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Compile Data Set for Download or QSAR

Found 381 hits with Last Name = 'hong' and Initial = 'kh'   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255109
PNG
(CHEMBL4081196)
Show SMILES [H][C@@]12CC[C@]3(O)C[C@@H](O)C[C@@H](O)[C@]3(CO)[C@@]1([H])[C@H](O)C[C@]1(C)[C@H](CC[C@]21O)c1cn(Cc2ccccc2)nn1 |r|
Show InChI InChI=1S/C28H39N3O6/c1-25-13-22(34)24-20(7-9-26(36)12-18(33)11-23(35)27(24,26)16-32)28(25,37)10-8-19(25)21-15-31(30-29-21)14-17-5-3-2-4-6-17/h2-6,15,18-20,22-24,32-37H,7-14,16H2,1H3/t18-,19+,20+,22+,23+,24+,25+,26-,27+,28-/m0/s1
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n/an/a 0.00200n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255111
PNG
(CHEMBL4092961)
Show SMILES [H][C@@]12C[C@@H](C[C@@]3(O)CC[C@]4([H])[C@]([H])([C@@H](C[C@]5(C)[C@@H](CO)CC[C@]45OCOC)OCOC)[C@@]13COC(C)(C)O2)OCOC |r|
Show InChI InChI=1S/C29H50O10/c1-25(2)37-15-28-23(39-25)11-20(35-16-32-4)12-27(28,31)9-8-21-24(28)22(36-17-33-5)13-26(3)19(14-30)7-10-29(21,26)38-18-34-6/h19-24,30-31H,7-18H2,1-6H3/t19-,20+,21-,22-,23-,24-,26-,27+,28-,29+/m1/s1
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n/an/a 0.0110n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255122
PNG
(CHEMBL4059538)
Show SMILES [H][C@]12OC(C)(C)O[C@@]1([H])[C@]([H])(O[C@H]1C[C@@]3([H])OC(C)(C)OC[C@]33[C@@]4([H])[C@@H](C[C@]5(C)[C@@H](CO)CC[C@]5(O)[C@]4([H])CC[C@]3(O)C1)OCOC)O[C@@H](C)[C@@H]2OCOC |r|
Show InChI InChI=1S/C36H60O13/c1-20-27(43-19-41-8)28-29(49-32(4,5)48-28)30(45-20)46-22-13-25-35(17-44-31(2,3)47-25)26-23(10-11-34(35,38)14-22)36(39)12-9-21(16-37)33(36,6)15-24(26)42-18-40-7/h20-30,37-39H,9-19H2,1-8H3/t20-,21+,22-,23+,24+,25+,26+,27-,28+,29+,30-,33+,34-,35+,36-/m0/s1
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n/an/a 0.600n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Cyclin-A1/Cyclin-dependent kinase 2


(Homo sapiens (Human))
BDBM2579
PNG
((2S,3R,4R,6R)-3-methoxy-2-methyl-4-(methylamino)-2...)
Show SMILES CN[C@@H]1C[C@H]2O[C@@](C)([C@@H]1OC)n1c3ccccc3c3c4CNC(=O)c4c4c5ccccc5n2c4c13 |r|
Show InChI InChI=1S/C28H26N4O3/c1-28-26(34-3)17(29-2)12-20(35-28)31-18-10-6-4-8-14(18)22-23-16(13-30-27(23)33)21-15-9-5-7-11-19(15)32(28)25(21)24(22)31/h4-11,17,20,26,29H,12-13H2,1-3H3,(H,30,33)/t17-,20-,26-,28+/m1/s1
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n/an/a 1.40n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of CDK2/Cyclin A1 (unknown origin) using histone H1 as substrate preincubated for 20 mins followed by 33P-ATP addition and measured after ...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113232
BindingDB Entry DOI: 10.7270/Q22J6GMW
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255138
PNG
(CHEMBL4066361)
Show SMILES [H][C@@]12C[C@@H](C[C@@]3(O)CC[C@]4([H])[C@]([H])([C@@H](C[C@]5(C)[C@H](CC[C@]45OCOC)\C=N\O)OCOC)[C@@]13COC(C)(C)O2)OCOC |r|
Show InChI InChI=1S/C29H49NO10/c1-25(2)38-15-28-23(40-25)11-20(36-16-33-4)12-27(28,31)9-8-21-24(28)22(37-17-34-5)13-26(3)19(14-30-32)7-10-29(21,26)39-18-35-6/h14,19-24,31-32H,7-13,15-18H2,1-6H3/b30-14+/t19-,20+,21-,22-,23-,24-,26-,27+,28-,29+/m1/s1
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n/an/a 1.40n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Cyclin-O


(Homo sapiens)
BDBM2579
PNG
((2S,3R,4R,6R)-3-methoxy-2-methyl-4-(methylamino)-2...)
Show SMILES CN[C@@H]1C[C@H]2O[C@@](C)([C@@H]1OC)n1c3ccccc3c3c4CNC(=O)c4c4c5ccccc5n2c4c13 |r|
Show InChI InChI=1S/C28H26N4O3/c1-28-26(34-3)17(29-2)12-20(35-28)31-18-10-6-4-8-14(18)22-23-16(13-30-27(23)33)21-15-9-5-7-11-19(15)32(28)25(21)24(22)31/h4-11,17,20,26,29H,12-13H2,1-3H3,(H,30,33)/t17-,20-,26-,28+/m1/s1
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n/an/a 1.5n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of CDK2/Cyclin-O (unknown origin) using histone H1 as substrate preincubated for 20 mins followed by 33P-ATP addition and measured after 2...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113232
BindingDB Entry DOI: 10.7270/Q22J6GMW
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1


