Compile Data Set for Download or QSAR

Found 134 hits with Last Name = 'kim' and Initial = 'gt'   

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
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121552 (US8729273, 22) Show SMILES OC(=O)c1ccnc(c1)-c1ccc2n(CC3CC3)cc(C#N)c2c1 Show InChI InChI=1S/C19H15N3O2/c20-9-15-11-22(10-12-1-2-12)18-4-3-13(7-16(15)18)17-8-14(19(23)24)5-6-21-17/h3-8,11-12H,1-2,10H2,(H,23,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	2.10	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121532 (US8729273, 2) Show SMILES OC(=O)c1cnn(c1)-c1ccc2n(CC3CC3)cc(C#N)c2c1 Show InChI InChI=1S/C17H14N4O2/c18-6-12-9-20(8-11-1-2-11)16-4-3-14(5-15(12)16)21-10-13(7-19-21)17(22)23/h3-5,7,9-11H,1-2,8H2,(H,22,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	2.80	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121531 (US8729273, 1) Show SMILES CC(C)n1cc(C#N)c2cc(ccc12)-n1cc(cn1)C(O)=O Show InChI InChI=1S/C16H14N4O2/c1-10(2)19-8-11(6-17)14-5-13(3-4-15(14)19)20-9-12(7-18-20)16(21)22/h3-5,7-10H,1-2H3,(H,21,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Similars	US Patent	n/a	n/a	3.40	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121536 (US8729273, 6) Show SMILES COCCn1cc(C#N)c2cc(ccc12)-n1cc(cn1)C(O)=O Show InChI InChI=1S/C16H14N4O3/c1-23-5-4-19-9-11(7-17)14-6-13(2-3-15(14)19)20-10-12(8-18-20)16(21)22/h2-3,6,8-10H,4-5H2,1H3,(H,21,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	3.80	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121534 (US8729273, 4) Show SMILES CC(C)Cn1cc(C#N)c2cc(ccc12)-n1cc(cn1)C(O)=O Show InChI InChI=1S/C17H16N4O2/c1-11(2)8-20-9-12(6-18)15-5-14(3-4-16(15)20)21-10-13(7-19-21)17(22)23/h3-5,7,9-11H,8H2,1-2H3,(H,22,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	4.5	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121547 (US8729273, 17) Show SMILES CC(C)n1cc([N+]([O-])=O)c2cc(ccc12)-n1cc(cn1)C(O)=O Show InChI InChI=1S/C15H14N4O4/c1-9(2)17-8-14(19(22)23)12-5-11(3-4-13(12)17)18-7-10(6-16-18)15(20)21/h3-9H,1-2H3,(H,20,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	4.60	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121539 (US8729273, 9) Show SMILES OC(=O)c1cnn(c1)-c1ccc2n(cc(C#N)c2c1)C1CCCC1 Show InChI InChI=1S/C18H16N4O2/c19-8-12-10-21(14-3-1-2-4-14)17-6-5-15(7-16(12)17)22-11-13(9-20-22)18(23)24/h5-7,9-11,14H,1-4H2,(H,23,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	4.60	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121550 (US8729273, 20) Show SMILES CC(C)n1cc(C#N)c2cc(ccc12)-c1ccc(s1)C(O)=O Show InChI InChI=1S/C17H14N2O2S/c1-10(2)19-9-12(8-18)13-7-11(3-4-14(13)19)15-5-6-16(22-15)17(20)21/h3-7,9-10H,1-2H3,(H,20,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	4.70	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121543 (US8729273, 13) Show SMILES Cc1nn(cc1C(O)=O)-c1ccc2n(CC3CC3)cc(C#N)c2c1 Show InChI InChI=1S/C18H16N4O2/c1-11-16(18(23)24)10-22(20-11)14-4-5-17-15(6-14)13(7-19)9-21(17)8-12-2-3-12/h4-6,9-10,12H,2-3,8H2,1H3,(H,23,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	4.80	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121559 (US8729273, 29) Show SMILES CC(C)c1cc2cc(cc(C#N)c2[nH]1)-n1cc(cn1)C(O)=O Show InChI InChI=1S/C16H14N4O2/c1-9(2)14-5-10-3-13(4-11(6-17)15(10)19-14)20-8-12(7-18-20)16(21)22/h3-5,7-9,19H,1-2H3,(H,21,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121535 (US8729273, 5) Show SMILES CC(C)(C)Cn1cc(C#N)c2cc(ccc12)-n1cc(cn1)C(O)=O Show InChI InChI=1S/C18H18N4O2/c1-18(2,3)11-21-9-12(7-19)15-6-14(4-5-16(15)21)22-10-13(8-20-22)17(23)24/h4-6,8-10H,11H2,1-3H3,(H,23,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121540 (US8729273, 10) Show SMILES CC(CF)n1cc(C#N)c2cc(ccc12)-n1cc(cn1)C(O)=O Show InChI InChI=1S/C16H13FN4O2/c1-10(5-17)20-8-11(6-18)14-4-13(2-3-15(14)20)21-9-12(7-19-21)16(22)23/h2-4,7-10H,5H2,1H3,(H,22,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	5.20	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121541 (US8729273, 11) Show SMILES OC(=O)c1cnn(c1)-c1ccc2n(cc(C#N)c2c1)C1CCOC1 Show InChI InChI=1S/C17H14N4O3/c18-6-11-8-20(14-3-4-24-10-14)16-2-1-13(5-15(11)16)21-9-12(7-19-21)17(22)23/h1-2,5,7-9,14H,3-4,10H2,(H,22,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	5.40	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121533 (US8729273, 3) Show SMILES OC(=O)c1cnn(c1)-c1ccc2n(cc(C#N)c2c1)C1CC1 Show InChI InChI=1S/C16H12N4O2/c17-6-10-8-19(12-1-2-12)15-4-3-13(5-14(10)15)20-9-11(7-18-20)16(21)22/h3-5,7-9,12H,1-2H2,(H,21,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	6	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121551 (US8729273, 21) Show SMILES CC(C)n1cc(C#N)c2cc(ccc12)-c1cc(ccn1)C(O)=O Show InChI InChI=1S/C18H15N3O2/c1-11(2)21-10-14(9-19)15-7-12(3-4-17(15)21)16-8-13(18(22)23)5-6-20-16/h3-8,10-11H,1-2H3,(H,22,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	6.20	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121554 (US8729273, 24) Show SMILES CC(CF)n1cc(C#N)c2cc(ccc12)-c1cc(ccn1)C(O)=O Show InChI InChI=1S/C18H14FN3O2/c1-11(8-19)22-10-14(9-20)15-6-12(2-3-17(15)22)16-7-13(18(23)24)4-5-21-16/h2-7,10-11H,8H2,1H3,(H,23,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	6.20	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121537 (US8729273, 7) Show SMILES CCC(C)n1cc(C#N)c2cc(ccc12)-n1cc(cn1)C(O)=O Show InChI InChI=1S/C17H16N4O2/c1-3-11(2)20-9-12(7-18)15-6-14(4-5-16(15)20)21-10-13(8-19-21)17(22)23/h4-6,8-11H,3H2,1-2H3,(H,22,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	6.70	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121538 (US8729273, 8) Show SMILES OC(=O)c1cnn(c1)-c1ccc2n(cc(C#N)c2c1)C1CCC1 Show InChI InChI=1S/C17H14N4O2/c18-7-11-9-20(13-2-1-3-13)16-5-4-14(6-15(11)16)21-10-12(8-19-21)17(22)23/h4-6,8-10,13H,1-3H2,(H,22,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	6.90	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121555 (US8729273, 25) Show SMILES COCCn1cc(C#N)c2cc(ccc12)-c1cc(ccn1)C(O)=O Show InChI InChI=1S/C18H15N3O3/c1-24-7-6-21-11-14(10-19)15-8-12(2-3-17(15)21)16-9-13(18(22)23)4-5-20-16/h2-5,8-9,11H,6-7H2,1H3,(H,22,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	8.5	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214714 ((S)-2-(tert-butylamino)-1-(2-(2-(1-methylcyclohexy...) Show