Compile Data Set for Download or QSAR

Found 256 hits with Last Name = 'bian' and Initial = 'x'   

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
Lysosomal alpha-glucosidase (Rattus norvegicus)	BDBM50438500 (CHEMBL2414822) Show SMILES CC(=O)Oc1ccc(\C=C\C(=O)NC[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1OC(C)=O |r| Show InChI InChI=1S/C20H25NO10/c1-10(23)29-13-5-3-12(7-14(13)30-11(2)24)4-6-17(25)21-8-15-18(26)20(28)19(27)16(9-22)31-15/h3-7,15-16,18-20,22,26-28H,8-9H2,1-2H3,(H,21,25)/b6-4+/t15-,16+,18-,19+,20+/m0/s1	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Competitive inhibition of rat intestinal maltase using maltose as substrate by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Sucrase-isomaltase, intestinal (Rattus norvegicus (Rat))	BDBM50438500 (CHEMBL2414822) Show SMILES CC(=O)Oc1ccc(\C=C\C(=O)NC[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1OC(C)=O |r| Show InChI InChI=1S/C20H25NO10/c1-10(23)29-13-5-3-12(7-14(13)30-11(2)24)4-6-17(25)21-8-15-18(26)20(28)19(27)16(9-22)31-15/h3-7,15-16,18-20,22,26-28H,8-9H2,1-2H3,(H,21,25)/b6-4+/t15-,16+,18-,19+,20+/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.71E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Competitive inhibition of rat intestinal sucrase using sucrose as substrate by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50506694 (CHEMBL4524414) Show SMILES [O-][N+](=O)OCCCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C22H24F6N6O5/c23-15-11-17(25)16(24)9-13(15)8-14(29-19(35)4-2-1-3-7-39-34(37)38)10-20(36)32-5-6-33-18(12-32)30-31-21(33)22(26,27)28/h9,11,14H,1-8,10,12H2,(H,29,35)/t14-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human DPP-4 using Ala-Pro-AMC as substrate preincubated for 10 mins followed by substrate addition and measured after 5 to 10 mins by f...				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM11162 ((1R)-3-oxo-3-[3-(trifluoroethyl)-5,6-dihydro[1,2,4...) Show SMILES N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C16H15F6N5O/c17-10-6-12(19)11(18)4-8(10)3-9(23)5-14(28)26-1-2-27-13(7-26)24-25-15(27)16(20,21)22/h4,6,9H,1-3,5,7,23H2/t9-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid PDB UniChem Similars	DrugBank PDB Article PubMed	n/a	n/a	120	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human DPP-4 using Ala-Pro-AMC as substrate preincubated for 10 mins followed by substrate addition and measured after 5 to 10 mins by f...				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair				3D Structure (crystal)
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50506698 (CHEMBL4577865) Show SMILES [O-][N+](=O)OCCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C21H22F6N6O5/c22-14-10-16(24)15(23)8-12(14)7-13(28-18(34)3-1-2-6-38-33(36)37)9-19(35)31-4-5-32-17(11-31)29-30-20(32)21(25,26)27/h8,10,13H,1-7,9,11H2,(H,28,34)/t13-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	170	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human DPP-4 using Ala-Pro-AMC as substrate preincubated for 10 mins followed by substrate addition and measured after 5 to 10 mins by f...				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50506696 (CHEMBL4434648) Show SMILES [O-][N+](=O)OCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C18H16F6N6O5/c19-11-6-13(21)12(20)4-9(11)3-10(25-15(31)8-35-30(33)34)5-16(32)28-1-2-29-14(7-28)26-27-17(29)18(22,23)24/h4,6,10H,1-3,5,7-8H2,(H,25,31)/t10-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	190	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human DPP-4 using Ala-Pro-AMC as substrate preincubated for 10 mins followed by substrate addition and measured after 5 to 10 mins by f...				