Compile Data Set for Download or QSAR

Found 97 hits Enz. Inhib. hit(s) with all data for entry = 5966   

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
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308460 ((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-(thiophen-3-yl)...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2ccsc2)c1 |r| Show InChI InChI=1S/C19H19ClN2O5S2/c20-12-2-1-9(18-17(26)16(25)15(24)13(7-23)27-18)5-11(12)6-14-21-22-19(29-14)10-3-4-28-8-10/h1-5,8,13,15-18,23-26H,6-7H2/t13-,15-,16+,17-,18+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	3.51	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308448 (2-(2-Chloro-5-((2S,3S,4R,5R,6R)-3,4,5-tris(benzylo...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2cnccn2)c1 |r| Show InChI InChI=1S/C19H19ClN4O5S/c20-11-2-1-9(18-17(28)16(27)15(26)13(8-25)29-18)5-10(11)6-14-23-24-19(30-14)12-7-21-3-4-22-12/h1-5,7,13,15-18,25-28H,6,8H2/t13-,15-,16+,17-,18+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	4.06	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM103019 (US8541380, 97) Show SMILES COc1cc(Cl)c(Cc2nnc(s2)-c2ccco2)cc1[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C20H21ClN2O7S/c1-28-13-7-11(21)9(6-15-22-23-20(31-15)12-3-2-4-29-12)5-10(13)19-18(27)17(26)16(25)14(8-24)30-19/h2-5,7,14,16-19,24-27H,6,8H2,1H3/t14-,16-,17+,18-,19+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	5.55	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308450 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((5-(furan-2-yl)-1,...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2ccco2)c1 |r| Show InChI InChI=1S/C19H19ClN2O6S/c20-11-4-3-9(18-17(26)16(25)15(24)13(8-23)28-18)6-10(11)7-14-21-22-19(29-14)12-2-1-5-27-12/h1-6,13,15-18,23-26H,7-8H2/t13-,15-,16+,17-,18+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	7.03	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308454 ((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-(5-phenylfuran-...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2ccc(o2)-c2ccccc2)c1 |r| Show InChI InChI=1S/C25H23ClN2O6S/c26-16-7-6-14(24-23(32)22(31)21(30)19(12-29)34-24)10-15(16)11-20-27-28-25(35-20)18-9-8-17(33-18)13-4-2-1-3-5-13/h1-10,19,21-24,29-32H,11-12H2/t19-,21-,22+,23-,24+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	10.6	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM103015 (US8541380, 93) Show SMILES COc1c(Cc2nnc(s2)-c2ccco2)cc([C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)c2ccccc12 |r| Show InChI InChI=1S/C24H24N2O7S/c1-31-22-12(10-18-25-26-24(34-18)16-7-4-8-32-16)9-15(13-5-2-3-6-14(13)22)23-21(30)20(29)19(28)17(11-27)33-23/h2-9,17,19-21,23,27-30H,10-11H2,1H3/t17-,19-,20+,21-,23+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	10.7	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308436 ((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-(methylthio)-1,...) Show SMILES CSc1nnc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)s1 |r| Show InChI InChI=1S/C16H19ClN2O5S2/c1-25-16-19-18-11(26-16)5-8-4-7(2-3-9(8)17)15-14(23)13(22)12(21)10(6-20)24-15/h2-4,10,12-15,20-23H,5-6H2,1H3/t10-,12-,13+,14-,15+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	10.9	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319070 ((2S,3R,4R,5S,6R)-2-(3-((6-(1,3,4-thiadiazol-2-yl)p...