Compile Data Set for Download or QSAR

Found 25 hits with Last Name = 'jones' and Initial = 'sh'   

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
DNA polymerase beta (Homo sapiens (Human))	BDBM50079577 ((4aS,6aS,6bR,10S,12aR,14bS)-10-Hydroxy-2,2,6a,6b,9...) Show SMILES CC1(C)CC[C@@]2(CC[C@]3(C)C(=CCC4[C@@]5(C)CC[C@H](O)C(C)(C)C5CC[C@@]34C)[C@@H]2C1)C(O)=O |c:10| Show InChI InChI=1S/C30H48O3/c1-25(2)14-16-30(24(32)33)17-15-28(6)19(20(30)18-25)8-9-22-27(5)12-11-23(31)26(3,4)21(27)10-13-29(22,28)7/h8,20-23,31H,9-18H2,1-7H3,(H,32,33)/t20-,21?,22?,23-,27-,28+,29+,30-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase 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
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 964-7 (2004) Article DOI: 10.1021/np030507y BindingDB Entry DOI: 10.7270/Q2FQ9WDF
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50346601 (NSC-114945 | OLEANOLIC_ACID | Oleanolic acid | Ole...) Show SMILES CC1(C)CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2C1)C(O)=O |r,c:10| Show InChI InChI=1S/C30H48O3/c1-25(2)14-16-30(24(32)33)17-15-28(6)19(20(30)18-25)8-9-22-27(5)12-11-23(31)26(3,4)21(27)10-13-29(22,28)7/h8,20-23,31H,9-18H2,1-7H3,(H,32,33)/t20-,21-,22+,23-,27-,28+,29+,30-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	8.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta lyase activity by deoxyribose phosphate excision assay				J Nat Prod 66: 1463-5 (2003) Article DOI: 10.1021/np0301893 BindingDB Entry DOI: 10.7270/Q2K35VJB
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50242105 (CHEMBL470873 | armenin-B) Show SMILES CO[C@@H]1C[C@]2(CC=C)[C@H](C)[C@H](OC2=C(OC)C1=O)c1ccc2OCOc2c1 |r,t:13| Show InChI InChI=1S/C21H24O6/c1-5-8-21-10-16(23-3)17(22)19(24-4)20(21)27-18(12(21)2)13-6-7-14-15(9-13)26-11-25-14/h5-7,9,12,16,18H,1,8,10-11H2,2-4H3/t12-,16-,18+,21-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.23E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 964-7 (2004) Article DOI: 10.1021/np030507y BindingDB Entry DOI: 10.7270/Q2FQ9WDF
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50222205 ((1S,2R,4aS,6aS,6bR,8aR,10R,11R,12aR,12bR,14bS)-10,...) Show SMILES C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)C[C@@H](O)[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2[C@H]1C)C(O)=O |r,c:9| Show InChI InChI=1S/C30H48O4/c1-17-10-13-30(25(33)34)15-14-28(6)19(23(30)18(17)2)8-9-22-27(5)16-20(31)24(32)26(3,4)21(27)11-12-29(22,28)7/h8,17-18,20-24,31-32H,9-16H2,1-7H3,(H,33,34)/t17-,18+,20-,21+,22-,23+,24+,27+,28-,29-,30+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.26E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 899-901 (2004) Article DOI: 10.1021/np030531b BindingDB Entry DOI: 10.7270/Q2KH0N38