SMILES CC(C)(C)NCC(=O)N1CCC[C@H]1C(=O)c1nnc(o1)C1(C)CCCCC1 Show InChI InChI=1S/C20H32N4O3/c1-19(2,3)21-13-15(25)24-12-8-9-14(24)16(26)17-22-23-18(27-17)20(4)10-6-5-7-11-20/h14,21H,5-13H2,1-4H3/t14-/m0/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	10	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121553 (US8729273, 23) Show SMILES OC(=O)c1ccnc(c1)-c1ccc2n(cc(C#N)c2c1)C1CCOC1 Show InChI InChI=1S/C19H15N3O3/c20-9-14-10-22(15-4-6-25-11-15)18-2-1-12(7-16(14)18)17-8-13(19(23)24)3-5-21-17/h1-3,5,7-8,10,15H,4,6,11H2,(H,23,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121557 (US8729273, 27) Show SMILES CC(C)n1cc([N+]([O-])=O)c2cc(ccc12)-c1cc(ccn1)C(O)=O Show InChI InChI=1S/C17H15N3O4/c1-10(2)19-9-16(20(23)24)13-7-11(3-4-15(13)19)14-8-12(17(21)22)5-6-18-14/h3-10H,1-2H3,(H,21,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121542 (US8729273, 12) Show SMILES CC(C)n1cc(C#N)c2cc(ccc12)-n1cc(C(O)=O)c(C)n1 Show InChI InChI=1S/C17H16N4O2/c1-10(2)20-8-12(7-18)14-6-13(4-5-16(14)20)21-9-15(17(22)23)11(3)19-21/h4-6,8-10H,1-3H3,(H,22,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	11.6	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121544 (US8729273, 14) Show SMILES COCCn1cc(C#N)c2cc(ccc12)-n1cc(C(O)=O)c(C)n1 Show InChI InChI=1S/C17H16N4O3/c1-11-15(17(22)23)10-21(19-11)13-3-4-16-14(7-13)12(8-18)9-20(16)5-6-24-2/h3-4,7,9-10H,5-6H2,1-2H3,(H,22,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	12	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121548 (US8729273, 18) Show SMILES CC(C)n1cc(C#N)c2cc(ccc12)-n1cnc(n1)C(O)=O Show InChI InChI=1S/C15H13N5O2/c1-9(2)19-7-10(6-16)12-5-11(3-4-13(12)19)20-8-17-14(18-20)15(21)22/h3-5,7-9H,1-2H3,(H,21,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	13	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214713 ((S)-2-(tert-butylamino)-1-(2-(5-(4-fluorophenyl)-1...) Show SMILES CC(C)(C)NCC(=O)N1CCC[C@H]1C(=O)c1noc(n1)-c1ccc(F)cc1 Show InChI InChI=1S/C19H23FN4O3/c1-19(2,3)21-11-15(25)24-10-4-5-14(24)16(26)17-22-18(27-23-17)12-6-8-13(20)9-7-12/h6-9,14,21H,4-5,10-11H2,1-3H3/t14-/m0/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	15	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121560 (US8729273, 30) Show SMILES COCc1cc2cc(cc(C#N)c2[nH]1)-n1cc(cn1)C(O)=O Show InChI InChI=1S/C15H12N4O3/c1-22-8-12-2-9-3-13(4-10(5-16)14(9)18-12)19-7-11(6-17-19)15(20)21/h2-4,6-7,18H,8H2,1H3,(H,20,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214723 ((S)-2-(tert-butylamino)-1-(2-(2-mesityl-1,3,4-oxad...) Show SMILES Cc1cc(C)c(-c2nnc(o2)C(=O)[C@@H]2CCCN2C(=O)CNC(C)(C)C)c(C)c1 Show InChI InChI=1S/C22H30N4O3/c1-13-10-14(2)18(15(3)11-13)20-24-25-21(29-20)19(28)16-8-7-9-26(16)17(27)12-23-22(4,5)6/h10-11,16,23H,7-9,12H2,1-6H3/t16-/m0/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	17	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214720 (2-(tert-butylamino)-1-((2S,4S)-4-fluoro-2-(2-tert-...) Show SMILES CCC(C)(C)c1nnc(o1)C(=O)[C@@H]1C[C@H](F)CN1C(=O)CNC(C)(C)C Show InChI