(Homo sapiens (Human))
BDBM2579
PNG
((2S,3R,4R,6R)-3-methoxy-2-methyl-4-(methylamino)-2...)
Show SMILES CN[C@@H]1C[C@H]2O[C@@](C)([C@@H]1OC)n1c3ccccc3c3c4CNC(=O)c4c4c5ccccc5n2c4c13 |r|
Show InChI InChI=1S/C28H26N4O3/c1-28-26(34-3)17(29-2)12-20(35-28)31-18-10-6-4-8-14(18)22-23-16(13-30-27(23)33)21-15-9-5-7-11-19(15)32(28)25(21)24(22)31/h4-11,17,20,26,29H,12-13H2,1-3H3,(H,30,33)/t17-,20-,26-,28+/m1/s1
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n/an/a 1.60n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of CDK2/Cyclin E (unknown origin) using histone H1 as substrate preincubated for 20 mins followed by 33P-ATP addition and measured after 2...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113232
BindingDB Entry DOI: 10.7270/Q22J6GMW
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-3


(Rattus norvegicus)
BDBM50286739
PNG
(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
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n/an/a 1.80n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta3 expressed in baculovirus infected Sf9 cell membranes using [gamma-32P]ATP as substrate prein...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1


(Homo sapiens (Human))
BDBM50563174
PNG
(CHEMBL1708376)
Show SMILES Cc1nn(-c2nccs2)c2C(Br)C(C)(C)CC(=O)c12
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n/an/a 2.30n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of CDK2/Cyclin E (unknown origin) using histone H1 as substrate preincubated for 20 mins followed by 33P-ATP addition and measured after 2...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113232
BindingDB Entry DOI: 10.7270/Q22J6GMW
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255120
PNG
(CHEBI:38178 | STROPHANTHIDIN)
Show SMILES [H][C@@]12CC[C@]3(O)C[C@@H](O)CC[C@]3(C=O)[C@@]1([H])CC[C@]1(C)[C@H](CC[C@]21O)C1=CC(=O)OC1 |r,t:29|
Show InChI InChI=1S/C23H32O6/c1-20-6-3-17-18(4-8-22(27)11-15(25)2-7-21(17,22)13-24)23(20,28)9-5-16(20)14-10-19(26)29-12-14/h10,13,15-18,25,27-28H,2-9,11-12H2,1H3/t15-,16+,17-,18+,20+,21-,22-,23-/m0/s1
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n/an/a 2.40n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Endothelin-1 receptor


(RAT)
BDBM50064000
PNG
(CHEMBL3400988)
Show SMILES CC(=O)c1ccc(OCc2ccc3OCOc3c2)cc1OC(CCC(O)=O)c1ccccc1
Show InChI InChI=1S/C26H24O7/c1-17(27)21-9-8-20(30-15-18-7-10-23-25(13-18)32-16-31-23)14-24(21)33-22(11-12-26(28)29)19-5-3-2-4-6-19/h2-10,13-14,22H,11-12,15-16H2,1H3,(H,28,29)
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n/an/a 3.30n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Displacement of PD156707 from rat ETA receptor after 1 hr by Lowry method


Bioorg Med Chem 23: 657-67 (2015)


Article DOI: 10.1016/j.bmc.2015.01.003
BindingDB Entry DOI: 10.7270/Q28K7BRM
More data for this
Ligand-Target Pair
Endothelin-1 receptor


(RAT)
BDBM50063998
PNG
(CHEMBL3400989)
Show SMILES CC(=O)c1ccc(OCc2ccc3nsnc3c2)cc1OC(CCC(O)=O)c1ccccc1
Show InChI InChI=1S/C25H22N2O5S/c1-16(28)20-9-8-19(31-15-17-7-10-21-22(13-17)27-33-26-21)14-24(20)32-23(11-12-25(29)30)18-5-3-2-4-6-18/h2-10,13-14,23H,11-12,15H2,1H3,(H,29,30)
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n/an/a 3.90n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Displacement of [125I]ET-1 from rat ETA receptor after 1 hr by Lowry method


Bioorg Med Chem 23: 657-67 (2015)


Article DOI: 10.1016/j.bmc.2015.01.003
BindingDB Entry DOI: 10.7270/Q28K7BRM
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255119
PNG
(CHEMBL4071710)
Show SMILES [H][C@]12OC(C)(C)O[C@@]1([H])[C@]([H])(O[C@H]1C[C@@]3([H])OC(C)(C)OC[C@]33[C@@]4([H])[C@H](O)C[C@]5(C)[C@H](CC[C@]5(O)[C@]4([H])CC[C@]3(O)C1)C1=CC(=O)OC1)O[C@@H](C)[C@@H]2O |r,t:48|
Show InChI InChI=1S/C35H52O12/c1-17-26(38)27-28(47-31(4,5)46-27)29(43-17)44-19-12-23-34(16-42-30(2,3)45-23)25-21(7-9-33(34,39)13-19)35(40)10-8-20(18-11-24(37)41-15-18)32(35,6)14-22(25)36/h11,17,19-23,25-29,36,38-40H,7-10,12-16H2,1-6H3/t17-,19-,20+,21+,22+,23+,25+,26-,27+,28+,29-,32+,33-,34+,35-/m0/s1
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n/an/a 4n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50286739
PNG
(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
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n/an/a 4.30n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Endothelin-1 receptor


