Compile Data Set for Download or QSAR

Found 45 hits of ic50 for UniProtKB: P15309   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50272706 ((+/-)-rac-alpha-(N-benzylamino)benzylphosphonic ac...) Show SMILES OP(O)(=O)C(NCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C14H16NO3P/c16-19(17,18)14(13-9-5-2-6-10-13)15-11-12-7-3-1-4-8-12/h1-10,14-15H,11H2,(H2,16,17,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
National Academy of Sciences of Ukraine Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase				Bioorg Med Chem Lett 18: 4620-3 (2008) Checked by Author Article DOI: 10.1016/j.bmcl.2008.07.021 BindingDB Entry DOI: 10.7270/Q26Q1X3M
					More data for this Ligand-Target Pair				3D Structure (crystal)
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50272707 ((R)-N-benzyl(phenyl)(phosphono)methanaminium chlor...) Show SMILES OP(O)(=O)[C@@H]([NH2+]Cc1ccccc1)c1ccccc1 |r| Show InChI InChI=1S/C14H16NO3P/c16-19(17,18)14(13-9-5-2-6-10-13)15-11-12-7-3-1-4-8-12/h1-10,14-15H,11H2,(H2,16,17,18)/p+1/t14-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
National Academy of Sciences of Ukraine Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase				Bioorg Med Chem Lett 18: 4620-3 (2008) Checked by Author Article DOI: 10.1016/j.bmcl.2008.07.021 BindingDB Entry DOI: 10.7270/Q26Q1X3M
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50289997 ((Benzylamino-naphthalen-1-yl-methyl)-phosphonic ac...) Show SMILES OP(O)(=O)C(NCc1ccccc1)c1cccc2ccccc12 Show InChI InChI=1S/C18H18NO3P/c20-23(21,22)18(19-13-14-7-2-1-3-8-14)17-12-6-10-15-9-4-5-11-16(15)17/h1-12,18-19H,13H2,(H2,20,21,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	8.60	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for its inhibitory activity against human prostatic acid phosphatase				Bioorg Med Chem Lett 7: 2169-2172 (1997) Article DOI: 10.1016/S0960-894X(97)00390-9 BindingDB Entry DOI: 10.7270/Q2416X2J
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50272138 ((R)-N-((S)-(4-methoxyphenyl)(phosphono)methyl)-1-p...) Show SMILES COc1ccc(cc1)[C@@H]([NH2+][C@H](C)c1ccccc1)P(O)(O)=O |r| Show InChI InChI=1S/C16H20NO4P/c1-12(13-6-4-3-5-7-13)17-16(22(18,19)20)14-8-10-15(21-2)11-9-14/h3-12,16-17H,1-2H3,(H2,18,19,20)/p+1/t12-,16+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	18	n/a	n/a	n/a	n/a	n/a	n/a
National Academy of Sciences of Ukraine Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase				Bioorg Med Chem Lett 18: 4620-3 (2008) Checked by Author Article DOI: 10.1016/j.bmcl.2008.07.021 BindingDB Entry DOI: 10.7270/Q26Q1X3M
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50272136 ((R)-1-phenyl-N-((S)-phenyl(phosphono)methyl)ethana...) Show SMILES C[C@@H]([NH2+][C@H](c1ccccc1)P(O)(O)=O)c1ccccc1 |r| Show InChI InChI=1S/C15H18NO3P/c1-12(13-8-4-2-5-9-13)16-15(20(17,18)19)14-10-6-3-7-11-14/h2-12,15-16H,1H3,(H2,17,18,19)/p+1/t12-,15+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	26	n/a	n/a	n/a	n/a	n/a	n/a
National Academy of Sciences of Ukraine Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase				Bioorg Med Chem Lett 18: 4620-3 (2008) Checked by Author Article DOI: 10.1016/j.bmcl.2008.07.021 BindingDB Entry DOI: 10.7270/Q26Q1X3M
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50272708 ((S)-N-benzyl(phenyl)(phosphono)methanaminium chlor...) Show SMILES OP(O)(=O)[C@H]([NH2+]Cc1ccccc1)c1ccccc1 |r| Show InChI InChI=1S/C14H16NO3P/c16-19(17,18)14(13-9-5-2-6-10-13)15-11-12-7-3-1-4-8-12/h1-10,14-15H,11H2,(H2,16,17,18)/p+1/t14-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	198	n/a	n/a	n/a	n/a	n/a	n/a
