Compile Data Set for Download or QSAR

Found 20 hits of affinity data for UniProtKB/TrEMBL: P07379   

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
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM181109 (3-Mercaptopicolinic acid (MPA)) Show SMILES OC(=O)c1ncccc1S Show InChI InChI=1S/C6H5NO2S/c8-6(9)5-4(10)2-1-3-7-5/h1-3,10H,(H,8,9)	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem	PDB Article PubMed	3.70E+4	-25.3	n/a	n/a	n/a	n/a	n/a	n/a	25
The University of Kansas Medical Center					Assay Description OAA/PEP binding site. When the enzyme was assayed in the direction of PEP →OAA, the standard reaction mixture contained 50 mM HEPES (pH 7.5), 2...				Biochemistry 54: 5878-87 (2015) Article DOI: 10.1021/acs.biochem.5b00822 BindingDB Entry DOI: 10.7270/Q2M61J1Q
					More data for this Ligand-Target Pair				3D Structure (crystal)
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] [H477R] (Rattus norvegicus (Rat))	BDBM223201 (β-Sulfopyruvate) Show SMILES OC(=O)C(=O)CS(O)(=O)=O Show InChI InChI=1S/C3H4O6S/c4-2(3(5)6)1-10(7,8)9/h1H2,(H,5,6)(H,7,8,9)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	DrugBank KEGG PC cid PC sid PDB UniChem	PDB Article PubMed	3.70E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Waterloo					Assay Description The inhibition of H477R PEPCK by β-sulfopyruvate (βSP), oxalate, and GMPPCP was conducted in the direction of PEP synthesis (OAA → PE...				Biochemistry 56: 2106-2115 (2017) Article DOI: 10.1021/acs.biochem.7b00178 BindingDB Entry DOI: 10.7270/Q2D50KTV
					More data for this Ligand-Target Pair				3D Structure (crystal)
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM181109 (3-Mercaptopicolinic acid (MPA)) Show SMILES OC(=O)c1ncccc1S Show InChI InChI=1S/C6H5NO2S/c8-6(9)5-4(10)2-1-3-7-5/h1-3,10H,(H,8,9)	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem	PDB Article PubMed	4.50E+4	-24.8	n/a	n/a	n/a	n/a	n/a	n/a	25
The University of Kansas Medical Center					Assay Description OAA/PEP binding site. The activity of PEPCK in the direction from OAA to PEP was assayed with 50 mM HEPES (pH 7.5), 10 mM DTT, 4 mM MgCl2, 0.5 mM GTP...				Biochemistry 54: 5878-87 (2015) Article DOI: 10.1021/acs.biochem.5b00822 BindingDB Entry DOI: 10.7270/Q2M61J1Q
					More data for this Ligand-Target Pair				3D Structure (crystal)
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM181109 (3-Mercaptopicolinic acid (MPA)) Show SMILES OC(=O)c1ncccc1S Show InChI InChI=1S/C6H5NO2S/c8-6(9)5-4(10)2-1-3-7-5/h1-3,10H,(H,8,9)	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem	PDB Article PubMed	8.30E+4	-23.3	n/a	n/a	n/a	n/a	n/a	n/a	25
The University of Kansas Medical Center					Assay Description Allosteric binding site. When the enzyme was assayed in the direction of PEP →OAA, the standard reaction mixture contained 50 mM HEPES (pH 7.5)...				Biochemistry 54: 5878-87 (2015) Article DOI: 10.1021/acs.biochem.5b00822 BindingDB Entry DOI: 10.7270/Q2M61J1Q
					More data for this Ligand-Target Pair				3D Structure (crystal)