(RAT)
BDBM50061101
PNG
(4-(1,1-Dimethylethyl)-N-(6-(2-hydroxyethoxy)-5-(2-...)
Show SMILES COc1ccccc1Oc1c(NS(=O)(=O)c2ccc(cc2)C(C)(C)C)nc(nc1OCCO)-c1ncccn1
Show InChI InChI=1S/C27H29N5O6S/c1-27(2,3)18-10-12-19(13-11-18)39(34,35)32-23-22(38-21-9-6-5-8-20(21)36-4)26(37-17-16-33)31-25(30-23)24-28-14-7-15-29-24/h5-15,33H,16-17H2,1-4H3,(H,30,31,32)
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n/an/a 4.70n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Displacement of [125I]ET-1 from rat ETA receptor after 1 hr by Lowry method


Bioorg Med Chem 23: 657-67 (2015)


Article DOI: 10.1016/j.bmc.2015.01.003
BindingDB Entry DOI: 10.7270/Q28K7BRM
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255140
PNG
(CHEMBL4076623)
Show SMILES [H][C@]12OC(C)(C)O[C@@]1([H])[C@]([H])(O[C@H]1C[C@@]3([H])OC(C)(C)OC[C@]33[C@@]4([H])[C@@H](C[C@]5(C)[C@H](CC[C@]5(O)[C@]4([H])CC[C@]3(O)C1)C=O)OCOC)O[C@@H](C)[C@@H]2OCOC |r|
Show InChI InChI=1S/C36H58O13/c1-20-27(43-19-41-8)28-29(49-32(4,5)48-28)30(45-20)46-22-13-25-35(17-44-31(2,3)47-25)26-23(10-11-34(35,38)14-22)36(39)12-9-21(16-37)33(36,6)15-24(26)42-18-40-7/h16,20-30,38-39H,9-15,17-19H2,1-8H3/t20-,21+,22-,23+,24+,25+,26+,27-,28+,29+,30-,33+,34-,35+,36-/m0/s1
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n/an/a 4.90n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255139
PNG
(CHEMBL4085219)
Show SMILES [H][C@@]12C[C@@H](C[C@@]3(O)CC[C@]4([H])[C@]([H])([C@@H](C[C@]5(C)[C@H](CC[C@]45OCOC)c4cn(Cc5ccccc5)nn4)OCOC)[C@@]13COC(C)(C)O2)OCOC |r|
Show InChI InChI=1S/C37H55N3O9/c1-33(2)47-21-36-31(49-33)16-26(45-22-42-4)17-35(36,41)14-12-28-32(36)30(46-23-43-5)18-34(3)27(13-15-37(28,34)48-24-44-6)29-20-40(39-38-29)19-25-10-8-7-9-11-25/h7-11,20,26-28,30-32,41H,12-19,21-24H2,1-6H3/t26-,27+,28+,30+,31+,32+,34+,35-,36+,37-/m0/s1
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n/an/a 5n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM46355
PNG
(DIGOXIN | MLS000069819 | SMR000059217 | US10668094...)
Show SMILES C[C@H]1O[C@H](C[C@H](O)[C@@H]1O)O[C@H]1[C@@H](O)C[C@H](O[C@H]2[C@@H](O)C[C@H](O[C@H]3CC[C@@]4(C)[C@H](CC[C@@H]5[C@@H]4C[C@@H](O)[C@]4(C)[C@H](CC[C@]54O)C4=CC(=O)OC4)C3)O[C@@H]2C)O[C@@H]1C |t:46|
Show InChI InChI=1S/C41H64O14/c1-19-36(47)28(42)15-34(50-19)54-38-21(3)52-35(17-30(38)44)55-37-20(2)51-33(16-29(37)43)53-24-8-10-39(4)23(13-24)6-7-26-27(39)14-31(45)40(5)25(9-11-41(26,40)48)22-12-32(46)49-18-22/h12,19-21,23-31,33-38,42-45,47-48H,6-11,13-18H2,1-5H3/t19-,20-,21-,23-,24+,25-,26-,27+,28+,29+,30+,31-,33+,34+,35+,36-,37-,38-,39+,40+,41+/m1/s1
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n/an/a 5.5n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Endothelin-1 receptor


(RAT)
BDBM50063997
PNG
(CHEMBL3400996)
Show SMILES OC(=O)CCC(Oc1cc(OCc2ccc3nonc3c2)ccc1C#N)c1ccccc1
Show InChI InChI=1S/C24H19N3O5/c25-14-18-7-8-19(30-15-16-6-9-20-21(12-16)27-32-26-20)13-23(18)31-22(10-11-24(28)29)17-4-2-1-3-5-17/h1-9,12-13,22H,10-11,15H2,(H,28,29)
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n/an/a 5.5n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Displacement of [125I]ET-1 from rat ETA receptor after 1 hr by Lowry method


Bioorg Med Chem 23: 657-67 (2015)


Article DOI: 10.1016/j.bmc.2015.01.003
BindingDB Entry DOI: 10.7270/Q28K7BRM
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM11162
PNG
((1R)-3-oxo-3-[3-(trifluoroethyl)-5,6-dihydro[1,2,4...)
Show SMILES N[C@@H](CC(=O)N1CCn2c(C1)nnc2C(F)(F)F)Cc1cc(F)c(F)cc1F |r|
Show InChI InChI=1S/C16H15F6N5O/c17-10-6-12(19)11(18)4-8(10)3-9(23)5-14(28)26-1-2-27-13(7-26)24-25-15(27)16(20,21)22/h4,6,9H,1-3,5,7,23H2/t9-/m1/s1
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n/an/a 7.80n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant human DPP4 using Gly-Pro-AMC as substrate incubated for 1 hr by fluorogenic assay