National Academy of Sciences of Ukraine Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase				Bioorg Med Chem Lett 18: 4620-3 (2008) Checked by Author Article DOI: 10.1016/j.bmcl.2008.07.021 BindingDB Entry DOI: 10.7270/Q26Q1X3M
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50272137 ((S)-N-((R)-(4-methoxyphenyl)(phosphono)methyl)-1-p...) Show SMILES COc1ccc(cc1)[C@H]([NH2+][C@@H](C)c1ccccc1)P(O)(O)=O |r| Show InChI InChI=1S/C16H20NO4P/c1-12(13-6-4-3-5-7-13)17-16(22(18,19)20)14-8-10-15(21-2)11-9-14/h3-12,16-17H,1-2H3,(H2,18,19,20)/p+1/t12-,16+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.07E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Academy of Sciences of Ukraine Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase				Bioorg Med Chem Lett 18: 4620-3 (2008) Checked by Author Article DOI: 10.1016/j.bmcl.2008.07.021 BindingDB Entry DOI: 10.7270/Q26Q1X3M
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50272135 ((S)-1-phenyl-N-((R)-phenyl(phosphono)methyl)ethana...) Show SMILES C[C@H]([NH2+][C@@H](c1ccccc1)P(O)(O)=O)c1ccccc1 |r| Show InChI InChI=1S/C15H18NO3P/c1-12(13-8-4-2-5-9-13)16-15(20(17,18)19)14-10-6-3-7-11-14/h2-12,15-16H,1H3,(H2,17,18,19)/p+1/t12-,15+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.21E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Academy of Sciences of Ukraine Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase				Bioorg Med Chem Lett 18: 4620-3 (2008) Checked by Author Article DOI: 10.1016/j.bmcl.2008.07.021 BindingDB Entry DOI: 10.7270/Q26Q1X3M
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50240513 ((1-Benzoyl-1-naphthalen-1-yl-2-oxo-2-phenyl-ethyl)...) Show SMILES OP(O)(=O)C(C(=O)c1ccccc1)(C(=O)c1ccccc1)c1cccc2ccccc12 Show InChI InChI=1S/C25H19O5P/c26-23(19-11-3-1-4-12-19)25(31(28,29)30,24(27)20-13-5-2-6-14-20)22-17-9-15-18-10-7-8-16-21(18)22/h1-17H,(H2,28,29,30)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for 50% of inhibition of Osteoclastic acid phosphatase (OAP) activity, determined using dose-response curve				Bioorg Med Chem Lett 5: 1801-1806 (1995) Article DOI: 10.1016/0960-894X(95)00299-9 BindingDB Entry DOI: 10.7270/Q2CC10NQ
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50139758 ((2-Naphthalen-2-yl-1-naphthalen-1-yl-2-oxo-ethyl)-...) Show SMILES OP(O)(=O)C(C(=O)c1ccc2ccccc2c1)c1cccc2ccccc12 Show InChI InChI=1S/C22H17O4P/c23-21(18-13-12-15-6-1-2-8-17(15)14-18)22(27(24,25)26)20-11-5-9-16-7-3-4-10-19(16)20/h1-14,22H,(H2,24,25,26)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Patents Similars	Article	n/a	n/a	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for 50% of inhibition of Osteoclastic acid phosphatase (OAP) activity, determined using dose-response curve				Bioorg Med Chem Lett 5: 1801-1806 (1995) Article DOI: 10.1016/0960-894X(95)00299-9 BindingDB Entry DOI: 10.7270/Q2CC10NQ
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50284958 ((2-Biphenyl-4-yl-1-naphthalen-1-yl-ethyl)-phosphon...) Show SMILES OP(O)(=O)C(Cc1ccc(cc1)-c1ccccc1)c1cccc2ccccc12 Show InChI InChI=1S/C24H21O3P/c25-28(26,27)24(23-12-6-10-21-9-4-5-11-22(21)23)17-18-13-15-20(16-14-18)19-7-2-1-3-8-19/h1-16,24H,17H2,(H2,25,26,27)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 Tested for 50% of inhibition of Osteoclastic acid phosphatase (OAP) activity, determined using dose-response curve				Bioorg Med Chem Lett 5: 1801-1806 (1995) Article DOI: 10.1016/0960-894X(95)00299-9 BindingDB Entry DOI: 10.7270/Q2CC10NQ