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50506695 (CHEMBL4437841) Show SMILES [O-][N+](=O)OCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C20H20F6N6O5/c21-13-9-15(23)14(22)7-11(13)6-12(27-17(33)2-1-5-37-32(35)36)8-18(34)30-3-4-31-16(10-30)28-29-19(31)20(24,25)26/h7,9,12H,1-6,8,10H2,(H,27,33)/t12-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	197	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human DPP-4 using Ala-Pro-AMC as substrate preincubated for 10 mins followed by substrate addition and measured after 5 to 10 mins by f...				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50506697 (CHEMBL4458307) Show SMILES OCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C20H21F6N5O3/c21-13-9-15(23)14(22)7-11(13)6-12(27-17(33)2-1-5-32)8-18(34)30-3-4-31-16(10-30)28-29-19(31)20(24,25)26/h7,9,12,32H,1-6,8,10H2,(H,27,33)/t12-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	208	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human DPP-4 using Ala-Pro-AMC as substrate preincubated for 10 mins followed by substrate addition and measured after 5 to 10 mins by f...				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50506693 (CHEMBL4537702) Show SMILES OCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C18H17F6N5O3/c19-11-6-13(21)12(20)4-9(11)3-10(25-15(31)8-30)5-16(32)28-1-2-29-14(7-28)26-27-17(29)18(22,23)24/h4,6,10,30H,1-3,5,7-8H2,(H,25,31)/t10-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	217	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human DPP-4 using Ala-Pro-AMC as substrate preincubated for 10 mins followed by substrate addition and measured after 5 to 10 mins by f...				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50506699 (CHEMBL4516388) Show SMILES OCCCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C22H25F6N5O3/c23-15-11-17(25)16(24)9-13(15)8-14(29-19(35)4-2-1-3-7-34)10-20(36)32-5-6-33-18(12-32)30-31-21(33)22(26,27)28/h9,11,14,34H,1-8,10,12H2,(H,29,35)/t14-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	223	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human DPP-4 using Ala-Pro-AMC as substrate preincubated for 10 mins followed by substrate addition and measured after 5 to 10 mins by f...				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50506692 (CHEMBL4464592) Show SMILES OCCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C21H23F6N5O3/c22-14-10-16(24)15(23)8-12(14)7-13(28-18(34)3-1-2-6-33)9-19(35)31-4-5-32-17(11-31)29-30-20(32)21(25,26)27/h8,10,13,33H,1-7,9,11H2,(H,28,34)/t13-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	226	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human DPP-4 using Ala-Pro-AMC as substrate preincubated for 10 mins followed by substrate addition and measured after 5 to 10 mins by f...				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Sucrase-isomaltase, intestinal (Rattus norvegicus (Rat))	BDBM50333465 ((2R,3R,4R,5R,6R)-5-((2R,3R,4R,5S,6R)-5-((2R,3R,4S,...) Show SMILES C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O |r,t:37| Show InChI InChI=1S/C25H43NO18/c1-6-11(26-8-2-7(3-27)12(30)15(33)13(8)31)14(32)19(37)24(40-6)43-22-10(5-29)42-25(20(38)17(22)35)44-21-9(4-28)41-23(39)18(36)16(21)34/h2,6,8-39H,3-5H2,1H3/t6-,8+,9-,10-,11-,12-,13+,14+,15+,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal sucrase using sucrose as substrate assessed as D-glucose release from substrate preincubated for 15 mins measured after ...