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Compile Data Set for Download or QSAR

Found 153 hits of ic50 for UniProtKB: Q9UEE5   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50585203
PNG
(CHEMBL5085430)
Show SMILES Brc1cnc(Nc2cccc(NC(=O)N3CCCC3)c2)nc1NCCCNC(=O)C1CCC1
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n/an/a 4.5n/an/an/an/an/an/a


TBA

Assay Description
Displacement of tracer K9 from NLuc fused DRAK1 (unknown origin) expressed in HEK293 cells by NanoBRET assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00440
BindingDB Entry DOI: 10.7270/Q27S7SND
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50274640
PNG
(CHEMBL4126445)
Show SMILES C[C@@H](C1CC1)N1Cc2cc(cc(C)c2C1=O)-c1sc(NC(C)=O)nc1C |r|
Show InChI InChI=1S/C20H23N3O2S/c1-10-7-15(18-11(2)21-20(26-18)22-13(4)24)8-16-9-23(19(25)17(10)16)12(3)14-5-6-14/h7-8,12,14H,5-6,9H2,1-4H3,(H,21,22,24)/t12-/m0/s1
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n/an/a 10n/an/an/an/an/an/a



Pharmaron-Beijing Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of recombinant human full length GST-tagged DRAK1 expressed in baculovirus expression system


J Med Chem 61: 5435-5441 (2018)


Article DOI: 10.1021/acs.jmedchem.8b00447
BindingDB Entry DOI: 10.7270/Q27M0BFZ
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441855
PNG
(US10647686, Example (3))
Show SMILES CC(C)c1ccc(Nc2ncc(Cl)c(NCCCN)n2)cc1
Show InChI InChI=1S/C16H22ClN5/c1-11(2)12-4-6-13(7-5-12)21-16-20-10-14(17)15(22-16)19-9-3-8-18/h4-7,10-11H,3,8-9,18H2,1-2H3,(H2,19,20,21,22)
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n/an/a 11n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50166076
PNG
(CHEMBL3799585)
Show SMILES CCCC(=O)Nc1ccc2NC(=O)\C(=C3/Nc4ccccc4/C/3=N\O)c2c1
Show InChI InChI=1S/C20H18N4O3/c1-2-5-16(25)21-11-8-9-15-13(10-11)17(20(26)23-15)19-18(24-27)12-6-3-4-7-14(12)22-19/h3-4,6-10,22,27H,2,5H2,1H3,(H,21,25)(H,23,26)/b19-17-,24-18+
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n/an/a 12n/an/an/an/an/an/a



Korea Research Institute of Chemical Technology

Curated by ChEMBL


Assay Description
Inhibition of DRAK1 (unknown origin)


Bioorg Med Chem Lett 26: 2719-23 (2016)


Article DOI: 10.1016/j.bmcl.2016.03.111
BindingDB Entry DOI: 10.7270/Q2N29ZTZ
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50154342
PNG
(CHEMBL3774448)
Show SMILES O=C1NC(=S)S\C1=C/c1ccc2ncccc2c1
Show InChI InChI=1S/C13H8N2OS2/c16-12-11(18-13(17)15-12)7-8-3-4-10-9(6-8)2-1-5-14-10/h1-7H,(H,15,16,17)/b11-7-
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n/an/a 13n/an/an/an/an/an/a



Saarland University

Curated by ChEMBL


Assay Description
Inhibition of STK17A (unknown origin)


Eur J Med Chem 112: 209-16 (2016)