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50250720 (3beta,16beta,23-triacetoxyolean-12-en-28-oic acid ...) Show SMILES CC(=O)OC[C@]1(C)[C@H](CC[C@@]2(C)[C@H]1CC[C@]1(C)[C@@H]2CC=C2[C@@H]3CC(C)(C)CC[C@@]3([C@H](C[C@@]12C)OC(C)=O)C(O)=O)OC(C)=O |r,t:21| Show InChI InChI=1S/C36H54O8/c1-21(37)42-20-33(7)26-12-15-34(8)27(32(26,6)14-13-28(33)43-22(2)38)11-10-24-25-18-31(4,5)16-17-36(25,30(40)41)29(44-23(3)39)19-35(24,34)9/h10,25-29H,11-20H2,1-9H3,(H,40,41)/t25-,26+,27+,28-,29-,32-,33-,34+,35+,36+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta lyase activity by deoxyribose phosphate excision assay				J Nat Prod 66: 1463-5 (2003) Article DOI: 10.1021/np0301893 BindingDB Entry DOI: 10.7270/Q2K35VJB
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50242088 ((7S,8R,1'S,5'S,6'R)-delta 2',8'-5',6'-Dihydroxy-3'...) Show SMILES COC1=C[C@]2(CC=C)[C@H](C)[C@@H](c3ccc4OCOc4c3)[C@](O)([C@@H]2O)C1=O |r,t:2,TLB:23:22:10.8:3.24.2| Show InChI InChI=1S/C20H22O6/c1-4-7-19-9-15(24-3)17(21)20(23,18(19)22)16(11(19)2)12-5-6-13-14(8-12)26-10-25-13/h4-6,8-9,11,16,18,22-23H,1,7,10H2,2-3H3/t11-,16+,18-,19-,20-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.53E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 964-7 (2004) Article DOI: 10.1021/np030507y BindingDB Entry DOI: 10.7270/Q2FQ9WDF
					More data for this Ligand-Target Pair
DNA polymerase beta (Rattus norvegicus)	BDBM23417 (α-CA inhibitor, 4 | (-)-Epicatechin | (2R,3R)...) Show SMILES O[C@@H]1Cc2c(O)cc(O)cc2O[C@@H]1c1ccc(O)c(O)c1 |r| Show InChI InChI=1S/C15H14O6/c16-8-4-11(18)9-6-13(20)15(21-14(9)5-8)7-1-2-10(17)12(19)3-7/h1-5,13,15-20H,6H2/t13-,15-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.85E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Virginia Curated by ChEMBL					Assay Description Inhibition of lyase activity of rat DNA polymerase beta after 30 mins by deoxyribose phosphate excision assay				J Nat Prod 67: 1744-7 (2004) Article DOI: 10.1021/np040057p BindingDB Entry DOI: 10.7270/Q2251K28
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50242090 (2,4-Dimethoxy-5,6-methylenedioxy-1-(2-propenyl)ben...) Show SMILES COc1cc(OC)c(CC=C)c2OCOc12 Show InChI InChI=1S/C12H14O4/c1-4-5-8-9(13-2)6-10(14-3)12-11(8)15-7-16-12/h4,6H,1,5,7H2,2-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.86E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 964-7 (2004) Article DOI: 10.1021/np030507y BindingDB Entry DOI: 10.7270/Q2FQ9WDF
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50148911 ((3beta)-3-hydroxyurs-12-en-28-oic acid | 3beta-hyd...) Show SMILES C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2[C@H]1C)C(O)=O |r,c:9| Show InChI InChI=1S/C30H48O3/c1-18-10-15-30(25(32)33)17-16-28(6)20(24(30)19(18)2)8-9-22-27(5)13-12-23(31)26(3,4)21(27)11-14-29(22,28)7/h8,18-19,21-24,31H,9-17H2,1-7H3,(H,32,33)/t18-,19+,21+,22-,23+,24+,27+,28-,29-,30+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.86E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 899-901 (2004) Article DOI: 10.1021/np030531b BindingDB Entry DOI: 10.7270/Q2KH0N38
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50242129 (3-beta-acetoxy-2-alpha-hydroxyurs-12-en-28-oic aci...) Show SMILES C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)C[C@@H](O)[C@H](OC(C)=O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2[C@H]1C)C(O)=O |r,c:9| Show InChI InChI=1S/C32H50O5/c1-18-11-14-32(27(35)36)16-15-30(7)21(25(32)19(18)2)9-10-24-29(6)17-22(34)26(37-20(3)33)28(4,5)23(29)12-13-31(24,30)8/h9,18-19,22-26,34H,10-17H2,1-8H3,(H,35,36)/t18-,19+,22-,23+,24-,25+,26+,29+,30-,31-,32+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.15E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 899-901 (2004) Article DOI: 10.1021/np030531b BindingDB Entry DOI: 10.7270/Q2KH0N38