InChI=1S/C18H29FN4O3/c1-7-18(5,6)16-22-21-15(26-16)14(25)12-8-11(19)10-23(12)13(24)9-20-17(2,3)4/h11-12,20H,7-10H2,1-6H3/t11-,12-/m0/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	20	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214709 (1-((2S,4S)-2-(2-tert-butyl-1,3,4-oxadiazole-5-carb...) Show SMILES CC(C)(CO)NCC(=O)N1C[C@@H](F)C[C@H]1C(=O)c1nnc(o1)C(C)(C)C Show InChI InChI=1S/C17H27FN4O4/c1-16(2,3)15-21-20-14(26-15)13(25)11-6-10(18)8-22(11)12(24)7-19-17(4,5)9-23/h10-11,19,23H,6-9H2,1-5H3/t10-,11-/m0/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	22	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121549 (US8729273, 19) Show SMILES CC(C)n1cc(C#N)c2cc(ccc12)-n1cnc(c1)C(O)=O Show InChI InChI=1S/C16H14N4O2/c1-10(2)20-7-11(6-17)13-5-12(3-4-15(13)20)19-8-14(16(21)22)18-9-19/h3-5,7-10H,1-2H3,(H,21,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	24	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121558 (US8729273, 28) Show SMILES OC(=O)c1cnn(c1)-c1cc(C#N)c2[nH]c(cc2c1)-c1ccccc1 Show InChI InChI=1S/C19H12N4O2/c20-9-14-7-16(23-11-15(10-21-23)19(24)25)6-13-8-17(22-18(13)14)12-4-2-1-3-5-12/h1-8,10-11,22H,(H,24,25)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	24	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214727 (1-((2S,4S)-2-(2-tert-butyl-1,3,4-oxadiazole-5-carb...) Show SMILES CC(C)(Cc1ccc(F)cc1)NCC(=O)N1C[C@@H](F)C[C@H]1C(=O)c1nnc(o1)C(C)(C)C Show InChI InChI=1S/C23H30F2N4O3/c1-22(2,3)21-28-27-20(32-21)19(31)17-10-16(25)13-29(17)18(30)12-26-23(4,5)11-14-6-8-15(24)9-7-14/h6-9,16-17,26H,10-13H2,1-5H3/t16-,17-/m0/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	25	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214725 (2-(tert-butylamino)-1-((2S,4S)-2-(2-cyclohexyl-1,3...) Show SMILES CC(C)(C)NCC(=O)N1C[C@@H](F)C[C@H]1C(=O)c1nnc(o1)C1CCCCC1 Show InChI InChI=1S/C19H29FN4O3/c1-19(2,3)21-10-15(25)24-11-13(20)9-14(24)16(26)18-23-22-17(27-18)12-7-5-4-6-8-12/h12-14,21H,4-11H2,1-3H3/t13-,14-/m0/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	30	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214726 ((S)-1-(2-(1,2,4-oxadiazole-3-carbonyl)pyrrolidin-1...) Show SMILES CC(C)(Cc1ccc(F)cc1)NCC(=O)N1CCC[C@H]1C(=O)c1ncon1 Show InChI InChI=1S/C19H23FN4O3/c1-19(2,10-13-5-7-14(20)8-6-13)22-11-16(25)24-9-3-4-15(24)17(26)18-21-12-27-23-18/h5-8,12,15,22H,3-4,9-11H2,1-2H3/t15-/m0/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	35	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Xanthine dehydrogenase/oxidase (Bos taurus (Bovine))	BDBM121561 (US8729273, 31) Show SMILES OC(=O)c1cnn(c1)-c1cc(C#N)c2[nH]ccc2c1 Show InChI InChI=1S/C13H8N4O2/c14-5-9-4-11(3-8-1-2-15-12(8)9)17-7-10(6-16-17)13(18)19/h1-4,6-7,15H,(H,18,19)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	40	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences Ltd. US Patent					Assay Description Xanthine oxidase originated from bovine milk was incubated for 3 min with test compounds, and the initial velocity of uric acid formation was determi...				US Patent US8729273 (2014) BindingDB Entry DOI: 10.7270/Q2D79937