Citation and Details

Article DOI: 10.1016/j.bmc.2020.115861
BindingDB Entry DOI: 10.7270/Q2930XTC
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1


(Homo sapiens (Human))
BDBM50563177
PNG
(CHEMBL4763182)
Show SMILES Cc1nn(c2C(Br)C(C)(C)CC(=O)c12)-c1ccncn1
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n/an/a 8.90n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of CDK2/Cyclin E (unknown origin) using histone H1 as substrate preincubated for 20 mins followed by 33P-ATP addition and measured after 2...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113232
BindingDB Entry DOI: 10.7270/Q22J6GMW
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255128
PNG
(CHEMBL4067657)
Show SMILES [H][C@@]12C[C@@H](C[C@@]3(O)CC[C@]4([H])[C@]([H])([C@@H](C[C@]5(C)[C@H](CC[C@]45OCOC)C(O)C#C)OCOC)[C@@]13COC(C)(C)O2)OCOC |r|
Show InChI InChI=1S/C31H50O10/c1-8-23(32)21-10-12-31(40-19-36-7)22-9-11-29(33)14-20(37-17-34-5)13-25-30(29,16-39-27(2,3)41-25)26(22)24(38-18-35-6)15-28(21,31)4/h1,20-26,32-33H,9-19H2,2-7H3/t20-,21+,22+,23?,24+,25+,26+,28+,29-,30+,31-/m0/s1
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n/an/a 10n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255117
PNG
(CHEMBL4072996)
Show SMILES [H][C@]12OC(C)(C)O[C@@]1([H])[C@]([H])(O[C@H]1C[C@@]3([H])OC(C)(C)OC[C@]33[C@@]4([H])[C@@H](C[C@]5(C)[C@H](CC[C@]5(O)[C@]4([H])CC[C@]3(O)C1)C(O)c1cn(Cc3ccc(F)cc3)nn1)OCOC)O[C@@H](C)[C@@H]2OCOC |r|
Show InChI InChI=1S/C45H66FN3O13/c1-25-36(56-24-54-8)37-38(62-41(4,5)61-37)39(58-25)59-28-17-33-44(22-57-40(2,3)60-33)34-29(13-15-43(44,51)18-28)45(52)16-14-30(42(45,6)19-32(34)55-23-53-7)35(50)31-21-49(48-47-31)20-26-9-11-27(46)12-10-26/h9-12,21,25,28-30,32-39,50-52H,13-20,22-24H2,1-8H3/t25-,28-,29+,30+,32+,33+,34+,35?,36-,37+,38+,39-,42+,43-,44+,45-/m0/s1
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n/an/a 12n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255121
PNG
(CHEBI:4037 | CHEMBL1075788)
Show SMILES [H][C@@]1(CC[C@]2(O)[C@]3([H])CC[C@]4(O)C[C@H](CC[C@]4(C=O)[C@@]3([H])CC[C@]12C)O[C@H]1C[C@H](OC)[C@H](O)[C@@H](C)O1)C1=CC(=O)OC1 |t:41|
Show InChI InChI=1S/C30H44O9/c1-17-26(33)23(36-3)13-25(38-17)39-19-4-9-28(16-31)21-5-8-27(2)20(18-12-24(32)37-15-18)7-11-30(27,35)22(21)6-10-29(28,34)14-19/h12,16-17,19-23,25-26,33-35H,4-11,13-15H2,1-3H3/t17-,19+,20-,21+,22-,23+,25+,26-,27-,28+,29+,30+/m1/s1
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n/an/a 12n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Endothelin-1 receptor


(RAT)
BDBM50063999
PNG
(CHEMBL3400984)
Show SMILES CC(=O)c1ccc(OCc2ccccc2)cc1OC(CCC(O)=O)c1ccccc1
Show InChI InChI=1S/C25H24O5/c1-18(26)22-13-12-21(29-17-19-8-4-2-5-9-19)16-24(22)30-23(14-15-25(27)28)20-10-6-3-7-11-20/h2-13,16,23H,14-15,17H2,1H3,(H,27,28)
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n/an/a 12n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Displacement of [125I]ET-1 from rat ETA receptor after 1 hr by Lowry method


Bioorg Med Chem 23: 657-67 (2015)


Article DOI: 10.1016/j.bmc.2015.01.003
BindingDB Entry DOI: 10.7270/Q28K7BRM
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255116
PNG
(CHEMBL4074239)
Show SMILES [H][C@@]1(O[C@H]2C[C@@H](O)[C@]3(CO)[C@@]4([H])[C@H](O)C[C@]5(C)[C@H](CC[C@]5(O)[C@]4([H])CC[C@]3(O)C2)C(O)c2cn(Cc3ccc(F)cc3)nn2)O[C@@H](C)[C@H](O)[C@@H](O)[C@H]1O |r|
Show InChI InChI=1S/C35H50FN3O11/c1-17-27(43)29(45)30(46)31(49-17)50-20-11-25(42)34(16-40)26-21(7-9-33(34,47)12-20)35(48)10-8-22(32(35,2)13-24(26)41)28(44)23-15-39(38-37-23)14-18-3-5-19(36)6-4-18/h3-6,15,17,20-22,24-31,40-48H,7-14,16H2,1-2H3/t17-,20-,21+,22+,24+,25+,26+,27-,28?,29+,30+,31-,32+,33-,34+,35-/m0/s1
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n/an/a 13n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM50462415
PNG
(CHEMBL4250492)
Show SMILES N[C@@H](CCn1cc(nn1)-c1ccncc1)Cc1cc(F)c(F)cc1F |r|
Show InChI InChI=1S/C17H16F3N5/c18-14-9-16(20)15(19)8-12(14)7-13(21)3-6-25-10-17(23-24-25)11-1-4-22-5-2-11/h1-2,4-5,8-10,13H,3,6-7,21H2/t13-/m0/s1
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n/an/a 14n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant human DPP4 using Gly-Pro-AMC as substrate incubated for 1 hr by fluorogenic assay


