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Found 9 hits Enz. Inhib. hit(s) with Target = 'RAC-beta serine/threonine-protein kinase' and Ligand = 'BDBM50398379'   
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
RAC-beta serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50398379
PNG
(CHEMBL2177390 | US10550114, Compound GDC-0068 | US...)
Show SMILES CC(C)NC[C@@H](C(=O)N1CCN(CC1)c1ncnc2[C@H](O)C[C@@H](C)c12)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C24H32ClN5O2/c1-15(2)26-13-19(17-4-6-18(25)7-5-17)24(32)30-10-8-29(9-11-30)23-21-16(3)12-20(31)22(21)27-14-28-23/h4-7,14-16,19-20,26,31H,8-13H2,1-3H3/t16-,19-,20-/m1/s1
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US Patent
n/an/a 1.70n/an/an/an/an/an/a



CELGENE QUANTICEL RESEARCH, INC.

US Patent




US Patent US10815234 (2020)


BindingDB Entry DOI: 10.7270/Q2RV0STB
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
RAC-beta serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50398379
PNG
(CHEMBL2177390 | US10550114, Compound GDC-0068 | US...)
Show SMILES CC(C)NC[C@@H](C(=O)N1CCN(CC1)c1ncnc2[C@H](O)C[C@@H](C)c12)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C24H32ClN5O2/c1-15(2)26-13-19(17-4-6-18(25)7-5-17)24(32)30-10-8-29(9-11-30)23-21-16(3)12-20(31)22(21)27-14-28-23/h4-7,14-16,19-20,26,31H,8-13H2,1-3H3/t16-,19-,20-/m1/s1
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n/an/a 1.70n/an/an/an/an/an/a


TBA



Citation and Details

BindingDB Entry DOI: 10.7270/Q2W95F93
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
RAC-beta serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50398379
PNG
(CHEMBL2177390 | US10550114, Compound GDC-0068 | US...)
Show SMILES CC(C)NC[C@@H](C(=O)N1CCN(CC1)c1ncnc2[C@H](O)C[C@@H](C)c12)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C24H32ClN5O2/c1-15(2)26-13-19(17-4-6-18(25)7-5-17)24(32)30-10-8-29(9-11-30)23-21-16(3)12-20(31)22(21)27-14-28-23/h4-7,14-16,19-20,26,31H,8-13H2,1-3H3/t16-,19-,20-/m1/s1
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n/an/a 1.70n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
RAC-beta serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50398379
PNG
(CHEMBL2177390 | US10550114, Compound GDC-0068 | US...)
Show SMILES CC(C)NC[C@@H](C(=O)N1CCN(CC1)c1ncnc2[C@H](O)C[C@@H](C)c12)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C24H32ClN5O2/c1-15(2)26-13-19(17-4-6-18(25)7-5-17)24(32)30-10-8-29(9-11-30)23-21-16(3)12-20(31)22(21)27-14-28-23/h4-7,14-16,19-20,26,31H,8-13H2,1-3H3/t16-,19-,20-/m1/s1
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Article
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n/an/a 3.80n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of N-terminal GST-tagged human AKT2 (120 to 481 residues) expressed in baculovirus infected Sf21 cells incubated for 1 hr in presence of A...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00815
BindingDB Entry DOI: 10.7270/Q2GF0Z92
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
RAC-beta serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50398379
PNG
(CHEMBL2177390 | US10550114, Compound GDC-0068 | US...)
Show SMILES CC(C)NC[C@@H](C(=O)N1CCN(CC1)c1ncnc2[C@H](O)C[C@@H](C)c12)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C24H32ClN5O2/c1-15(2)26-13-19(17-4-6-18(25)7-5-17)24(32)30-10-8-29(9-11-30)23-21-16(3)12-20(31)22(21)27-14-28-23/h4-7,14-16,19-20,26,31H,8-13H2,1-3H3/t16-,19-,20-/m1/s1
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n/an/a 18n/an/an/an/an/an/a



Array BioPharma Inc.

Curated by ChEMBL


Assay Description
Competitive inhibition of wild-type full-length amino-terminal polyhistidine-tagged human Akt2 expressed in recombinant baculovirus system using fluo...


J Med Chem 55: 8110-27 (2012)


Article DOI: 10.1021/jm301024w
BindingDB Entry DOI: 10.7270/Q20P1160
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
RAC-beta serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50398379
PNG
(CHEMBL2177390 | US10550114, Compound GDC-0068 | US...)
Show SMILES CC(C)NC[C@@H](C(=O)N1CCN(CC1)c1ncnc2[C@H](O)C[C@@H](C)c12)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C24H32ClN5O2/c1-15(2)26-13-19(17-4-6-18(25)7-5-17)24(32)30-10-8-29(9-11-30)23-21-16(3)12-20(31)22(21)27-14-28-23/h4-7,14-16,19-20,26,31H,8-13H2,1-3H3/t16-,19-,20-/m1/s1
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n/an/a 18n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
RAC-beta serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50398379
PNG
(CHEMBL2177390 | US10550114, Compound GDC-0068 | US...)
Show SMILES CC(C)NC[C@@H](C(=O)N1CCN(CC1)c1ncnc2[C@H](O)C[C@@H](C)c12)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C24H32ClN5O2/c1-15(2)26-13-19(17-4-6-18(25)7-5-17)24(32)30-10-8-29(9-11-30)23-21-16(3)12-20(31)22(21)27-14-28-23/h4-7,14-16,19-20,26,31H,8-13H2,1-3H3/t16-,19-,20-/m1/s1
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n/an/a 32n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of full length human Akt2 S474D mutant using GRPRTSSFAEGKK as substrate incubated for 40 mins by scintillation counting method


Citation and Details

Article DOI: 10.1016/j.ejmech.2020.112076
BindingDB Entry DOI: 10.7270/Q2NP282C
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
RAC-beta serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50398379
PNG
(CHEMBL2177390 | US10550114, Compound GDC-0068 | US...)
Show SMILES CC(C)NC[C@@H](C(=O)N1CCN(CC1)c1ncnc2[C@H](O)C[C@@H](C)c12)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C24H32ClN5O2/c1-15(2)26-13-19(17-4-6-18(25)7-5-17)24(32)30-10-8-29(9-11-30)23-21-16(3)12-20(31)22(21)27-14-28-23/h4-7,14-16,19-20,26,31H,8-13H2,1-3H3/t16-,19-,20-/m1/s1
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n/an/a 48n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00527
BindingDB Entry DOI: 10.7270/Q2TX3KGT
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
RAC-beta serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50398379
PNG
(CHEMBL2177390 | US10550114, Compound GDC-0068 | US...)
Show SMILES CC(C)NC[C@@H](C(=O)N1CCN(CC1)c1ncnc2[C@H](O)C[C@@H](C)c12)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C24H32ClN5O2/c1-15(2)26-13-19(17-4-6-18(25)7-5-17)24(32)30-10-8-29(9-11-30)23-21-16(3)12-20(31)22(21)27-14-28-23/h4-7,14-16,19-20,26,31H,8-13H2,1-3H3/t16-,19-,20-/m1/s1
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n/an/an/a 35n/an/an/an/an/a


TBA

Assay Description
Binding affinity to wild-type human partial length AKT2 expressed in bacterial expression system assessed as residual binding level by Kinomescan met...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c01476
BindingDB Entry DOI: 10.7270/Q2DZ0D73
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)