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214712 ((S)-1-(2-(2-tert-butyl-1,3,4-oxadiazole-5-carbonyl...) Show SMILES CC(C)(CO)NCC(=O)N1CCC[C@H]1C(=O)c1nnc(o1)C(C)(C)C Show InChI InChI=1S/C17H28N4O4/c1-16(2,3)15-20-19-14(25-15)13(24)11-7-6-8-21(11)12(23)9-18-17(4,5)10-22/h11,18,22H,6-10H2,1-5H3/t11-/m0/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	47	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214719 (2-(adamantan-1-ylamino)-1-[(2S,4S)-4-fluoro-2-(5-m...) Show SMILES Cc1nnc(o1)C(=O)[C@@H]1C[C@H](F)CN1C(=O)CNC12CC3CC(CC(C3)C1)C2 |TLB:17:18:21:25.24.23,THB:19:20:23:27.18.26,19:18:21.20.25:23,26:18:21:25.24.23,26:24:21:27.19.18| Show InChI InChI=1S/C20H27FN4O3/c1-11-23-24-19(28-11)18(27)16-5-15(21)10-25(16)17(26)9-22-20-6-12-2-13(7-20)4-14(3-12)8-20/h12-16,22H,2-10H2,1H3/t12?,13?,14?,15-,16-,20?/m0/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
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214717 ((S)-1-(2-(2-tert-butyl-1,3,4-oxadiazole-5-carbonyl...) Show SMILES CC(C)(C)NCC(=O)N1CCC[C@H]1C(=O)c1nnc(o1)C(C)(C)C Show InChI InChI=1S/C17H28N4O3/c1-16(2,3)15-20-19-14(24-15)13(23)11-8-7-9-21(11)12(22)10-18-17(4,5)6/h11,18H,7-10H2,1-6H3/t11-/m0/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	56	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214718 (1-((2S,4S)-2-(5-tert-butyl-1,2,4-oxadiazole-3-carb...) Show SMILES CC(C)(C)NCC(=O)N1C[C@@H](F)C[C@H]1C(=O)c1noc(n1)C(C)(C)C Show InChI InChI=1S/C17H27FN4O3/c1-16(2,3)15-20-14(21-25-15)13(24)11-7-10(18)9-22(11)12(23)8-19-17(4,5)6/h10-11,19H,7-9H2,1-6H3/t10-,11-/m0/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	63	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214724 (1-((2S,4S)-2-(5-tert-butyl-1,2,4-oxadiazole-3-carb...) Show SMILES CC(C)(CO)NCC(=O)N1C[C@@H](F)C[C@H]1C(=O)c1noc(n1)C(C)(C)C Show InChI InChI=1S/C17H27FN4O4/c1-16(2,3)15-20-14(21-26-15)13(25)11-6-10(18)8-22(11)12(24)7-19-17(4,5)9-23/h10-11,19,23H,6-9H2,1-5H3/t10-,11-/m0/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	67	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214722 ((S)-2-(1-hydroxy-2-methylpropan-2-ylamino)-1-(2-(5...) Show SMILES Cc1nc(no1)C(=O)[C@@H]1CCCN1C(=O)CNC(C)(C)CO Show InChI InChI=1S/C14H22N4O4/c1-9-16-13(17-22-9)12(21)10-5-4-6-18(10)11(20)7-15-14(2,3)8-19/h10,15,19H,4-8H2,1-3H3/t10-/m0/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	77	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214728 (2-(adamantan-1-ylamino)-1-[(S)-2-(5-methyl-[1,3,4]...) Show SMILES Cc1nnc(o1)C(=O)[C@@H]1CCCN1C(=O)CNC12CC3CC(CC(C3)C1)C2 |TLB:16:17:20:24.23.22,THB:18:19:22:26.17.25,18:17:20.19.24:22,25:17:20:24.23.22,25:23:20:26.18.17| Show InChI InChI=1S/C20H28N4O3/c1-12-22-23-19(27-12)18(26)16-3-2-4-24(16)17(25)11-21-20-8-13-5-14(9-20)7-15(6-13)10-20/h13-16,21H,2-11H2,1H3/t13?,14?,15?,16-,20?