BDBM231662 DMeCF3 (13)::US10668094, Compound DCF3

SMILES: C[C@@H]1O[C@H](C[C@H](O)[C@@H]1O[C@H]1C[C@H](O)[C@H](OC2CCN(CC(F)(F)F)CC(C)O2)[C@H](C)O1)O[C@H]1CC[C@@]2(C)C(CCC3C2C[C@H](O)[C@]2(C)[C@H](CC[C@]32O)C2=CC(=O)OC2)C1

InChI Key: InChIKey=UNYFXQCNOFHMAF-NVAUYEMTSA-N

Data: 6 KI

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 231662   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Na,K-ATPase alpha2beta3 (Homo sapiens (Human))	BDBM231662 (DMeCF3 (13) | US10668094, Compound DCF3) Show SMILES C[C@@H]1O[C@H](C[C@H](O)[C@@H]1O[C@H]1C[C@H](O)[C@H](OC2CCN(CC(F)(F)F)CC(C)O2)[C@H](C)O1)O[C@H]1CC[C@@]2(C)C(CCC3C2C[C@H](O)[C@]2(C)[C@H](CC[C@]32O)C2=CC(=O)OC2)C1 |r,t:58| Show InChI InChI=1S/C43H66F3NO12/c1-22-19-47(21-43(44,45)46)13-10-35(54-22)58-38-23(2)56-37(18-32(38)49)59-39-24(3)55-36(17-31(39)48)57-27-8-11-40(4)26(15-27)6-7-29-30(40)16-33(50)41(5)28(9-12-42(29,41)52)25-14-34(51)53-20-25/h14,22-24,26-33,35-39,48-50,52H,6-13,15-21H2,1-5H3/t22?,23-,24-,26?,27-,28+,29?,30?,31-,32-,33-,35?,36-,37-,38+,39+,40-,41-,42-/m0/s1	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	12.4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yeda Research and Development Co. Ltd. US Patent					Assay Description To screen for isoform selectivity of the digoxin derivatives we compared inhibition of Na,K-ATPase activity of purified detergent-soluble human isofo...				US Patent US10668094 (2020)
					More data for this Ligand-Target Pair
Na,K-ATPase alpha2beta2 (Homo sapiens (Human))	BDBM231662 (DMeCF3 (13) | US10668094, Compound DCF3) Show SMILES C[C@@H]1O[C@H](C[C@H](O)[C@@H]1O[C@H]1C[C@H](O)[C@H](OC2CCN(CC(F)(F)F)CC(C)O2)[C@H](C)O1)O[C@H]1CC[C@@]2(C)C(CCC3C2C[C@H](O)[C@]2(C)[C@H](CC[C@]32O)C2=CC(=O)OC2)C1 |r,t:58| Show InChI InChI=1S/C43H66F3NO12/c1-22-19-47(21-43(44,45)46)13-10-35(54-22)58-38-23(2)56-37(18-32(38)49)59-39-24(3)55-36(17-31(39)48)57-27-8-11-40(4)26(15-27)6-7-29-30(40)16-33(50)41(5)28(9-12-42(29,41)52)25-14-34(51)53-20-25/h14,22-24,26-33,35-39,48-50,52H,6-13,15-21H2,1-5H3/t22?,23-,24-,26?,27-,28+,29?,30?,31-,32-,33-,35?,36-,37-,38+,39+,40-,41-,42-/m0/s1	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	18.1	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yeda Research and Development Co. Ltd. US Patent					Assay Description To screen for isoform selectivity of the digoxin derivatives we compared inhibition of Na,K-ATPase activity of purified detergent-soluble human isofo...				US Patent US10668094 (2020)
					More data for this Ligand-Target Pair
Na,K-ATPase alpha2beta1 (Homo sapiens (Human))	BDBM231662 (DMeCF3 (13) | US10668094, Compound DCF3) Show SMILES C[C@@H]1O[C@H](C[C@H](O)[C@@H]1O[C@H]1C[C@H](O)[C@H](OC2CCN(CC(F)(F)F)CC(C)O2)[C@H](C)O1)O[C@H]1CC[C@@]2(C)C(CCC3C2C[C@H](O)[C@]2(C)[C@H](CC[C@]32O)C2=CC(=O)OC2)C1 |r,t:58| Show InChI InChI=1S/C43H66F3NO12/c1-22-19-47(21-43(44,45)46)13-10-35(54-22)58-38-23(2)56-37(18-32(38)49)59-39-24(3)55-36(17-31(39)48)57-27-8-11-40(4)26(15-27)6-7-29-30(40)16-33(50)41(5)28(9-12-42(29,41)52)25-14-34(51)53-20-25/h14,22-24,26-33,35-39,48-50,52H,6-13,15-21H2,1-5H3/t22?,23-,24-,26?,27-,28+,29?,30?,31-,32-,33-,35?,36-,37-,38+,39+,40-,41-,42-/m0/s1	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	28.6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yeda Research and Development Co. Ltd. US Patent					Assay Description To screen for isoform selectivity of the digoxin derivatives we compared inhibition of Na,K-ATPase activity of purified detergent-soluble human isofo...				US Patent US10668094 (2020)