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Oligo-1,6-glucosidase IMA1 (Saccharomyces cerevisiae S288c (Baker's yeast))	BDBM50438504 (CHEMBL2414818) Show SMILES OC[C@H]1O[C@@H](CNC(=O)\C=C\c2ccccc2)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C16H21NO6/c18-9-12-15(21)16(22)14(20)11(23-12)8-17-13(19)7-6-10-4-2-1-3-5-10/h1-7,11-12,14-16,18,20-22H,8-9H2,(H,17,19)/b7-6+/t11-,12+,14-,15+,16+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of Saccharomyces cerevisiae alpha-glucosidase assessed as 4-nitrophenol release from 4-nitrophenyl alpha-D-glucopyranoside preincubated fo...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Rattus norvegicus)	BDBM50333465 ((2R,3R,4R,5R,6R)-5-((2R,3R,4R,5S,6R)-5-((2R,3R,4S,...) Show SMILES C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O |r,t:37| Show InChI InChI=1S/C25H43NO18/c1-6-11(26-8-2-7(3-27)12(30)15(33)13(8)31)14(32)19(37)24(40-6)43-22-10(5-29)42-25(20(38)17(22)35)44-21-9(4-28)41-23(39)18(36)16(21)34/h2,6,8-39H,3-5H2,1H3/t6-,8+,9-,10-,11-,12-,13+,14+,15+,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-/m1/s1	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	3.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal maltase using maltose as substrate assessed as D-glucose release from substrate preincubated for 15 mins measured after ...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Rattus norvegicus)	BDBM50438500 (CHEMBL2414822) Show SMILES CC(=O)Oc1ccc(\C=C\C(=O)NC[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1OC(C)=O |r| Show InChI InChI=1S/C20H25NO10/c1-10(23)29-13-5-3-12(7-14(13)30-11(2)24)4-6-17(25)21-8-15-18(26)20(28)19(27)16(9-22)31-15/h3-7,15-16,18-20,22,26-28H,8-9H2,1-2H3,(H,21,25)/b6-4+/t15-,16+,18-,19+,20+/m0/s1	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal maltase using maltose as substrate assessed as D-glucose release from substrate preincubated for 15 mins measured after ...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Oligo-1,6-glucosidase IMA1 (Saccharomyces cerevisiae S288c (Baker's yeast))	BDBM50438503 (CHEMBL2414819) Show SMILES OC[C@H]1O[C@@H](CNC(=O)\C=C\c2ccc(O)cc2)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C16H21NO7/c18-8-12-15(22)16(23)14(21)11(24-12)7-17-13(20)6-3-9-1-4-10(19)5-2-9/h1-6,11-12,14-16,18-19,21-23H,7-8H2,(H,17,20)/b6-3+/t11-,12+,14-,15+,16+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of Saccharomyces cerevisiae alpha-glucosidase assessed as 4-nitrophenol release from 4-nitrophenyl alpha-D-glucopyranoside preincubated fo...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Rattus norvegicus)	BDBM50438505 (CHEMBL2414817) Show SMILES CC(=O)Oc1cc(cc(OC(C)=O)c1OC(C)=O)C(=O)NC[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C20H25NO12/c1-8(23)30-12-4-11(5-13(31-9(2)24)19(12)32-10(3)25)20(29)21-6-14-16(26)18(28)17(27)15(7-22)33-14/h4-5,14-18,22,26-28H,6-7H2,1-3H3,(H,21,29)/t14-,15+,16-,17+,18+/m0/s1	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal maltase using maltose as substrate assessed as D-glucose release from substrate preincubated for 15 mins measured after ...