Compile Data Set for Download or QSAR

Found 19 hits Enz. Inhib. hit(s) with Target = 'Potassium-transporting ATPase alpha chain 2'   

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
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50408438 (CHEMBL2068911) Show SMILES CN(C)CCOC(=O)\C=C\[C@H]1CC[C@]2(O)[C@@H]3CC[C@@H]4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C Show InChI InChI=1S/C26H43NO4/c1-24-12-10-20(28)17-19(24)5-7-22-21(24)11-13-25(2)18(9-14-26(22,25)30)6-8-23(29)31-16-15-27(3)4/h6,8,18-22,28,30H,5,7,9-17H2,1-4H3/b8-6+/t18-,19+,20-,21-,22+,24-,25+,26-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
Prassis Istituto di Ricerche Sigma-Tau Curated by ChEMBL					Assay Description Compound was evaluated for its ability to inhibit the specific [3H]-ouabain binding to dog kidney Na+/K+ ATPase				J Med Chem 41: 3033-40 (1998) Article DOI: 10.1021/jm980108d BindingDB Entry DOI: 10.7270/Q2VX0H6K
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50408439 (CHEMBL2068890) Show SMILES C[C@]12CC[C@H]3[C@@H](CC[C@@H]4C[C@@H](O)CC[C@]34C)[C@@]1(O)CC[C@@H]2\C=C\C=O Show InChI InChI=1S/C22H34O3/c1-20-10-8-17(24)14-16(20)5-6-19-18(20)9-11-21(2)15(4-3-13-23)7-12-22(19,21)25/h3-4,13,15-19,24-25H,5-12,14H2,1-2H3/b4-3+/t15-,16+,17-,18-,19+,20-,21+,22-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
Prassis Istituto di Ricerche Sigma-Tau Curated by ChEMBL					Assay Description Compound was evaluated for its ability to inhibit the specific [3H]-ouabain binding to dog kidney Na+/K+ ATPase				J Med Chem 41: 3033-40 (1998) Article DOI: 10.1021/jm980108d BindingDB Entry DOI: 10.7270/Q2VX0H6K
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM66977 (3-[(3S,5R,8R,9S,10S,13R,14S,17R)-10,13-dimethyl-3,...) Show SMILES C[C@]12CC[C@H]3[C@@H](CC[C@@H]4C[C@@H](O)CC[C@]34C)[C@@]1(O)CC[C@@H]2C1=CC(=O)OC1 |t:25| Show InChI InChI=1S/C23H34O4/c1-21-8-5-16(24)12-15(21)3-4-19-18(21)6-9-22(2)17(7-10-23(19,22)26)14-11-20(25)27-13-14/h11,15-19,24,26H,3-10,12-13H2,1-2H3/t15-,16+,17-,18+,19-,21+,22-,23+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	80	n/a	n/a	n/a	n/a	n/a	n/a
Prassis Istituto di Ricerche Sigma-Tau Curated by ChEMBL					Assay Description Compound was evaluated for its ability to inhibit the specific [3H]-ouabain binding to dog kidney Na+/K+ ATPase				J Med Chem 41: 3033-40 (1998) Article DOI: 10.1021/jm980108d BindingDB Entry DOI: 10.7270/Q2VX0H6K
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50066032 (CHEMBL323301 | [(1R,4bR,7S,8aR)-7-Hydroxy-1,4b,8,8...) Show SMILES C[C@@H]1C2C(CC\C1=C/C(=O)OCCN(C)C)[C@@]1(C)CC[C@H](O)C(C)(C)[C@@H]1CC2=O Show InChI InChI=1S/C24H39NO4/c1-15-16(13-21(28)29-12-11-25(5)6)7-8-17-22(15)18(26)14-19-23(2,3)20(27)9-10-24(17,19)4/h13,15,17,19-20,22,27H,7-12,14H2,1-6H3/b16-13+/t15-,17?,19-,20-,22?,24+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	100	n/a	n/a	n/a	n/a	n/a	n/a
Prassis Istituto di Ricerche Sigma-Tau Curated by ChEMBL					Assay Description Compound was evaluated for its ability to inhibit the specific [3H]-ouabain binding to dog kidney Na+/K+ ATPase				J Med Chem 41: 3033-40 (1998) Article DOI: 10.1021/jm980108d BindingDB Entry DOI: 10.7270/Q2VX0H6K