Citation and Details

Article DOI: 10.1016/j.bmc.2020.115861
BindingDB Entry DOI: 10.7270/Q2930XTC
More data for this
Ligand-Target Pair
Endothelin-1 receptor


(RAT)
BDBM50063996
PNG
(CHEMBL3400998)
Show SMILES OC(=O)c1ccc(OCc2ccccc2)cc1OC(CCC#N)c1ccccc1
Show InChI InChI=1S/C24H21NO4/c25-15-7-12-22(19-10-5-2-6-11-19)29-23-16-20(13-14-21(23)24(26)27)28-17-18-8-3-1-4-9-18/h1-6,8-11,13-14,16,22H,7,12,17H2,(H,26,27)
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n/an/a 19n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Displacement of [125I]ET-1 from rat ETA receptor after 1 hr by Lowry method


Bioorg Med Chem 23: 657-67 (2015)


Article DOI: 10.1016/j.bmc.2015.01.003
BindingDB Entry DOI: 10.7270/Q28K7BRM
More data for this
Ligand-Target Pair
Cyclin-A1/Cyclin-dependent kinase 2


(Homo sapiens (Human))
BDBM50563174
PNG
(CHEMBL1708376)
Show SMILES Cc1nn(-c2nccs2)c2C(Br)C(C)(C)CC(=O)c12
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n/an/a 24n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of CDK2/Cyclin A1 (unknown origin) using histone H1 as substrate preincubated for 20 mins followed by 33P-ATP addition and measured after ...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113232
BindingDB Entry DOI: 10.7270/Q22J6GMW
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1


(Homo sapiens (Human))
BDBM50563140
PNG
(CHEMBL1906448)
Show SMILES Cc1nn(c2C(Br)C(C)(C)CC(=O)c12)-c1ccccn1
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n/an/a 27n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of CDK2/Cyclin E (unknown origin) using histone H1 as substrate preincubated for 20 mins followed by 33P-ATP addition and measured after 2...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113232
BindingDB Entry DOI: 10.7270/Q22J6GMW
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM50552244
PNG
(CHEMBL4790735)
Show SMILES N[C@@H](CCn1cc(nn1)-c1cccnc1)Cc1cc(F)c(F)cc1F |r|
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n/an/a 28n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant human DPP4 using Gly-Pro-AMC as substrate incubated for 1 hr by fluorogenic assay


Citation and Details

Article DOI: 10.1016/j.bmc.2020.115861
BindingDB Entry DOI: 10.7270/Q2930XTC
More data for this
Ligand-Target Pair
Endothelin-1 receptor


(RAT)
BDBM50029352
PNG
(CHEMBL336033 | [(5S,8S,11R,14S,16aR)-8-(1H-Indol-3...)
Show SMILES CC(C)C[C@H]1NC(=O)[C@@H](NC(=O)[C@H]2CCCN2C(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC1=O)C(C)C
Show InChI InChI=1S/C31H42N6O7/c1-16(2)12-21-27(40)33-22(13-18-15-32-20-9-6-5-8-19(18)20)28(41)35-23(14-25(38)39)31(44)37-11-7-10-24(37)29(42)36-26(17(3)4)30(43)34-21/h5-6,8-9,15-17,21-24,26,32H,7,10-14H2,1-4H3,(H,33,40)(H,34,43)(H,35,41)(H,36,42)(H,38,39)/t21-,22+,23+,24-,26+/m1/s1
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n/an/a 28n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Displacement of [125I]ET-1 from rat ETA receptor after 1 hr by Lowry method


Bioorg Med Chem 23: 657-67 (2015)


Article DOI: 10.1016/j.bmc.2015.01.003
BindingDB Entry DOI: 10.7270/Q28K7BRM
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-3/beta-1