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Sucrase-isomaltase, intestinal (Rattus norvegicus (Rat))	BDBM50438500 (CHEMBL2414822) Show SMILES CC(=O)Oc1ccc(\C=C\C(=O)NC[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1OC(C)=O |r| Show InChI InChI=1S/C20H25NO10/c1-10(23)29-13-5-3-12(7-14(13)30-11(2)24)4-6-17(25)21-8-15-18(26)20(28)19(27)16(9-22)31-15/h3-7,15-16,18-20,22,26-28H,8-9H2,1-2H3,(H,21,25)/b6-4+/t15-,16+,18-,19+,20+/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.04E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal sucrase using sucrose as substrate assessed as D-glucose release from substrate preincubated for 15 mins measured after ...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Sucrase-isomaltase, intestinal (Rattus norvegicus (Rat))	BDBM50438505 (CHEMBL2414817) Show SMILES CC(=O)Oc1cc(cc(OC(C)=O)c1OC(C)=O)C(=O)NC[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C20H25NO12/c1-8(23)30-12-4-11(5-13(31-9(2)24)19(12)32-10(3)25)20(29)21-6-14-16(26)18(28)17(27)15(7-22)33-14/h4-5,14-18,22,26-28H,6-7H2,1-3H3,(H,21,29)/t14-,15+,16-,17+,18+/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.56E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal sucrase using sucrose as substrate assessed as D-glucose release from substrate preincubated for 15 mins measured after ...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Rattus norvegicus)	BDBM50333465 ((2R,3R,4R,5R,6R)-5-((2R,3R,4R,5S,6R)-5-((2R,3R,4S,...) Show SMILES C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O |r,t:37| Show InChI InChI=1S/C25H43NO18/c1-6-11(26-8-2-7(3-27)12(30)15(33)13(8)31)14(32)19(37)24(40-6)43-22-10(5-29)42-25(20(38)17(22)35)44-21-9(4-28)41-23(39)18(36)16(21)34/h2,6,8-39H,3-5H2,1H3/t6-,8+,9-,10-,11-,12-,13+,14+,15+,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-/m1/s1	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	2.55E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal maltase using maltose as substrate by colorimetric analysis				Bioorg Med Chem Lett 23: 2022-6 (2013) Article DOI: 10.1016/j.bmcl.2013.02.011 BindingDB Entry DOI: 10.7270/Q2CV4K3J
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Rattus norvegicus)	BDBM50432216 (CHEMBL2347149) Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1ccc2C(=O)N(CCNc3ccc(O)c(O)c3)C(=O)c2c1 Show InChI InChI=1S/C23H21N3O6S/c1-14-2-6-17(7-3-14)33(31,32)25-16-4-8-18-19(12-16)23(30)26(22(18)29)11-10-24-15-5-9-20(27)21(28)13-15/h2-9,12-13,24-25,27-28H,10-11H2,1H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.88E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal maltase using maltose as substrate by colorimetric analysis				Bioorg Med Chem Lett 23: 2022-6 (2013) Article DOI: 10.1016/j.bmcl.2013.02.011 BindingDB Entry DOI: 10.7270/Q2CV4K3J
					More data for this Ligand-Target Pair
Oligo-1,6-glucosidase IMA1 (Saccharomyces cerevisiae S288c (Baker's yeast))	BDBM50438514 (CHEMBL2414746) Show SMILES OC[C@H]1O[C@@H](CNC(=O)c2ccc(cc2)[N+]([O-])=O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C14H18N2O8/c17-6-10-12(19)13(20)11(18)9(24-10)5-15-14(21)7-1-3-8(4-2-7)16(22)23/h1-4,9-13,17-20H,5-6H2,(H,15,21)/t9-,10+,11-,12+,13+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.62E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of Saccharomyces cerevisiae alpha-glucosidase assessed as 4-nitrophenol release from 4-nitrophenyl alpha-D-glucopyranoside preincubated fo...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Oligo-1,6-glucosidase IMA1 (Saccharomyces cerevisiae S288c (Baker's yeast))	BDBM50438498 (CHEMBL2414823) Show SMILES OC[C@H]1O[C@@H](CNCc2ccccc2)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C14H21NO5/c16-8-11-13(18)14(19)12(17)10(20-11)7-15-6-9-4-2-1-3-5-9/h1-5,10-19H,6-8H2/t10-,11+,12-,13+,14+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.92E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of Saccharomyces cerevisiae alpha-glucosidase assessed as 4-nitrophenol release from 4-nitrophenyl alpha-D-glucopyranoside preincubated fo...