Compile Data Set for Download or QSAR

Found 73 hits with Last Name = 'zhang' and Initial = 'gc'   

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
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431782 (CHEMBL2347039) Show SMILES CC#CCn1c(nc2ccn(Cc3nc(C)c4ccccc4n3)c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C25H27N7O/c1-3-4-13-32-24(33)23-21(29-25(32)31-12-7-8-18(26)15-31)11-14-30(23)16-22-27-17(2)19-9-5-6-10-20(19)28-22/h5-6,9-11,14,18H,7-8,12-13,15-16,26H2,1-2H3/t18-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.60	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431785 (CHEMBL2347036) Show SMILES CC#CCn1c(nc2ccn(Cc3ccc4ccc(F)cc4n3)c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C25H25FN6O/c1-2-3-12-32-24(33)23-21(29-25(32)31-11-4-5-19(27)15-31)10-13-30(23)16-20-9-7-17-6-8-18(26)14-22(17)28-20/h6-10,13-14,19H,4-5,11-12,15-16,27H2,1H3/t19-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.70	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431784 (CHEMBL2347037) Show SMILES CC#CCn1c(nc2ccn(Cc3cnc4ccccc4n3)c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C24H25N7O/c1-2-3-12-31-23(32)22-21(28-24(31)30-11-6-7-17(25)15-30)10-13-29(22)16-18-14-26-19-8-4-5-9-20(19)27-18/h4-5,8-10,13-14,17H,6-7,11-12,15-16,25H2,1H3/t17-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL 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
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431791 (CHEMBL2346926) Show SMILES CC#CCn1c(nc2ccn(Cc3ccc4ccccc4n3)c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C25H26N6O/c1-2-3-14-31-24(32)23-22(28-25(31)30-13-6-8-19(26)16-30)12-15-29(23)17-20-11-10-18-7-4-5-9-21(18)27-20/h4-5,7,9-12,15,19H,6,8,13-14,16-17,26H2,1H3/t19-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.10	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431786 (CHEMBL2347035) Show SMILES CC#CCn1c(nc2ccn(Cc3ccc4ccc(Cl)cc4n3)c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C25H25ClN6O/c1-2-3-12-32-24(33)23-21(29-25(32)31-11-4-5-19(27)15-31)10-13-30(23)16-20-9-7-17-6-8-18(26)14-22(17)28-20/h6-10,13-14,19H,4-5,11-12,15-16,27H2,1H3/t19-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431788 (CHEMBL2346929) Show SMILES CC#CCn1c(nc2ccn(Cc3ccc4cc(F)ccc4n3)c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C25H25FN6O/c1-2-3-12-32-24(33)23-22(29-25(32)31-11-4-5-19(27)15-31)10-13-30(23)16-20-8-6-17-14-18(26)7-9-21(17)28-20/h6-10,13-14,19H,4-5,11-12,15-16,27H2,1H3/t19-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	15	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431783 (CHEMBL2347038) Show SMILES CC#CCn1c(nc2ccn(Cc3nc4ccccc4nc3C)c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C25H27N7O/c1-3-4-13-32-24(33)23-21(29-25(32)31-12-7-8-18(26)15-31)11-14-30(23)16-22-17(2)27-19-9-5-6-10-20(19)28-22/h5-6,9-11,14,18H,7-8,12-13,15-16,26H2,1-2H3/t18-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM256459 (US10329256, Example 3 | US9487512, 3 | US9944601, ...) Show SMILES C1[C@@H](NC2CCNCC2)[C@@H]1c1ccccc1 |r| Show InChI InChI=1S/C14H20N2/c1-2-4-11(5-3-1)13-10-14(13)16-12-6-8-15-9-7-12/h1-5,12-16H,6-10H2/t13-,14+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem	Article PubMed	n/a	n/a	24	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431793 (CHEMBL2346924) Show SMILES CC#CCn1c(nc2ccn(Cc3nc4ccccc4[nH]3)c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C23H25N7O/c1-2-3-12-30-22(31)21-19(27-23(30)29-11-6-7-16(24)14-29)10-13-28(21)15-20-25-17-8-4-5-9-18(17)26-20/h4-5,8-10,13,16H,6-7,11-12,14-15,24H2,1H3,(H,25,26)/t16-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	