(Rattus norvegicus)
BDBM50286739
PNG
(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
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n/an/a 31n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha3/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255108
PNG
(CHEMBL4077606)
Show SMILES [H][C@@]12CC[C@]3(O)C[C@@H](O)C[C@@H](O)[C@]3(CO)[C@@]1([H])[C@H](O)C[C@]1(C)[C@H](CC[C@]21O)c1cn(Cc2ccc(Cl)cc2)nn1 |r|
Show InChI InChI=1S/C28H38ClN3O6/c1-25-12-22(35)24-20(6-8-26(37)11-18(34)10-23(36)27(24,26)15-33)28(25,38)9-7-19(25)21-14-32(31-30-21)13-16-2-4-17(29)5-3-16/h2-5,14,18-20,22-24,33-38H,6-13,15H2,1H3/t18-,19+,20+,22+,23+,24+,25+,26-,27+,28-/m0/s1
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n/an/a 32n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255107
PNG
(CHEMBL4093925)
Show SMILES [H][C@@]12CC[C@]3(O)C[C@@H](O)C[C@@H](O)[C@]3(CO)[C@@]1([H])[C@H](O)C[C@]1(C)[C@H](CC[C@]21O)c1cn(Cc2ccc(F)cc2)nn1 |r|
Show InChI InChI=1S/C28H38FN3O6/c1-25-12-22(35)24-20(6-8-26(37)11-18(34)10-23(36)27(24,26)15-33)28(25,38)9-7-19(25)21-14-32(31-30-21)13-16-2-4-17(29)5-3-16/h2-5,14,18-20,22-24,33-38H,6-13,15H2,1H3/t18-,19+,20+,22+,23+,24+,25+,26-,27+,28-/m0/s1
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n/an/a 32n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255114
PNG
(CHEMBL4072200)
Show SMILES [H][C@]12OC(C)(C)O[C@@]1([H])[C@]([H])(O[C@H]1C[C@@]3([H])OC(C)(C)OC[C@]33[C@@]4([H])[C@@H](C[C@]5(C)[C@H](CC[C@]5(O)[C@]4([H])CC[C@]3(O)C1)C#N)OCOC)O[C@@H](C)[C@@H]2OCOC |r|
Show InChI InChI=1S/C36H57NO12/c1-20-27(43-19-41-8)28-29(49-32(4,5)48-28)30(45-20)46-22-13-25-35(17-44-31(2,3)47-25)26-23(10-11-34(35,38)14-22)36(39)12-9-21(16-37)33(36,6)15-24(26)42-18-40-7/h20-30,38-39H,9-15,17-19H2,1-8H3/t20-,21+,22-,23+,24+,25+,26+,27-,28+,29+,30-,33+,34-,35+,36-/m0/s1
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n/an/a 33n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Cyclin-O


(Homo sapiens)
BDBM50563174
PNG
(CHEMBL1708376)
Show SMILES Cc1nn(-c2nccs2)c2C(Br)C(C)(C)CC(=O)c12
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n/an/a 33n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of CDK2/Cyclin-O (unknown origin) using histone H1 as substrate preincubated for 20 mins followed by 33P-ATP addition and measured after 2...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113232
BindingDB Entry DOI: 10.7270/Q22J6GMW
More data for this
Ligand-Target Pair
Sodium/potassium-transporting ATPase subunit alpha-4/beta-1


(Rattus norvegicus)
BDBM50255127
PNG
(CHEMBL4095064)
Show SMILES [H][C@@]12C[C@@H](C[C@@]3(O)CC[C@]4([H])[C@]([H])([C@@H](C[C@]5(C)[C@H](CC[C@]45OCOC)C(O)=O)OCOC)[C@@]13COC(C)(C)O2)OCOC |r|
Show InChI InChI=1S/C29H48O11/c1-25(2)38-14-28-22(40-25)11-18(36-15-33-4)12-27(28,32)9-7-19-23(28)21(37-16-34-5)13-26(3)20(24(30)31)8-10-29(19,26)39-17-35-6/h18-23,32H,7-17H2,1-6H3,(H,30,31)/t18-,19+,20+,21+,22+,23+,26+,27-,28+,29-/m0/s1
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n/an/a 39n/an/an/an/an/an/a



Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy , University of Minnesota , Minneapolis , Minnesota 55414 , United States.

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat Na+/K+-ATPase alpha4/beta1 expressed in baculovirus infected insect Sf9 cell membranes using [gamma-32P]ATP as substrat...


J Med Chem 61: 1800-1820 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00925
BindingDB Entry DOI: 10.7270/Q2T43WJH
More data for this
Ligand-Target Pair
Cyclin-O


(Homo sapiens)
BDBM50563177
PNG
(CHEMBL4763182)
Show SMILES Cc1nn(c2C(Br)C(C)(C)CC(=O)c12)-c1ccncn1
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n/an/a 42n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of CDK2/Cyclin-O (unknown origin) using histone H1 as substrate preincubated for 20 mins followed by 33P-ATP addition and measured after 2...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113232
BindingDB Entry DOI: 10.7270/Q22J6GMW
More data for this
Ligand-Target Pair
Cyclin-A1/Cyclin-dependent kinase 2


(Homo sapiens (Human))
BDBM50563177
PNG
(CHEMBL4763182)
Show SMILES Cc1nn(c2C(Br)C(C)(C)CC(=O)c12)-c1ccncn1
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n/an/a 46n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of CDK2/Cyclin A1 (unknown origin) using histone H1 as substrate preincubated for 20 mins followed by 33P-ATP addition and measured after ...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113232
BindingDB Entry DOI: 10.7270/Q22J6GMW
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50082211
PNG
(CHEMBL3421742)
Show SMILES Nc1ccccc1NC(=O)c1ccc(CNCc2nc(no2)-c2ccc(cc2)[N+]([O-])=O)cc1
Show InChI InChI=1S/C23H20N6O4/c24-19-3-1-2-4-20(19)26-23(30)17-7-5-15(6-8-17)13-25-14-21-27-22(28-33-21)16-9-11-18(12-10-16)29(31)32/h1-12,25H,13-14,24H2,(H,26,30)
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n/an/a 60n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Inhibition of recombinant HDAC1 (unknown origin) using fluorogenic substrate Boc-Lys (acetyl)-AMC after 20 mins by homogeneous fluorescence release a...