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Oligo-1,6-glucosidase IMA1 (Saccharomyces cerevisiae S288c (Baker's yeast))	BDBM50438494 (CHEMBL2414827) Show SMILES OC[C@H]1O[C@@H](CNCc2cccc(c2)[N+]([O-])=O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C14H20N2O7/c17-7-11-13(19)14(20)12(18)10(23-11)6-15-5-8-2-1-3-9(4-8)16(21)22/h1-4,10-15,17-20H,5-7H2/t10-,11+,12-,13+,14+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.43E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of Saccharomyces cerevisiae alpha-glucosidase assessed as 4-nitrophenol release from 4-nitrophenyl alpha-D-glucopyranoside preincubated fo...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Lactase/phlorizin hydrolase (Rattus norvegicus)	BDBM50432219 (CHEMBL2347146) Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1ccc2C(=O)N(Cc3ccc(C(O)=O)c(O)c3)C(=O)c2c1 Show InChI InChI=1S/C23H18N2O7S/c1-13-2-6-16(7-3-13)33(31,32)24-15-5-9-17-19(11-15)22(28)25(21(17)27)12-14-4-8-18(23(29)30)20(26)10-14/h2-11,24,26H,12H2,1H3,(H,29,30)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.47E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal lactase using lactose as substrate by colorimetric analysis				Bioorg Med Chem Lett 23: 2022-6 (2013) Article DOI: 10.1016/j.bmcl.2013.02.011 BindingDB Entry DOI: 10.7270/Q2CV4K3J
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Rattus norvegicus)	BDBM50432214 (CHEMBL2347151) Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1ccc2C(=O)N(CCOc3ccc(O)cc3)C(=O)c2c1 Show InChI InChI=1S/C23H20N2O6S/c1-15-2-9-19(10-3-15)32(29,30)24-16-4-11-20-21(14-16)23(28)25(22(20)27)12-13-31-18-7-5-17(26)6-8-18/h2-11,14,24,26H,12-13H2,1H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.77E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal maltase using maltose as substrate by colorimetric analysis				Bioorg Med Chem Lett 23: 2022-6 (2013) Article DOI: 10.1016/j.bmcl.2013.02.011 BindingDB Entry DOI: 10.7270/Q2CV4K3J
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 8 (Homo sapiens (Human))	BDBM11162 ((1R)-3-oxo-3-[3-(trifluoroethyl)-5,6-dihydro[1,2,4...) Show SMILES N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C16H15F6N5O/c17-10-6-12(19)11(18)4-8(10)3-9(23)5-14(28)26-1-2-27-13(7-26)24-25-15(27)16(20,21)22/h4,6,9H,1-3,5,7,23H2/t9-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	5.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-8 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Rattus norvegicus)	BDBM50432213 (CHEMBL2347152) Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1ccc2C(=O)N(CCOc3ccccc3)C(=O)c2c1 Show InChI InChI=1S/C23H20N2O5S/c1-16-7-10-19(11-8-16)31(28,29)24-17-9-12-20-21(15-17)23(27)25(22(20)26)13-14-30-18-5-3-2-4-6-18/h2-12,15,24H,13-14H2,1H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.11E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal maltase using maltose as substrate by colorimetric analysis				Bioorg Med Chem Lett 23: 2022-6 (2013) Article DOI: 10.1016/j.bmcl.2013.02.011 BindingDB Entry DOI: 10.7270/Q2CV4K3J