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288643 (CHEMBL106132 | [Phenyl-(2-trifluoromethyl-phenyl)-...) Show SMILES OP(O)(=O)C(c1ccccc1)c1ccccc1C(F)(F)F Show InChI InChI=1S/C14H12F3O3P/c15-14(16,17)12-9-5-4-8-11(12)13(21(18,19)20)10-6-2-1-3-7-10/h1-9,13H,(H2,18,19,20)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article	n/a	n/a	9.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50284955 (CHEMBL416111 | [1-(4-Chloro-benzyl)-2-(4-chloro-ph...) Show SMILES OP(O)(=O)C(Cc1ccc(Cl)cc1)(Cc1ccc(Cl)cc1)c1cccc2ccccc12 Show InChI InChI=1S/C25H21Cl2O3P/c26-21-12-8-18(9-13-21)16-25(31(28,29)30,17-19-10-14-22(27)15-11-19)24-7-3-5-20-4-1-2-6-23(20)24/h1-15H,16-17H2,(H2,28,29,30)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	9.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for 50% of inhibition of Osteoclastic acid phosphatase (OAP) activity, determined using dose-response curve				Bioorg Med Chem Lett 5: 1801-1806 (1995) Article DOI: 10.1016/0960-894X(95)00299-9 BindingDB Entry DOI: 10.7270/Q2CC10NQ
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50284954 (CHEMBL53536 | [2-Cyclohexyl-1-(2-methyl-naphthalen...) Show SMILES Cc1ccc2ccccc2c1C(CC1CCCCC1)P(O)(O)=O Show InChI InChI=1S/C19H25O3P/c1-14-11-12-16-9-5-6-10-17(16)19(14)18(23(20,21)22)13-15-7-3-2-4-8-15/h5-6,9-12,15,18H,2-4,7-8,13H2,1H3,(H2,20,21,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL 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 Tested for 50% of inhibition of Osteoclastic acid phosphatase (OAP) activity, determined using dose-response curve				Bioorg Med Chem Lett 5: 1801-1806 (1995) Article DOI: 10.1016/0960-894X(95)00299-9 BindingDB Entry DOI: 10.7270/Q2CC10NQ
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50284957 ((2-Cyclohexyl-1-naphthalen-1-yl-ethyl)-phosphonic ...) Show SMILES OP(O)(=O)C(CC1CCCCC1)c1cccc2ccccc12 Show InChI InChI=1S/C18H23O3P/c19-22(20,21)18(13-14-7-2-1-3-8-14)17-12-6-10-15-9-4-5-11-16(15)17/h4-6,9-12,14,18H,1-3,7-8,13H2,(H2,19,20,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1.14E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for 50% of inhibition of Osteoclastic acid phosphatase (OAP) activity, determined using dose-response curve				Bioorg Med Chem Lett 5: 1801-1806 (1995) Article DOI: 10.1016/0960-894X(95)00299-9 BindingDB Entry DOI: 10.7270/Q2CC10NQ
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288656 ((Phenyl-m-tolyl-methyl)-phosphonic acid | CHEMBL71...) Show SMILES Cc1cccc(c1)C(c1ccccc1)P(O)(O)=O Show InChI InChI=1S/C14H15O3P/c1-11-6-5-9-13(10-11)14(18(15,16)17)12-7-3-2-4-8-12/h2-10,14H,1H3,(H2,15,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for its inhibitory activity against human prostatic acid phosphatase				Bioorg Med Chem Lett 7: 2169-2172 (1997) Article DOI: 10.1016/S0960-894X(97)00390-9 BindingDB Entry DOI: 10.7270/Q2416X2J