Article DOI: 10.1016/j.ejmech.2016.02.017
BindingDB Entry DOI: 10.7270/Q2GF0WC4
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441866
PNG
(US10647686, Example (13))
Show SMILES NCCCNc1nc(Nc2ccc(cc2)S(=O)(=O)c2ccc(cc2)[N+]([O-])=O)ncc1Cl
Show InChI InChI=1S/C19H19ClN6O4S/c20-17-12-23-19(25-18(17)22-11-1-10-21)24-13-2-6-15(7-3-13)31(29,30)16-8-4-14(5-9-16)26(27)28/h2-9,12H,1,10-11,21H2,(H2,22,23,24,25)
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n/an/a 14n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50520157
PNG
(CHEMBL4436188)
Show SMILES C[C@@H](N1CCN(CC1)C(=O)CC(F)(F)F)c1ccnc(Nc2nc3ccc(cc3[nH]2)-c2cnn(CC3CCC3)c2)c1 |r|
Show InChI InChI=1S/C29H33F3N8O/c1-19(38-9-11-39(12-10-38)27(41)15-29(30,31)32)21-7-8-33-26(14-21)37-28-35-24-6-5-22(13-25(24)36-28)23-16-34-40(18-23)17-20-3-2-4-20/h5-8,13-14,16,18-20H,2-4,9-12,15,17H2,1H3,(H2,33,35,36,37)/t19-/m1/s1
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n/an/a 15n/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Inhibition of wild-type human partial length DRAK1 (R32 to E363 residues) expressed in bacterial expression system by Kinomescan method


J Med Chem 63: 601-612 (2020)


Article DOI: 10.1021/acs.jmedchem.9b01460
BindingDB Entry DOI: 10.7270/Q2CN7795
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50606011
PNG
(CHEMBL5191892)
Show SMILES C[C@H](NC(=O)c1ccc-2cc1OCCOCCNc1ccn3ncc-2c3n1)c1ccncc1 |r|
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n/an/a 15n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00173
BindingDB Entry DOI: 10.7270/Q2NC6587
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441876
PNG
(US10647686, Example (23))
Show SMILES NCCCNc1nc(Nc2ccc3CCCCc3c2)ncc1Cl
Show InChI InChI=1S/C17H22ClN5/c18-15-11-21-17(23-16(15)20-9-3-8-19)22-14-7-6-12-4-1-2-5-13(12)10-14/h6-7,10-11H,1-5,8-9,19H2,(H2,20,21,22,23)
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n/an/a 15n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441873
PNG
(US10647686, Example (20))
Show SMILES NCCCNc1nc(Nc2ccc3OCOc3c2)ncc1Cl
Show InChI InChI=1S/C14H16ClN5O2/c15-10-7-18-14(20-13(10)17-5-1-4-16)19-9-2-3-11-12(6-9)22-8-21-11/h2-3,6-7H,1,4-5,8,16H2,(H2,17,18,19,20)
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n/an/a 16n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441862
PNG
(US10647686, Example (9))
Show SMILES NCCCNc1nc(Nc2ccc(F)cc2)ncc1Cl
Show InChI InChI=1S/C13H15ClFN5/c14-11-8-18-13(20-12(11)17-7-1-6-16)19-10-4-2-9(15)3-5-10/h2-5,8H,1,6-7,16H2,(H2,17,18,19,20)
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n/an/a 19n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441882
PNG
(US10647686, Example (26))
Show SMILES NCCCNc1nc(Nc2ccc(cc2)C2CCNCC2)ncc1Cl
Show InChI InChI=1S/C18H25ClN6/c19-16-12-23-18(25-17(16)22-9-1-8-20)24-15-4-2-13(3-5-15)14-6-10-21-11-7-14/h2-5,12,14,21H,1,6-11,20H2,(H2,22,23,24,25)
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n/an/a 19n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441878
PNG
(US10647686, Example (24))
Show SMILES NCCCNc1nc(Nc2ccc3C(=O)CCCc3c2)ncc1Cl
Show InChI InChI=1S/C17H20ClN5O/c18-14-10-21-17(23-16(14)20-8-2-7-19)22-12-5-6-13-11(9-12)3-1-4-15(13)24/h5-6,9-10H,1-4,7-8,19H2,(H2,20,21,22,23)
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n/an/a 19n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50166251
PNG
(CHEMBL3799389)
Show SMILES O\N=C1\C(\Nc2ccccc\12)=C1\C(=O)Nc2ccc(NC(=O)C3CC3)cc12
Show InChI InChI=1S/C20H16N4O3/c25-19(10-5-6-10)21-11-7-8-15-13(9-11)16(20(26)23-15)18-17(24-27)12-3-1-2-4-14(12)22-18/h1-4,7-10,22,27H,5-6H2,(H,21,25)(H,23,26)/b18-16-,24-17+
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n/an/a 21n/an/an/an/an/an/a