28	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431795 (CHEMBL2346922) Show SMILES CC#CCn1c(nc2ccn(Cc3ncccn3)c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C20H23N7O/c1-2-3-11-27-19(28)18-16(24-20(27)26-10-4-6-15(21)13-26)7-12-25(18)14-17-22-8-5-9-23-17/h5,7-9,12,15H,4,6,10-11,13-14,21H2,1H3/t15-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	44	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50381853 (CHEMBL2023067) Show SMILES N[C@@H]1CCCN(C1)c1nc2c(Br)c[nH]c2c(=O)n1Cc1ccccc1C#N |r| Show InChI InChI=1S/C19H19BrN6O/c20-15-9-23-17-16(15)24-19(25-7-3-6-14(22)11-25)26(18(17)27)10-13-5-2-1-4-12(13)8-21/h1-2,4-5,9,14,23H,3,6-7,10-11,22H2/t14-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	44	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431794 (CHEMBL2346923) Show SMILES CC#CCn1c(nc2ccn(Cc3c[nH]c4ccccc34)c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C24H26N6O/c1-2-3-12-30-23(31)22-21(27-24(30)29-11-6-7-18(25)16-29)10-13-28(22)15-17-14-26-20-9-5-4-8-19(17)20/h4-5,8-10,13-14,18,26H,6-7,11-12,15-16,25H2,1H3/t18-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	44	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431792 (CHEMBL2346925) Show SMILES CC#CCn1c(nc2ccn(Cc3ccnc4ccccc34)c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C25H26N6O/c1-2-3-14-31-24(32)23-22(28-25(31)30-13-6-7-19(26)17-30)11-15-29(23)16-18-10-12-27-21-9-5-4-8-20(18)21/h4-5,8-12,15,19H,6-7,13-14,16-17,26H2,1H3/t19-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	48	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431787 (CHEMBL2346930) Show SMILES CC#CCn1c(nc2ccn(Cc3ccc4cc(C)ccc4n3)c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C26H28N6O/c1-3-4-13-32-25(33)24-23(29-26(32)31-12-5-6-20(27)16-31)11-14-30(24)17-21-9-8-19-15-18(2)7-10-22(19)28-21/h7-11,14-15,20H,5-6,12-13,16-17,27H2,1-2H3/t20-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	53	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431789 (CHEMBL2346928) Show SMILES CC#CCn1c(nc2ccn(Cc3ccc4cc(Cl)ccc4n3)c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C25H25ClN6O/c1-2-3-12-32-24(33)23-22(29-25(32)31-11-4-5-19(27)15-31)10-13-30(23)16-20-8-6-17-14-18(26)7-9-21(17)28-20/h6-10,13-14,19H,4-5,11-12,15-16,27H2,1H3/t19-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431790 (CHEMBL2346927) Show SMILES CC#CCn1c(nc2ccn(Cc3ccc4cc(Br)ccc4n3)c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C25H25BrN6O/c1-2-3-12-32-24(33)23-22(29-25(32)31-11-4-5-19(27)15-31)10-13-30(23)16-20-8-6-17-14-18(26)7-9-21(17)28-20/h6-10,13-14,19H,4-5,11-12,15-16,27H2,1H3/t19-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	139	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431781 (CHEMBL2346919) Show SMILES CC#CCn1c(nc2ccn(C)c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C16H21N5O/c1-3-4-9-21-15(22)14-13(7-10-19(14)2)18-16(21)20-8-5-6-12(17)11-20/h7,10,12H,5-6,8-9,11,17H2,1-2H3/t12-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	212	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431796 (CHEMBL2346921) Show SMILES CC#CCn1c(nc2cc[nH]c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C15H19N5O/c1-2-3-9-20-14(21)13-12(6-7-17-13)18-15(20)19-8-4-5-11(16)10-19/h6-7,11,17H,4-5,8-10,16H2,1H3/t11-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	460	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50431797 (CHEMBL2346920) Show SMILES