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50066031 ((E)-(S)-4-((2S,4bS,7S,8aR)-7-Hydroxy-2,4b-dimethyl...) Show SMILES CC[C@@H](\C=C\C(=O)OCCN(C)C)[C@]1(C)CCC2C(CC[C@@H]3C[C@@H](O)CC[C@]23C)C1=O Show InChI InChI=1S/C26H43NO4/c1-6-18(8-10-23(29)31-16-15-27(4)5)26(3)14-12-22-21(24(26)30)9-7-19-17-20(28)11-13-25(19,22)2/h8,10,18-22,28H,6-7,9,11-17H2,1-5H3/b10-8+/t18-,19+,20-,21?,22?,25-,26-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	120	n/a	n/a	n/a	n/a	n/a	n/a
Prassis Istituto di Ricerche Sigma-Tau Curated by ChEMBL					Assay Description Compound was evaluated for its ability to inhibit the specific [3H]-ouabain binding to dog kidney Na+/K+ ATPase				J Med Chem 41: 3033-40 (1998) Article DOI: 10.1021/jm980108d BindingDB Entry DOI: 10.7270/Q2VX0H6K
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50066029 (4-[(S)-1-((2S,4bS,7S,8aR)-7-Hydroxy-2,4b-dimethyl-...) Show SMILES CC[C@H](C1=CC(=O)OC1)[C@@]1(C)CCC2C(CC[C@@H]3C[C@@H](O)CC[C@]23C)C1 |t:3| Show InChI InChI=1S/C23H36O3/c1-4-19(16-11-21(25)26-14-16)22(2)9-8-20-15(13-22)5-6-17-12-18(24)7-10-23(17,20)3/h11,15,17-20,24H,4-10,12-14H2,1-3H3/t15?,17-,18+,19-,20?,22+,23+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	130	n/a	n/a	n/a	n/a	n/a	n/a
Prassis Istituto di Ricerche Sigma-Tau Curated by ChEMBL					Assay Description Compound was evaluated for its ability to inhibit the specific [3H]-ouabain binding to dog kidney Na+/K+ ATPase				J Med Chem 41: 3033-40 (1998) Article DOI: 10.1021/jm980108d BindingDB Entry DOI: 10.7270/Q2VX0H6K
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50066036 (4-[(R)-1-((2R,4bS,7S,8aR)-7-Hydroxy-2,4b-dimethyl-...) Show SMILES CC[C@H](C1=CC(=O)OC1)[C@@]1(C)CCC2C(CC[C@@H]3C[C@@H](O)CC[C@]23C)C1=O |t:3| Show InChI InChI=1S/C23H34O4/c1-4-18(14-11-20(25)27-13-14)23(3)10-8-19-17(21(23)26)6-5-15-12-16(24)7-9-22(15,19)2/h11,15-19,24H,4-10,12-13H2,1-3H3/t15-,16+,17?,18-,19?,22+,23-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a	n/a
Prassis Istituto di Ricerche Sigma-Tau Curated by ChEMBL					Assay Description Compound was evaluated for its ability to inhibit the specific [3H]-ouabain binding to dog kidney Na+/K+ ATPase				J Med Chem 41: 3033-40 (1998) Article DOI: 10.1021/jm980108d BindingDB Entry DOI: 10.7270/Q2VX0H6K
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50131828 ((E,Z)10,13-Dimethyl-tetradecahydro-cyclopenta[a]ph...) Show SMILES C[C@]12CCC3C(CC(=O)[C@H]4C\C(CC[C@]34C)=N\OCCN)[C@@H]1CCC2=O Show InChI InChI=1S/C21H32N2O3/c1-20-7-5-13(23-26-10-9-22)11-17(20)18(24)12-14-15-3-4-19(25)21(15,2)8-6-16(14)20/h14-17H,3-12,22H2,1-2H3/b23-13+/t14?,15-,16?,17+,20+,21-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a	n/a
Prassis Istituto di Ricerche Sigma-Tau Curated by ChEMBL					Assay Description Inhibitory activity against Na+/K+ ATPase				J Med Chem 46: 3644-54 (2003) Article DOI: 10.1021/jm030830y BindingDB Entry DOI: 10.7270/Q24T6K47
