SMILES NOCc1cccc(c1)N1CCCC1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	240	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c00142 BindingDB Entry DOI: 10.7270/Q25T3QJF
					More data for this Ligand-Target Pair
Ephrin type-A receptor 2 (Homo sapiens (Human))	BDBM50551201 (CHEMBL4761556) Show SMILES [H][C@@]1(CC[C@@]2([H])[C@]3([H])CC[C@]4([H])C[C@@H](CC[C@]4(C)[C@@]3([H])CC[C@]12C)OC(=O)NCC)[C@H](C)CCC(=O)N[C@H](CC(O)=O)Cc1c[nH]c2ccccc12 |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem	Article PubMed	300	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Competitive inhibition of biotinylated ephrin-A1-Fc binding to EphA2 (unknown origin)				Citation and Details Article DOI: 10.1016/j.ejmech.2020.112083 BindingDB Entry DOI: 10.7270/Q2X35233
					More data for this Ligand-Target Pair
Ephrin type-A receptor 2 (Homo sapiens (Human))	BDBM50234957 (CHEMBL3735125) Show SMILES [H][C@@]1(CC[C@@]2([H])[C@]3([H])CC[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCC(=O)N[C@H](CC(O)=O)Cc1c[nH]c2ccccc12 |r| Show InChI InChI=1S/C36H52N2O4/c1-22(8-13-33(40)38-25(20-34(41)42)18-23-21-37-32-7-5-4-6-27(23)32)29-11-12-30-28-10-9-24-19-26(39)14-16-35(24,2)31(28)15-17-36(29,30)3/h4-7,21-22,24-26,28-31,37,39H,8-20H2,1-3H3,(H,38,40)(H,41,42)/t22-,24-,25+,26-,28+,29-,30+,31+,35+,36-/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	400	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Competitive inhibition of biotinylated ephrin-A1-Fc binding to EphA2 (unknown origin)				Citation and Details Article DOI: 10.1016/j.ejmech.2020.112083 BindingDB Entry DOI: 10.7270/Q2X35233
					More data for this Ligand-Target Pair
Alanine--glyoxylate aminotransferase (Homo sapiens)	BDBM50601013 (CHEMBL5179589) Show SMILES Cl.Cc1ccc(CON)cc1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	400	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c00142 BindingDB Entry DOI: 10.7270/Q25T3QJF
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541733 (CHEMBL4641147) Show SMILES CCCCCn1c2cn(CCO)nc2c(O)c(C(=O)NC23CC4CC(CC(O)(C4)C2)C3)c1=O |TLB:23:24:22.21.28:29,THB:23:22:30.24.25:29,25:24:21:28.26.29,25:26:30.24.23:21,27:26:30.24.23:21| Show InChI InChI=1S/C24H34N4O5/c1-2-3-4-5-28-17-13-27(6-7-29)26-19(17)20(30)18(22(28)32)21(31)25-23-9-15-8-16(10-23)12-24(33,11-15)14-23/h13,15-16,29-30,33H,2-12,14H2,1H3,(H,25,31)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	492	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541721 (CHEMBL4633927) Show SMILES Cn1cc2n(CCCCF)c(=O)c(C(=O)NC34CC5CC(CC(C5)C3)C4)c(O)c2n1 |TLB:19:20:18.17.23:24,THB:19:18:25.20.21:24,21:20:17:23.22.24,21:22:25.20.19:17| Show InChI InChI=1S/C22H29FN4O3/c1-26-12-16-18(25-26)19(28)17(21(30)27(16)5-3-2-4-23)20(29)24-22-9-13-6-14(10-22)8-15(7-13)11-22/h12-15,28H,2-11H2,1H3,(H,24,29)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	532	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Alanine--glyoxylate aminotransferase (Homo sapiens)	BDBM50146579 (Benzyl-O-Hydroxylamine | CHEMBL443652 | O-Benzylhy...) Show SMILES NOCc1ccccc1 Show InChI InChI=1S/C7H9NO/c8-9-6-7-4-2-1-3-5-7/h1-5H,6,8H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	Article PubMed	600	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c00142 BindingDB Entry DOI: 10.7270/Q25T3QJF
					More data for this Ligand-Target Pair
Alanine--glyoxylate aminotransferase (Homo sapiens)	BDBM50601019 (CHEMBL5199538) Show SMILES NOCc1cccc(c1)-c1ccc(cc1)C(F)(F)F Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	720	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c00142 BindingDB Entry DOI: 10.7270/Q25T3QJF
					More data for this Ligand-Target Pair
