Compile Data Set for Download or QSAR

Found 106 hits with Last Name = 'taylor' and Initial = 'aj'   

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
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50160371 (7-Methoxy-6-oxazol-5-yl-3-(2-pyridin-4-yl-ethyl)-2...) Show SMILES COc1cc2[nH]c(=S)n(CCc3ccncc3)c(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C19H16N4O3S/c1-25-16-9-15-13(8-14(16)17-10-21-11-26-17)18(24)23(19(27)22-15)7-4-12-2-5-20-6-3-12/h2-3,5-6,8-11H,4,7H2,1H3,(H,22,27)	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	13	n/a	n/a	n/a	n/a	n/a	n/a
Celltech R and D Curated by ChEMBL					Assay Description In vitro inhibitory concentration against inosine-5'-monophosphate dehydrogenase				Bioorg Med Chem Lett 15: 751-4 (2005) Article DOI: 10.1016/j.bmcl.2004.11.015 BindingDB Entry DOI: 10.7270/Q2RN37CZ
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50160379 (7-Methoxy-3-methyl-6-oxazol-5-yl-2-thioxo-2,3-dihy...) Show SMILES COc1cc2[nH]c(=S)n(C)c(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C13H11N3O3S/c1-16-12(17)7-3-8(11-5-14-6-19-11)10(18-2)4-9(7)15-13(16)20/h3-6H,1-2H3,(H,15,20)	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	17	n/a	n/a	n/a	n/a	n/a	n/a
Celltech R and D Curated by ChEMBL					Assay Description In vitro inhibitory concentration against inosine-5'-monophosphate dehydrogenase				Bioorg Med Chem Lett 15: 751-4 (2005) Article DOI: 10.1016/j.bmcl.2004.11.015 BindingDB Entry DOI: 10.7270/Q2RN37CZ
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50160378 (3-(3-Imidazol-1-yl-propyl)-7-methoxy-6-oxazol-5-yl...) Show SMILES COc1cc2[nH]c(=S)n(CCCn3ccnc3)c(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C18H17N5O3S/c1-25-15-8-14-12(7-13(15)16-9-20-11-26-16)17(24)23(18(27)21-14)5-2-4-22-6-3-19-10-22/h3,6-11H,2,4-5H2,1H3,(H,21,27)	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
Celltech R and D Curated by ChEMBL					Assay Description In vitro inhibitory concentration against inosine-5'-monophosphate dehydrogenase				Bioorg Med Chem Lett 15: 751-4 (2005) Article DOI: 10.1016/j.bmcl.2004.11.015 BindingDB Entry DOI: 10.7270/Q2RN37CZ
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50160375 (7-Methoxy-6-oxazol-5-yl-2-thioxo-2,3-dihydro-1H-qu...) Show SMILES COc1cc2[nH]c(=S)[nH]c(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C12H9N3O3S/c1-17-9-3-8-6(11(16)15-12(19)14-8)2-7(9)10-4-13-5-18-10/h2-5H,1H3,(H2,14,15,16,19)	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
Celltech R and D Curated by ChEMBL					Assay Description In vitro inhibitory concentration against inosine-5'-monophosphate dehydrogenase				Bioorg Med Chem Lett 15: 751-4 (2005) Article DOI: 10.1016/j.bmcl.2004.11.015 BindingDB Entry DOI: 10.7270/Q2RN37CZ