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50242104 ((7S,8R,1'S,5'S,6'R)-delta 2',8'-3',6'-dihydroxy-5'...) Show SMILES CO[C@@]12[C@H](O)[C@](CC=C)(CC(=O)C1=O)[C@H](C)[C@H]2c1ccc2OCOc2c1 |r,THB:4:3:16.14:9.12.10| Show InChI InChI=1S/C20H22O6/c1-4-7-19-9-13(21)17(22)20(24-3,18(19)23)16(11(19)2)12-5-6-14-15(8-12)26-10-25-14/h4-6,8,11,16,18,23H,1,7,9-10H2,2-3H3/t11-,16+,18-,19-,20-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.16E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 964-7 (2004) Article DOI: 10.1021/np030507y BindingDB Entry DOI: 10.7270/Q2FQ9WDF
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50218197 ((-)-beta-Sitosterol | (24R)-Ethylcholest-5-en-3bet...) Show SMILES CC[C@H](CC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C |r,t:13| Show InChI InChI=1S/C29H50O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h10,19-21,23-27,30H,7-9,11-18H2,1-6H3/t20-,21-,23+,24+,25-,26+,27+,28+,29-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.63E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta lyase activity by deoxyribose phosphate excision assay				J Nat Prod 66: 1463-5 (2003) Article DOI: 10.1021/np0301893 BindingDB Entry DOI: 10.7270/Q2K35VJB
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50242092 (CHEMBL511441 | canellin A) Show SMILES CO[C@H]1C[C@@]2(CC=C)[C@@H](C)[C@H](c3ccc4OCOc4c3)[C@](OC)([C@@H]2O)[C@@H]1O |r,TLB:24:23:10.8:3.25.2| Show InChI InChI=1S/C21H28O6/c1-5-8-20-10-16(24-3)18(22)21(25-4,19(20)23)17(12(20)2)13-6-7-14-15(9-13)27-11-26-14/h5-7,9,12,16-19,22-23H,1,8,10-11H2,2-4H3/t12-,16-,17+,18+,19+,20-,21+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.65E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 964-7 (2004) Article DOI: 10.1021/np030507y BindingDB Entry DOI: 10.7270/Q2FQ9WDF
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50257635 ((-)-BETA-SITOSTEROL-BETA-D-GLUCOPYRANOSIDE | (2R,3...) Show SMILES CC[C@H](CC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(C)C |r,t:13| Show InChI InChI=1S/C35H60O6/c1-7-22(20(2)3)9-8-21(4)26-12-13-27-25-11-10-23-18-24(14-16-34(23,5)28(25)15-17-35(26,27)6)40-33-32(39)31(38)30(37)29(19-36)41-33/h10,20-22,24-33,36-39H,7-9,11-19H2,1-6H3/t21-,22-,24+,25+,26-,27+,28+,29-,30-,31+,32-,33-,34+,35-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.65E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 899-901 (2004) Article DOI: 10.1021/np030531b BindingDB Entry DOI: 10.7270/Q2KH0N38