Eur J Med Chem 96: 1-13 (2015)


Article DOI: 10.1016/j.ejmech.2015.04.002
BindingDB Entry DOI: 10.7270/Q21G0P01
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (Human))
BDBM50029422
PNG
(CHEMBL3343311)
Show SMILES CC1CCCCN1CCCOc1ccc2c(Nc3ccc(NC(=O)NCc4ccccc4)cc3)ncnc2c1
Show InChI InChI=1S/C31H36N6O2/c1-23-8-5-6-17-37(23)18-7-19-39-27-15-16-28-29(20-27)33-22-34-30(28)35-25-11-13-26(14-12-25)36-31(38)32-21-24-9-3-2-4-10-24/h2-4,9-16,20,22-23H,5-8,17-19,21H2,1H3,(H2,32,36,38)(H,33,34,35)
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n/an/a 61n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Inhibition of Aurora-A (unknown origin) using STK substrate 2-biotin by HTRF-KinEASE-STK assay


Bioorg Med Chem 22: 5813-23 (2014)


Article DOI: 10.1016/j.bmc.2014.09.029
BindingDB Entry DOI: 10.7270/Q279468G
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50094049
PNG
(CHEMBL3585965)
Show SMILES ONC(=O)CCCCCCc1nc(no1)-c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C149H249N47O42/c1-9-10-11-12-16-45-118(209)238-78-106(137(227)176-88(36-19-23-60-152)123(213)182-96(37-20-24-61-153)142(232)196-68-31-44-110(196)145(235)195-67-30-41-107(195)138(228)170-83(8)120(210)172-86(34-17-21-58-150)124(214)185-99(69-80(2)3)131(221)183-97(49-55-114(158)203)143(233)193-65-28-43-109(193)140(230)184-98(146(236)237)40-27-64-168-149(163)164)191-129(219)94(50-56-116(205)206)178-121(211)87(35-18-22-59-151)173-122(212)89(38-25-62-166-147(159)160)174-125(215)91(46-52-111(155)200)177-127(217)93(48-54-113(157)202)181-141(231)119(82(6)7)192-130(220)90(39-26-63-167-148(161)162)175-126(216)92(47-53-112(156)201)179-134(224)102(72-85-74-165-79-169-85)188-128(218)95(51-57-117(207)208)180-139(229)108-42-29-66-194(108)144(234)105(77-199)190-132(222)100(70-81(4)5)186-133(223)101(71-84-32-14-13-15-33-84)187-136(226)104(76-198)189-135(225)103(75-197)171-115(204)73-154/h13-15,32-33,74,79-83,86-110,119,197-199H,9-12,16-31,34-73,75-78,150-154H2,1-8H3,(H2,155,200)(H2,156,201)(H2,157,202)(H2,158,203)(H,165,169)(H,170,228)(H,171,204)(H,172,210)(H,173,212)(H,174,215)(H,175,216)(H,176,227)(H,177,217)(H,178,211)(H,179,224)(H,180,229)(H,181,231)(H,182,213)(H,183,221)(H,184,230)(H,185,214)(H,186,223)(H,187,226)(H,188,218)(H,189,225)(H,190,222)(H,191,219)(H,192,220)(H,205,206)(H,207,208)(H,236,237)(H4,159,160,166)(H4,161,162,167)(H4,163,164,168)/t83-,86-,87-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107?,108+,109?,110?,119-/m0/s1
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n/an/a 70n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Inhibition of recombinant HDAC1 (unknown origin) incubated for 10 mins using Boc-Lys(acetyl)-AMC fluorogenic substrate by homogeneous fluorescence re...


Bioorg Med Chem 23: 3457-71 (2015)


Article DOI: 10.1016/j.bmc.2015.04.028
BindingDB Entry DOI: 10.7270/Q2W95BXX
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50082261
PNG
(CHEMBL3421746)
Show SMILES Nc1ccccc1NC(=O)c1ccc(CNCc2nc(no2)-c2ccccc2Cl)cc1
Show InChI InChI=1S/C23H20ClN5O2/c24-18-6-2-1-5-17(18)22-28-21(31-29-22)14-26-13-15-9-11-16(12-10-15)23(30)27-20-8-4-3-7-19(20)25/h1-12,26H,13-14,25H2,(H,27,30)
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n/an/a 70n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Inhibition of recombinant HDAC1 (unknown origin) using fluorogenic substrate Boc-Lys (acetyl)-AMC after 20 mins by homogeneous fluorescence release a...


Eur J Med Chem 96: 1-13 (2015)


Article DOI: 10.1016/j.ejmech.2015.04.002
BindingDB Entry DOI: 10.7270/Q21G0P01
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (Human))
BDBM50029416
PNG
(CHEMBL3343310)
Show SMILES O=C(NCc1ccccc1)Nc1ccc(Nc2ncnc3cc(OCCCN4CCCCC4)ccc23)cc1
Show InChI InChI=1S/C30H34N6O2/c37-30(31-21-23-8-3-1-4-9-23)35-25-12-10-24(11-13-25)34-29-27-15-14-26(20-28(27)32-22-33-29)38-19-7-18-36-16-5-2-6-17-36/h1,3-4,8-15,20,22H,2,5-7,16-19,21H2,(H2,31,35,37)(H,32,33,34)
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n/an/a 78n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Inhibition of Aurora-A (unknown origin) using STK substrate 2-biotin by HTRF-KinEASE-STK assay


Bioorg Med Chem 22: 5813-23 (2014)