Ephrin type-A receptor 2 (Homo sapiens (Human))	BDBM50234948 (CHEMBL4078429) Show SMILES [H][C@@]1(CC[C@@]2([H])[C@]3([H])CC[C@]4([H])C[C@@H](CC[C@]4(C)[C@@]3([H])CC[C@]12C)OC(N)=O)[C@H](C)CCC(=O)N[C@H](CC(O)=O)Cc1c[nH]c2ccccc12 |r| Show InChI InChI=1S/C37H53N3O5/c1-22(8-13-33(41)40-25(20-34(42)43)18-23-21-39-32-7-5-4-6-27(23)32)29-11-12-30-28-10-9-24-19-26(45-35(38)44)14-16-36(24,2)31(28)15-17-37(29,30)3/h4-7,21-22,24-26,28-31,39H,8-20H2,1-3H3,(H2,38,44)(H,40,41)(H,42,43)/t22-,24-,25+,26-,28+,29-,30+,31+,36+,37-/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	800	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Competitive inhibition of biotinylated ephrin-A1-Fc binding to EphA2 (unknown origin)				Citation and Details Article DOI: 10.1016/j.ejmech.2020.112083 BindingDB Entry DOI: 10.7270/Q2X35233
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541730 (CHEMBL4641784) Show SMILES CCCn1c2cn(CCO)nc2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:21:22:20.19.25:26,THB:21:20:27.22.23:26,23:22:19:25.24.26,23:24:27.22.21:19| Show InChI InChI=1S/C22H30N4O4/c1-2-3-26-16-12-25(4-5-27)24-18(16)19(28)17(21(26)30)20(29)23-22-9-13-6-14(10-22)8-15(7-13)11-22/h12-15,27-28H,2-11H2,1H3,(H,23,29)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541722 (CHEMBL4641997) Show SMILES Cn1cc2n(CCCCF)c(=O)c(C(=O)NC34CC5CC(CC(O)(C5)C3)C4)c(O)c2n1 |TLB:19:20:18.17.24:25,THB:19:18:26.20.21:25,21:20:17:24.22.25,21:22:26.20.19:17,23:22:26.20.19:17| Show InChI InChI=1S/C22H29FN4O4/c1-26-11-15-17(25-26)18(28)16(20(30)27(15)5-3-2-4-23)19(29)24-21-7-13-6-14(8-21)10-22(31,9-13)12-21/h11,13-14,28,31H,2-10,12H2,1H3,(H,24,29)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541720 (CHEMBL4649714) Show SMILES CCCCn1c2cn(C)nc2c(O)c(C(=O)NC23CC4CC(CC(O)(C4)C2)C3)c1=O |TLB:20:21:19.18.25:26,THB:20:19:27.21.22:26,22:21:18:25.23.26,22:23:27.21.20:18,24:23:27.21.20:18| Show InChI InChI=1S/C22H30N4O4/c1-3-4-5-26-15-11-25(2)24-17(15)18(27)16(20(26)29)19(28)23-21-7-13-6-14(8-21)10-22(30,9-13)12-21/h11,13-14,27,30H,3-10,12H2,1-2H3,(H,23,28)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541731 (CHEMBL4643391) Show SMILES CCCCn1c2cn(CCO)nc2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:22:23:21.20.26:27,THB:22:21:28.23.24:27,24:23:20:26.25.27,24:25:28.23.22:20| Show InChI InChI=1S/C23H32N4O4/c1-2-3-4-27-17-13-26(5-6-28)25-19(17)20(29)18(22(27)31)21(30)24-23-10-14-7-15(11-23)9-16(8-14)12-23/h13-16,28-29H,2-12H2,1H3,(H,24,30)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541734 (CHEMBL4633168) Show SMILES CCCCn1c2cnn(CCO)c2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:22:23:21.20.26:27,THB:22:21:28.23.24:27,24:23:20:26.25.27,24:25:28.23.22:20| Show InChI InChI=1S/C23H32N4O4/c1-2-3-4-26-17-13-24-27(5-6-28)19(17)20(29)18(22(26)31)21(30)25-23-10-14-7-15(11-23)9-16(8-14)12-23/h13-16,28-29H,2-12H2,1H3,(H,25,30)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50541735 (CHEMBL4641494) Show SMILES Cn1cc2n(CCCCO)c(=O)c(C(=O)NC34CC5CC(CC(C5)C3)C4)c(O)c2n1 |TLB:19:20:18.17.23:24,THB:19:18:25.20.21:24,21:20:17:23.22.24,21:22:25.20.19:17| Show InChI InChI=1S/C22H30N4O4/c1-25-12-16-18(24-25)19(28)17(21(30)26(16)4-2-3-5-27)20(29)23-22-9-13-6-14(10-22)8-15(7-13)11-22/h12-15,27-28H,2-11H2,1H3,(H,23,29)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Siena Curated by ChEMBL					Assay Description Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes				J Med Chem 63: 7369-7391 (2020) Article DOI: 10.1021/acs.jmedchem.0c00595 BindingDB Entry DOI: 10.7270/Q2N01B3C
					More data for this Ligand-Target Pair

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