Korea Research Institute of Chemical Technology

Curated by ChEMBL


Assay Description
Inhibition of DRAK1 (unknown origin)


Bioorg Med Chem Lett 26: 2719-23 (2016)


Article DOI: 10.1016/j.bmcl.2016.03.111
BindingDB Entry DOI: 10.7270/Q2N29ZTZ
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441874
PNG
(US10647686, Example (21))
Show SMILES NCCCNc1nc(Nc2ccc3CCCc3c2)ncc1Cl
Show InChI InChI=1S/C16H20ClN5/c17-14-10-20-16(22-15(14)19-8-2-7-18)21-13-6-5-11-3-1-4-12(11)9-13/h5-6,9-10H,1-4,7-8,18H2,(H2,19,20,21,22)
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n/an/a 21n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441881
PNG
(US10647686, Example (25))
Show SMILES NCCCNc1nc(Nc2ccc(cc2)N2CCNCC2)ncc1Cl
Show InChI InChI=1S/C17H24ClN7/c18-15-12-22-17(24-16(15)21-7-1-6-19)23-13-2-4-14(5-3-13)25-10-8-20-9-11-25/h2-5,12,20H,1,6-11,19H2,(H2,21,22,23,24)
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n/an/a 22n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441872
PNG
(US10647686, Example (19) | US10647686, Example 19)
Show SMILES Cc1cnc(Nc2ccc(Cl)cc2)nc1NCCCN
Show InChI InChI=1S/C14H18ClN5/c1-10-9-18-14(20-13(10)17-8-2-7-16)19-12-5-3-11(15)4-6-12/h3-6,9H,2,7-8,16H2,1H3,(H2,17,18,19,20)
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n/an/a 23n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441872
PNG
(US10647686, Example (19) | US10647686, Example 19)
Show SMILES Cc1cnc(Nc2ccc(Cl)cc2)nc1NCCCN
Show InChI InChI=1S/C14H18ClN5/c1-10-9-18-14(20-13(10)17-8-2-7-16)19-12-5-3-11(15)4-6-12/h3-6,9H,2,7-8,16H2,1H3,(H2,17,18,19,20)
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n/an/a 23n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441870
PNG
(US10647686, Example (17))
Show SMILES NCCCNc1nc(Nc2ccc(Br)cc2)ncc1Cl
Show InChI InChI=1S/C13H15BrClN5/c14-9-2-4-10(5-3-9)19-13-18-8-11(15)12(20-13)17-7-1-6-16/h2-5,8H,1,6-7,16H2,(H2,17,18,19,20)
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n/an/a 23n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441872
PNG
(US10647686, Example (19) | US10647686, Example 19)
Show SMILES Cc1cnc(Nc2ccc(Cl)cc2)nc1NCCCN
Show InChI InChI=1S/C14H18ClN5/c1-10-9-18-14(20-13(10)17-8-2-7-16)19-12-5-3-11(15)4-6-12/h3-6,9H,2,7-8,16H2,1H3,(H2,17,18,19,20)
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KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441858
PNG
(US10647686, Example (6))
Show SMILES Cc1ccc(Nc2ncc(Cl)c(NCCCN)n2)cc1Cl
Show InChI InChI=1S/C14H17Cl2N5/c1-9-3-4-10(7-11(9)15)20-14-19-8-12(16)13(21-14)18-6-2-5-17/h3-4,7-8H,2,5-6,17H2,1H3,(H2,18,19,20,21)
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n/an/a 24n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50166260
PNG
(CHEMBL3799505)
Show SMILES CC(C)(C)CC(=O)Nc1ccc2NC(=O)\C(=C3/Nc4ccccc4/C/3=N\O)c2c1
Show InChI InChI=1S/C22H22N4O3/c1-22(2,3)11-17(27)23-12-8-9-16-14(10-12)18(21(28)25-16)20-19(26-29)13-6-4-5-7-15(13)24-20/h4-10,24,29H,11H2,1-3H3,(H,23,27)(H,25,28)/b20-18-,26-19+
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Korea Research Institute of Chemical Technology