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM181109 (3-Mercaptopicolinic acid (MPA)) Show SMILES OC(=O)c1ncccc1S Show InChI InChI=1S/C6H5NO2S/c8-6(9)5-4(10)2-1-3-7-5/h1-3,10H,(H,8,9)	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem	PDB Article PubMed	8.30E+4	-23.3	n/a	n/a	n/a	n/a	n/a	n/a	25
The University of Kansas Medical Center					Assay Description OAA/PEP binding site. When the enzyme was assayed in the direction of PEP →OAA, the standard reaction mixture contained 50 mM HEPES (pH 7.5), 2...				Biochemistry 54: 5878-87 (2015) Article DOI: 10.1021/acs.biochem.5b00822 BindingDB Entry DOI: 10.7270/Q2M61J1Q
					More data for this Ligand-Target Pair				3D Structure (crystal)
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM181109 (3-Mercaptopicolinic acid (MPA)) Show SMILES OC(=O)c1ncccc1S Show InChI InChI=1S/C6H5NO2S/c8-6(9)5-4(10)2-1-3-7-5/h1-3,10H,(H,8,9)	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem	PDB Article PubMed	1.21E+5	-22.4	n/a	n/a	n/a	n/a	n/a	n/a	25
The University of Kansas Medical Center					Assay Description Allosteric binding site. The activity of PEPCK in the direction from OAA to PEP was assayed with 50 mM HEPES (pH 7.5), 10 mM DTT, 4 mM MgCl2, 0.5 mM ...				Biochemistry 54: 5878-87 (2015) Article DOI: 10.1021/acs.biochem.5b00822 BindingDB Entry DOI: 10.7270/Q2M61J1Q
					More data for this Ligand-Target Pair				3D Structure (crystal)
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM223202 (β,γ-methyleneguanosine 5′-triphosp...) Show SMILES Nc1nc([O-])c2ncn([C@@H]3O[C@H](COP(O)(=O)OP(O)(=O)C[P+](O)(O)[O-])[C@@H](O)[C@H]3O)c2n1 Show InChI InChI=1S/C11H18N5O13P3/c12-11-14-8-5(9(19)15-11)13-2-16(8)10-7(18)6(17)4(28-10)1-27-32(25,26)29-31(23,24)3-30(20,21)22/h2,4,6-7,10,17-18H,1,3H2,(H,23,24)(H,25,26)(H2,20,21,22)(H3,12,14,15,19)/p-1/t4-,6-,7-,10-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Waterloo					Assay Description The inhibition of H477R PEPCK by β-sulfopyruvate (βSP), oxalate, and GMPPCP was conducted in the direction of PEP synthesis (OAA → PE...				Biochemistry 56: 2106-2115 (2017) Article DOI: 10.1021/acs.biochem.7b00178 BindingDB Entry DOI: 10.7270/Q2D50KTV
					More data for this Ligand-Target Pair
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM181109 (3-Mercaptopicolinic acid (MPA)) Show SMILES OC(=O)c1ncccc1S Show InChI InChI=1S/C6H5NO2S/c8-6(9)5-4(10)2-1-3-7-5/h1-3,10H,(H,8,9)	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem	PDB Article PubMed	1.80E+5	-21.4	n/a	n/a	n/a	n/a	n/a	n/a	25
The University of Kansas Medical Center					Assay Description Allosteric binding site. When the enzyme was assayed in the direction of PEP →OAA, the standard reaction mixture contained 50 mM HEPES (pH 7.5)...				Biochemistry 54: 5878-87 (2015) Article DOI: 10.1021/acs.biochem.5b00822 BindingDB Entry DOI: 10.7270/Q2M61J1Q
					More data for this Ligand-Target Pair				3D Structure (crystal)