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50066034 ((E)-(R)-4-((2R,4bS,7S,8aR)-7-Hydroxy-2,4b-dimethyl...) Show SMILES CC[C@H](\C=C\C(=O)OCCN(C)C)[C@@]1(C)CCC2C(CC[C@@H]3C[C@@H](O)CC[C@]23C)C1=O Show InChI InChI=1S/C26H43NO4/c1-6-18(8-10-23(29)31-16-15-27(4)5)26(3)14-12-22-21(24(26)30)9-7-19-17-20(28)11-13-25(19,22)2/h8,10,18-22,28H,6-7,9,11-17H2,1-5H3/b10-8+/t18-,19-,20+,21?,22?,25+,26-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	250	n/a	n/a	n/a	n/a	n/a	n/a
Prassis Istituto di Ricerche Sigma-Tau Curated by ChEMBL					Assay Description Compound was evaluated for its ability to inhibit the specific [3H]-ouabain binding to dog kidney Na+/K+ ATPase				J Med Chem 41: 3033-40 (1998) Article DOI: 10.1021/jm980108d BindingDB Entry DOI: 10.7270/Q2VX0H6K
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50408437 (CHEMBL2068917) Show SMILES COC(=O)\C=C\[C@H]1CC[C@]2(O)[C@@H]3CC[C@@H]4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C Show InChI InChI=1S/C23H36O4/c1-21-11-9-17(24)14-16(21)4-6-19-18(21)10-12-22(2)15(5-7-20(25)27-3)8-13-23(19,22)26/h5,7,15-19,24,26H,4,6,8-14H2,1-3H3/b7-5+/t15-,16+,17-,18-,19+,21-,22+,23-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	350	n/a	n/a	n/a	n/a	n/a	n/a
Prassis Istituto di Ricerche Sigma-Tau Curated by ChEMBL					Assay Description Compound was evaluated for its ability to inhibit the specific [3H]-ouabain binding to dog kidney Na+/K+ ATPase				J Med Chem 41: 3033-40 (1998) Article DOI: 10.1021/jm980108d BindingDB Entry DOI: 10.7270/Q2VX0H6K
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50408440 (CHEMBL2068987) Show SMILES CN(C)CCOC(=O)\C=C\[C@@H]1CC[C@]2(O)[C@@H]3CC[C@@H]4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@@]12C Show InChI InChI=1S/C26H43NO4/c1-24-12-10-20(28)17-19(24)5-7-22-21(24)11-13-25(2)18(9-14-26(22,25)30)6-8-23(29)31-16-15-27(3)4/h6,8,18-22,28,30H,5,7,9-17H2,1-4H3/b8-6+/t18-,19-,20+,21+,22-,24+,25+,26+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.89E+3	n/a	n/a	n/a	n/a	n/a	n/a
Prassis Istituto di Ricerche Sigma-Tau Curated by ChEMBL					Assay Description Compound was evaluated for its ability to inhibit the specific [3H]-ouabain binding to dog kidney Na+/K+ ATPase				J Med Chem 41: 3033-40 (1998) Article DOI: 10.1021/jm980108d BindingDB Entry DOI: 10.7270/Q2VX0H6K
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50131829 ((E)4,10,13-Trimethyl-tetradecahydro-cyclopenta[a]p...) Show SMILES C[C@H]1[C@@H]2C(=O)CC3[C@@H]4CCC(=O)[C@@]4(C)CCC3[C@@]2(C)CC\C1=N/OCCN Show InChI InChI=1S/C22H34N2O3/c1-13-17(24-27-11-10-23)7-9-22(3)16-6-8-21(2)15(4-5-19(21)26)14(16)12-18(25)20(13)22/h13-16,20H,4-12,23H2,1-3H3/b24-17+/t13-,14?,15+,16?,20-,21+,22-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Prassis Istituto di Ricerche Sigma-Tau Curated by ChEMBL					Assay Description Inhibitory activity against Na+/K+ ATPase				J Med Chem 46: 3644-54 (2003) Article DOI: 10.1021/jm030830y BindingDB Entry DOI: 10.7270/Q24T6K47