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2ccc(nn2)-c2nncs2)c1 |r| Show InChI InChI=1S/C19H19ClN4O5S/c20-12-3-1-9(18-17(28)16(27)15(26)14(7-25)29-18)5-10(12)6-11-2-4-13(23-22-11)19-24-21-8-30-19/h1-5,8,14-18,25-28H,6-7H2/t14-,15-,16+,17-,18+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	US Patent	n/a	n/a	11.4	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319048 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((6-(methylthio)pyr...) Show SMILES CSc1ccc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)nn1 |r| Show InChI InChI=1S/C18H21ClN2O5S/c1-27-14-5-3-11(20-21-14)7-10-6-9(2-4-12(10)19)18-17(25)16(24)15(23)13(8-22)26-18/h2-6,13,15-18,22-25H,7-8H2,1H3/t13-,15-,16+,17-,18+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	13.4	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308459 ((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-(thiophen-2-yl)...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2cccs2)c1 |r| Show InChI InChI=1S/C19H19ClN2O5S2/c20-11-4-3-9(18-17(26)16(25)15(24)12(8-23)27-18)6-10(11)7-14-21-22-19(29-14)13-2-1-5-28-13/h1-6,12,15-18,23-26H,7-8H2/t12-,15-,16+,17-,18+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	14.4	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308440 ((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-phenyl-1,3,4-th...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2ccccc2)c1 |r| Show InChI InChI=1S/C21H21ClN2O5S/c22-14-7-6-12(20-19(28)18(27)17(26)15(10-25)29-20)8-13(14)9-16-23-24-21(30-16)11-4-2-1-3-5-11/h1-8,15,17-20,25-28H,9-10H2/t15-,17-,18+,19-,20+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	16.6	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319044 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((6-(pentyloxy)pyri...) Show SMILES CCCCCOc1ccc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)nn1 |r| Show InChI InChI=1S/C22H29ClN2O6/c1-2-3-4-9-30-18-8-6-15(24-25-18)11-14-10-13(5-7-16(14)23)22-21(29)20(28)19(27)17(12-26)31-22/h5-8,10,17,19-22,26-29H,2-4,9,11-12H2,1H3/t17-,19-,20+,21-,22+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319045 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((6-(hexyloxy)pyrid...) Show SMILES CCCCCCOc1ccc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)nn1 |r| Show InChI InChI=1S/C23H31ClN2O6/c1-2-3-4-5-10-31-19-9-7-16(25-26-19)12-15-11-14(6-8-17(15)24)23-22(30)21(29)20(28)18(13-27)32-23/h6-9,11,18,20-23,27-30H,2-5,10,12-13H2,1H3/t18-,20-,21+,22-,23+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	17.3	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM103018 (US8541380, 96) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1cc(Cc2nnc(s2)-c2ccco2)c(Cl)cc1Cl |r| Show InChI InChI=1S/C19H18Cl2N2O6S/c20-10-6-11(21)9(18-17(27)16(26)15(25)13(7-24)29-18)4-8(10)5-14-22-23-19(30-14)12-2-1-3-28-12/h1-4,6,13,15-18,24-27H,5,7H2/t13-,15-,16+,17-,18+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	17.6	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308451 ((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-(furan-3-yl)-1,...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2ccoc2)c1 |r| Show InChI InChI=1S/C19H19ClN2O6S/c20-12-2-1-9(18-17(26)16(25)15(24)13(7-23)28-18)5-11(12)6-14-21-22-19(29-14)10-3-4-27-8-10/h1-5,8,13,15-18,23-26H,6-7H2/t13-,15-,16+,17-,18+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	17.7	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308463 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((5-(5-chlorothioph...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2ccc(Cl)s2)c1 |r| Show InChI InChI=1S/C19H18Cl2N2O5S2/c20-10-2-1-8(18-17(27)16(26)15(25)11(7-24)28-18)5-9(10)6-14-22-23-19(30-14)12-3-4-13(21)29-12/h1-5,11,15-18,24-27H,6-7H2/t11-,15-,16+,17-,18+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	18.2	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308465 ((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-(thiazol-4-yl)-...