CC#CCn1c(nc2c(Br)c[nH]c2c1=O)N1CCC[C@@H](N)C1 |r| Show InChI InChI=1S/C15H18BrN5O/c1-2-3-7-21-14(22)13-12(11(16)8-18-13)19-15(21)20-6-4-5-10(17)9-20/h8,10,18H,4-7,9,17H2,1H3/t10-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	860	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Science Curated by ChEMBL					Assay Description Inhibition of human DPP4 using Gly-Pro-AMC as substrate treated with enzyme 10 mins prior to substrate addition measured after 10 mins				Bioorg Med Chem 21: 1749-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.062 BindingDB Entry DOI: 10.7270/Q2R78GMR
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524592 (CHEMBL4550944) Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccc(F)cc2)c2ccc(Cl)cc12 Show InChI InChI=1S/C21H17ClFNO3/c1-12-18(11-27-21(12)26)20(25)17-10-24(9-13-2-5-15(23)6-3-13)19-7-4-14(22)8-16(17)19/h2-8,10,18,20,25H,1,9,11H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.23E+3	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524624 (CHEMBL4470161) Show SMILES Cc1ccc(cc1)S(=O)(=O)n1cc(C(O)C2COC(=O)C2=C)c2cc(Cl)ccc12 Show InChI InChI=1S/C21H18ClNO5S/c1-12-3-6-15(7-4-12)29(26,27)23-10-17(16-9-14(22)5-8-19(16)23)20(24)18-11-28-21(25)13(18)2/h3-10,18,20,24H,2,11H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.78E+3	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524625 (CHEMBL4545973) Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccc(F)cc2)c2ccccc12 Show InChI InChI=1S/C21H18FNO3/c1-13-18(12-26-21(13)25)20(24)17-11-23(19-5-3-2-4-16(17)19)10-14-6-8-15(22)9-7-14/h2-9,11,18,20,24H,1,10,12H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.47E+3	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524596 (CHEMBL4545461) Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccccc2F)c2ccccc12 Show InChI InChI=1S/C21H18FNO3/c1-13-17(12-26-21(13)25)20(24)16-11-23(19-9-5-3-7-15(16)19)10-14-6-2-4-8-18(14)22/h2-9,11,17,20,24H,1,10,12H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.85E+3	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524640 (CHEMBL4456313) Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccc(Cl)nc2)c2ccccc12 Show InChI InChI=1S/C20H17ClN2O3/c1-12-16(11-26-20(12)25)19(24)15-10-23(17-5-3-2-4-14(15)17)9-13-6-7-18(21)22-8-13/h2-8,10,16,19,24H,1,9,11H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524598 (CHEMBL4591471) Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccc(Cl)c(Cl)c2)c2ccccc12 Show InChI InChI=1S/C21H17Cl2NO3/c1-12-16(11-27-21(12)26)20(25)15-10-24(19-5-3-2-4-14(15)19)9-13-6-7-17(22)18(23)8-13/h2-8,10,16,20,25H,1,9,11H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.58E+3	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524602 (CHEMBL4592421) Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccc(Cl)nc2)c2ccc(Cl)cc12 Show InChI InChI=1S/C20H16Cl2N2O3/c1-11-16(10-27-20(11)26)19(25)15-9-24(8-12-2-5-18(22)23-7-12)17-4-3-13(21)6-14(15)17/h2-7,9,16,19,25H,1,8,10H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.34E+3	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524603 (CHEMBL4439541) Show SMILES COCCCOc1ccnc(Cn2cc(C(O)C3COC(=O)C3=C)c3cc(Cl)ccc23)c1C Show InChI InChI=1S/C25H27ClN2O5/c1-15-20(14-33-25(15)30)24(29)19-12-28(22-6-5-17(26)11-18(19)22)13-21-16(2)23(7-8-27-21)32-10-4-9-31-3/h5-8,11-12,20,24,29H,1,4,9-10,13-14H2,2-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.41E+3	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524629 (CHEMBL4527359) Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccccc2C(F)(F)F)c2ccccc12 