Compile Data Set for Download or QSAR

Found 19 hits with Last Name = 'sakai' and Initial = 's'   

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
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50002692 ((AZT) 1-(4-Azido-5-hydroxymethyl-tetrahydro-furan-...) Show SMILES Cc1cn([C@H]2C[C@H](N=[N+]=[N-])[C@@H](CO)O2)c(=O)[nH]c1=O |r| Show InChI InChI=1S/C10H13N5O4/c1-5-3-15(10(18)12-9(5)17)8-2-6(13-14-11)7(4-16)19-8/h3,6-8,16H,2,4H2,1H3,(H,12,17,18)/t6-,7+,8+/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	6	n/a	n/a	n/a	n/a	n/a	n/a
Tosoh Company, Ltd. Curated by ChEMBL					Assay Description Inhibitory effect of the compound on HIV-1 RT activity using template primer,poly (rA)-oligo (dT)				J Med Chem 38: 2038-40 (1995) BindingDB Entry DOI: 10.7270/Q2BZ6532
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50030532 (CHEMBL62196 | Ethyl-methyl-carbamic acid 4-(2,6-di...) Show SMILES CCN(C)C(=O)Oc1nsnc1-c1c(Cl)cccc1Cl |(12.79,-1.52,;12.16,-.12,;10.62,.04,;9.99,1.44,;9.71,-1.21,;10.34,-2.62,;8.19,-1.05,;7.29,-2.29,;7.75,-3.76,;6.52,-4.67,;5.26,-3.76,;5.75,-2.29,;4.84,-1.05,;3.31,-1.22,;2.69,-2.62,;2.4,.02,;3.03,1.44,;4.56,1.6,;5.47,.35,;7.01,.35,)| Show InChI InChI=1S/C12H11Cl2N3O2S/c1-3-17(2)12(18)19-11-10(15-20-16-11)9-7(13)5-4-6-8(9)14/h4-6H,3H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	300	n/a	n/a	n/a	n/a	n/a	n/a
Tosoh Company, Ltd. Curated by ChEMBL					Assay Description Inhibitory effect of the compound on HIV-1 RT activity using template primer,poly (rC)-oligo (dG)				J Med Chem 38: 2038-40 (1995) BindingDB Entry DOI: 10.7270/Q2BZ6532
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50030537 (CHEMBL60314 | Methyl-propyl-carbamic acid 4-(2,6-d...) Show SMILES CCCN(C)C(=O)Oc1nsnc1-c1c(Cl)cccc1Cl |(15.73,-8.85,;14.26,-9.32,;13.12,-8.28,;11.65,-8.76,;10.51,-7.71,;11.32,-10.25,;12.47,-11.29,;9.85,-10.73,;9.53,-12.23,;10.55,-13.38,;9.78,-14.71,;8.27,-14.38,;8.12,-12.86,;6.79,-12.09,;5.46,-12.84,;5.46,-14.38,;4.14,-12.09,;4.14,-10.55,;5.46,-9.76,;6.79,-10.55,;8.13,-9.78,)| Show InChI InChI=1S/C13H13Cl2N3O2S/c1-3-7-18(2)13(19)20-12-11(16-21-17-12)10-8(14)5-4-6-9(10)15/h4-6H,3,7H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	800	n/a	n/a	n/a	n/a	n/a	n/a
Tosoh Company, Ltd. Curated by ChEMBL					Assay Description Inhibitory effect of the compound on HIV-1 RT activity using template primer,poly (rC)-oligo (dG)				J Med Chem 38: 2038-40 (1995) BindingDB Entry DOI: 10.7270/Q2BZ6532
					More data for this Ligand-Target Pair
Aldo-keto reductase family 1 member B1 (Sus scrofa)	BDBM50292354 (CHEMBL463755 | Isorhamnetin 3,7-disulfate) Show SMILES COc1cc(ccc1O)-c1oc2cc(OS([O-])(=O)=O)cc(O)c2c(=O)c1OS([O-])(=O)=O Show InChI InChI=1S/C16H12O13S2/c1-26-11-4-7(2-3-9(11)17)15-16(29-31(23,24)25)14(19)13-10(18)5-8(6-12(13)27-15)28-30(20,21)22/h2-6,17-18H,1H3,(H,20,21,22)(H,23,24,25)/p-2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG 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
Fukuyama University Curated by ChEMBL					Assay Description Inhibition of pig lens aldose reductase by spectrophotometry				J Nat Prod 59: 443-5 (1996) Article DOI: 10.1021/np9601622 BindingDB Entry DOI: 10.7270/Q29Z94X7