Curated by ChEMBL


Assay Description
Inhibition of DRAK1 (unknown origin)


Bioorg Med Chem Lett 26: 2719-23 (2016)


Article DOI: 10.1016/j.bmcl.2016.03.111
BindingDB Entry DOI: 10.7270/Q2N29ZTZ
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441875
PNG
(US10647686, Example (22))
Show SMILES NCCCNc1nc(Nc2ccc3OCCOc3c2)ncc1Cl
Show InChI InChI=1S/C15H18ClN5O2/c16-11-9-19-15(21-14(11)18-5-1-4-17)20-10-2-3-12-13(8-10)23-7-6-22-12/h2-3,8-9H,1,4-7,17H2,(H2,18,19,20,21)
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KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50166271
PNG
(CHEMBL3798563)
Show SMILES O\N=C1\C(\Nc2ccccc\12)=C1\C(=O)Nc2ccc(NC(=O)c3cc(cc(c3)[N+]([O-])=O)[N+]([O-])=O)cc12
Show InChI InChI=1S/C23H14N6O7/c30-22(11-7-13(28(33)34)10-14(8-11)29(35)36)24-12-5-6-18-16(9-12)19(23(31)26-18)21-20(27-32)15-3-1-2-4-17(15)25-21/h1-10,25,32H,(H,24,30)(H,26,31)/b21-19-,27-20+
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Korea Research Institute of Chemical Technology

Curated by ChEMBL


Assay Description
Inhibition of DRAK1 (unknown origin)


Bioorg Med Chem Lett 26: 2719-23 (2016)


Article DOI: 10.1016/j.bmcl.2016.03.111
BindingDB Entry DOI: 10.7270/Q2N29ZTZ
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50520152
PNG
(CHEMBL4594167 | US10894784, Example 150.02)
Show SMILES CNc1cc(ncn1)-c1ccc2nc(Nc3cc(CN4CCN(CC4)C(=O)CC(F)(F)F)ccn3)[nH]c2c1
Show InChI InChI=1S/C25H26F3N9O/c1-29-21-12-19(31-15-32-21)17-2-3-18-20(11-17)34-24(33-18)35-22-10-16(4-5-30-22)14-36-6-8-37(9-7-36)23(38)13-25(26,27)28/h2-5,10-12,15H,6-9,13-14H2,1H3,(H,29,31,32)(H2,30,33,34,35)
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Bayer AG

Curated by ChEMBL


Assay Description
Inhibition of wild-type human partial length DRAK1 (R32 to E363 residues) expressed in bacterial expression system by Kinomescan method


J Med Chem 63: 601-612 (2020)