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Rattus norvegicus)	BDBM50432215 (CHEMBL2347150) Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1ccc2C(=O)N(CCOc3cccc(O)c3)C(=O)c2c1 Show InChI InChI=1S/C23H20N2O6S/c1-15-5-8-19(9-6-15)32(29,30)24-16-7-10-20-21(13-16)23(28)25(22(20)27)11-12-31-18-4-2-3-17(26)14-18/h2-10,13-14,24,26H,11-12H2,1H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.56E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal maltase using maltose as substrate by colorimetric analysis				Bioorg Med Chem Lett 23: 2022-6 (2013) Article DOI: 10.1016/j.bmcl.2013.02.011 BindingDB Entry DOI: 10.7270/Q2CV4K3J
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Rattus norvegicus)	BDBM50432221 (CHEMBL2347144) Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1ccc2C(=O)N(Cc3ccc(cc3)C(N)=O)C(=O)c2c1 Show InChI InChI=1S/C23H19N3O5S/c1-14-2-9-18(10-3-14)32(30,31)25-17-8-11-19-20(12-17)23(29)26(22(19)28)13-15-4-6-16(7-5-15)21(24)27/h2-12,25H,13H2,1H3,(H2,24,27)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.14E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal maltase using maltose as substrate by colorimetric analysis				Bioorg Med Chem Lett 23: 2022-6 (2013) Article DOI: 10.1016/j.bmcl.2013.02.011 BindingDB Entry DOI: 10.7270/Q2CV4K3J
					More data for this Ligand-Target Pair
Lactase/phlorizin hydrolase (Rattus norvegicus)	BDBM50432216 (CHEMBL2347149) Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1ccc2C(=O)N(CCNc3ccc(O)c(O)c3)C(=O)c2c1 Show InChI InChI=1S/C23H21N3O6S/c1-14-2-6-17(7-3-14)33(31,32)25-16-4-8-18-19(12-16)23(30)26(22(18)29)11-10-24-15-5-9-20(27)21(28)13-15/h2-9,12-13,24-25,27-28H,10-11H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.66E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal lactase using lactose as substrate by colorimetric analysis				Bioorg Med Chem Lett 23: 2022-6 (2013) Article DOI: 10.1016/j.bmcl.2013.02.011 BindingDB Entry DOI: 10.7270/Q2CV4K3J
					More data for this Ligand-Target Pair
Lactase/phlorizin hydrolase (Rattus norvegicus)	BDBM50432221 (CHEMBL2347144) Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1ccc2C(=O)N(Cc3ccc(cc3)C(N)=O)C(=O)c2c1 Show InChI InChI=1S/C23H19N3O5S/c1-14-2-9-18(10-3-14)32(30,31)25-17-8-11-19-20(12-17)23(29)26(22(19)28)13-15-4-6-16(7-5-15)21(24)27/h2-12,25H,13H2,1H3,(H2,24,27)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.42E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal lactase using lactose as substrate by colorimetric analysis				Bioorg Med Chem Lett 23: 2022-6 (2013) Article DOI: 10.1016/j.bmcl.2013.02.011 BindingDB Entry DOI: 10.7270/Q2CV4K3J
					More data for this Ligand-Target Pair
Oligo-1,6-glucosidase IMA1 (Saccharomyces cerevisiae S288c (Baker's yeast))	BDBM50438508 (CHEMBL2414814) Show SMILES CC(=O)Oc1ccc(cc1)C(=O)NC[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C16H21NO8/c1-8(19)24-10-4-2-9(3-5-10)16(23)17-6-11-13(20)15(22)14(21)12(7-18)25-11/h2-5,11-15,18,20-22H,6-7H2,1H3,(H,17,23)/t11-,12+,13-,14+,15+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.65E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of Saccharomyces cerevisiae alpha-glucosidase assessed as 4-nitrophenol release from 4-nitrophenyl alpha-D-glucopyranoside preincubated fo...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Sucrase-isomaltase, intestinal (Rattus norvegicus (Rat))	BDBM50438519 (CHEMBL2414741) Show SMILES OC[C@H]1O[C@@H](CNC\C=C\c2ccccc2)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C16H23NO5/c18-10-13-15(20)16(21)14(19)12(22-13)9-17-8-4-7-11-5-2-1-3-6-11/h1-7,12-21H,8-10H2/b7-4+/t12-,13+,14-,15+,16+/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.74E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal sucrase using sucrose as substrate assessed as D-glucose release from substrate preincubated for 15 mins measured after ...