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50242093 (CHEMBL469849 | canellin C) Show SMILES CO[C@@]12[C@H](O)[C@@](CC=C)(CC(=O)[C@H]1O)[C@@H](C)[C@@H]2c1ccc2OCOc2c1 |r,THB:4:3:16.14:9.12.10| Show InChI InChI=1S/C20H24O6/c1-4-7-19-9-13(21)17(22)20(24-3,18(19)23)16(11(19)2)12-5-6-14-15(8-12)26-10-25-14/h4-6,8,11,16-18,22-23H,1,7,9-10H2,2-3H3/t11-,16+,17+,18+,19-,20+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.24E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 964-7 (2004) Article DOI: 10.1021/np030507y BindingDB Entry DOI: 10.7270/Q2FQ9WDF
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50242107 (1-allyl-2,6-dimethoxy-3,4-methylenedioxybenzene | ...) Show SMILES COc1cc2OCOc2c(OC)c1CC=C Show InChI InChI=1S/C12H14O4/c1-4-5-8-9(13-2)6-10-12(11(8)14-3)16-7-15-10/h4,6H,1,5,7H2,2-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.42E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 964-7 (2004) Article DOI: 10.1021/np030507y BindingDB Entry DOI: 10.7270/Q2FQ9WDF
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50376364 (STIGMASTEROL) Show SMILES CC[C@H](\C=C\[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C |r,t:13| Show InChI InChI=1S/C29H48O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h8-10,19-21,23-27,30H,7,11-18H2,1-6H3/b9-8+/t20-,21-,23+,24+,25-,26+,27+,28+,29-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.34E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta lyase activity by deoxyribose phosphate excision assay				J Nat Prod 66: 1463-5 (2003) Article DOI: 10.1021/np0301893 BindingDB Entry DOI: 10.7270/Q2K35VJB
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50242091 (2,6-Dimethoxy-3,4-methylenedioxycinnamyl alcohol |...) Show SMILES COc1cc2OCOc2c(OC)c1\C=C\CO Show InChI InChI=1S/C12H14O5/c1-14-9-6-10-12(17-7-16-10)11(15-2)8(9)4-3-5-13/h3-4,6,13H,5,7H2,1-2H3/b4-3+	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	4.35E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 964-7 (2004) Article DOI: 10.1021/np030507y BindingDB Entry DOI: 10.7270/Q2FQ9WDF
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM23208 ((1R,2R,5S,8R,9R,10R,13R,14R,17S,19R)-17-hydroxy-1,...) Show SMILES [H][C@]12[C@@H](CC[C@@]1(CC[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](O)C(C)(C)[C@]3([H])CC[C@@]12C)C(O)=O)C(C)=C Show InChI InChI=1S/C30H48O3/c1-18(2)19-10-15-30(25(32)33)17-16-28(6)20(24(19)30)8-9-22-27(5)13-12-23(31)26(3,4)21(27)11-14-29(22,28)7/h19-24,31H,1,8-17H2,2-7H3,(H,32,33)/t19-,20+,21-,22+,23-,24+,27-,28+,29+,30-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	4.36E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta lyase activity by deoxyribose phosphate excision assay				J Nat Prod 66: 1463-5 (2003) Article DOI: 10.1021/np0301893 BindingDB Entry DOI: 10.7270/Q2K35VJB
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50242106 (CHEMBL470874 | dillapiol | dillapiole) Show SMILES COc1c2OCOc2cc(CC=C)c1OC Show InChI InChI=1S/C12H14O4/c1-4-5-8-6-9-11(16-7-15-9)12(14-3)10(8)13-2/h4,6H,1,5,7H2,2-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 964-7 (2004) Article DOI: 10.1021/np030507y BindingDB Entry DOI: 10.7270/Q2FQ9WDF