Article DOI: 10.1016/j.bmc.2014.09.029
BindingDB Entry DOI: 10.7270/Q279468G
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50094054
PNG
(CHEMBL3585968)
Show SMILES ONC(=O)CCCCCCc1nc(no1)-c1cccnc1
Show InChI InChI=1S/C152H255N47O42/c1-9-10-11-12-13-14-15-19-48-121(212)241-81-109(194-138(228)106(78-200)174-118(207)76-157)140(230)190-104(74-87-35-17-16-18-36-87)136(226)189-103(73-84(4)5)135(225)193-108(80-202)147(237)197-69-32-45-111(197)142(232)183-98(54-60-120(210)211)131(221)191-105(75-88-77-168-82-172-88)137(227)182-95(50-56-115(159)204)129(219)178-93(42-29-66-170-151(164)165)133(223)195-122(85(6)7)144(234)184-96(51-57-116(160)205)130(220)180-94(49-55-114(158)203)128(218)177-92(41-28-65-169-150(162)163)125(215)176-90(38-21-25-62-154)124(214)181-97(53-59-119(208)209)132(222)192-107(79-201)139(229)179-91(39-22-26-63-155)126(216)185-99(40-23-27-64-156)145(235)199-71-34-47-113(199)148(238)198-70-33-44-110(198)141(231)173-86(8)123(213)175-89(37-20-24-61-153)127(217)188-102(72-83(2)3)134(224)186-100(52-58-117(161)206)146(236)196-68-31-46-112(196)143(233)187-101(149(239)240)43-30-67-171-152(166)167/h16-18,35-36,77,82-86,89-113,122,200-202H,9-15,19-34,37-76,78-81,153-157H2,1-8H3,(H2,158,203)(H2,159,204)(H2,160,205)(H2,161,206)(H,168,172)(H,173,231)(H,174,207)(H,175,213)(H,176,215)(H,177,218)(H,178,219)(H,179,229)(H,180,220)(H,181,214)(H,182,227)(H,183,232)(H,184,234)(H,185,216)(H,186,224)(H,187,233)(H,188,217)(H,189,226)(H,190,230)(H,191,221)(H,192,222)(H,193,225)(H,194,228)(H,195,223)(H,208,209)(H,210,211)(H,239,240)(H4,162,163,169)(H4,164,165,170)(H4,166,167,171)/t86-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110?,111+,112?,113?,122-/m0/s1
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n/an/a 80n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Inhibition of recombinant HDAC1 (unknown origin) incubated for 10 mins using Boc-Lys(acetyl)-AMC fluorogenic substrate by homogeneous fluorescence re...


Bioorg Med Chem 23: 3457-71 (2015)


Article DOI: 10.1016/j.bmc.2015.04.028
BindingDB Entry DOI: 10.7270/Q2W95BXX
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (Human))
BDBM50029449
PNG
(CHEMBL3343321)
Show SMILES CC1CCCCN1CCCOC1=CC2N=CN=C(Nc3ccc(NC(=O)NC4CCCCC4)cc3)C2C=C1 |c:15,40,t:12,17|
Show InChI InChI=1S/C30H42N6O2/c1-22-8-5-6-17-36(22)18-7-19-38-26-15-16-27-28(20-26)31-21-32-29(27)33-24-11-13-25(14-12-24)35-30(37)34-23-9-3-2-4-10-23/h11-16,20-23,27-28H,2-10,17-19H2,1H3,(H,31,32,33)(H2,34,35,37)
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n/an/a 82n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Inhibition of Aurora-A (unknown origin) using STK substrate 2-biotin by HTRF-KinEASE-STK assay


Bioorg Med Chem 22: 5813-23 (2014)


Article DOI: 10.1016/j.bmc.2014.09.029
BindingDB Entry DOI: 10.7270/Q279468G
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50082210
PNG
(CHEMBL3421741)
Show SMILES Nc1ccccc1NC(=O)c1ccc(CNCc2nc(no2)-c2ccc(Cl)cc2)cc1
Show InChI InChI=1S/C23H20ClN5O2/c24-18-11-9-16(10-12-18)22-28-21(31-29-22)14-26-13-15-5-7-17(8-6-15)23(30)27-20-4-2-1-3-19(20)25/h1-12,26H,13-14,25H2,(H,27,30)
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n/an/a 90n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Inhibition of recombinant HDAC1 (unknown origin) using fluorogenic substrate Boc-Lys (acetyl)-AMC after 20 mins by homogeneous fluorescence release a...


Eur J Med Chem 96: 1-13 (2015)


Article DOI: 10.1016/j.ejmech.2015.04.002
BindingDB Entry DOI: 10.7270/Q21G0P01
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50559361
PNG
(CHEMBL4782213)
Show SMILES Clc1ccc(C(Cn2ccnc2)OCc2ccc3ccccc3c2)c(Cl)c1
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n/an/a 90n/an/an/an/an/an/a


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Assay Description
Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and measured aft...


Citation and Details

Article DOI: 10.1016/j.bmcl.2020.127756
BindingDB Entry DOI: 10.7270/Q2CF9TS5
More data for this
Ligand-Target Pair
Endothelin receptor type B


(RAT)
BDBM50061101
PNG
(4-(1,1-Dimethylethyl)-N-(6-(2-hydroxyethoxy)-5-(2-...)
Show SMILES COc1ccccc1Oc1c(NS(=O)(=O)c2ccc(cc2)C(C)(C)C)nc(nc1OCCO)-c1ncccn1
Show InChI InChI=1S/C27H29N5O6S/c1-27(2,3)18-10-12-19(13-11-18)39(34,35)32-23-22(38-21-9-6-5-8-20(21)36-4)26(37-17-16-33)31-25(30-23)24-28-14-7-15-29-24/h5-15,33H,16-17H2,1-4H3,(H,30,31,32)
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n/an/a 95n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Displacement of [125I]ET-1 from rat ETB receptor after 1 hr by Lowry method


Bioorg Med Chem 23: 657-67 (2015)


Article DOI: 10.1016/j.bmc.2015.01.003
BindingDB Entry DOI: 10.7270/Q28K7BRM
More data for this
Ligand-Target Pair
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