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] [H477R] (Rattus norvegicus (Rat))	BDBM50366413 (PHOSPHOENOLPYRUVATE) Show SMILES OC(=O)C(=C)OP(O)(O)=O Show InChI InChI=1S/C3H5O6P/c1-2(3(4)5)9-10(6,7)8/h1H2,(H,4,5)(H2,6,7,8)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Similars	PDB Article PubMed	2.89E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Waterloo					Assay Description The inhibition of H477R PEPCK by β-sulfopyruvate (βSP), oxalate, and GMPPCP was conducted in the direction of PEP synthesis (OAA → PE...				Biochemistry 56: 2106-2115 (2017) Article DOI: 10.1021/acs.biochem.7b00178 BindingDB Entry DOI: 10.7270/Q2D50KTV
					More data for this Ligand-Target Pair				3D Structure (crystal)
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] [H477R] (Rattus norvegicus (Rat))	BDBM23230 (2-Oxosuccinic acid | 2-oxobutanedioic acid | Oxalo...) Show SMILES OC(=O)CC(=O)C(O)=O Show InChI InChI=1S/C4H4O5/c5-2(4(8)9)1-3(6)7/h1H2,(H,6,7)(H,8,9)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase MCE KEGG MMDB PC cid PC sid PDB UniChem Patents	PDB Article PubMed	4.41E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Waterloo					Assay Description The inhibition of H477R PEPCK by β-sulfopyruvate (βSP), oxalate, and GMPPCP was conducted in the direction of PEP synthesis (OAA → PE...				Biochemistry 56: 2106-2115 (2017) Article DOI: 10.1021/acs.biochem.7b00178 BindingDB Entry DOI: 10.7270/Q2D50KTV
					More data for this Ligand-Target Pair				3D Structure (crystal)
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] [H477R] (Rattus norvegicus (Rat))	BDBM223202 (β,γ-methyleneguanosine 5′-triphosp...) Show SMILES Nc1nc([O-])c2ncn([C@@H]3O[C@H](COP(O)(=O)OP(O)(=O)C[P+](O)(O)[O-])[C@@H](O)[C@H]3O)c2n1 Show InChI InChI=1S/C11H18N5O13P3/c12-11-14-8-5(9(19)15-11)13-2-16(8)10-7(18)6(17)4(28-10)1-27-32(25,26)29-31(23,24)3-30(20,21)22/h2,4,6-7,10,17-18H,1,3H2,(H,23,24)(H,25,26)(H2,20,21,22)(H3,12,14,15,19)/p-1/t4-,6-,7-,10-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	6.96E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Waterloo					Assay Description The inhibition of H477R PEPCK by β-sulfopyruvate (βSP), oxalate, and GMPPCP was conducted in the direction of PEP synthesis (OAA → PE...				Biochemistry 56: 2106-2115 (2017) Article DOI: 10.1021/acs.biochem.7b00178 BindingDB Entry DOI: 10.7270/Q2D50KTV
					More data for this Ligand-Target Pair
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM50133801 (CHEMBL120708 | N-(4-((1-(2-fluorobenzyl)-3-butyl-2...) Show SMILES CCCCn1c2nc(Cc3ccc(NC(C)=O)cc3)[nH]c2c(=O)n(Cc2ccccc2F)c1=O Show InChI InChI=1S/C25H26FN5O3/c1-3-4-13-30-23-22(24(33)31(25(30)34)15-18-7-5-6-8-20(18)26)28-21(29-23)14-17-9-11-19(12-10-17)27-16(2)32/h5-12H,3-4,13-15H2,1-2H3,(H,27,32)(H,28,29)	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	n/a	n/a	8.60E+3	n/a	n/a	n/a	n/a
Roche Research Center Curated by ChEMBL					Assay Description Inhibition of cPEPCK in rat H4IIE cells assessed as effect on glucose production				Bioorg Med Chem Lett 17: 3835-9 (2007) Article DOI: 10.1016/j.bmcl.2007.05.013 BindingDB Entry DOI: 10.7270/Q2BV7HF1
					More data for this Ligand-Target Pair				3D Structure (crystal)