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174783 (1-tert-butyl 5-methyl (3S,5R)-7'-methoxy-3'-methyl...) Show SMILES COC(=O)[C@H]1C[C@]2(CN1C(=O)OC(C)(C)C)Nc1cc(OC)c(cc1C(=O)N2C)-c1cnco1 Show InChI InChI=1S/C23H28N4O7/c1-22(2,3)34-21(30)27-11-23(9-16(27)20(29)32-6)25-15-8-17(31-5)14(18-10-24-12-33-18)7-13(15)19(28)26(23)4/h7-8,10,12,16,25H,9,11H2,1-6H3/t16-,23+/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	35	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174782 (CHEMBL198729 | N,N-diethyl-7'-methoxy-3'-methyl-6'...) Show SMILES CCN(CC)C(=O)N1CCC2(C1)Nc1cc(OC)c(cc1C(=O)N2C)-c1cnco1 Show InChI InChI=1S/C21H27N5O4/c1-5-25(6-2)20(28)26-8-7-21(12-26)23-16-10-17(29-4)15(18-11-22-13-30-18)9-14(16)19(27)24(21)3/h9-11,13,23H,5-8,12H2,1-4H3	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	45	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50160374 (3-[2-(1H-Imidazol-4-yl)-ethyl]-7-methoxy-6-oxazol-...) Show SMILES COc1cc2[nH]c(=O)n(CCc3cnc[nH]3)c(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C17H15N5O4/c1-25-14-5-13-11(4-12(14)15-7-19-9-26-15)16(23)22(17(24)21-13)3-2-10-6-18-8-20-10/h4-9H,2-3H2,1H3,(H,18,20)(H,21,24)	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
Celltech R and D Curated by ChEMBL					Assay Description In vitro inhibitory concentration against inosine-5'-monophosphate dehydrogenase				Bioorg Med Chem Lett 15: 751-4 (2005) Article DOI: 10.1016/j.bmcl.2004.11.015 BindingDB Entry DOI: 10.7270/Q2RN37CZ
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174790 (7-methoxy-2,3-dimethyl-6-(oxazol-5-yl)-2-styryl-2,...) Show SMILES COc1cc2NC(C)(\C=C\c3ccccc3)N(C)C(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C22H21N3O3/c1-22(10-9-15-7-5-4-6-8-15)24-18-12-19(27-3)17(20-13-23-14-28-20)11-16(18)21(26)25(22)2/h4-14,24H,1-3H3/b10-9+	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	49	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174792 (CHEMBL199075 | N-(2,4-difluorophenyl)-7'-methoxy-N...) Show SMILES COc1cc2NC3(CCN(C3)C(=O)N(C)c3ccc(F)cc3F)N(C)C(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C24H23F2N5O4/c1-29(19-5-4-14(25)8-17(19)26)23(33)31-7-6-24(12-31)28-18-10-20(34-3)16(21-11-27-13-35-21)9-15(18)22(32)30(24)2/h4-5,8-11,13,28H,6-7,12H2,1-3H3	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	51	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174796 (7'-methoxy-N,3'-dimethyl-6'-(1,3-oxazol-5-yl)-4'-o...) Show SMILES COc1cc2NC3(CCN(C3)C(=O)N(C)c3ccccc3)N(C)C(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C24H25N5O4/c1-27(16-7-5-4-6-8-16)23(31)29-10-9-24(14-29)26-19-12-20(32-3)18(21-13-25-15-33-21)11-17(19)22(30)28(24)2/h4-8,11-13,15,26H,9-10,14H2,1-3H3	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	64	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174795 (7'-methoxy-3'-methyl-6'-(1,3-oxazol-5-yl)-1-[(pipe...) Show SMILES COc1cc2NC3(CCN(C3)C(=O)N3CCCCC3)N(C)C(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C22H27N5O4/c1-25-20(28)15-10-16(19-12-23-14-31-19)18(30-2)11-17(15)24-22(25)6-9-27(13-22)21(29)26-7-4-3-5-8-26/h10-12,14,24H,3-9,13H2,1-2H3	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	68	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174789 (7'-methoxy-3'-methyl-6'-(1,3-oxazol-5-yl)-4'-oxo-N...) Show SMILES COc1cc2NC3(CCN(C3)C(=O)N(C(C)C)C(C)C)N(C)C(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C23H31N5O4/c1-14(2)28(15(3)4)22(30)27-8-7-23(12-27)25-18-10-19(31-6)17(20-11-24-13-32-20)9-16(18)21(29)26(23)5/h9-11,13-15,25H,7-8,12H2,1-6H3	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	71	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50160368 (7-Methoxy-3-(2-morpholin-4-yl-ethyl)-6-oxazol-5-yl...) Show SMILES COc1cc2[nH]c(=S)n(CCN3CCOCC3)c(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C18H20N4O4S/c1-24-15-9-14-12(8-13(15)16-10-19-11-26-16)17(23)22(18(27)20-14)3-2-21-4-6-25-7-5-21/h8-11H,2-7H2,1H3,(H,20,27)	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	71	n/a	n/a	n/a	n/a	n/a	n/a