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50242103 (3'-methoxyguianin | CHEMBL513395) Show SMILES COC1=C[C@]2(CC=C)[C@H](C)[C@@H](c3ccc4OCOc4c3)[C@](OC)([C@@H]2O)C1=O |r,t:2,TLB:24:23:10.8:3.25.2| Show InChI InChI=1S/C21H24O6/c1-5-8-20-10-16(24-3)18(22)21(25-4,19(20)23)17(12(20)2)13-6-7-14-15(9-13)27-11-26-14/h5-7,9-10,12,17,19,23H,1,8,11H2,2-4H3/t12-,17+,19-,20-,21-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 964-7 (2004) Article DOI: 10.1021/np030507y BindingDB Entry DOI: 10.7270/Q2FQ9WDF
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50242135 (3-(p-coumaroyl)ursolic acid | CHEMBL463917) Show SMILES C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](OC(=O)\C=C\c6ccc(O)cc6)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2[C@H]1C)C(O)=O |r,c:9| Show InChI InChI=1S/C39H54O5/c1-24-16-21-39(34(42)43)23-22-37(6)28(33(39)25(24)2)13-14-30-36(5)19-18-31(35(3,4)29(36)17-20-38(30,37)7)44-32(41)15-10-26-8-11-27(40)12-9-26/h8-13,15,24-25,29-31,33,40H,14,16-23H2,1-7H3,(H,42,43)/b15-10+/t24-,25+,29+,30-,31+,33+,36+,37-,38-,39+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 899-901 (2004) Article DOI: 10.1021/np030531b BindingDB Entry DOI: 10.7270/Q2KH0N38
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50242089 ((7S,8R,1'S,5'S,6'R)-delta 2',8'-3',5',6'-Trihydrox...) Show SMILES C[C@@H]1[C@@H](c2ccc3OCOc3c2)[C@]2(O)[C@H](O)[C@]1(CC=C)CC(=O)C2=O |r,TLB:15:14:2.1:20.23.21| Show InChI InChI=1S/C19H20O6/c1-3-6-18-8-12(20)16(21)19(23,17(18)22)15(10(18)2)11-4-5-13-14(7-11)25-9-24-13/h3-5,7,10,15,17,22-23H,1,6,8-9H2,2H3/t10-,15+,17-,18-,19-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 964-7 (2004) Article DOI: 10.1021/np030507y BindingDB Entry DOI: 10.7270/Q2FQ9WDF
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50242108 (CHEMBL506422 | omega-hydroxyisodillapiole) Show SMILES COc1c2OCOc2cc(\C=C\CO)c1OC Show InChI InChI=1S/C12H14O5/c1-14-10-8(4-3-5-13)6-9-11(12(10)15-2)17-7-16-9/h3-4,6,13H,5,7H2,1-2H3/b4-3+	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	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Polytechnic Institute and State University Curated by ChEMBL					Assay Description Inhibition of DNA polymerase beta (unknown origin) lyase activity				J Nat Prod 67: 964-7 (2004) Article DOI: 10.1021/np030507y BindingDB Entry DOI: 10.7270/Q2FQ9WDF
					More data for this Ligand-Target Pair
DNA polymerase beta (Rattus norvegicus)	BDBM50260079 (30-(4'-hydroxybenzoyloxy)-11alpha-hydroxylupane-20...) Show SMILES C[C@]12CC[C@H]([C@@H]1[C@H]1C[C@@H](O)[C@@H]3[C@@]4(C)CCC(=O)C(C)(C)[C@@H]4CC[C@@]3(C)[C@]1(C)CC2)C(=C)COC(=O)c1ccc(O)cc1 |r| Show InChI InChI=1S/C37H52O5/c1-22(21-42-32(41)23-8-10-24(38)11-9-23)25-12-15-34(4)18-19-36(6)26(30(25)34)20-27(39)31-35(5)16-14-29(40)33(2,3)28(35)13-17-37(31,36)7/h8-11,25-28,30-31,38-39H,1,12-21H2,2-7H3/t25-,26+,27+,28-,30+,31+,34+,35-,36+,37+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.28E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Virginia Curated by ChEMBL					Assay Description Inhibition of lyase activity of rat DNA polymerase beta after 30 mins by deoxyribose phosphate excision assay				J Nat Prod 67: 1744-7 (2004) Article DOI: 10.1021/np040057p BindingDB Entry DOI: 10.7270/Q2251K28
					More data for this Ligand-Target Pair