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM50214004 (CHEMBL243116 | N-(4-((1-(2-fluorobenzyl)-3-butyl-2...) Show SMILES CCCCn1c2nc(Cc3ccc(NS(=O)(=O)c4c(C)nn(C)c4Cl)cc3)[nH]c2c(=O)n(Cc2ccccc2F)c1=O Show InChI InChI=1S/C28H29ClFN7O4S/c1-4-5-14-36-26-23(27(38)37(28(36)39)16-19-8-6-7-9-21(19)30)31-22(32-26)15-18-10-12-20(13-11-18)34-42(40,41)24-17(2)33-35(3)25(24)29/h6-13,34H,4-5,14-16H2,1-3H3,(H,31,32)	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	3.97E+3	n/a	n/a	n/a	n/a
Roche Research Center Curated by ChEMBL					Assay Description Inhibition of cPEPCK in rat H4IIE cells assessed as effect on glucose production				Bioorg Med Chem Lett 17: 3835-9 (2007) Article DOI: 10.1016/j.bmcl.2007.05.013 BindingDB Entry DOI: 10.7270/Q2BV7HF1
					More data for this Ligand-Target Pair
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM50214012 (CHEMBL394368 | N-(4-((1-(2-fluorobenzyl)-3-(cyclop...) Show SMILES Cc1noc(C)c1S(=O)(=O)Nc1ccc(Cc2nc3n(CC4CC4)c(=O)n(Cc4ccccc4F)c(=O)c3[nH]2)cc1 Show InChI InChI=1S/C28H27FN6O5S/c1-16-25(17(2)40-32-16)41(38,39)33-21-11-9-18(10-12-21)13-23-30-24-26(31-23)34(14-19-7-8-19)28(37)35(27(24)36)15-20-5-3-4-6-22(20)29/h3-6,9-12,19,33H,7-8,13-15H2,1-2H3,(H,30,31)	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	3.40E+3	n/a	n/a	n/a	n/a
Roche Research Center Curated by ChEMBL					Assay Description Inhibition of cPEPCK in rat H4IIE cells assessed as effect on glucose production				Bioorg Med Chem Lett 17: 3835-9 (2007) Article DOI: 10.1016/j.bmcl.2007.05.013 BindingDB Entry DOI: 10.7270/Q2BV7HF1
					More data for this Ligand-Target Pair
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM50214013 (CHEMBL242486 | N-(4-((1-(2-fluorobenzyl)-3-(cyclop...) Show SMILES Fc1ccccc1Cn1c(=O)n(CC2CC2)c2nc(Cc3ccc(NS(=O)(=O)c4cccnc4)cc3)[nH]c2c1=O Show InChI InChI=1S/C28H25FN6O4S/c29-23-6-2-1-4-20(23)17-35-27(36)25-26(34(28(35)37)16-19-7-8-19)32-24(31-25)14-18-9-11-21(12-10-18)33-40(38,39)22-5-3-13-30-15-22/h1-6,9-13,15,19,33H,7-8,14,16-17H2,(H,31,32)	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	5.50E+3	n/a	n/a	n/a	n/a
Roche Research Center Curated by ChEMBL					Assay Description Inhibition of cPEPCK in rat H4IIE cells assessed as effect on glucose production				Bioorg Med Chem Lett 17: 3835-9 (2007) Article DOI: 10.1016/j.bmcl.2007.05.013 BindingDB Entry DOI: 10.7270/Q2BV7HF1
					More data for this Ligand-Target Pair
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM50214016 (CHEMBL243342 | N-(4-((1-(2-fluorobenzyl)-3-(cyclop...) Show SMILES Cc1nc(N)sc1S(=O)(=O)Nc1ccc(Cc2nc3n(CC4CC4)c(=O)n(Cc4ccccc4F)c(=O)c3[nH]2)cc1 Show InChI InChI=1S/C27H26FN7O4S2/c1-15-25(40-26(29)30-15)41(38,39)33-19-10-8-16(9-11-19)12-21-31-22-23(32-21)34(13-17-6-7-17)27(37)35(24(22)36)14-18-4-2-3-5-20(18)28/h2-5,8-11,17,33H,6-7,12-14H2,1H3,(H2,29,30)(H,31,32)	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	8.20E+3	n/a	n/a	n/a	n/a
Roche Research Center Curated by ChEMBL					Assay Description Inhibition of cPEPCK in rat H4IIE cells assessed as effect on glucose production				Bioorg Med Chem Lett 17: 3835-9 (2007) Article DOI: 10.1016/j.bmcl.2007.05.013 BindingDB Entry DOI: 10.7270/Q2BV7HF1
					More data for this Ligand-Target Pair
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM50214010 (CHEMBL244165 | N-(4-((1-(2-fluorobenzyl)-3-(cyclop...) Show SMILES CC(=O)Nc1ccc(Cc2nc3n(CC4CC4)c(=O)n(Cc4ccccc4F)c(=O)c3[nH]2)cc1 Show InChI InChI=1S/C25H24FN5O3/c1-15(32)27-19-10-8-16(9-11-19)12-21-28-22-23(29-21)30(13-17-6-7-17)25(34)31(24(22)33)14-18-4-2-3-5-20(18)26/h2-5,8-11,17H,6-7,12-14H2,1H3,(H,27,32)(H,28,29)	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	4.70E+3	n/a	n/a	n/a	n/a
Roche Research Center Curated by ChEMBL					Assay Description Inhibition of cPEPCK in rat H4IIE cells assessed as effect on glucose production				Bioorg Med Chem Lett 17: 3835-9 (2007) Article DOI: 10.1016/j.bmcl.2007.05.013 BindingDB Entry DOI: 10.7270/Q2BV7HF1
					More data for this Ligand-Target Pair
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM50214001 (CHEMBL389494 | N-(4-((1-(2-fluorobenzyl)-3-(cyclop...) Show SMILES Cc1nn(C)c(Cl)c1S(=O)(=O)Nc1ccc(Cc2nc3n(CC4CC4)c(=O)n(Cc4ccccc4F)c(=O)c3[nH]2)cc1 Show InChI InChI=1S/C28H27ClFN7O4S/c1-16-24(25(29)35(2)33-16)42(40,41)34-20-11-9-17(10-12-20)13-22-31-23-26(32-22)36(14-18-7-8-18)28(39)37(27(23)38)15-19-5-3-4-6-21(19)30/h3-6,9-12,18,34H,7-8,13-15H2,1-2H3,(H,31,32)	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	2.17E+3	n/a	n/a	n/a	n/a
Roche Research Center Curated by ChEMBL					Assay Description Inhibition of cPEPCK in rat H4IIE cells assessed as effect on glucose production				Bioorg Med Chem Lett 17: 3835-9 (2007) Article DOI: 10.1016/j.bmcl.2007.05.013 BindingDB Entry DOI: 10.7270/Q2BV7HF1
					More data for this Ligand-Target Pair
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM50214003 (CHEMBL243134 | N-(4-((1-(2-fluorobenzyl)-3-(cyclop...) Show SMILES Cn1cc(cn1)S(=O)(=O)Nc1ccc(Cc2nc3n(CC4CC4)c(=O)n(Cc4ccccc4F)c(=O)c3[nH]2)cc1 Show InChI InChI=1S/C27H26FN7O4S/c1-33-16-21(13-29-33)40(38,39)32-20-10-8-17(9-11-20)12-23-30-24-25(31-23)34(14-18-6-7-18)27(37)35(26(24)36)15-19-4-2-3-5-22(19)28/h2-5,8-11,13,16,18,32H,6-7,12,14-15H2,1H3,(H,30,31)	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	8.75E+3	n/a	n/a	n/a	n/a
Roche Research Center Curated by ChEMBL					Assay Description Inhibition of cPEPCK in rat H4IIE cells assessed as effect on glucose production				Bioorg Med Chem Lett 17: 3835-9 (2007) Article DOI: 10.1016/j.bmcl.2007.05.013 BindingDB Entry DOI: 10.7270/Q2BV7HF1
					More data for this Ligand-Target Pair
Phosphoenolpyruvate carboxykinase, cytosolic [GTP] (Rattus norvegicus (Rat))	BDBM50214007 (CHEMBL394621 | N-(4-((1-(2-fluorobenzyl)-3-(cyclop...) Show SMILES Cc1nn(C)cc1S(=O)(=O)Nc1ccc(Cc2nc3n(CC4CC4)c(=O)n(Cc4ccccc4F)c(=O)c3[nH]2)cc1 Show InChI InChI=1S/C28H28FN7O4S/c1-17-23(16-34(2)32-17)41(39,40)33-21-11-9-18(10-12-21)13-24-30-25-26(31-24)35(14-19-7-8-19)28(38)36(27(25)37)15-20-5-3-4-6-22(20)29/h3-6,9-12,16,19,33H,7-8,13-15H2,1-2H3,(H,30,31)	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	5.57E+3	n/a	n/a	n/a	n/a
Roche Research Center Curated by ChEMBL					Assay Description Inhibition of cPEPCK in rat H4IIE cells assessed as effect on glucose production				Bioorg Med Chem Lett 17: 3835-9 (2007) Article DOI: 10.1016/j.bmcl.2007.05.013 BindingDB Entry DOI: 10.7270/Q2BV7HF1
					More data for this Ligand-Target Pair