Celltech R and D Curated by ChEMBL					Assay Description In vitro inhibitory concentration against inosine-5'-monophosphate dehydrogenase				Bioorg Med Chem Lett 15: 751-4 (2005) Article DOI: 10.1016/j.bmcl.2004.11.015 BindingDB Entry DOI: 10.7270/Q2RN37CZ
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174785 (CHEMBL372753 | N,7'-dimethoxy-N,3'-dimethyl-6'-(1,...) Show SMILES CON(C)C(=O)N1CCC2(C1)Nc1cc(OC)c(cc1C(=O)N2C)-c1cnco1 Show InChI InChI=1S/C19H23N5O5/c1-22-17(25)12-7-13(16-9-20-11-29-16)15(27-3)8-14(12)21-19(22)5-6-24(10-19)18(26)23(2)28-4/h7-9,11,21H,5-6,10H2,1-4H3	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	79	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174791 (CHEMBL197163 | ethyl 7'-methoxy-3'-methyl-6'-(1,3-...) Show SMILES CCOC(=O)N1CCC2(C1)Nc1cc(OC)c(cc1C(=O)N2C)-c1cnco1 Show InChI InChI=1S/C19H22N4O5/c1-4-27-18(25)23-6-5-19(10-23)21-14-8-15(26-3)13(16-9-20-11-28-16)7-12(14)17(24)22(19)2/h7-9,11,21H,4-6,10H2,1-3H3	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	80	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50160370 (3-(2-Imidazol-1-yl-ethyl)-7-methoxy-6-oxazol-5-yl-...) Show SMILES COc1cc2[nH]c(=O)n(CCn3ccnc3)c(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C17H15N5O4/c1-25-14-7-13-11(6-12(14)15-8-19-10-26-15)16(23)22(17(24)20-13)5-4-21-3-2-18-9-21/h2-3,6-10H,4-5H2,1H3,(H,20,24)	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	86	n/a	n/a	n/a	n/a	n/a	n/a
Celltech R and D Curated by ChEMBL					Assay Description In vitro inhibitory concentration against inosine-5'-monophosphate dehydrogenase				Bioorg Med Chem Lett 15: 751-4 (2005) Article DOI: 10.1016/j.bmcl.2004.11.015 BindingDB Entry DOI: 10.7270/Q2RN37CZ
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50160372 (7-Methoxy-6-oxazol-5-yl-3-(2-pyridin-2-yl-ethyl)-2...) Show SMILES COc1cc2[nH]c(=S)n(CCc3ccccn3)c(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C19H16N4O3S/c1-25-16-9-15-13(8-14(16)17-10-20-11-26-17)18(24)23(19(27)22-15)7-5-12-4-2-3-6-21-12/h2-4,6,8-11H,5,7H2,1H3,(H,22,27)	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	91	n/a	n/a	n/a	n/a	n/a	n/a
Celltech R and D Curated by ChEMBL					Assay Description In vitro inhibitory concentration against inosine-5'-monophosphate dehydrogenase				Bioorg Med Chem Lett 15: 751-4 (2005) Article DOI: 10.1016/j.bmcl.2004.11.015 BindingDB Entry DOI: 10.7270/Q2RN37CZ