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288656 ((Phenyl-m-tolyl-methyl)-phosphonic acid | CHEMBL71...) Show SMILES Cc1cccc(c1)C(c1ccccc1)P(O)(O)=O Show InChI InChI=1S/C14H15O3P/c1-11-6-5-9-13(10-11)14(18(15,16)17)12-7-3-2-4-8-12/h2-10,14H,1H3,(H2,15,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288649 ((1,3-Diphenyl-propyl)-phosphonic acid | CHEMBL1062...) Show SMILES OP(O)(=O)C(CCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C15H17O3P/c16-19(17,18)15(14-9-5-2-6-10-14)12-11-13-7-3-1-4-8-13/h1-10,15H,11-12H2,(H2,16,17,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288653 (CHEMBL104125 | [(3-Chloro-phenyl)-phenyl-methyl]-p...) Show SMILES OP(O)(=O)C(c1ccccc1)c1cccc(Cl)c1 Show InChI InChI=1S/C13H12ClO3P/c14-12-8-4-7-11(9-12)13(18(15,16)17)10-5-2-1-3-6-10/h1-9,13H,(H2,15,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288651 ((2-Biphenyl-4-yl-1-phenyl-ethyl)-phosphonic acid |...) Show SMILES OP(O)(=O)C(Cc1ccc(cc1)-c1ccccc1)c1ccccc1 Show InChI InChI=1S/C20H19O3P/c21-24(22,23)20(19-9-5-2-6-10-19)15-16-11-13-18(14-12-16)17-7-3-1-4-8-17/h1-14,20H,15H2,(H2,21,22,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288665 (CHEMBL322700 | [(3-Nitro-phenyl)-phenyl-methyl]-ph...) Show SMILES OP(O)(=O)C(c1ccccc1)c1cccc(c1)[N+]([O-])=O Show InChI InChI=1S/C13H12NO5P/c15-14(16)12-8-4-7-11(9-12)13(20(17,18)19)10-5-2-1-3-6-10/h1-9,13H,(H2,17,18,19)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	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 Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50284959 (CHEMBL300425 | [2-(4-Chloro-phenyl)-1-naphthalen-1...) Show SMILES OP(O)(=O)C(Cc1ccc(Cl)cc1)c1cccc2ccccc12 Show InChI InChI=1S/C18H16ClO3P/c19-15-10-8-13(9-11-15)12-18(23(20,21)22)17-7-3-5-14-4-1-2-6-16(14)17/h1-11,18H,12H2,(H2,20,21,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents 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 Tested for 50% of inhibition of Osteoclastic acid phosphatase (OAP) activity, determined using dose-response curve				Bioorg Med Chem Lett 5: 1801-1806 (1995) Article DOI: 10.1016/0960-894X(95)00299-9 BindingDB Entry DOI: 10.7270/Q2CC10NQ
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50284956 ((1-Naphthalen-1-yl-2-phenyl-ethyl)-phosphonic acid...) Show SMILES OP(O)(=O)C(Cc1ccccc1)c1cccc2ccccc12 Show InChI InChI=1S/C18H17O3P/c19-22(20,21)18(13-14-7-2-1-3-8-14)17-12-6-10-15-9-4-5-11-16(15)17/h1-12,18H,13H2,(H2,19,20,21)	PDB MMDB 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 Tested for 50% of inhibition of Osteoclastic acid phosphatase (OAP) activity, determined using dose-response curve				Bioorg Med Chem Lett 5: 1801-1806 (1995) Article DOI: 10.1016/0960-894X(95)00299-9 BindingDB Entry DOI: 10.7270/Q2CC10NQ
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288666 ((9H-Xanthen-9-yl)-phosphonic acid | CHEMBL106688) Show SMILES OP(O)(O)=c1c2ccccc2oc2ccccc12 Show InChI InChI=1S/C13H11O4P/c14-18(15,16)13-9-5-1-3-7-11(9)17-12-8-4-2-6-10(12)13/h1-8,14-16H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	2.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50080269 (1-naphthalenemethylphosphonate | CHEMBL37851 | Nap...) Show SMILES OP(O)(=O)Cc1cccc2ccccc12 Show InChI InChI=1S/C11H11O3P/c12-15(13,14)8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7H,8H2,(H2,12,13,14)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for 50% of inhibition of Osteoclastic acid phosphatase (OAP) activity, determined using dose-response curve				Bioorg Med Chem Lett 5: 1801-1806 (1995) Article DOI: 10.1016/0960-894X(95)00299-9 BindingDB Entry DOI: 10.7270/Q2CC10NQ