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50131821 ((E,Z)10,13-Dimethyl-tetradecahydro-cyclopenta[a]ph...) Show SMILES CN(C)CCO\N=C1/CC[C@]2(C)C3CC[C@@]4(C)[C@@H](CCC4=O)C3CC(=O)[C@H]2C1 Show InChI InChI=1S/C23H36N2O3/c1-22-9-7-15(24-28-12-11-25(3)4)13-19(22)20(26)14-16-17-5-6-21(27)23(17,2)10-8-18(16)22/h16-19H,5-14H2,1-4H3/b24-15+/t16?,17-,18?,19+,22+,23-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
Prassis Istituto di Ricerche Sigma-Tau Curated by ChEMBL					Assay Description Inhibitory activity against Na+/K+ ATPase measured by 32P-ATP hydrolysis method				J Med Chem 46: 3644-54 (2003) Article DOI: 10.1021/jm030830y BindingDB Entry DOI: 10.7270/Q24T6K47
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50286741 (CHEMBL168713 | methyl 18-[6-(2-{2-[4,5-dihydroxy-3...) Show SMILES COC(=O)C12CCC(C)(C)CC1C1=CCC3[C@@]4(C)CCC(OC5OC(CCOCCC6OCC(O)C(O)C6OC6OCC(O)C(O)C6O)C(O)C(O)C5O)C(C)(C)C4CC[C@@]3(C)[C@]1(C)C[C@H]2O |t:13| Show InChI InChI=1S/C50H82O17/c1-45(2)17-18-50(44(60)61-8)26(21-45)25-9-10-32-47(5)15-12-34(46(3,4)31(47)11-16-48(32,6)49(25,7)22-33(50)53)66-43-40(59)38(57)37(56)29(65-43)13-19-62-20-14-30-41(36(55)28(52)23-63-30)67-42-39(58)35(54)27(51)24-64-42/h9,26-43,51-59H,10-24H2,1-8H3/t26?,27?,28?,29?,30?,31?,32?,33-,34?,35?,36?,37?,38?,39?,40?,41?,42?,43?,47+,48-,49-,50?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	2.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity of the compound against rat kidney Na+/K+ ATPase was determined by fiske subbarow method				Bioorg Med Chem Lett 5: 827-830 (1995) Article DOI: 10.1016/0960-894X(95)00121-9 BindingDB Entry DOI: 10.7270/Q2XK8FJF
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50131832 ((E)2,10,13-Trimethyl-tetradecahydro-cyclopenta[a]p...) Show SMILES C[C@@H]1C[C@]2(C)C3CC[C@@]4(C)[C@@H](CCC4=O)C3CC(=O)[C@H]2C\C1=N\OCCN Show InChI InChI=1S/C22H34N2O3/c1-13-12-22(3)16-6-7-21(2)15(4-5-20(21)26)14(16)10-19(25)17(22)11-18(13)24-27-9-8-23/h13-17H,4-12,23H2,1-3H3/b24-18-/t13-,14?,15+,16?,17-,21+,22-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Prassis Istituto di Ricerche Sigma-Tau Curated by ChEMBL					Assay Description Inhibitory activity against Na+/K+ ATPase				J Med Chem 46: 3644-54 (2003) Article DOI: 10.1021/jm030830y BindingDB Entry DOI: 10.7270/Q24T6K47
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50013297 (CHEMBL149689 | N-[4-(5-Methyl-1H-pyrrol-3-yl)-thia...) Show SMILES Cc1cc(c[nH]1)-c1csc(N=C(N)N)n1 |(18.9,-14.7,;17.37,-14.88,;16.59,-16.21,;15.08,-15.91,;14.92,-14.38,;16.33,-13.73,;13.86,-16.84,;13.89,-18.36,;12.45,-18.88,;11.52,-17.64,;9.97,-17.68,;9.23,-19.03,;7.69,-19.06,;10.04,-20.34,;12.41,-16.39,)| Show InChI InChI=1S/C9H11N5S/c1-5-2-6(3-12-5)7-4-15-9(13-7)14-8(10)11/h2-4,12H,1H3,(H4,10,11,13,14)	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Inc. Curated by ChEMBL					Assay Description Tested against canine renal Na+/K+ ATPase				J Med Chem 33: 543-52 (1990) BindingDB Entry DOI: 10.7270/Q2K35V79