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174788 (1-(2,2-dimethylpropanoyl)-7'-methoxy-3'-methyl-6'-...) Show SMILES COc1cc2NC3(CCN(C3)C(=O)C(C)(C)C)N(C)C(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C21H26N4O4/c1-20(2,3)19(27)25-7-6-21(11-25)23-15-9-16(28-5)14(17-10-22-12-29-17)8-13(15)18(26)24(21)4/h8-10,12,23H,6-7,11H2,1-5H3	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	94	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174781 (7'-methoxy-3'-methyl-6'-(1,3-oxazol-5-yl)-3',4',1,...) Show SMILES COc1cc2NC3(Cc4ccsc4C3)N(C)C(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C19H17N3O3S/c1-22-18(23)12-5-13(16-9-20-10-25-16)15(24-2)6-14(12)21-19(22)7-11-3-4-26-17(11)8-19/h3-6,9-10,21H,7-8H2,1-2H3	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	96	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50160373 (7-Methoxy-6-oxazol-5-yl-3-pyridin-4-ylmethyl-2-thi...) Show SMILES COc1cc2[nH]c(=S)n(Cc3ccncc3)c(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C18H14N4O3S/c1-24-15-7-14-12(6-13(15)16-8-20-10-25-16)17(23)22(18(26)21-14)9-11-2-4-19-5-3-11/h2-8,10H,9H2,1H3,(H,21,26)	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	100	n/a	n/a	n/a	n/a	n/a	n/a
Celltech R and D Curated by ChEMBL					Assay Description In vitro inhibitory concentration against inosine-5'-monophosphate dehydrogenase				Bioorg Med Chem Lett 15: 751-4 (2005) Article DOI: 10.1016/j.bmcl.2004.11.015 BindingDB Entry DOI: 10.7270/Q2RN37CZ
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50160367 (7-Methoxy-3-methyl-6-oxazol-5-yl-1H-quinazoline-2,...) Show SMILES COc1cc2[nH]c(=O)n(C)c(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C13H11N3O4/c1-16-12(17)7-3-8(11-5-14-6-20-11)10(19-2)4-9(7)15-13(16)18/h3-6H,1-2H3,(H,15,18)	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	104	n/a	n/a	n/a	n/a	n/a	n/a
Celltech R and D Curated by ChEMBL					Assay Description In vitro inhibitory concentration against inosine-5'-monophosphate dehydrogenase				Bioorg Med Chem Lett 15: 751-4 (2005) Article DOI: 10.1016/j.bmcl.2004.11.015 BindingDB Entry DOI: 10.7270/Q2RN37CZ
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50160367 (7-Methoxy-3-methyl-6-oxazol-5-yl-1H-quinazoline-2,...) Show SMILES COc1cc2[nH]c(=O)n(C)c(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C13H11N3O4/c1-16-12(17)7-3-8(11-5-14-6-20-11)10(19-2)4-9(7)15-13(16)18/h3-6H,1-2H3,(H,15,18)	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	104	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174793 (CHEMBL371533 | tert-butyl 7'-methoxy-6'-(1,3-oxazo...) Show SMILES COc1cc2NC3(CCN(C3)C(=O)OC(C)(C)C)N(C)C(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C21H26N4O5/c1-20(2,3)30-19(27)25-7-6-21(11-25)23-15-9-16(28-5)14(17-10-22-12-29-17)8-13(15)18(26)24(21)4/h8-10,12,23H,6-7,11H2,1-5H3	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	104	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174798 (CHEMBL373029 | N-ethyl-7'-methoxy-3'-methyl-6'-(1,...) Show SMILES CCNC(=O)N1CCC2(C1)Nc1cc(OC)c(cc1C(=O)N2C)-c1cnco1 Show InChI InChI=1S/C19H23N5O4/c1-4-21-18(26)24-6-5-19(10-24)22-14-8-15(27-3)13(16-9-20-11-28-16)7-12(14)17(25)23(19)2/h7-9,11,22H,4-6,10H2,1-3H3,(H,21,26)	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	119	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50160369 (7-Methoxy-6-oxazol-5-yl-3-(2-pyridin-4-yl-ethyl)-1...) Show SMILES COc1cc2[nH]c(=O)n(CCc3ccncc3)c(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C19H16N4O4/c1-26-16-9-15-13(8-14(16)17-10-21-11-27-17)18(24)23(19(25)22-15)7-4-12-2-5-20-6-3-12/h2-3,5-6,8-11H,4,7H2,1H3,(H,22,25)	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	188	n/a	n/a	n/a	n/a	n/a	n/a