					More data for this Ligand-Target Pair
Na,K-ATPase alpha2beta1 (Homo sapiens (Human))	BDBM231662 (DMeCF3 (13) | US10668094, Compound DCF3) Show SMILES C[C@@H]1O[C@H](C[C@H](O)[C@@H]1O[C@H]1C[C@H](O)[C@H](OC2CCN(CC(F)(F)F)CC(C)O2)[C@H](C)O1)O[C@H]1CC[C@@]2(C)C(CCC3C2C[C@H](O)[C@]2(C)[C@H](CC[C@]32O)C2=CC(=O)OC2)C1 |r,t:58| Show InChI InChI=1S/C43H66F3NO12/c1-22-19-47(21-43(44,45)46)13-10-35(54-22)58-38-23(2)56-37(18-32(38)49)59-39-24(3)55-36(17-31(39)48)57-27-8-11-40(4)26(15-27)6-7-29-30(40)16-33(50)41(5)28(9-12-42(29,41)52)25-14-34(51)53-20-25/h14,22-24,26-33,35-39,48-50,52H,6-13,15-21H2,1-5H3/t22?,23-,24-,26?,27-,28+,29?,30?,31-,32-,33-,35?,36-,37-,38+,39+,40-,41-,42-/m0/s1	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	44	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Weizmann Institute of Science					Assay Description Inhibition of Na,K-ATPase activity of the detergent-soluble α1β1, α2β1, and α3β1 complexes by CGs was done exactly as d...				J Biol Chem 289: 21153-62 (2014) Article DOI: 10.1074/jbc.M114.557629 BindingDB Entry DOI: 10.7270/Q2G44P6T
					More data for this Ligand-Target Pair
Na,K-ATPase alpha1beta1 (Homo sapiens (Human))	BDBM231662 (DMeCF3 (13) | US10668094, Compound DCF3) Show SMILES C[C@@H]1O[C@H](C[C@H](O)[C@@H]1O[C@H]1C[C@H](O)[C@H](OC2CCN(CC(F)(F)F)CC(C)O2)[C@H](C)O1)O[C@H]1CC[C@@]2(C)C(CCC3C2C[C@H](O)[C@]2(C)[C@H](CC[C@]32O)C2=CC(=O)OC2)C1 |r,t:58| Show InChI InChI=1S/C43H66F3NO12/c1-22-19-47(21-43(44,45)46)13-10-35(54-22)58-38-23(2)56-37(18-32(38)49)59-39-24(3)55-36(17-31(39)48)57-27-8-11-40(4)26(15-27)6-7-29-30(40)16-33(50)41(5)28(9-12-42(29,41)52)25-14-34(51)53-20-25/h14,22-24,26-33,35-39,48-50,52H,6-13,15-21H2,1-5H3/t22?,23-,24-,26?,27-,28+,29?,30?,31-,32-,33-,35?,36-,37-,38+,39+,40-,41-,42-/m0/s1	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	119	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yeda Research and Development Co. Ltd. US Patent					Assay Description To screen for isoform selectivity of the digoxin derivatives we compared inhibition of Na,K-ATPase activity of purified detergent-soluble human isofo...				US Patent US10668094 (2020)
					More data for this Ligand-Target Pair
Na,K-ATPase alpha1beta1 (Homo sapiens (Human))	BDBM231662 (DMeCF3 (13) | US10668094, Compound DCF3) Show SMILES C[C@@H]1O[C@H](C[C@H](O)[C@@H]1O[C@H]1C[C@H](O)[C@H](OC2CCN(CC(F)(F)F)CC(C)O2)[C@H](C)O1)O[C@H]1CC[C@@]2(C)C(CCC3C2C[C@H](O)[C@]2(C)[C@H](CC[C@]32O)C2=CC(=O)OC2)C1 |r,t:58| Show InChI InChI=1S/C43H66F3NO12/c1-22-19-47(21-43(44,45)46)13-10-35(54-22)58-38-23(2)56-37(18-32(38)49)59-39-24(3)55-36(17-31(39)48)57-27-8-11-40(4)26(15-27)6-7-29-30(40)16-33(50)41(5)28(9-12-42(29,41)52)25-14-34(51)53-20-25/h14,22-24,26-33,35-39,48-50,52H,6-13,15-21H2,1-5H3/t22?,23-,24-,26?,27-,28+,29?,30?,31-,32-,33-,35?,36-,37-,38+,39+,40-,41-,42-/m0/s1	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	199	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Weizmann Institute of Science					Assay Description Inhibition of Na,K-ATPase activity of the detergent-soluble α1β1, α2β1, and α3β1 complexes by CGs was done exactly as d...				J Biol Chem 289: 21153-62 (2014) Article DOI: 10.1074/jbc.M114.557629 BindingDB Entry DOI: 10.7270/Q2G44P6T
					More data for this Ligand-Target Pair