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2cscn2)c1 |r| Show InChI InChI=1S/C18H18ClN3O5S2/c19-10-2-1-8(17-16(26)15(25)14(24)12(5-23)27-17)3-9(10)4-13-21-22-18(29-13)11-6-28-7-20-11/h1-3,6-7,12,14-17,23-26H,4-5H2/t12-,14-,15+,16-,17+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	21.8	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM103016 (US8541380, 94) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1cc(Cc2nnc(s2)-c2ccco2)c(O)c2ccccc12 |r| Show InChI InChI=1S/C23H22N2O7S/c26-10-16-19(28)20(29)21(30)22(32-16)14-8-11(18(27)13-5-2-1-4-12(13)14)9-17-24-25-23(33-17)15-6-3-7-31-15/h1-8,16,19-22,26-30H,9-10H2/t16-,19-,20+,21-,22+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	24.8	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM103013 (US8541380, 91) Show SMILES CC(=O)c1cnc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)nn1 |r| Show InChI InChI=1S/C18H20ClN3O6/c1-8(24)12-6-20-14(22-21-12)5-10-4-9(2-3-11(10)19)18-17(27)16(26)15(25)13(7-23)28-18/h2-4,6,13,15-18,23,25-27H,5,7H2,1H3/t13-,15-,16+,17-,18+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	24.9	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM102998 (US8541380, 23) Show SMILES CCCc1ccc(cc1)-c1nnc(Cc2cc(ccc2Cl)C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)s1 |r,w:21.22| Show InChI InChI=1S/C24H27ClN2O5S/c1-2-3-13-4-6-14(7-5-13)24-27-26-19(33-24)11-16-10-15(8-9-17(16)25)23-22(31)21(30)20(29)18(12-28)32-23/h4-10,18,20-23,28-31H,2-3,11-12H2,1H3/t18-,20-,21+,22-,23?/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	24.9	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308442 ((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-(pyridin-2-yl)-...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2ccccn2)c1 |r| Show InChI InChI=1S/C20H20ClN3O5S/c21-12-5-4-10(19-18(28)17(27)16(26)14(9-25)29-19)7-11(12)8-15-23-24-20(30-15)13-3-1-2-6-22-13/h1-7,14,16-19,25-28H,8-9H2/t14-,16-,17+,18-,19+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	30.3	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308445 ((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-(2-methylpyridi...) Show SMILES Cc1cc(ccn1)-c1nnc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)s1 |r| Show InChI InChI=1S/C21H22ClN3O5S/c1-10-6-12(4-5-23-10)21-25-24-16(31-21)8-13-7-11(2-3-14(13)22)20-19(29)18(28)17(27)15(9-26)30-20/h2-7,15,17-20,26-29H,8-9H2,1H3/t15-,17-,18+,19-,20+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	36.4	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319039 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((6-ethoxypyridazin...) Show SMILES CCOc1ccc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)nn1 |r| Show InChI InChI=1S/C19H23ClN2O6/c1-2-27-15-6-4-12(21-22-15)8-11-7-10(3-5-13(11)20)19-18(26)17(25)16(24)14(9-23)28-19/h3-7,14,16-19,23-26H,2,8-9H2,1H3/t14-,16-,17+,18-,19+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	43	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308464 ((2S,3R,4R,5S,6R)-2-(3-((5-(Benzo[b]thiophen-2-yl)-...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2cc3ccccc3s2)c1 |r| Show InChI InChI=1S/C23H21ClN2O5S2/c24-14-6-5-12(22-21(30)20(29)19(28)15(10-27)31-22)7-13(14)9-18-25-26-23(33-18)17-8-11-3-1-2-4-16(11)32-17/h1-8,15,19-22,27-30H,9-10H2/t15-,19-,20+,21-,22+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	44.5	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM102996 (US8541380, 21) Show SMILES OC[C@H]1OC([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2cccnc2)c1 |r,w:4.11| Show InChI InChI=1S/C20H20ClN3O5S/c21-13-4-3-10(19-18(28)17(27)16(26)14(9-25)29-19)6-12(13)7-15-23-24-20(30-15)11-2-1-5-22-8-11/h1-6,8,14,16-19,25-28H,7,9H2/t14-,16-,17+,18-,19?