Celltech R and D Curated by ChEMBL					Assay Description In vitro inhibitory concentration against inosine-5'-monophosphate dehydrogenase				Bioorg Med Chem Lett 15: 751-4 (2005) Article DOI: 10.1016/j.bmcl.2004.11.015 BindingDB Entry DOI: 10.7270/Q2RN37CZ
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174786 (7-methoxy-2,2,3-trimethyl-6-(oxazol-5-yl)-2,3-dihy...) Show SMILES COc1cc2NC(C)(C)N(C)C(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C15H17N3O3/c1-15(2)17-11-6-12(20-4)10(13-7-16-8-21-13)5-9(11)14(19)18(15)3/h5-8,17H,1-4H3	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	192	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50160380 (7-Methoxy-3-(2-morpholin-4-yl-ethyl)-6-oxazol-5-yl...) Show SMILES COc1cc2[nH]c(=O)n(CCN3CCOCC3)c(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C18H20N4O5/c1-25-15-9-14-12(8-13(15)16-10-19-11-27-16)17(23)22(18(24)20-14)3-2-21-4-6-26-7-5-21/h8-11H,2-7H2,1H3,(H,20,24)	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	297	n/a	n/a	n/a	n/a	n/a	n/a
Celltech R and D Curated by ChEMBL					Assay Description In vitro inhibitory concentration against inosine-5'-monophosphate dehydrogenase				Bioorg Med Chem Lett 15: 751-4 (2005) Article DOI: 10.1016/j.bmcl.2004.11.015 BindingDB Entry DOI: 10.7270/Q2RN37CZ
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174780 (7-methoxy-2,2-dimethyl-6-(oxazol-5-yl)-3-(2-(pyrid...) Show SMILES COc1cc2NC(C)(C)N(CCc3ccncc3)C(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C21H22N4O3/c1-21(2)24-17-11-18(27-3)16(19-12-23-13-28-19)10-15(17)20(26)25(21)9-6-14-4-7-22-8-5-14/h4-5,7-8,10-13,24H,6,9H2,1-3H3	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	300	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174784 (7'-methoxy-3'-methyl-6'-(1,3-oxazol-5-yl)-1'H-spir...) Show SMILES COc1cc2NC3(CCCC3)N(C)C(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C17H19N3O3/c1-20-16(21)11-7-12(15-9-18-10-23-15)14(22-2)8-13(11)19-17(20)5-3-4-6-17/h7-10,19H,3-6H2,1-2H3	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	328	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174799 (1-tert-butyl 5-methyl (3S,5S)-7'-methoxy-3'-methyl...) Show SMILES COC(=O)[C@@H]1C[C@]2(CN1C(=O)OC(C)(C)C)Nc1cc(OC)c(cc1C(=O)N2C)-c1cnco1 Show InChI InChI=1S/C23H28N4O7/c1-22(2,3)34-21(30)27-11-23(9-16(27)20(29)32-6)25-15-8-17(31-5)14(18-10-24-12-33-18)7-13(15)19(28)26(23)4/h7-8,10,12,16,25H,9,11H2,1-6H3/t16-,23-/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	369	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174797 (7'-methoxy-3'-methyl-6'-(1,3-oxazol-5-yl)-4'-oxo-N...) Show SMILES COc1cc2NC3(CCN(C3)C(=O)Nc3ccccc3)N(C)C(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C23H23N5O4/c1-27-21(29)16-10-17(20-12-24-14-32-20)19(31-2)11-18(16)26-23(27)8-9-28(13-23)22(30)25-15-6-4-3-5-7-15/h3-7,10-12,14,26H,8-9,13H2,1-2H3,(H,25,30)	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	393	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174787 (7'-methoxy-3'-methyl-6'-(1,3-oxazol-5-yl)-2,3,5,6-...) Show