Article DOI: 10.1021/acs.jmedchem.9b01460
BindingDB Entry DOI: 10.7270/Q2CN7795
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441863
PNG
(US10647686, Example (10))
Show SMILES NCCCNc1nc(Nc2ccc(Oc3ccccc3)cc2)ncc1Cl
Show InChI InChI=1S/C19H20ClN5O/c20-17-13-23-19(25-18(17)22-12-4-11-21)24-14-7-9-16(10-8-14)26-15-5-2-1-3-6-15/h1-3,5-10,13H,4,11-12,21H2,(H2,22,23,24,25)
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KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441854
PNG
(US10647686, Example (2))
Show SMILES NCCCNc1nc(Nc2cc(Cl)cc(Cl)c2)ncc1Cl
Show InChI InChI=1S/C13H14Cl3N5/c14-8-4-9(15)6-10(5-8)20-13-19-7-11(16)12(21-13)18-3-1-2-17/h4-7H,1-3,17H2,(H2,18,19,20,21)
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KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441868
PNG
(US10647686, Example (15))
Show SMILES NCCCNc1nc(Nc2ccc(F)c(c2)C(F)(F)F)ncc1Cl
Show InChI InChI=1S/C14H14ClF4N5/c15-10-7-22-13(24-12(10)21-5-1-4-20)23-8-2-3-11(16)9(6-8)14(17,18)19/h2-3,6-7H,1,4-5,20H2,(H2,21,22,23,24)
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KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441904
PNG
(US10647686, Comparative Example 6)
Show SMILES NCCCNc1nc(Nc2ccc(Cl)cc2)ncc1Br
Show InChI InChI=1S/C13H15BrClN5/c14-11-8-18-13(20-12(11)17-7-1-6-16)19-10-4-2-9(15)3-5-10/h2-5,8H,1,6-7,16H2,(H2,17,18,19,20)
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KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441904
PNG
(US10647686, Comparative Example 6)
Show SMILES NCCCNc1nc(Nc2ccc(Cl)cc2)ncc1Br
Show InChI InChI=1S/C13H15BrClN5/c14-11-8-18-13(20-12(11)17-7-1-6-16)19-10-4-2-9(15)3-5-10/h2-5,8H,1,6-7,16H2,(H2,17,18,19,20)
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KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50520150
PNG
(CHEMBL4566796)
Show SMILES COCc1cc(ncn1)-c1ccc2nc(Nc3cc(ccn3)[C@@H](C)N3CCN(CC3)C(=O)CC(F)(F)F)[nH]c2c1 |r|
Show InChI InChI=1S/C27H29F3N8O2/c1-17(37-7-9-38(10-8-37)25(39)14-27(28,29)30)18-5-6-31-24(12-18)36-26-34-21-4-3-19(11-23(21)35-26)22-13-20(15-40-2)32-16-33-22/h3-6,11-13,16-17H,7-10,14-15H2,1-2H3,(H2,31,34,35,36)/t17-/m1/s1
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Bayer AG

Curated by ChEMBL


Assay Description
Inhibition of wild-type human partial length DRAK1 (R32 to E363 residues) expressed in bacterial expression system by Kinomescan method


J Med Chem 63: 601-612 (2020)


Article DOI: 10.1021/acs.jmedchem.9b01460
BindingDB Entry DOI: 10.7270/Q2CN7795
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(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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University of Florida

Curated by ChEMBL


Assay Description
Inhibition of human DRAK1 using KKLNRTLSFAEPG as substrate by [gamma-33P]-ATP assay


Eur J Med Chem 161: 456-467 (2019)


Article DOI: 10.1016/j.ejmech.2018.10.052
BindingDB Entry DOI: 10.7270/Q2W380MT
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441898
PNG
(US10647686, Example (41))
Show SMILES NCCCCNc1nc(Nc2cc(Cl)cc(Cl)c2)ncc1Cl
Show InChI InChI=1S/C14H16Cl3N5/c15-9-5-10(16)7-11(6-9)21-14-20-8-12(17)13(22-14)19-4-2-1-3-18/h5-8H,1-4,18H2,(H2,19,20,21,22)
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KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50606014
PNG
(CHEMBL5193635)
Show SMILES CC(NC(=O)c1ccc-2cc1OCCOCCNc1ccn3ncc-2c3n1)c1ccccc1
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TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00173
BindingDB Entry DOI: 10.7270/Q2NC6587
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(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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TBA