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288662 (CHEMBL320504 | [(2-Chloro-phenyl)-phenyl-methyl]-p...) Show SMILES OP(O)(=O)C(c1ccccc1)c1ccccc1Cl Show InChI InChI=1S/C13H12ClO3P/c14-12-9-5-4-8-11(12)13(18(15,16)17)10-6-2-1-3-7-10/h1-9,13H,(H2,15,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	3.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50284960 (CHEMBL50626 | H3VO4 | Vanadiumsaeure | [VO(OH)3] |...) Show SMILES O[V](O)(O)=O Show InChI InChI=1S/3H2O.O.V/h3*1H2;;/q;;;;+3/p-3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	3.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for 50% of inhibition of Osteoclastic acid phosphatase (OAP) activity, determined using dose-response curve				Bioorg Med Chem Lett 5: 1801-1806 (1995) Article DOI: 10.1016/0960-894X(95)00299-9 BindingDB Entry DOI: 10.7270/Q2CC10NQ
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288661 (CHEMBL107858 | [2-Biphenyl-4-yl-1-(3-trifluorometh...) Show SMILES OP(O)(=O)C(Cc1ccc(cc1)-c1ccccc1)c1cccc(c1)C(F)(F)F Show InChI InChI=1S/C21H18F3O3P/c22-21(23,24)19-8-4-7-18(14-19)20(28(25,26)27)13-15-9-11-17(12-10-15)16-5-2-1-3-6-16/h1-12,14,20H,13H2,(H2,25,26,27)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	3.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288658 (CHEMBL107347 | [(4-Methoxy-phenyl)-phenyl-methyl]-...) Show SMILES COc1ccc(cc1)C(c1ccccc1)P(O)(O)=O Show InChI InChI=1S/C14H15O4P/c1-18-13-9-7-12(8-10-13)14(19(15,16)17)11-5-3-2-4-6-11/h2-10,14H,1H3,(H2,15,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	3.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288655 ((Phenyl-o-tolyl-methyl)-phosphonic acid | CHEMBL10...) Show SMILES Cc1ccccc1C(c1ccccc1)P(O)(O)=O Show InChI InChI=1S/C14H15O3P/c1-11-7-5-6-10-13(11)14(18(15,16)17)12-8-3-2-4-9-12/h2-10,14H,1H3,(H2,15,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	3.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288644 (CHEMBL104389 | [Phenyl-(4-trifluoromethyl-phenyl)-...) Show SMILES OP(O)(=O)C(c1ccccc1)c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C14H12F3O3P/c15-14(16,17)12-8-6-11(7-9-12)13(21(18,19)20)10-4-2-1-3-5-10/h1-9,13H,(H2,18,19,20)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	4.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288660 (CHEMBL107374 | [Phenyl-(3-trifluoromethyl-phenyl)-...) Show SMILES OP(O)(=O)C(c1ccccc1)c1cccc(c1)C(F)(F)F Show InChI InChI=1S/C14H12F3O3P/c15-14(16,17)12-8-4-7-11(9-12)13(21(18,19)20)10-5-2-1-3-6-10/h1-9,13H,(H2,18,19,20)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	6.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288652 ((Biphenyl-4-yl-phenyl-methyl)-phosphonic acid | CH...) Show SMILES OP(O)(=O)C(c1ccccc1)c1ccc(cc1)-c1ccccc1 Show InChI InChI=1S/C19H17O3P/c20-23(21,22)19(17-9-5-2-6-10-17)18-13-11-16(12-14-18)15-7-3-1-4-8-15/h1-14,19H,(H2,20,21,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	6.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288648 ((Bis-biphenyl-4-yl-methyl)-phosphonic acid | CHEMB...) Show SMILES OP(O)(=O)C(c1ccc(cc1)-c1ccccc1)c1ccc(cc1)-c1ccccc1 Show InChI InChI=1S/C25H21O3P/c26-29(27,28)25(23-15-11-21(12-16-23)19-7-3-1-4-8-19)24-17-13-22(14-18-24)20-9-5-2-6-10-20/h1-18,25H,(H2,26,27,28)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	7.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288667 ((3-Trifluoromethyl-benzyl)-phosphonic acid | CHEMB...) Show SMILES OP(O)(=O)Cc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C8H8F3O3P/c9-8(10,11)7-3-1-2-6(4-7)5-15(12,13)14/h1-4H,5H2,(H2,12,13,14)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	8.