/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	45.3	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM103006 (US8541380, 56) Show SMILES CCCCCCCCOc1ccc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)nn1 |r| Show InChI InChI=1S/C25H35ClN2O6/c1-2-3-4-5-6-7-12-33-21-11-9-18(27-28-21)14-17-13-16(8-10-19(17)26)25-24(32)23(31)22(30)20(15-29)34-25/h8-11,13,20,22-25,29-32H,2-7,12,14-15H2,1H3/t20-,22-,23+,24-,25+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	50.5	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM102995 (US8541380, 20) Show SMILES OC[C@H]1OC([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2ccncc2)c1 |r,w:4.11| Show InChI InChI=1S/C20H20ClN3O5S/c21-13-2-1-11(19-18(28)17(27)16(26)14(9-25)29-19)7-12(13)8-15-23-24-20(30-15)10-3-5-22-6-4-10/h1-7,14,16-19,25-28H,8-9H2/t14-,16-,17+,18-,19?/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	53	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308453 ((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-(5-methylfuran-...) Show SMILES Cc1ccc(o1)-c1nnc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)s1 |r| Show InChI InChI=1S/C20H21ClN2O6S/c1-9-2-5-13(28-9)20-23-22-15(30-20)7-11-6-10(3-4-12(11)21)19-18(27)17(26)16(25)14(8-24)29-19/h2-6,14,16-19,24-27H,7-8H2,1H3/t14-,16-,17+,18-,19+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	58.3	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319060 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((6-(furan-3-yl)pyr...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2ccc(nn2)-c2ccoc2)c1 |r| Show InChI InChI=1S/C21H21ClN2O6/c22-15-3-1-11(21-20(28)19(27)18(26)17(9-25)30-21)7-13(15)8-14-2-4-16(24-23-14)12-5-6-29-10-12/h1-7,10,17-21,25-28H,8-9H2/t17-,18-,19+,20-,21+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	61.3	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319059 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((6-(furan-2-yl)pyr...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2ccc(nn2)-c2ccco2)c1 |r| Show InChI InChI=1S/C21H21ClN2O6/c22-14-5-3-11(21-20(28)19(27)18(26)17(10-25)30-21)8-12(14)9-13-4-6-15(24-23-13)16-2-1-7-29-16/h1-8,17-21,25-28H,9-10H2/t17-,18-,19+,20-,21+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	64.3	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319067 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((6-(pyridin-3-yl)p...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2ccc(nn2)-c2cccnc2)c1 |r| Show InChI InChI=1S/C22H22ClN3O5/c23-16-5-3-12(22-21(30)20(29)19(28)18(11-27)31-22)8-14(16)9-15-4-6-17(26-25-15)13-2-1-7-24-10-13/h1-8,10,18-22,27-30H,9,11H2/t18-,19-,20+,21-,22+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	64.9	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319040 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((6-propoxypyridazi...) Show SMILES CCCOc1ccc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)nn1 |r| Show InChI InChI=1S/C20H25ClN2O6/c1-2-7-28-16-6-4-13(22-23-16)9-12-8-11(3-5-14(12)21)20-19(27)18(26)17(25)15(10-24)29-20/h3-6,8,15,17-20,24-27H,2,7,9-10H2,1H3/t15-,17-,18+,19-,20+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	70.8	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319049 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((6-(ethylthio)pyri...) Show SMILES CCSc1ccc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)nn1 |r| Show InChI InChI=1S/C19H23ClN2O5S/c1-2-28-15-6-4-12(21-22-15)8-11-7-10(3-5-13(11)20)19-18(26)17(25)16(24)14(9-23)27-19/h3-7,14,16-19,23-26H,2,8-9H2,1H3/t14-,16-,17+,18-,19+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	71.3	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319061 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((6-(thiophen-2-yl)...