SMILES COc1cc2NC3(CCOCC3)N(C)C(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C17H19N3O4/c1-20-16(21)11-7-12(15-9-18-10-24-15)14(22-2)8-13(11)19-17(20)3-5-23-6-4-17/h7-10,19H,3-6H2,1-2H3	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	526	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50160377 (3-(2,2-Dimethyl-propyl)-7-methoxy-6-oxazol-5-yl-2-...) Show SMILES COc1cc2[nH]c(=S)n(CC(C)(C)C)c(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C17H19N3O3S/c1-17(2,3)8-20-15(21)10-5-11(14-7-18-9-23-14)13(22-4)6-12(10)19-16(20)24/h5-7,9H,8H2,1-4H3,(H,19,24)	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	821	n/a	n/a	n/a	n/a	n/a	n/a
Celltech R and D Curated by ChEMBL					Assay Description In vitro inhibitory concentration against inosine-5'-monophosphate dehydrogenase				Bioorg Med Chem Lett 15: 751-4 (2005) Article DOI: 10.1016/j.bmcl.2004.11.015 BindingDB Entry DOI: 10.7270/Q2RN37CZ
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50174794 (1-tert-butyl 5-methyl (3R,5S)-7'-methoxy-3'-methyl...) Show SMILES COC(=O)[C@@H]1C[C@@]2(CN1C(=O)OC(C)(C)C)Nc1cc(OC)c(cc1C(=O)N2C)-c1cnco1 Show InChI InChI=1S/C23H28N4O7/c1-22(2,3)34-21(30)27-11-23(9-16(27)20(29)32-6)25-15-8-17(31-5)14(18-10-24-12-33-18)7-13(15)19(28)26(23)4/h7-8,10,12,16,25H,9,11H2,1-6H3/t16-,23+/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	948	n/a	n/a	n/a	n/a	n/a	n/a
UCB Celltech Curated by ChEMBL					Assay Description Inhibitory activity against IMPDH II				Bioorg Med Chem Lett 15: 5335-9 (2005) Article DOI: 10.1016/j.bmcl.2005.06.108 BindingDB Entry DOI: 10.7270/Q2CZ36P8
					More data for this Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase 2 (Homo sapiens (Human))	BDBM50160376 (7-Methoxy-6-oxazol-5-yl-3-pyridin-3-yl-2-thioxo-2,...) Show SMILES COc1cc2[nH]c(=S)n(-c3cccnc3)c(=O)c2cc1-c1cnco1 Show InChI InChI=1S/C17H12N4O3S/c1-23-14-6-13-11(5-12(14)15-8-19-9-24-15)16(22)21(17(25)20-13)10-3-2-4-18-7-10/h2-9H,1H3,(H,20,25)	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	1.71E+3	n/a	n/a	n/a	n/a	n/a	n/a
Celltech R and D Curated by ChEMBL					Assay Description In vitro inhibitory concentration against inosine-5'-monophosphate dehydrogenase				Bioorg Med Chem Lett 15: 751-4 (2005) Article DOI: 10.1016/j.bmcl.2004.11.015 BindingDB Entry DOI: 10.7270/Q2RN37CZ
					More data for this Ligand-Target Pair
Taste receptor type 1 member 1/3 (Homo sapiens (Human))	BDBM525923 (US11185100, TABLE 6.1) Show SMILES Nc1ncnc2n(cnc12)[C@H]1C[C@@H](OP(O)(O)=O)[C@@H](COP(O)(O)=O)O1 |r| Show InChI	UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	2.00E+4	n/a	n/a	n/a	n/a
TBA					Assay Description HEK293 cells that stably express T1R3 and inducibly express T1R1 were exposed to nucleotide derivatives alone to activate the umami receptor. Activat...				Citation and Details BindingDB Entry DOI: 10.7270/Q2KP859X
					More data for this Ligand-Target Pair
Taste receptor type 1 member 1/3 (Homo sapiens (Human))	BDBM525923 (US11185100, TABLE 6.1) Show SMILES Nc1ncnc2n(cnc12)[C@H]1C[C@@H](OP(O)(O)=O)[C@@H](COP(O)(O)=O)O1 |r| Show InChI	UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	2.00E+4	n/a	n/a	n/a	n/a