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Rattus norvegicus)	BDBM50432223 (CHEMBL2347142) Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1ccc2C(=O)N(CCNc3ccccc3)C(=O)c2c1 Show InChI InChI=1S/C23H21N3O4S/c1-16-7-10-19(11-8-16)31(29,30)25-18-9-12-20-21(15-18)23(28)26(22(20)27)14-13-24-17-5-3-2-4-6-17/h2-12,15,24-25H,13-14H2,1H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.96E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal maltase using maltose as substrate by colorimetric analysis				Bioorg Med Chem Lett 23: 2022-6 (2013) Article DOI: 10.1016/j.bmcl.2013.02.011 BindingDB Entry DOI: 10.7270/Q2CV4K3J
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 9 (Homo sapiens (Human))	BDBM50506699 (CHEMBL4516388) Show SMILES OCCCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C22H25F6N5O3/c23-15-11-17(25)16(24)9-13(15)8-14(29-19(35)4-2-1-3-7-34)10-20(36)32-5-6-33-18(12-32)30-31-21(33)22(26,27)28/h9,11,14,34H,1-8,10,12H2,(H,29,35)/t14-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-9 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 8 (Homo sapiens (Human))	BDBM50506696 (CHEMBL4434648) Show SMILES [O-][N+](=O)OCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C18H16F6N6O5/c19-11-6-13(21)12(20)4-9(11)3-10(25-15(31)8-35-30(33)34)5-16(32)28-1-2-29-14(7-28)26-27-17(29)18(22,23)24/h4,6,10H,1-3,5,7-8H2,(H,25,31)/t10-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-8 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 8 (Homo sapiens (Human))	BDBM50506699 (CHEMBL4516388) Show SMILES OCCCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C22H25F6N5O3/c23-15-11-17(25)16(24)9-13(15)8-14(29-19(35)4-2-1-3-7-34)10-20(36)32-5-6-33-18(12-32)30-31-21(33)22(26,27)28/h9,11,14,34H,1-8,10,12H2,(H,29,35)/t14-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-8 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 8 (Homo sapiens (Human))	BDBM50506694 (CHEMBL4524414) Show SMILES [O-][N+](=O)OCCCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C22H24F6N6O5/c23-15-11-17(25)16(24)9-13(15)8-14(29-19(35)4-2-1-3-7-39-34(37)38)10-20(36)32-5-6-33-18(12-32)30-31-21(33)22(26,27)28/h9,11,14H,1-8,10,12H2,(H,29,35)/t14-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-8 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 9 (Homo sapiens (Human))	BDBM50506697 (CHEMBL4458307) Show SMILES OCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C20H21F6N5O3/c21-13-9-15(23)14(22)7-11(13)6-12(27-17(33)2-1-5-32)8-18(34)30-3-4-31-16(10-30)28-29-19(31)20(24,25)26/h7,9,12,32H,1-6,8,10H2,(H,27,33)/t12-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-9 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 8 (Homo sapiens (Human))	BDBM50506698 (CHEMBL4577865) Show SMILES [O-][N+](=O)OCCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C21H22F6N6O5/c22-14-10-16(24)15(23)8-12(14)7-13(28-18(34)3-1-2-6-38-33(36)37)9-19(35)31-4-5-32-17(11-31)29-30-20(32)21(25,26)27/h8,10,13H,1-7,9,11H2,(H,28,34)/t13-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-8 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 8 (Homo sapiens (Human))	BDBM50506695 (CHEMBL4437841) Show SMILES [O-][N+](=O)OCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C20H20F6N6O5/c21-13-9-15(23)14(22)7-11(13)6-12(27-17(33)2-1-5-37-32(35)36)8-18(34)30-3-4-31-16(10-30)28-29-19(31)20(24,25)26/h7,9,12H,1-6,8,10H2,(H,27,33)/t12-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-8 