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50030532 (CHEMBL62196 | Ethyl-methyl-carbamic acid 4-(2,6-di...) Show SMILES CCN(C)C(=O)Oc1nsnc1-c1c(Cl)cccc1Cl |(12.79,-1.52,;12.16,-.12,;10.62,.04,;9.99,1.44,;9.71,-1.21,;10.34,-2.62,;8.19,-1.05,;7.29,-2.29,;7.75,-3.76,;6.52,-4.67,;5.26,-3.76,;5.75,-2.29,;4.84,-1.05,;3.31,-1.22,;2.69,-2.62,;2.4,.02,;3.03,1.44,;4.56,1.6,;5.47,.35,;7.01,.35,)| Show InChI InChI=1S/C12H11Cl2N3O2S/c1-3-17(2)12(18)19-11-10(15-20-16-11)9-7(13)5-4-6-8(9)14/h4-6H,3H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tosoh Company, Ltd. Curated by ChEMBL					Assay Description Inhibitory effect of the compound on HIV-1 RT activity using template primer,poly (rA)-oligo (dT)				J Med Chem 38: 2038-40 (1995) BindingDB Entry DOI: 10.7270/Q2BZ6532
					More data for this Ligand-Target Pair
Aldo-keto reductase family 1 member B1 (Sus scrofa)	BDBM50292357 (CHEMBL458251 | Tamarixetin 3-glucoside-7-sulfate) Show SMILES COc1ccc(cc1O)-c1oc2cc(OS([O-])(=O)=O)cc(O)c2c(=O)c1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C22H22O15S/c1-33-12-3-2-8(4-10(12)24)20-21(36-22-19(29)18(28)16(26)14(7-23)35-22)17(27)15-11(25)5-9(6-13(15)34-20)37-38(30,31)32/h2-6,14,16,18-19,22-26,28-29H,7H2,1H3,(H,30,31,32)/p-1/t14-,16-,18+,19-,22+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Fukuyama University Curated by ChEMBL					Assay Description Inhibition of pig lens aldose reductase by spectrophotometry				J Nat Prod 59: 443-5 (1996) Article DOI: 10.1021/np9601622 BindingDB Entry DOI: 10.7270/Q29Z94X7
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50030537 (CHEMBL60314 | Methyl-propyl-carbamic acid 4-(2,6-d...) Show SMILES CCCN(C)C(=O)Oc1nsnc1-c1c(Cl)cccc1Cl |(15.73,-8.85,;14.26,-9.32,;13.12,-8.28,;11.65,-8.76,;10.51,-7.71,;11.32,-10.25,;12.47,-11.29,;9.85,-10.73,;9.53,-12.23,;10.55,-13.38,;9.78,-14.71,;8.27,-14.38,;8.12,-12.86,;6.79,-12.09,;5.46,-12.84,;5.46,-14.38,;4.14,-12.09,;4.14,-10.55,;5.46,-9.76,;6.79,-10.55,;8.13,-9.78,)| Show InChI InChI=1S/C13H13Cl2N3O2S/c1-3-7-18(2)13(19)20-12-11(16-21-17-12)10-8(14)5-4-6-9(10)15/h4-6H,3,7H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tosoh Company, Ltd. Curated by ChEMBL					Assay Description Inhibitory effect of the compound on HIV-1 RT activity using template primer,poly (rA)-oligo (dT)				J Med Chem 38: 2038-40 (1995) BindingDB Entry DOI: 10.7270/Q2BZ6532
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50030540 (Butyl-methyl-carbamic acid 4-(2,6-dichloro-phenyl)...) Show SMILES CCCCN(C)C(=O)Oc1nsnc1-c1c(Cl)cccc1Cl |(14.94,-3.1,;14.31,-1.69,;12.79,-1.52,;12.16,-.12,;10.62,.04,;9.99,1.44,;9.71,-1.21,;10.34,-2.62,;8.19,-1.05,;7.29,-2.29,;7.75,-3.76,;6.52,-4.67,;5.26,-3.76,;5.75,-2.29,;4.84,-1.05,;3.31,-1.22,;2.69,-2.62,;2.4,.02,;3.03,1.44,;4.56,1.6,;5.47,.35,;7.01,.35,)| Show InChI InChI=1S/C14H15Cl2N3O2S/c1-3-4-8-19(2)14(20)21-13-12(17-22-18-13)11-9(15)6-5-7-10(11)16/h5-7H,3-4,8H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
Tosoh Company, Ltd. Curated by ChEMBL					Assay Description Inhibitory effect of the compound on HIV-1 RT activity using template primer,poly (rA)-oligo (dT)				J Med Chem 38: 2038-40 (1995) BindingDB Entry DOI: 10.7270/Q2BZ6532
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50030540 (Butyl-methyl-carbamic acid 4-(2,6-dichloro-phenyl)...) Show SMILES CCCCN(C)C(=O)Oc1nsnc1-c1c(Cl)cccc1Cl |(14.94,-3.1,;14.31,-1.69,;12.79,-1.52,;12.16,-.12,;10.62,.04,;9.99,1.44,;9.71,-1.21,;10.34,-2.62,;8.19,-1.05,;7.29,-2.29,;7.75,-3.76,;6.52,-4.67,;5.26,-3.76,;5.75,-2.29,;4.84,-1.05,;3.31,-1.22,;2.69,-2.62,;2.4,.02,;3.03,1.44,;4.56,1.6,;5.47,.35,;7.01,.35,)| Show InChI InChI=1S/C14H15Cl2N3O2S/c1-3-4-8-19(2)14(20)21-13-12(17-22-18-13)11-9(15)6-5-7-10(11)16/h5-7H,3-4,8H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