TBA					Assay Description The concentration of alanine is 20 mM.				Citation and Details BindingDB Entry DOI: 10.7270/Q2KP859X
					More data for this Ligand-Target Pair
Taste receptor type 1 member 1/3 (Homo sapiens (Human))	BDBM525931 (US11185100, TABLE 6.2) Show SMILES O[C@@H]1[C@@H](COP([O-])(=O)OP([O-])([O-])=O)O[C@H]([C@@H]1O)n1cnc2c1nc[nH]c2=O |r| Show InChI	UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase KEGG PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	6.50E+5	n/a	n/a	n/a	n/a
TBA					Assay Description The concentration of alanine is 20 mM.				Citation and Details BindingDB Entry DOI: 10.7270/Q2KP859X
					More data for this Ligand-Target Pair
Taste receptor type 1 member 1/3 (Homo sapiens (Human))	BDBM525941 (US11185100, TABLE 6.3) Show SMILES Nc1nc2n(cnc2c(=O)[nH]1)[C@@H]1O[C@H](COP(O)(O)=O)[C@H](O)C1O |r| Show InChI	UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	7.00E+4	n/a	n/a	n/a	n/a
TBA					Assay Description HEK293 cells that stably express T1R3 and inducibly express T1R1 were exposed to nucleotide derivatives alone to activate the umami receptor. Activat...				Citation and Details BindingDB Entry DOI: 10.7270/Q2KP859X
					More data for this Ligand-Target Pair
Taste receptor type 1 member 1/3 (Homo sapiens (Human))	BDBM525941 (US11185100, TABLE 6.3) Show SMILES Nc1nc2n(cnc2c(=O)[nH]1)[C@@H]1O[C@H](COP(O)(O)=O)[C@H](O)C1O |r| Show InChI	UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	1.40E+5	n/a	n/a	n/a	n/a
TBA					Assay Description The concentration of alanine is 20 mM.				Citation and Details BindingDB Entry DOI: 10.7270/Q2KP859X
					More data for this Ligand-Target Pair
Taste receptor type 1 member 1/3 (Homo sapiens (Human))	BDBM525941 (US11185100, TABLE 6.3) Show SMILES Nc1nc2n(cnc2c(=O)[nH]1)[C@@H]1O[C@H](COP(O)(O)=O)[C@H](O)C1O |r| Show InChI	UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	>3.00E+6	n/a	n/a	n/a	n/a
TBA					Assay Description The concentration of IMP is 0.2 mM.				Citation and Details BindingDB Entry DOI: 10.7270/Q2KP859X
					More data for this Ligand-Target Pair
Taste receptor type 1 member 1/3 (Homo sapiens (Human))	BDBM525941 (US11185100, TABLE 6.3) Show SMILES Nc1nc2n(cnc2c(=O)[nH]1)[C@@H]1O[C@H](COP(O)(O)=O)[C@H](O)C1O |r| Show InChI	UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	>3.00E+6	n/a	n/a	n/a	n/a
TBA					Assay Description The concentration of alanine is 20 mM, and the concentration of IMP is 0.2 mM.				Citation and Details BindingDB Entry DOI: 10.7270/Q2KP859X
					More data for this Ligand-Target Pair
Taste receptor type 1 member 1/3 (Homo sapiens (Human))	BDBM525945 (US11185100, TABLE 6.4) Show SMILES O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)OC([C@@H]1O)n1cnc2c1[nH]cnc2=O |r| Show InChI	UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	5.00E+4	n/a	n/a	n/a	n/a
TBA					Assay Description HEK293 cells that stably express T1R3 and inducibly express T1R1 were exposed to nucleotide derivatives alone to activate the umami receptor. Activat...				Citation and Details BindingDB Entry DOI: 10.7270/Q2KP859X
					More data for this Ligand-Target Pair