Show InChI InChI=1S/C22H18F3NO3/c1-13-17(12-29-21(13)28)20(27)16-11-26(19-9-5-3-7-15(16)19)10-14-6-2-4-8-18(14)22(23,24)25/h2-9,11,17,20,27H,1,10,12H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.96E+3	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524597 (CHEMBL4445502) Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccc(Cl)cc2)c2ccccc12 Show InChI InChI=1S/C21H18ClNO3/c1-13-18(12-26-21(13)25)20(24)17-11-23(19-5-3-2-4-16(17)19)10-14-6-8-15(22)9-7-14/h2-9,11,18,20,24H,1,10,12H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	9.47E+3	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524590 (CHEMBL4447670) Show SMILES OC(C1COC(=O)C1=C)c1cn(CC2CC2)c2ccc(Cl)cc12 Show InChI InChI=1S/C18H18ClNO3/c1-10-15(9-23-18(10)22)17(21)14-8-20(7-11-2-3-11)16-5-4-12(19)6-13(14)16/h4-6,8,11,15,17,21H,1-3,7,9H2	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524591 (CHEMBL4592269) Show SMILES COc1ccc2c(cn(Cc3ccc(Cl)cc3)c2c1)C(O)C1COC(=O)C1=C Show InChI InChI=1S/C22H20ClNO4/c1-13-19(12-28-22(13)26)21(25)18-11-24(10-14-3-5-15(23)6-4-14)20-9-16(27-2)7-8-17(18)20/h3-9,11,19,21,25H,1,10,12H2,2H3	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524593 (CHEMBL4543148) Show SMILES O\N=C(\c1cn(Cc2ccc(F)cc2)c2ccc(Cl)cc12)c1ccccc1 Show InChI InChI=1S/C22H16ClFN2O/c23-17-8-11-21-19(12-17)20(22(25-27)16-4-2-1-3-5-16)14-26(21)13-15-6-9-18(24)10-7-15/h1-12,14,27H,13H2/b25-22+	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524594 (CHEMBL4476237) Show SMILES Fc1ccc(Cn2cc(C(=O)c3ccco3)c3cc(Cl)ccc23)cc1 Show InChI InChI=1S/C20H13ClFNO2/c21-14-5-8-18-16(10-14)17(20(24)19-2-1-9-25-19)12-23(18)11-13-3-6-15(22)7-4-13/h1-10,12H,11H2	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524599 (CHEMBL4456857) Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2cnc(Cl)s2)c2ccc(Cl)cc12 Show InChI InChI=1S/C18H14Cl2N2O3S/c1-9-14(8-25-17(9)24)16(23)13-7-22(6-11-5-21-18(20)26-11)15-3-2-10(19)4-12(13)15/h2-5,7,14,16,23H,1,6,8H2	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524600 (CHEMBL4589600) Show SMILES Nc1nc(Cn2cc(C(O)C3COC(=O)C3=C)c3cc(Cl)ccc23)cs1 Show InChI InChI=1S/C18H16ClN3O3S/c1-9-14(7-25-17(9)24)16(23)13-6-22(5-11-8-26-18(20)21-11)15-3-2-10(19)4-12(13)15/h2-4,6,8,14,16,23H,1,5,7H2,(H2,20,21)	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524601 (CHEMBL4583255) Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccncc2)c2ccc(Cl)cc12 Show InChI InChI=1S/C20H17ClN2O3/c1-12-17(11-26-20(12)25)19(24)16-10-23(9-13-4-6-22-7-5-13)18-3-2-14(21)8-15(16)18/h2-8,10,17,19,24H,1,9,11H2	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524604 (CHEMBL4461712) Show SMILES Cc1nc(Cn2cc(C(O)C3COC(=O)C3=C)c3cc(Cl)ccc23)nc2ccccc12 Show InChI InChI=1S/C24H20ClN3O3/c1-13-19(12-31-24(13)30)23(29)18-10-28(21-8-7-15(25)9-17(18)21)11-22-26-14(2)16-5-3-4-6-20(16)27-22/h3-10,19,23,29H,1,11-12H2,2H3	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524605 (CHEMBL4586915) Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2nc3ccccc3o2)c2ccc(Cl)cc12 Show InChI InChI=1S/C22H17ClN2O4/c1-12-16(11-28-22(12)27)21(26)15-9-25(18-7-6-13(23)8-14(15)18)10-20-24-17-4-2-3-5-19(17)29-20/h2-9,16,21,26H,1,10-11H2	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524606 (CHEMBL4574897) Show SMILES Cc1ccsc1C(=O)n1cc(C(O)C2COC(=O)C2=C)c2cc(Cl)ccc12 Show InChI InChI=1S/C20H16ClNO4S/c1-10-5-6-27-18(10)19(24)22-8-14(13-7-12(21)3-4-16(13)22)17(23)15-9-26-20(25)11(15)2/h3-8,15,17,23H,2,9H2,1H3	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524607 (CHEMBL4559325) Show SMILES OC(C1COC(=O)C1=C)c1cn(C(=O)c2ccco2)c2ccc(Cl)cc12 Show InChI InChI=1S/C19H14ClNO5/c1-10-14(9-26-19(10)24)17(22)13-8-21(18(23)16-3-2-6-25-16)15-5-4-11(20)7-12(13)15/h2-8,14,17,22H,1,9H2	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524608 (CHEMBL4553752) Show SMILES Cc1noc(C)c1C(=O)n1cc(C(O)C2COC(=O)C2=C)c2cc(Cl)ccc12 Show InChI InChI=1S/C20H17ClN2O5/c1-9-15(8-27-20(9)26)18(24)14-7-23(16-5-4-12(21)6-13(14)16)19(25)17-10(2)22-28-11(17)3/h4-7,15,18,24H,1,8H2,2-3H3	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524609 (CHEMBL4443586) Show SMILES OC(C1COC(=O)C1=C)c1cn(C(=O)C2CC2)c2ccc(Cl)cc12 Show InChI InChI=1S/C18H16ClNO4/c1-9-14(8-24-18(9)23)16(21)13-7-20(17(22)10-2-3-10)15-5-4-11(19)6-12(13)15/h4-7,10,14,16,21H,1-3,8H2	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524610 (CHEMBL4459346) Show SMILES COc1cccc2n(Cc3ccc(Cl)cc3)cc(C(O)C3COC(=O)C3=C)c12 Show InChI InChI=1S/C22H20ClNO4/c1-13-17(12-28-22(13)26)21(25)16-11-24(10-14-6-8-15(23)9-7-14)18-4-3-5-19(27-2)20(16)18/h3-9,11,17,21,25H,1,10,12H2,2H3	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524611 (CHEMBL4462953) Show SMILES COc1cccc2c(cn(Cc3ccc(Cl)cc3)c12)C(O)C1COC(=O)C1=C Show InChI InChI=1S/C22H20ClNO4/c1-13-18(12-28-22(13)26)21(25)17-11-24(10-14-6-8-15(23)9-7-14)20-16(17)4-3-5-19(20)27-2/h3-9,11,18,21,25H,1,10,12H2,2H3	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524612 (CHEMBL4549040) Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccc(Cl)cc2)c2cccc(Cl)c12 Show InChI InChI=1S/C21H17Cl2NO3/c1-12-16(11-27-21(12)26)20(25)15-10-24(9-13-5-7-14(22)8-6-13)18-4-2-3-17(23)19(15)18/h2-8,10,16,20,25H,1,9,11H2	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524613 (CHEMBL4517041) Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccc(Cl)cc2)c2ccc(Cl)cc12 Show InChI InChI=1S/C21H17Cl2NO3/c1-12-18(11-27-21(12)26)20(25)17-10-24(9-13-2-4-14(22)5-3-13)19-7-6-15(23)8-16(17)19/h2-8,10,18,20,25H,1,9,11H2	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524614 (CHEMBL4468238) Show SMILES OC(C1COC(=O)C1=C)c1cn(Cc2ccc(Cl)cc2)c2ccc(F)cc12 Show InChI InChI=1S/C21H17ClFNO3/c1-12-18(11-27-21(12)26)20(25)17-10-24(9-13-2-4-14(22)5-3-13)19-7-6-15(23)8-16(17)19/h2-8,10,18,20,25H,1,9,11H2	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524615 (CHEMBL4446079) Show SMILES CC(=O)c1cn(Cc2ccc(F)cc2)c2ccc(Cl)cc12 Show InChI InChI=1S/C17H13ClFNO/c1-11(21)16-10-20(9-12-2-5-14(19)6-3-12)17-7-4-13(18)8-15(16)17/h2-8,10H,9H2,1H3	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524616 (CHEMBL4557004) Show SMILES Fc1ccc(Cn2cc(C(=O)c3ccccc3)c3cc(Cl)ccc23)cc1 Show InChI InChI=1S/C22H15ClFNO/c23-17-8-11-21-19(12-17)20(22(26)16-4-2-1-3-5-16)14-25(21)13-15-6-9-18(24)10-7-15/h1-12,14H,13H2	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50524617 (CHEMBL4451864) Show SMILES Fc1ccc(Cn2cc(C(=O)c3ccc(F)cc3)c3cc(Cl)ccc23)cc1 Show InChI InChI=1S/C22H14ClF2NO/c23-16-5-10-21-19(11-16)20(22(27)15-3-8-18(25)9-4-15)13-26(21)12-14-1-6-17(24)7-2-14/h1-11,13H,12H2	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+4	n/a	n/a	n/a	n/a	n/a	n/a
Zhengzhou University Curated by ChEMBL					Assay Description Inhibition of recombinant LSD1 (unknown origin) (catalytic domain 157 to 852 residues) expressed in Escherichia coli BL21 using H3K4me1 as substrate ...				Eur J Med Chem 175: 357-372 (2019) Article DOI: 10.1016/j.ejmech.2019.04.065 BindingDB Entry DOI: 10.7270/Q2X351W0
					More data for this Ligand-Target Pair

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