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288664 ((1,2-Diphenyl-ethyl)-phosphonic acid | CHEMBL53486) Show SMILES OP(O)(=O)C(Cc1ccccc1)c1ccccc1 Show InChI InChI=1S/C14H15O3P/c15-18(16,17)14(13-9-5-2-6-10-13)11-12-7-3-1-4-8-12/h1-10,14H,11H2,(H2,15,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	8.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288646 ((10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)-ph...) Show SMILES OP(O)(=O)C1c2ccccc2CCc2ccccc12 Show InChI InChI=1S/C15H15O3P/c16-19(17,18)15-13-7-3-1-5-11(13)9-10-12-6-2-4-8-14(12)15/h1-8,15H,9-10H2,(H2,16,17,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article	n/a	n/a	9.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288650 (CHEMBL107540 | [2-Phenyl-1-(3-trifluoromethyl-phen...) Show SMILES OP(O)(=O)C(Cc1ccccc1)c1cccc(c1)C(F)(F)F Show InChI InChI=1S/C15H14F3O3P/c16-15(17,18)13-8-4-7-12(10-13)14(22(19,20)21)9-11-5-2-1-3-6-11/h1-8,10,14H,9H2,(H2,19,20,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288663 ((9H-Thioxanthen-9-yl)-phosphonic acid | CHEMBL1043...) Show SMILES OP(O)(O)=c1c2ccccc2sc2ccccc12 Show InChI InChI=1S/C13H11O3PS/c14-17(15,16)13-9-5-1-3-7-11(9)18-12-8-4-2-6-10(12)13/h1-8,14-16H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288657 ((5H-Dibenzo[a,d]cyclohepten-5-yl)-phosphonic acid ...) Show SMILES OP(O)(O)=c1c2ccccc2ccc2ccccc12 Show InChI InChI=1S/C15H13O3P/c16-19(17,18)15-13-7-3-1-5-11(13)9-10-12-6-2-4-8-14(12)15/h1-10,16-18H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288647 (Benzhydryl-phosphonic acid | CHEMBL106165) Show SMILES OP(O)(=O)C(c1ccccc1)c1ccccc1 Show InChI InChI=1S/C13H13O3P/c14-17(15,16)13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13H,(H2,14,15,16)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	1.42E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288654 (CHEMBL107348 | [(4-Chloro-phenyl)-phenyl-methyl]-p...) Show SMILES OP(O)(=O)C(c1ccccc1)c1ccc(Cl)cc1 Show InChI InChI=1S/C13H12ClO3P/c14-12-8-6-11(7-9-12)13(18(15,16)17)10-4-2-1-3-5-10/h1-9,13H,(H2,15,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1.43E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288659 ((Phenyl-p-tolyl-methyl)-phosphonic acid | CHEMBL10...) Show SMILES Cc1ccc(cc1)C(c1ccccc1)P(O)(O)=O Show InChI InChI=1S/C14H15O3P/c1-11-7-9-13(10-8-11)14(18(15,16)17)12-5-3-2-4-6-12/h2-10,14H,1H3,(H2,15,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1.52E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50080274 (Benzyl-phosphonic acid | CHEMBL299737 | Phenyl-met...) Show SMILES OP(O)(=O)Cc1ccccc1 Show InChI InChI=1S/C7H9O3P/c8-11(9,10)6-7-4-2-1-3-5-7/h1-5H,6H2,(H2,8,9,10)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article	n/a	n/a	>5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair
Prostatic acid phosphatase (Homo sapiens (Human))	BDBM50288645 ((9H-Fluoren-9-yl)-phosphonic acid | CHEMBL105772) Show SMILES OP(O)(=O)C1c2ccccc2-c2ccccc12 Show InChI InChI=1S/C13H11O3P/c14-17(15,16)13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)13/h1-8,13H,(H2,14,15,16)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	>5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human prostatic acid phosphatase was determined as inhibition of the hydrolysis of tyrosine phosphate				Bioorg Med Chem Lett 6: 311-314 (1996) Article DOI: 10.1016/0960-894X(96)00018-2 BindingDB Entry DOI: 10.7270/Q21R6QGR
					More data for this Ligand-Target Pair