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2ccc(nn2)-c2cccs2)c1 |r| Show InChI InChI=1S/C21H21ClN2O5S/c22-14-5-3-11(21-20(28)19(27)18(26)16(10-25)29-21)8-12(14)9-13-4-6-15(24-23-13)17-2-1-7-30-17/h1-8,16,18-21,25-28H,9-10H2/t16-,18-,19+,20-,21+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	71.4	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM102994 (US8541380, 14) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2cnc(s2)-c2ccncc2)c1 |r| Show InChI InChI=1S/C23H21ClN4O5S2/c24-14-2-1-12(21-20(32)19(31)18(30)15(10-29)33-21)7-13(14)8-17-27-28-23(35-17)16-9-26-22(34-16)11-3-5-25-6-4-11/h1-7,9,15,18-21,29-32H,8,10H2/t15-,18-,19+,20-,21+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	72.6	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319062 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((6-(thiophen-3-yl)...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2ccc(nn2)-c2ccsc2)c1 |r| Show InChI InChI=1S/C21H21ClN2O5S/c22-15-3-1-11(21-20(28)19(27)18(26)17(9-25)29-21)7-13(15)8-14-2-4-16(24-23-14)12-5-6-30-10-12/h1-7,10,17-21,25-28H,8-9H2/t17-,18-,19+,20-,21+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	75.4	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319047 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((6-(tetrahydro-2H-...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2ccc(OC3CCOCC3)nn2)c1 |r| Show InChI InChI=1S/C22H27ClN2O7/c23-16-3-1-12(22-21(29)20(28)19(27)17(11-26)32-22)9-13(16)10-14-2-4-18(25-24-14)31-15-5-7-30-8-6-15/h1-4,9,15,17,19-22,26-29H,5-8,10-11H2/t17-,19-,20+,21-,22+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	77.6	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308446 ((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-(isoquinolin-3-...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2cc3ccccc3cn2)c1 |r| Show InChI InChI=1S/C24H22ClN3O5S/c25-16-6-5-13(23-22(32)21(31)20(30)18(11-29)33-23)7-15(16)9-19-27-28-24(34-19)17-8-12-3-1-2-4-14(12)10-26-17/h1-8,10,18,20-23,29-32H,9,11H2/t18-,20-,21+,22-,23+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	81.6	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319068 ((2S,3R,4R,5S,6R)-2-(3-((6-(benzo[d][1,3]dioxol-5-y...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2ccc(nn2)-c2ccc3OCOc3c2)c1 |r| Show InChI InChI=1S/C24H23ClN2O7/c25-16-4-1-13(24-23(31)22(30)21(29)20(10-28)34-24)7-14(16)8-15-3-5-17(27-26-15)12-2-6-18-19(9-12)33-11-32-18/h1-7,9,20-24,28-31H,8,10-11H2/t20-,21-,22+,23-,24+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	82.7	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM103014 (US8541380, 92) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1cc(Cc2nnc(s2)-c2ccco2)cc2ccccc12 |r| Show InChI InChI=1S/C23H22N2O6S/c26-11-17-19(27)20(28)21(29)22(31-17)15-9-12(8-13-4-1-2-5-14(13)15)10-18-24-25-23(32-18)16-6-3-7-30-16/h1-9,17,19-22,26-29H,10-11H2/t17-,19-,20+,21-,22+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	88.9	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308444 ((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-(6-methylpyridi...) Show SMILES Cc1ccc(cn1)-c1nnc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)s1 |r| Show InChI InChI=1S/C21H22ClN3O5S/c1-10-2-3-12(8-23-10)21-25-24-16(31-21)7-13-6-11(4-5-14(13)22)20-19(29)18(28)17(27)15(9-26)30-20/h2-6,8,15,17-20,26-29H,7,9H2,1H3/t15-,17-,18+,19-,20+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	97.4	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319069 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((6-(2,3-dihydroben...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2ccc(nn2)-c2ccc3OCCOc3c2)c1 |r| Show InChI InChI=1S/C25H25ClN2O7/c26-17-4-1-14(25-24(32)23(31)22(30)21(12-29)35-25)9-15(17)10-16-3-5-18(28-27-16)13-2-6-19-20(11-13)34-8-7-33-19/h1-6,9,11,21-25,29-32H,7-8,10,12H2/t21-,22-,23+,24-,25+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	103	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM102997 (US8541380, 22) Show SMILES Cc1ccc(cc1)-c1nnc(Cc2cc(ccc2Cl)C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)s1 |r,w:19.20| Show InChI InChI=1S/C22H23ClN2O5S/c1-11-2-4-12(5-3-11)22-25-24-17(31-22)9-14-8-13(6-7-15(14)23)21-20(29)19(28)18(27)16(10-26)30-21/h2-8,16,18-21,26-29H,9-10H2,1H3/t16-,18-,19+,20-,21?/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	n/a	n/a	103	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308452 ((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-(3-methylfuran-...) Show SMILES Cc1ccoc1-c1nnc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)s1 |r| Show InChI InChI=1S/C20H21ClN2O6S/c1-9-4-5-28-18(9)20-23-22-14(30-20)7-11-6-10(2-3-12(11)21)19-17(27)16(26)15(25)13(8-24)29-19/h2-6,13,15-17,19,24-27H,7-8H2,1H3/t13-,15-,16+,17-,19+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	106	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319042 ((2S,3R,4R,5S,6R)-2-(3-((6-butoxypyridazin-3-yl)met...) Show SMILES CCCCOc1ccc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)nn1 |r| Show InChI InChI=1S/C21H27ClN2O6/c1-2-3-8-29-17-7-5-14(23-24-17)10-13-9-12(4-6-15(13)22)21-20(28)19(27)18(26)16(11-25)30-21/h4-7,9,16,18-21,25-28H,2-3,8,10-11H2,1H3/t16-,18-,19+,20-,21+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	109	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319041 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((6-isopropoxypyrid...) Show SMILES CC(C)Oc1ccc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)nn1 |r| Show InChI InChI=1S/C20H25ClN2O6/c1-10(2)28-16-6-4-13(22-23-16)8-12-7-11(3-5-14(12)21)20-19(27)18(26)17(25)15(9-24)29-20/h3-7,10,15,17-20,24-27H,8-9H2,1-2H3/t15-,17-,18+,19-,20+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	110	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50319046 ((2S,3R,4R,5S,6R)-2-(4-chloro-3-((6-(cyclohexyloxy)...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2ccc(OC3CCCCC3)nn2)c1 |r| Show InChI InChI=1S/C23H29ClN2O6/c24-17-8-6-13(23-22(30)21(29)20(28)18(12-27)32-23)10-14(17)11-15-7-9-19(26-25-15)31-16-4-2-1-3-5-16/h6-10,16,18,20-23,27-30H,1-5,11-12H2/t18-,20-,21+,22-,23+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	111	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308457 (((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-(1-methyl-1Hpy...) Show SMILES Cn1cccc1-c1nnc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)s1 |r| Show InChI InChI=1S/C20H22ClN3O5S/c1-24-6-2-3-13(24)20-23-22-15(30-20)8-11-7-10(4-5-12(11)21)19-18(28)17(27)16(26)14(9-25)29-19/h2-7,14,16-19,25-28H,8-9H2,1H3/t14-,16-,17+,18-,19+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	119	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308484 ((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-heptyl-1,3,4-th...) Show SMILES CCCCCCCc1nnc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)s1 |r| Show InChI InChI=1S/C22H31ClN2O5S/c1-2-3-4-5-6-7-17-24-25-18(31-17)11-14-10-13(8-9-15(14)23)22-21(29)20(28)19(27)16(12-26)30-22/h8-10,16,19-22,26-29H,2-7,11-12H2,1H3/t16-,19-,20+,21-,22+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	122	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair
Sodium/glucose cotransporter 2 (Homo sapiens (Human))	BDBM50308441 ((2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-(4-chlorophenyl...) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1ccc(Cl)c(Cc2nnc(s2)-c2ccc(Cl)cc2)c1 |r| Show InChI InChI=1S/C21H20Cl2N2O5S/c22-13-4-1-10(2-5-13)21-25-24-16(31-21)8-12-7-11(3-6-14(12)23)20-19(29)18(28)17(27)15(9-26)30-20/h1-7,15,17-20,26-29H,8-9H2/t15-,17-,18+,19-,20+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	126	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation US Patent					Assay Description Inhibition assay using hSGLT2.				US Patent US8541380 (2013) BindingDB Entry DOI: 10.7270/Q2T43RQ3
					More data for this Ligand-Target Pair

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