Tosoh Company, Ltd. Curated by ChEMBL					Assay Description Inhibitory effect of the compound on HIV-1 RT activity using template primer,poly (rA)-oligo (dT)				J Med Chem 38: 2038-40 (1995) BindingDB Entry DOI: 10.7270/Q2BZ6532
					More data for this Ligand-Target Pair
Aldo-keto reductase family 1 member B1 (Sus scrofa)	BDBM50241354 (2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-tr...) Show SMILES OC[C@H]1O[C@@H](Oc2c(O)c3c(cc(O)cc3=O)oc2-c2ccc(O)c(O)c2)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C21H20O12/c22-6-13-15(27)17(29)18(30)21(32-13)33-20-16(28)14-11(26)4-8(23)5-12(14)31-19(20)7-1-2-9(24)10(25)3-7/h1-5,13,15,17-18,21-25,27-30H,6H2/t13-,15-,17+,18-,21+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
Fukuyama University Curated by ChEMBL					Assay Description Inhibition of pig lens aldose reductase by spectrophotometry				J Nat Prod 59: 443-5 (1996) Article DOI: 10.1021/np9601622 BindingDB Entry DOI: 10.7270/Q29Z94X7
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50030539 (2-(2-Acetyl-5-methyl-phenylamino)-2-(2,6-dichloro-...) Show SMILES CC(=O)c1ccc(C)cc1NC(C(N)=O)c1c(Cl)cccc1Cl Show InChI InChI=1S/C17H16Cl2N2O2/c1-9-6-7-11(10(2)22)14(8-9)21-16(17(20)23)15-12(18)4-3-5-13(15)19/h3-8,16,21H,1-2H3,(H2,20,23)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	1.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
Tosoh Company, Ltd. Curated by ChEMBL					Assay Description Inhibitory effect of the compound on HIV-1 RT activity using template primer,poly (rA)-oligo (dT)				J Med Chem 38: 2038-40 (1995) BindingDB Entry DOI: 10.7270/Q2BZ6532
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50030539 (2-(2-Acetyl-5-methyl-phenylamino)-2-(2,6-dichloro-...) Show SMILES CC(=O)c1ccc(C)cc1NC(C(N)=O)c1c(Cl)cccc1Cl Show InChI InChI=1S/C17H16Cl2N2O2/c1-9-6-7-11(10(2)22)14(8-9)21-16(17(20)23)15-12(18)4-3-5-13(15)19/h3-8,16,21H,1-2H3,(H2,20,23)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	1.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
Tosoh Company, Ltd. Curated by ChEMBL					Assay Description Inhibitory effect of the compound on HIV-1 RT activity using template primer,poly (rA)-oligo (dT)				J Med Chem 38: 2038-40 (1995) BindingDB Entry DOI: 10.7270/Q2BZ6532
					More data for this Ligand-Target Pair
Aldo-keto reductase family 1 member B1 (Sus scrofa)	BDBM50292356 (CHEMBL457815 | Rhamnazin-3-sulfate) Show SMILES COc1cc2oc(-c3ccc(O)c(OC)c3)c(OS([O-])(=O)=O)c(O)c2c(=O)c1 Show InChI InChI=1S/C17H14O10S/c1-24-9-6-11(19)14-13(7-9)26-16(17(15(14)20)27-28(21,22)23)8-3-4-10(18)12(5-8)25-2/h3-7,18,20H,1-2H3,(H,21,22,23)/p-1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.01E+4	n/a	n/a	n/a	n/a	n/a	n/a
Fukuyama University Curated by ChEMBL					Assay Description Inhibition of pig lens aldose reductase by spectrophotometry				J Nat Prod 59: 443-5 (1996) Article DOI: 10.1021/np9601622 BindingDB Entry DOI: 10.7270/Q29Z94X7
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50002692 ((AZT) 1-(4-Azido-5-hydroxymethyl-tetrahydro-furan-...) Show SMILES Cc1cn([C@H]2C[C@H](N=[N+]=[N-])[C@@H](CO)O2)c(=O)[nH]c1=O |r| Show InChI InChI=1S/C10H13N5O4/c1-5-3-15(10(18)12-9(5)17)8-2-6(13-14-11)7(4-16)19-8/h3,6-8,16H,2,4H2,1H3,(H,12,17,18)/t6-,7+,8+/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Tosoh Company, Ltd. Curated by ChEMBL					Assay Description Inhibitory effect of the compound on HIV-1 RT activity using template primer,poly (rA)-oligo (dT)				J Med Chem 38: 2038-40 (1995) BindingDB Entry DOI: 10.7270/Q2BZ6532