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50131823 ((E,Z)6,17-Dihydroxy-10,13-dimethyl-hexadecahydro-c...) Show SMILES CN(C)CCO\N=C1/CC[C@]2(C)C3CC[C@]4(C)C(O)CC[C@H]4C3C[C@@H](O)[C@H]2C1 Show InChI InChI=1S/C23H40N2O3/c1-22-9-7-15(24-28-12-11-25(3)4)13-19(22)20(26)14-16-17-5-6-21(27)23(17,2)10-8-18(16)22/h16-21,26-27H,5-14H2,1-4H3/b24-15+/t16?,17-,18?,19+,20+,21?,22+,23-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Prassis Istituto di Ricerche Sigma-Tau Curated by ChEMBL					Assay Description Inhibitory activity against Na+/K+ ATPase was determined in guinea pig				J Med Chem 46: 3644-54 (2003) Article DOI: 10.1021/jm030830y BindingDB Entry DOI: 10.7270/Q24T6K47
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50286739 (4-((1R,3S,5S,8R,10R,11R,13R,14S,17R)-1,5,11,14-tet...) Show SMILES C[C@@H]1O[C@@H](O[C@H]2C[C@@H](O)[C@]3(CO)[C@H]4[C@H](O)C[C@]5(C)[C@H](CC[C@]5(O)[C@@H]4CC[C@]3(O)C2)C2=CC(=O)OC2)[C@H](O)[C@H](O)[C@H]1O |r,t:33| Show InChI InChI=1S/C29H44O12/c1-13-22(34)23(35)24(36)25(40-13)41-15-8-19(32)28(12-30)21-17(3-5-27(28,37)9-15)29(38)6-4-16(14-7-20(33)39-11-14)26(29,2)10-18(21)31/h7,13,15-19,21-25,30-32,34-38H,3-6,8-12H2,1-2H3/t13-,15-,16+,17+,18+,19+,21+,22-,23+,24+,25-,26+,27-,28+,29-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article	n/a	n/a	2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity of the compound against rat kidney Na+/K+ ATPase was determined by fiske subbarow method				Bioorg Med Chem Lett 5: 827-830 (1995) Article DOI: 10.1016/0960-894X(95)00121-9 BindingDB Entry DOI: 10.7270/Q2XK8FJF
					More data for this Ligand-Target Pair
Potassium-transporting ATPase alpha chain 2 (Homo sapiens (Human))	BDBM50286740 (CHEMBL406262 | Saponin derivative) Show SMILES CC1OC(COCCCC2OC(CCCOOC(=O)C34CCC(C)(C)CC3C3=CCC5[C@@]6(C)CCC(OC7OC(CCOCCC8OCC(O)C(O)C8OC8OCC(O)C(O)C8O)C(O)C(O)C7O)C(C)(C)C6CC[C@@]5(C)[C@]3(C)C[C@H]4O)C(OCC3OC(C)C(OCCCCCCCCC4OCC(O)C(OC5OCC(O)C(O)C5O)C4O)C(O)C3O)C(O)C2O)C(OC(=O)C(C)=CCC[C@](C)(O)C=C)C(OC(=O)C(\CO)=C\CC[C@](C)(O)C=C)C1O |t:28| Show InChI InChI=1S/C112H184O44/c1-15-107(10,136)38-23-27-58(3)99(133)152-97-74(147-59(4)79(119)98(97)153-100(134)61(51-113)28-24-39-108(11,137)16-2)56-139-44-25-30-69-84(124)89(129)95(143-57-73-85(125)88(128)93(60(5)148-73)140-45-22-20-18-17-19-21-29-68-86(126)94(67(117)55-141-68)154-101-90(130)80(120)64(114)53-144-101)72(149-69)31-26-46-146-156-104(135)112-43-42-105(6,7)49-63(112)62-32-33-76-109(12)40-35-78(106(8,9)75(109)34-41-110(76,13)111(62,14)50-77(112)118)151-103-92(132)87(127)83(123)70(150-103)36-47-138-48-37-71-96(82(122)66(116)52-142-71)155-102-91(131)81(121)65(115)54-145-102/h15-16,27-28,32,59-60,63-98,101-103,113-132,136-137H,1-2,17-26,29-31,33-57H2,3-14H3/b58-27+,61-28+/t59?,60?,63?,64?,65?,66?,67?,68?,69?,70?,71?,72?,73?,74?,75?,76?,77-,78?,79?,80?,81?,82?,83?,84?,85?,86?,87?,88?,89?,90?,91?,92?,93?,94?,95?,96?,97?,98?,101?,102?,103?,107-,108-,109+,110-,111-,112?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	4.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity of the compound against rat kidney Na+/K+ ATPase was determined by fiske subbarow method				Bioorg Med Chem Lett 5: 827-830 (1995) Article DOI: 10.1016/0960-894X(95)00121-9 BindingDB Entry DOI: 10.7270/Q2XK8FJF
					More data for this Ligand-Target Pair