Taste receptor type 1 member 1/3 (Homo sapiens (Human))	BDBM525945 (US11185100, TABLE 6.4) Show SMILES O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)OC([C@@H]1O)n1cnc2c1[nH]cnc2=O |r| Show InChI	UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	8.00E+4	n/a	n/a	n/a	n/a
TBA					Assay Description The concentration of alanine is 20 mM.				Citation and Details BindingDB Entry DOI: 10.7270/Q2KP859X
					More data for this Ligand-Target Pair
Taste receptor type 1 member 1/3 (Homo sapiens (Human))	BDBM525945 (US11185100, TABLE 6.4) Show SMILES O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)OC([C@@H]1O)n1cnc2c1[nH]cnc2=O |r| Show InChI	UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	2.00E+4	n/a	n/a	n/a	n/a
TBA					Assay Description The concentration of IMP is 0.2 mM.				Citation and Details BindingDB Entry DOI: 10.7270/Q2KP859X
					More data for this Ligand-Target Pair
Taste receptor type 1 member 1/3 (Homo sapiens (Human))	BDBM525945 (US11185100, TABLE 6.4) Show SMILES O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)OC([C@@H]1O)n1cnc2c1[nH]cnc2=O |r| Show InChI	UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	3.00E+4	n/a	n/a	n/a	n/a
TBA					Assay Description The concentration of alanine is 20 mM, and the concentration of IMP is 0.2 mM.				Citation and Details BindingDB Entry DOI: 10.7270/Q2KP859X
					More data for this Ligand-Target Pair
Taste receptor type 1 member 1/3 (Homo sapiens (Human))	BDBM525952 (US11185100, TABLE 6.5) Show SMILES O[C@H]1[C@@H](COP(O)(O)=O)O[C@H](C1O)n1cnc2c(Nc3ccccc3)ncnc12 |r| Show InChI	UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a
TBA					Assay Description HEK293 cells that stably express T1R3 and inducibly express T1R1 were exposed to nucleotide derivatives alone to activate the umami receptor. Activat...				Citation and Details BindingDB Entry DOI: 10.7270/Q2KP859X
					More data for this Ligand-Target Pair
Taste receptor type 1 member 1/3 (Homo sapiens (Human))	BDBM525952 (US11185100, TABLE 6.5) Show SMILES O[C@H]1[C@@H](COP(O)(O)=O)O[C@H](C1O)n1cnc2c(Nc3ccccc3)ncnc12 |r| Show InChI	UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a
TBA					Assay Description The concentration of alanine is 20 mM.				Citation and Details BindingDB Entry DOI: 10.7270/Q2KP859X
					More data for this Ligand-Target Pair
Taste receptor type 1 member 1/3 (Homo sapiens (Human))	BDBM525952 (US11185100, TABLE 6.5) Show SMILES O[C@H]1[C@@H](COP(O)(O)=O)O[C@H](C1O)n1cnc2c(Nc3ccccc3)ncnc12 |r| Show InChI	UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	7.20E+5	n/a	n/a	n/a	n/a
TBA					Assay Description The concentration of IMP is 0.2 mM.				Citation and Details BindingDB Entry DOI: 10.7270/Q2KP859X
					More data for this Ligand-Target Pair
Taste receptor type 1 member 1/3 (Homo sapiens (Human))	BDBM525952 (US11185100, TABLE 6.5) Show SMILES O[C@H]1[C@@H](COP(O)(O)=O)O[C@H](C1O)n1cnc2c(Nc3ccccc3)ncnc12 |r| Show InChI	UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a
TBA					Assay Description The concentration of alanine is 20 mM, and the concentration of IMP is 0.2 mM.				Citation and Details BindingDB Entry DOI: 10.7270/Q2KP859X
					More data for this Ligand-Target Pair

Displayed 1 to 50 (of 106 total )  |  Next  |  Last  >>

Jump to: