Compile Data Set for Download or QSAR

Found 125 hits with Last Name = 'cebula' and Initial = 'r'   

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
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372752 (CHEMBL272547) Show SMILES O=C(Nc1ccc(cc1)C1CCCCC1)C1C(=O)CC(Cc2ccccc2)NC1=O Show InChI InChI=1S/C25H28N2O3/c28-22-16-21(15-17-7-3-1-4-8-17)27-25(30)23(22)24(29)26-20-13-11-19(12-14-20)18-9-5-2-6-10-18/h1,3-4,7-8,11-14,18,21,23H,2,5-6,9-10,15-16H2,(H,26,29)(H,27,30)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	40	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372771 (CHEMBL404127) Show SMILES O=C(Nc1ccc(cc1)C1CCCCC1)C1C(=O)CC(NC1=O)C1CCCCC1 Show InChI InChI=1S/C24H32N2O3/c27-21-15-20(18-9-5-2-6-10-18)26-24(29)22(21)23(28)25-19-13-11-17(12-14-19)16-7-3-1-4-8-16/h11-14,16,18,20,22H,1-10,15H2,(H,25,28)(H,26,29)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372766 (CHEMBL271482) Show SMILES O=C(NC1CCCCC1)C1C(=O)CC(Cc2ccccc2)NC1=O Show InChI InChI=1S/C19H24N2O3/c22-16-12-15(11-13-7-3-1-4-8-13)21-19(24)17(16)18(23)20-14-9-5-2-6-10-14/h1,3-4,7-8,14-15,17H,2,5-6,9-12H2,(H,20,23)(H,21,24)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	70	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372754 (CHEMBL272054) Show SMILES O=C(Nc1ccc(cc1)C1CCCCC1)C1C(=O)C[C@H](NC1=O)c1ccccc1 Show InChI InChI=1S/C24H26N2O3/c27-21-15-20(18-9-5-2-6-10-18)26-24(29)22(21)23(28)25-19-13-11-17(12-14-19)16-7-3-1-4-8-16/h2,5-6,9-14,16,20,22H,1,3-4,7-8,15H2,(H,25,28)(H,26,29)/t20-,22?/m0/s1	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	70	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372751 (CHEMBL256222) Show SMILES O=C(Nc1ccc(Oc2ccccc2)cc1)C1C(=O)CC(Cc2ccccc2)NC1=O Show InChI InChI=1S/C25H22N2O4/c28-22-16-19(15-17-7-3-1-4-8-17)27-25(30)23(22)24(29)26-18-11-13-21(14-12-18)31-20-9-5-2-6-10-20/h1-14,19,23H,15-16H2,(H,26,29)(H,27,30)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	110	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372750 (CHEMBL272914) Show SMILES O=C(Nc1ccc(cc1)N1CCCCC1)C1C(=O)CC(Cc2ccccc2)NC1=O Show InChI InChI=1S/C24H27N3O3/c28-21-16-19(15-17-7-3-1-4-8-17)26-24(30)22(21)23(29)25-18-9-11-20(12-10-18)27-13-5-2-6-14-27/h1,3-4,7-12,19,22H,2,5-6,13-16H2,(H,25,29)(H,26,30)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	110	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372760 (CHEMBL257948) Show SMILES O=C(Nc1ccc(cc1)-c1ccccc1)C1C(=O)NC(CCc2ccccc2)C1=O Show InChI InChI=1S/C25H22N2O3/c28-23-21(16-11-17-7-3-1-4-8-17)27-25(30)22(23)24(29)26-20-14-12-19(13-15-20)18-9-5-2-6-10-18/h1-10,12-15,21-22H,11,16H2,(H,26,29)(H,27,30)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	120	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372767 (CHEMBL272913) Show SMILES FC(F)(F)c1ccc(NC(=O)C2C(=O)CC(Cc3ccccc3)NC2=O)cn1 Show InChI InChI=1S/C19H16F3N3O3/c20-19(21,22)15-7-6-12(10-23-15)24-17(27)16-14(26)9-13(25-18(16)28)8-11-4-2-1-3-5-11/h1-7,10,13,16H,8-9H2,(H,24,27)(H,25,28)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	140	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372762 (CHEMBL272162) Show SMILES O=C(Nc1ccc(cc1)C1CCCCC1)C1C(=O)NC(CCc2ccccc2)C1=O Show InChI InChI=1S/C25H28N2O3/c28-23-21(16-11-17-7-3-1-4-8-17)27-25(30)22(23)24(29)26-20-14-12-19(13-15-20)18-9-5-2-6-10-18/h1,3-4,7-8,12-15,18,21-22H,2,5-6,9-11,16H2,(H,26,29)(H,27,30)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	160	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372753 (CHEMBL271845) Show SMILES O=C(Nc1ccc(cc1)C1CCCCC1)C1C(=O)C[C@@H](NC1=O)c1ccccc1 Show InChI InChI=1S/C24H26N2O3/c27-21-15-20(18-9-5-2-6-10-18)26-24(29)22(21)23(28)25-19-13-11-17(12-14-19)16-7-3-1-4-8-16/h2,5-6,9-14,16,20,22H,1,3-4,7-8,15H2,(H,25,28)(H,26,29)/t20-,22?/m1/s1	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	180	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372780 (CHEMBL404126) Show SMILES CC(C)CC1CC(=O)C(C(=O)Nc2ccc(cc2)C2CCCCC2)C(=O)N1 Show InChI InChI=1S/C22H30N2O3/c1-14(2)12-18-13-19(25)20(22(27)24-18)21(26)23-17-10-8-16(9-11-17)15-6-4-3-5-7-15/h8-11,14-15,18,20H,3-7,12-13H2,1-2H3,(H,23,26)(H,24,27)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372753 (CHEMBL271845) Show SMILES O=C(Nc1ccc(cc1)C1CCCCC1)C1C(=O)C[C@@H](NC1=O)c1ccccc1 Show InChI InChI=1S/C24H26N2O3/c27-21-15-20(18-9-5-2-6-10-18)26-24(29)22(21)23(28)25-19-13-11-17(12-14-19)16-7-3-1-4-8-16/h2,5-6,9-14,16,20,22H,1,3-4,7-8,15H2,(H,25,28)(H,26,29)/t20-,22?/m1/s1	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372758 (CHEMBL269960) Show SMILES O=C(Nc1ccc(cc1)C1CCCCC1)C1C(=O)CN(Cc2ccccc2)C1=O Show InChI InChI=1S/C24H26N2O3/c27-21-16-26(15-17-7-3-1-4-8-17)24(29)22(21)23(28)25-20-13-11-19(12-14-20)18-9-5-2-6-10-18/h1,3-4,7-8,11-14,18,22H,2,5-6,9-10,15-16H2,(H,25,28)	PDB KEGG UniProtKB/SwissProt 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
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372755 (CHEMBL255828) Show SMILES O=C(Nc1ccc(cc1)C1CCCCC1)C1C(=O)OC(Cc2ccccc2)C1=O Show InChI InChI=1S/C24H25NO4/c26-22-20(15-16-7-3-1-4-8-16)29-24(28)21(22)23(27)25-19-13-11-18(12-14-19)17-9-5-2-6-10-17/h1,3-4,7-8,11-14,17,20-21H,2,5-6,9-10,15H2,(H,25,27)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372768 (CHEMBL272696) Show SMILES O=C(Nc1ccc(cc1)-n1ccnc1)C1C(=O)CC(Cc2ccccc2)NC1=O Show InChI InChI=1S/C22H20N4O3/c27-19-13-17(12-15-4-2-1-3-5-15)25-22(29)20(19)21(28)24-16-6-8-18(9-7-16)26-11-10-23-14-26/h1-11,14,17,20H,12-13H2,(H,24,28)(H,25,29)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	630	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372759 (CHEMBL256476) Show SMILES O=C(Nc1ccc(cc1)N1CCCCC1)C1C(=O)NC(CCc2ccccc2)C1=O Show InChI InChI=1S/C24H27N3O3/c28-22-20(14-9-17-7-3-1-4-8-17)26-24(30)21(22)23(29)25-18-10-12-19(13-11-18)27-15-5-2-6-16-27/h1,3-4,7-8,10-13,20-21H,2,5-6,9,14-16H2,(H,25,29)(H,26,30)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	800	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372770 (CHEMBL256223) Show SMILES O=C(Nc1ccc(Nc2ccccc2)cc1)C1C(=O)CC(Cc2ccccc2)NC1=O Show InChI InChI=1S/C25H23N3O3/c29-22-16-21(15-17-7-3-1-4-8-17)28-25(31)23(22)24(30)27-20-13-11-19(12-14-20)26-18-9-5-2-6-10-18/h1-14,21,23,26H,15-16H2,(H,27,30)(H,28,31)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372772 (CHEMBL271293) Show SMILES O=C(Nc1ccc(cc1)-c1ccccc1)C1C(=O)OC(Cc2ccccc2)C1=O Show InChI InChI=1S/C24H19NO4/c26-22-20(15-16-7-3-1-4-8-16)29-24(28)21(22)23(27)25-19-13-11-18(12-14-19)17-9-5-2-6-10-17/h1-14,20-21H,15H2,(H,25,27)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372761 (CHEMBL272163) Show SMILES CC(C)CC1NC(=O)C(C(=O)Nc2ccc(cc2)C2CCCCC2)C1=O Show InChI InChI=1S/C21H28N2O3/c1-13(2)12-17-19(24)18(21(26)23-17)20(25)22-16-10-8-15(9-11-16)14-6-4-3-5-7-14/h8-11,13-14,17-18H,3-7,12H2,1-2H3,(H,22,25)(H,23,26)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372778 (CHEMBL403226) Show SMILES O=C(Nc1ccc(cc1)C1CCCCC1)C1C(=O)NC(Cc2ccccc2)C1=O Show InChI InChI=1S/C24H26N2O3/c27-22-20(15-16-7-3-1-4-8-16)26-24(29)21(22)23(28)25-19-13-11-18(12-14-19)17-9-5-2-6-10-17/h1,3-4,7-8,11-14,17,20-21H,2,5-6,9-10,15H2,(H,25,28)(H,26,29)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372756 (CHEMBL404337) Show SMILES Clc1cc(Cl)cc(NC(=O)C2C(=O)OC(C2=O)c2ccccc2)c1 Show InChI InChI=1S/C17H11Cl2NO4/c18-10-6-11(19)8-12(7-10)20-16(22)13-14(21)15(24-17(13)23)9-4-2-1-3-5-9/h1-8,13,15H,(H,20,22)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372765 (CHEMBL256483) Show SMILES O=C(Nc1ccc(cc1)-n1ccnc1)C1C(=O)NCC(CC2CCCCC2)C1=O Show InChI InChI=1S/C22H26N4O3/c27-20-16(12-15-4-2-1-3-5-15)13-24-21(28)19(20)22(29)25-17-6-8-18(9-7-17)26-11-10-23-14-26/h6-11,14-16,19H,1-5,12-13H2,(H,24,28)(H,25,29)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372774 (CHEMBL270170) Show SMILES Fc1ccc(NC(=O)C2C(=O)NC(CCc3ccccc3)C2=O)cc1 Show InChI InChI=1S/C19H17FN2O3/c20-13-7-9-14(10-8-13)21-18(24)16-17(23)15(22-19(16)25)11-6-12-4-2-1-3-5-12/h1-5,7-10,15-16H,6,11H2,(H,21,24)(H,22,25)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372763 (CHEMBL272377) Show SMILES O=C(Nc1ccc(cc1)C1CCCCC1)C1C(=O)NC(C1=O)c1ccccc1 Show InChI InChI=1S/C23H24N2O3/c26-21-19(23(28)25-20(21)17-9-5-2-6-10-17)22(27)24-18-13-11-16(12-14-18)15-7-3-1-4-8-15/h2,5-6,9-15,19-20H,1,3-4,7-8H2,(H,24,27)(H,25,28)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
M-phase inducer phosphatase 1 (Homo sapiens (Human))	BDBM50289899 (CHEMBL292556 | Sulfuric acid mono-[5-phenyl-1-((1S...) Show SMILES CC1=CC[C@H]2C(C)(C)CCC[C@]2(C)[C@H]1CC(CCCCc1ccccc1)OS(O)(=O)=O |t:1| Show InChI InChI=1S/C26H40O4S/c1-20-15-16-24-25(2,3)17-10-18-26(24,4)23(20)19-22(30-31(27,28)29)14-9-8-13-21-11-6-5-7-12-21/h5-7,11-12,15,22-24H,8-10,13-14,16-19H2,1-4H3,(H,27,28,29)/t22?,23-,24-,26+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	3.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against Cdc25A phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
M-phase inducer phosphatase 1 (Homo sapiens (Human))	BDBM50289900 (CHEMBL303581 | Sulfuric acid mono-[5-furan-3-yl-1-...) Show SMILES CC1=CC[C@H]2C(C)(C)CCC[C@]2(C)[C@H]1CC(CCCCc1ccoc1)OS(O)(=O)=O |t:1| Show InChI InChI=1S/C24H38O5S/c1-18-10-11-22-23(2,3)13-7-14-24(22,4)21(18)16-20(29-30(25,26)27)9-6-5-8-19-12-15-28-17-19/h10,12,15,17,20-22H,5-9,11,13-14,16H2,1-4H3,(H,25,26,27)/t20?,21-,22-,24+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	4.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against Cdc25A phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
M-phase inducer phosphatase 1 (Homo sapiens (Human))	BDBM50289900 (CHEMBL303581 | Sulfuric acid mono-[5-furan-3-yl-1-...) Show SMILES CC1=CC[C@H]2C(C)(C)CCC[C@]2(C)[C@H]1CC(CCCCc1ccoc1)OS(O)(=O)=O |t:1| Show InChI InChI=1S/C24H38O5S/c1-18-10-11-22-23(2,3)13-7-14-24(22,4)21(18)16-20(29-30(25,26)27)9-6-5-8-19-12-15-28-17-19/h10,12,15,17,20-22H,5-9,11,13-14,16H2,1-4H3,(H,25,26,27)/t20?,21-,22-,24+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	4.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against Cdc25A phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372776 (CHEMBL428250) Show SMILES O=C(Nc1ccc(cc1)C1CCCCC1)C1C(=O)NC(Cc2ncc[nH]2)C1=O Show InChI InChI=1S/C21H24N4O3/c26-19-16(12-17-22-10-11-23-17)25-21(28)18(19)20(27)24-15-8-6-14(7-9-15)13-4-2-1-3-5-13/h6-11,13,16,18H,1-5,12H2,(H,22,23)(H,24,27)(H,25,28)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Dual specificity protein phosphatase 3 (Homo sapiens (Human))	BDBM50289899 (CHEMBL292556 | Sulfuric acid mono-[5-phenyl-1-((1S...) Show SMILES CC1=CC[C@H]2C(C)(C)CCC[C@]2(C)[C@H]1CC(CCCCc1ccccc1)OS(O)(=O)=O |t:1| Show InChI InChI=1S/C26H40O4S/c1-20-15-16-24-25(2,3)17-10-18-26(24,4)23(20)19-22(30-31(27,28)29)14-9-8-13-21-11-6-5-7-12-21/h5-7,11-12,15,22-24H,8-10,13-14,16-19H2,1-4H3,(H,27,28,29)/t22?,23-,24-,26+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	4.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against VHR phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
Dual specificity protein phosphatase 3 (Homo sapiens (Human))	BDBM50286608 (CHEMBL60072 | Sulfircin analogue | Sulfuric acid m...) Show SMILES C[C@H](CCCc1ccoc1)[C@H](C[C@H]1C(C)=CC[C@H]2C(C)(C)CCC[C@]12C)OS([O-])(=O)=O |c:15| Show InChI InChI=1S/C25H40O5S/c1-18-10-11-23-24(3,4)13-7-14-25(23,5)21(18)16-22(30-31(26,27)28)19(2)8-6-9-20-12-15-29-17-20/h10,12,15,17,19,21-23H,6-9,11,13-14,16H2,1-5H3,(H,26,27,28)/p-1/t19-,21+,22+,23+,25-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	4.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against VHR phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50289899 (CHEMBL292556 | Sulfuric acid mono-[5-phenyl-1-((1S...) Show SMILES CC1=CC[C@H]2C(C)(C)CCC[C@]2(C)[C@H]1CC(CCCCc1ccccc1)OS(O)(=O)=O |t:1| Show InChI InChI=1S/C26H40O4S/c1-20-15-16-24-25(2,3)17-10-18-26(24,4)23(20)19-22(30-31(27,28)29)14-9-8-13-21-11-6-5-7-12-21/h5-7,11-12,15,22-24H,8-10,13-14,16-19H2,1-4H3,(H,27,28,29)/t22?,23-,24-,26+/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	5.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against PTB1B phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
Dual specificity protein phosphatase 3 (Homo sapiens (Human))	BDBM50289906 (2-[3-Phenyl-1-((1S,2S,4aS,8aR)-2,5,5,8a-tetramethy...) Show SMILES C[C@H]1CC[C@H]2C(C)(C)CCC[C@]2(C)[C@H]1CC(CCc1ccccc1)C(C(O)=O)C(O)=O Show InChI InChI=1S/C27H40O4/c1-18-11-14-22-26(2,3)15-8-16-27(22,4)21(18)17-20(23(24(28)29)25(30)31)13-12-19-9-6-5-7-10-19/h5-7,9-10,18,20-23H,8,11-17H2,1-4H3,(H,28,29)(H,30,31)/t18-,20?,21-,22-,27+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	5.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against VHR phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
M-phase inducer phosphatase 1 (Homo sapiens (Human))	BDBM50289906 (2-[3-Phenyl-1-((1S,2S,4aS,8aR)-2,5,5,8a-tetramethy...) Show SMILES C[C@H]1CC[C@H]2C(C)(C)CCC[C@]2(C)[C@H]1CC(CCc1ccccc1)C(C(O)=O)C(O)=O Show InChI InChI=1S/C27H40O4/c1-18-11-14-22-26(2,3)15-8-16-27(22,4)21(18)17-20(23(24(28)29)25(30)31)13-12-19-9-6-5-7-10-19/h5-7,9-10,18,20-23H,8,11-17H2,1-4H3,(H,28,29)(H,30,31)/t18-,20?,21-,22-,27+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	6.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against Cdc25A phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
M-phase inducer phosphatase 1 (Homo sapiens (Human))	BDBM50286608 (CHEMBL60072 | Sulfircin analogue | Sulfuric acid m...) Show SMILES C[C@H](CCCc1ccoc1)[C@H](C[C@H]1C(C)=CC[C@H]2C(C)(C)CCC[C@]12C)OS([O-])(=O)=O |c:15| Show InChI InChI=1S/C25H40O5S/c1-18-10-11-23-24(3,4)13-7-14-25(23,5)21(18)16-22(30-31(26,27)28)19(2)8-6-9-20-12-15-29-17-20/h10,12,15,17,19,21-23H,6-9,11,13-14,16H2,1-5H3,(H,26,27,28)/p-1/t19-,21+,22+,23+,25-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	7.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against Cdc25A phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
Dual specificity protein phosphatase 3 (Homo sapiens (Human))	BDBM50289897 (CHEMBL60297 | Sulfuric acid mono-[5-furan-3-yl-2-m...) Show SMILES CC(CCCc1ccoc1)C(C[C@H]1C(C)=CC[C@H]2C(C)(C)CCC[C@]12C)OS(O)(=O)=O |c:15| Show InChI InChI=1S/C25H40O5S/c1-18-10-11-23-24(3,4)13-7-14-25(23,5)21(18)16-22(30-31(26,27)28)19(2)8-6-9-20-12-15-29-17-20/h10,12,15,17,19,21-23H,6-9,11,13-14,16H2,1-5H3,(H,26,27,28)/t19?,21-,22?,23-,25+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	7.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against VHR phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
Farnesyl pyrophosphate synthase (Homo sapiens (Human))	BDBM50372758 (CHEMBL269960) Show SMILES O=C(Nc1ccc(cc1)C1CCCCC1)C1C(=O)CN(Cc2ccccc2)C1=O Show InChI InChI=1S/C24H26N2O3/c27-21-16-26(15-17-7-3-1-4-8-17)24(29)22(21)23(28)25-20-13-11-19(12-14-20)18-9-5-2-6-10-18/h1,3-4,7-8,11-14,18,22H,2,5-6,9-10,15-16H2,(H,25,28)	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	8.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of human FPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
M-phase inducer phosphatase 1 (Homo sapiens (Human))	BDBM50289897 (CHEMBL60297 | Sulfuric acid mono-[5-furan-3-yl-2-m...) Show SMILES CC(CCCc1ccoc1)C(C[C@H]1C(C)=CC[C@H]2C(C)(C)CCC[C@]12C)OS(O)(=O)=O |c:15| Show InChI InChI=1S/C25H40O5S/c1-18-10-11-23-24(3,4)13-7-14-25(23,5)21(18)16-22(30-31(26,27)28)19(2)8-6-9-20-12-15-29-17-20/h10,12,15,17,19,21-23H,6-9,11,13-14,16H2,1-5H3,(H,26,27,28)/t19?,21-,22?,23-,25+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	8.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against Cdc25A phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372769 (CHEMBL256017) Show SMILES O=C(Nc1ccc(cc1)S(=O)(=O)c1ccccc1)C1C(=O)CC(Cc2ccccc2)NC1=O Show InChI InChI=1S/C25H22N2O5S/c28-22-16-19(15-17-7-3-1-4-8-17)27-25(30)23(22)24(29)26-18-11-13-21(14-12-18)33(31,32)20-9-5-2-6-10-20/h1-14,19,23H,15-16H2,(H,26,29)(H,27,30)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Dual specificity protein phosphatase 3 (Homo sapiens (Human))	BDBM50289902 (2-[3-Oxo-3-phenyl-1-((4aS,8aS)-2,5,5,8a-tetramethy...) Show SMILES CC1=C(CC(CC(=O)c2ccccc2)C(C(O)=O)C(O)=O)[C@@]2(C)CCCC(C)(C)[C@@H]2CC1 |c:1| Show InChI InChI=1S/C27H36O5/c1-17-11-12-22-26(2,3)13-8-14-27(22,4)20(17)15-19(23(24(29)30)25(31)32)16-21(28)18-9-6-5-7-10-18/h5-7,9-10,19,22-23H,8,11-16H2,1-4H3,(H,29,30)(H,31,32)/t19?,22-,27+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	8.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against VHR phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372779 (CHEMBL271282) Show SMILES O=C(Nc1ccc(cc1)-n1ccnc1)C1C(=O)NCC(Cc2ccccc2)C1=O Show InChI InChI=1S/C22H20N4O3/c27-20-16(12-15-4-2-1-3-5-15)13-24-21(28)19(20)22(29)25-17-6-8-18(9-7-17)26-11-10-23-14-26/h1-11,14,16,19H,12-13H2,(H,24,28)(H,25,29)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Dual specificity protein phosphatase 3 (Homo sapiens (Human))	BDBM50289900 (CHEMBL303581 | Sulfuric acid mono-[5-furan-3-yl-1-...) Show SMILES CC1=CC[C@H]2C(C)(C)CCC[C@]2(C)[C@H]1CC(CCCCc1ccoc1)OS(O)(=O)=O |t:1| Show InChI InChI=1S/C24H38O5S/c1-18-10-11-22-23(2,3)13-7-14-24(22,4)21(18)16-20(29-30(25,26)27)9-6-5-8-19-12-15-28-17-19/h10,12,15,17,20-22H,5-9,11,13-14,16H2,1-4H3,(H,25,26,27)/t20?,21-,22-,24+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	1.08E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against Cdc25A phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
Dual specificity protein phosphatase 3 (Homo sapiens (Human))	BDBM50289900 (CHEMBL303581 | Sulfuric acid mono-[5-furan-3-yl-1-...) Show SMILES CC1=CC[C@H]2C(C)(C)CCC[C@]2(C)[C@H]1CC(CCCCc1ccoc1)OS(O)(=O)=O |t:1| Show InChI InChI=1S/C24H38O5S/c1-18-10-11-22-23(2,3)13-7-14-24(22,4)21(18)16-20(29-30(25,26)27)9-6-5-8-19-12-15-28-17-19/h10,12,15,17,20-22H,5-9,11,13-14,16H2,1-4H3,(H,25,26,27)/t20?,21-,22-,24+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	1.08E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against VHR phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50289900 (CHEMBL303581 | Sulfuric acid mono-[5-furan-3-yl-1-...) Show SMILES CC1=CC[C@H]2C(C)(C)CCC[C@]2(C)[C@H]1CC(CCCCc1ccoc1)OS(O)(=O)=O |t:1| Show InChI InChI=1S/C24H38O5S/c1-18-10-11-22-23(2,3)13-7-14-24(22,4)21(18)16-20(29-30(25,26)27)9-6-5-8-19-12-15-28-17-19/h10,12,15,17,20-22H,5-9,11,13-14,16H2,1-4H3,(H,25,26,27)/t20?,21-,22-,24+/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against PTB1B phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50289900 (CHEMBL303581 | Sulfuric acid mono-[5-furan-3-yl-1-...) Show SMILES CC1=CC[C@H]2C(C)(C)CCC[C@]2(C)[C@H]1CC(CCCCc1ccoc1)OS(O)(=O)=O |t:1| Show InChI InChI=1S/C24H38O5S/c1-18-10-11-22-23(2,3)13-7-14-24(22,4)21(18)16-20(29-30(25,26)27)9-6-5-8-19-12-15-28-17-19/h10,12,15,17,20-22H,5-9,11,13-14,16H2,1-4H3,(H,25,26,27)/t20?,21-,22-,24+/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against PTB1B phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
M-phase inducer phosphatase 1 (Homo sapiens (Human))	BDBM50289903 (CHEMBL64690 | Sulfuric acid mono-[3-phenyl-1-((1S,...) Show SMILES CC1=CC[C@H]2C(C)(C)CCC[C@]2(C)[C@H]1CC(CCc1ccccc1)OS(O)(=O)=O |t:1| Show InChI InChI=1S/C24H36O4S/c1-18-11-14-22-23(2,3)15-8-16-24(22,4)21(18)17-20(28-29(25,26)27)13-12-19-9-6-5-7-10-19/h5-7,9-11,20-22H,8,12-17H2,1-4H3,(H,25,26,27)/t20?,21-,22-,24+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	1.65E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against PTB1B phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
M-phase inducer phosphatase 1 (Homo sapiens (Human))	BDBM50289903 (CHEMBL64690 | Sulfuric acid mono-[3-phenyl-1-((1S,...) Show SMILES CC1=CC[C@H]2C(C)(C)CCC[C@]2(C)[C@H]1CC(CCc1ccccc1)OS(O)(=O)=O |t:1| Show InChI InChI=1S/C24H36O4S/c1-18-11-14-22-23(2,3)15-8-16-24(22,4)21(18)17-20(28-29(25,26)27)13-12-19-9-6-5-7-10-19/h5-7,9-11,20-22H,8,12-17H2,1-4H3,(H,25,26,27)/t20?,21-,22-,24+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	1.65E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against Cdc25A phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50289897 (CHEMBL60297 | Sulfuric acid mono-[5-furan-3-yl-2-m...) Show SMILES CC(CCCc1ccoc1)C(C[C@H]1C(C)=CC[C@H]2C(C)(C)CCC[C@]12C)OS(O)(=O)=O |c:15| Show InChI InChI=1S/C25H40O5S/c1-18-10-11-23-24(3,4)13-7-14-25(23,5)21(18)16-22(30-31(26,27)28)19(2)8-6-9-20-12-15-29-17-20/h10,12,15,17,19,21-23H,6-9,11,13-14,16H2,1-5H3,(H,26,27,28)/t19?,21-,22?,23-,25+/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	1.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against PTB1B phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372764 (CHEMBL272703) Show SMILES CCCCCCOc1ccc(NC(=O)C2C(=O)NC(Cc3ccccc3)C2=O)cc1 Show InChI InChI=1S/C24H28N2O4/c1-2-3-4-8-15-30-19-13-11-18(12-14-19)25-23(28)21-22(27)20(26-24(21)29)16-17-9-6-5-7-10-17/h5-7,9-14,20-21H,2-4,8,15-16H2,1H3,(H,25,28)(H,26,29)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50289906 (2-[3-Phenyl-1-((1S,2S,4aS,8aR)-2,5,5,8a-tetramethy...) Show SMILES C[C@H]1CC[C@H]2C(C)(C)CCC[C@]2(C)[C@H]1CC(CCc1ccccc1)C(C(O)=O)C(O)=O Show InChI InChI=1S/C27H40O4/c1-18-11-14-22-26(2,3)15-8-16-27(22,4)21(18)17-20(23(24(28)29)25(30)31)13-12-19-9-6-5-7-10-19/h5-7,9-10,18,20-23H,8,11-17H2,1-4H3,(H,28,29)(H,30,31)/t18-,20?,21-,22-,27+/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	2.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Concentration required for its inhibitory activity against PTB1B phosphatase				Bioorg Med Chem Lett 7: 2015-2020 (1997) Article DOI: 10.1016/S0960-894X(97)00357-0 BindingDB Entry DOI: 10.7270/Q28S4PXX
					More data for this Ligand-Target Pair
Isoprenyl transferase (Streptococcus pneumoniae)	BDBM50372757 (CHEMBL256033) Show SMILES Clc1ccc(NC(=O)C2C(=O)OC(C2=O)c2ccccc2)cc1 Show InChI InChI=1S/C17H12ClNO4/c18-11-6-8-12(9-7-11)19-16(21)13-14(20)15(23-17(13)22)10-4-2-1-3-5-10/h1-9,13,15H,(H,19,21)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for BioMedical Research Curated by ChEMBL					Assay Description Inhibition of Streptococcus pneumoniae UPPS				Bioorg Med Chem Lett 18: 1840-4 (2008) Article DOI: 10.1016/j.bmcl.2008.02.009 BindingDB Entry DOI: 10.7270/Q2CF9QZ5
					More data for this Ligand-Target Pair

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