/m0/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	84	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214711 ((S)-2-(tert-butylamino)-1-(2-(5-(1-methylcyclohexy...) Show SMILES CC(C)(C)NCC(=O)N1CCC[C@H]1C(=O)c1noc(n1)C1(C)CCCCC1 Show InChI InChI=1S/C20H32N4O3/c1-19(2,3)21-13-15(25)24-12-8-9-14(24)16(26)17-22-18(27-23-17)20(4)10-6-5-7-11-20/h14,21H,5-13H2,1-4H3/t14-/m0/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	95	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 2 (Homo sapiens (Human))	BDBM50214726 ((S)-1-(2-(1,2,4-oxadiazole-3-carbonyl)pyrrolidin-1...) Show SMILES CC(C)(Cc1ccc(F)cc1)NCC(=O)N1CCC[C@H]1C(=O)c1ncon1 Show InChI InChI=1S/C19H23FN4O3/c1-19(2,10-13-5-7-14(20)8-6-13)22-11-16(25)24-9-3-4-15(24)17(26)18-21-12-27-23-18/h5-8,12,15,22H,3-4,9-11H2,1-2H3/t15-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of DPP2				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214729 (2-(adamantan-1-ylamino)-1-[(S)-2-(5-methyl-[1,2,4]...) Show SMILES Cc1nc(no1)C(=O)[C@@H]1CCCN1C(=O)CNC12CC3CC(CC(C3)C1)C2 |TLB:16:17:20:24.23.22,THB:18:19:22:26.17.25,18:17:20.19.24:22,25:17:20:24.23.22,25:23:20:26.18.17| Show InChI InChI=1S/C20H28N4O3/c1-12-22-19(23-27-12)18(26)16-3-2-4-24(16)17(25)11-21-20-8-13-5-14(9-20)7-15(6-13)10-20/h13-16,21H,2-11H2,1H3/t13?,14?,15?,16-,20?/m0/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	210	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214715 ((S)-1-(2-(5-tert-butyl-1,2,4-oxadiazole-3-carbonyl...) Show SMILES CC(C)(CO)NCC(=O)N1CCC[C@H]1C(=O)c1noc(n1)C(C)(C)C Show InChI InChI=1S/C17H28N4O4/c1-16(2,3)15-19-14(20-25-15)13(24)11-7-6-8-21(11)12(23)9-18-17(4,5)10-22/h11,18,22H,6-10H2,1-5H3/t11-/m0/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	223	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214710 (2-(adamantan-1-ylamino)-1-[(R)-4-(5-methyl-[1,3,4]...) Show SMILES Cc1nnc(o1)C(=O)[C@@H]1CSCN1C(=O)CNC12CC3CC(CC(C3)C1)C2 |TLB:16:17:20:24.23.22,THB:18:19:22:26.17.25,18:17:20.19.24:22,25:17:20:24.23.22,25:23:20:26.18.17| Show InChI InChI=1S/C19H26N4O3S/c1-11-21-22-18(26-11)17(25)15-9-27-10-23(15)16(24)8-20-19-5-12-2-13(6-19)4-14(3-12)7-19/h12-15,20H,2-10H2,1H3/t12?,13?,14?,15-,19?/m0/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	224	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214731 ((S)-2-(1-hydroxy-2-methylpropan-2-ylamino)-1-(2-(2...) Show SMILES Cc1nnc(o1)C(=O)[C@@H]1CCCN1C(=O)CNC(C)(C)CO Show InChI InChI=1S/C14H22N4O4/c1-9-16-17-13(22-9)12(21)10-5-4-6-18(10)11(20)7-15-14(2,3)8-19/h10,15,19H,4-8H2,1-3H3/t10-/m0/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	255	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair
Dipeptidyl peptidase 4 (Homo sapiens (Human))	BDBM50214730 (2-(3-hydroxy-adamantan-1-ylamino)-1-[(S)-2-(5-meth...) Show SMILES Cc1nnc(o1)C(=O)[C@@H]1CCCN1C(=O)CNC12CC3CC(CC(O)(C3)C1)C2 |TLB:27:17:25:20.21.22,THB:18:19:22:26.17.27,18:17:25.19.20:22,27:21:25:26.18.17,16:17:25:20.21.22| Show InChI InChI=1S/C20H28N4O4/c1-12-22-23-18(28-12)17(26)15-3-2-4-24(15)16(25)10-21-19-6-13-5-14(7-19)9-20(27,8-13)11-19/h13-15,21,27H,2-11H2,1H3/t13?,14?,15-,19?,20?/m0/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	339	n/a	n/a	n/a	n/a	n/a	n/a
LG Life Sciences, Ltd Curated by ChEMBL					Assay Description Inhibition of human DPP4				Bioorg Med Chem Lett 17: 4167-72 (2007) Article DOI: 10.1016/j.bmcl.2007.05.046 BindingDB Entry DOI: 10.7270/Q2611006
					More data for this Ligand-Target Pair

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