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 9 (Homo sapiens (Human))	BDBM50506698 (CHEMBL4577865) Show SMILES [O-][N+](=O)OCCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C21H22F6N6O5/c22-14-10-16(24)15(23)8-12(14)7-13(28-18(34)3-1-2-6-38-33(36)37)9-19(35)31-4-5-32-17(11-31)29-30-20(32)21(25,26)27/h8,10,13H,1-7,9,11H2,(H,28,34)/t13-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-9 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 9 (Homo sapiens (Human))	BDBM50506692 (CHEMBL4464592) Show SMILES OCCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C21H23F6N5O3/c22-14-10-16(24)15(23)8-12(14)7-13(28-18(34)3-1-2-6-33)9-19(35)31-4-5-32-17(11-31)29-30-20(32)21(25,26)27/h8,10,13,33H,1-7,9,11H2,(H,28,34)/t13-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-9 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 8 (Homo sapiens (Human))	BDBM50506692 (CHEMBL4464592) Show SMILES OCCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C21H23F6N5O3/c22-14-10-16(24)15(23)8-12(14)7-13(28-18(34)3-1-2-6-33)9-19(35)31-4-5-32-17(11-31)29-30-20(32)21(25,26)27/h8,10,13,33H,1-7,9,11H2,(H,28,34)/t13-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-8 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 9 (Homo sapiens (Human))	BDBM11162 ((1R)-3-oxo-3-[3-(trifluoroethyl)-5,6-dihydro[1,2,4...) Show SMILES N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C16H15F6N5O/c17-10-6-12(19)11(18)4-8(10)3-9(23)5-14(28)26-1-2-27-13(7-26)24-25-15(27)16(20,21)22/h4,6,9H,1-3,5,7,23H2/t9-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-9 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 9 (Homo sapiens (Human))	BDBM50506693 (CHEMBL4537702) Show SMILES OCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C18H17F6N5O3/c19-11-6-13(21)12(20)4-9(11)3-10(25-15(31)8-30)5-16(32)28-1-2-29-14(7-28)26-27-17(29)18(22,23)24/h4,6,10,30H,1-3,5,7-8H2,(H,25,31)/t10-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-9 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 9 (Homo sapiens (Human))	BDBM50506694 (CHEMBL4524414) Show SMILES [O-][N+](=O)OCCCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C22H24F6N6O5/c23-15-11-17(25)16(24)9-13(15)8-14(29-19(35)4-2-1-3-7-39-34(37)38)10-20(36)32-5-6-33-18(12-32)30-31-21(33)22(26,27)28/h9,11,14H,1-8,10,12H2,(H,29,35)/t14-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-9 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 9 (Homo sapiens (Human))	BDBM50506695 (CHEMBL4437841) Show SMILES [O-][N+](=O)OCCCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C20H20F6N6O5/c21-13-9-15(23)14(22)7-11(13)6-12(27-17(33)2-1-5-37-32(35)36)8-18(34)30-3-4-31-16(10-30)28-29-19(31)20(24,25)26/h7,9,12H,1-6,8,10H2,(H,27,33)/t12-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-9 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 9 (Homo sapiens (Human))	BDBM50506696 (CHEMBL4434648) Show SMILES [O-][N+](=O)OCC(=O)N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r| Show InChI InChI=1S/C18H16F6N6O5/c19-11-6-13(21)12(20)4-9(11)3-10(25-15(31)8-35-30(33)34)5-16(32)28-1-2-29-14(7-28)26-27-17(29)18(22,23)24/h4,6,10H,1-3,5,7-8H2,(H,25,31)/t10-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of human recombinant DPP-9 using H-Gly-Pro-AMC as substrate after 10 mins by fluorescence assay				Bioorg Med Chem Lett 28: 3731-3735 (2018) Article DOI: 10.1016/j.bmcl.2018.10.019 BindingDB Entry DOI: 10.7270/Q2B85CFR
					More data for this Ligand-Target Pair

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