					More data for this Ligand-Target Pair
Aldo-keto reductase family 1 member B1 (Sus scrofa)	BDBM7460 (2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chrome...) Show SMILES Oc1cc(O)c2c(c1)oc(-c1ccc(O)c(O)c1)c(O)c2=O Show InChI InChI=1S/C15H10O7/c16-7-4-10(19)12-11(5-7)22-15(14(21)13(12)20)6-1-2-8(17)9(18)3-6/h1-5,16-19,21H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	5.01E+4	n/a	n/a	n/a	n/a	n/a	n/a
Fukuyama University Curated by ChEMBL					Assay Description Inhibition of pig lens aldose reductase by spectrophotometry				J Nat Prod 59: 443-5 (1996) Article DOI: 10.1021/np9601622 BindingDB Entry DOI: 10.7270/Q29Z94X7
					More data for this Ligand-Target Pair
Aldo-keto reductase family 1 member B1 (Sus scrofa)	BDBM50292352 (CHEMBL463753 | potassium 2-(3,4-dihydroxyphenyl)-5...) Show SMILES Oc1cc2oc(-c3ccc(O)c(O)c3)c(OS([O-])(=O)=O)c(O)c2c(=O)c1 Show InChI InChI=1S/C15H10O10S/c16-7-4-10(19)12-11(5-7)24-14(6-1-2-8(17)9(18)3-6)15(13(12)20)25-26(21,22)23/h1-5,16-18,20H,(H,21,22,23)/p-1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.09E+4	n/a	n/a	n/a	n/a	n/a	n/a
Fukuyama University Curated by ChEMBL					Assay Description Inhibition of pig lens aldose reductase by spectrophotometry				J Nat Prod 59: 443-5 (1996) Article DOI: 10.1021/np9601622 BindingDB Entry DOI: 10.7270/Q29Z94X7
					More data for this Ligand-Target Pair
Aldo-keto reductase family 1 member B1 (Sus scrofa)	BDBM50292353 (CHEMBL471479 | Percicarin | Persicarin) Show SMILES COc1cc(ccc1O)-c1oc2cc(O)cc(=O)c2c(O)c1OS([O-])(=O)=O Show InChI InChI=1S/C16H12O10S/c1-24-11-4-7(2-3-9(11)18)15-16(26-27(21,22)23)14(20)13-10(19)5-8(17)6-12(13)25-15/h2-6,17-18,20H,1H3,(H,21,22,23)/p-1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
Fukuyama University Curated by ChEMBL					Assay Description Inhibition of pig lens aldose reductase by spectrophotometry				J Nat Prod 59: 443-5 (1996) Article DOI: 10.1021/np9601622 BindingDB Entry DOI: 10.7270/Q29Z94X7
					More data for this Ligand-Target Pair
Aldo-keto reductase family 1 member B1 (Sus scrofa)	BDBM50292355 (CHEMBL457148 | Rhamnazin) Show SMILES COc1cc(O)c2c(c1)oc(-c1ccc(O)c(OC)c1)c(O)c2=O Show InChI InChI=1S/C17H14O7/c1-22-9-6-11(19)14-13(7-9)24-17(16(21)15(14)20)8-3-4-10(18)12(5-8)23-2/h3-7,18-19,21H,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>9.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Fukuyama University Curated by ChEMBL					Assay Description Inhibition of pig lens aldose reductase by spectrophotometry				J Nat Prod 59: 443-5 (1996) Article DOI: 10.1021/np9601622 BindingDB Entry DOI: 10.7270/Q29Z94X7
					More data for this Ligand-Target Pair
Aldo-keto reductase family 1 member B1 (Sus scrofa)	BDBM23409 (3,5,7-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-...) Show SMILES COc1cc(ccc1O)-c1oc2cc(O)cc(O)c2c(=O)c1O Show InChI InChI=1S/C16H12O7/c1-22-11-4-7(2-3-9(11)18)16-15(21)14(20)13-10(19)5-8(17)6-12(13)23-16/h2-6,17-19,21H,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	>9.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Fukuyama University Curated by ChEMBL					Assay Description Inhibition of pig lens aldose reductase by spectrophotometry				J Nat Prod 59: 443-5 (1996) Article DOI: 10.1021/np9601622 BindingDB Entry DOI: 10.7270/Q29Z94X7
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