Assay Description
Inhibition of human DRAK1 using KKLNRTLSFAEPG as substrate by [gamma-33P]-ATP assay


Citation and Details

Article DOI: 10.1016/j.bmc.2018.02.022
BindingDB Entry DOI: 10.7270/Q2DJ5KB8
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50166077
PNG
(CHEMBL513703)
Show SMILES CC(C)(C)C(=O)Nc1ccc2NC(=O)\C(=C3/Nc4ccccc4/C/3=N\O)c2c1
Show InChI InChI=1S/C21H20N4O3/c1-21(2,3)20(27)22-11-8-9-15-13(10-11)16(19(26)24-15)18-17(25-28)12-6-4-5-7-14(12)23-18/h4-10,23,28H,1-3H3,(H,22,27)(H,24,26)/b18-16-,25-17+
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Korea Research Institute of Chemical Technology

Curated by ChEMBL


Assay Description
Inhibition of DRAK1 (unknown origin)


Bioorg Med Chem Lett 26: 2719-23 (2016)


Article DOI: 10.1016/j.bmcl.2016.03.111
BindingDB Entry DOI: 10.7270/Q2N29ZTZ
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441905
PNG
(US10647686, Example 1)
Show SMILES CC(C)(C)OC(=O)NCCCNc1nc(Cl)ncc1Cl
Show InChI InChI=1S/C12H18Cl2N4O2/c1-12(2,3)20-11(19)16-6-4-5-15-9-8(13)7-17-10(14)18-9/h7H,4-6H2,1-3H3,(H,16,19)(H,15,17,18)
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KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441869
PNG
(US10647686, Example (16))
Show SMILES NCCCNc1nc(Nc2ccc(Br)c(c2)C(F)(F)F)ncc1Cl
Show InChI InChI=1S/C14H14BrClF3N5/c15-10-3-2-8(6-9(10)14(17,18)19)23-13-22-7-11(16)12(24-13)21-5-1-4-20/h2-3,6-7H,1,4-5,20H2,(H2,21,22,23,24)
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KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441895
PNG
(US10647686, Example (38))
Show SMILES Cc1cnc(Nc2ccc(F)c(Cl)c2)nc1NCCCN
Show InChI InChI=1S/C14H17ClFN5/c1-9-8-19-14(21-13(9)18-6-2-5-17)20-10-3-4-12(16)11(15)7-10/h3-4,7-8H,2,5-6,17H2,1H3,(H2,18,19,20,21)
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KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441871
PNG
(US10647686, Example (18))
Show SMILES COc1ccc(Nc2ncc(Cl)c(NCCCN)n2)cc1Cl
Show InChI InChI=1S/C14H17Cl2N5O/c1-22-12-4-3-9(7-10(12)15)20-14-19-8-11(16)13(21-14)18-6-2-5-17/h3-4,7-8H,2,5-6,17H2,1H3,(H2,18,19,20,21)
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KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441867
PNG
(US10647686, Example (14))
Show SMILES Cc1ccc(Nc2ncc(Cl)c(NCCCN)n2)cc1C
Show InChI InChI=1S/C15H20ClN5/c1-10-4-5-12(8-11(10)2)20-15-19-9-13(16)14(21-15)18-7-3-6-17/h4-5,8-9H,3,6-7,17H2,1-2H3,(H2,18,19,20,21)
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KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441905
PNG
(US10647686, Example 1)
Show SMILES CC(C)(C)OC(=O)NCCCNc1nc(Cl)ncc1Cl
Show InChI InChI=1S/C12H18Cl2N4O2/c1-12(2,3)20-11(19)16-6-4-5-15-9-8(13)7-17-10(14)18-9/h7H,4-6H2,1-3H3,(H,16,19)(H,15,17,18)
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KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441853
PNG
(US10647686, Example (1))
Show SMILES NCCCNc1nc(Nc2ccc(Cl)cc2)ncc1Cl
Show InChI InChI=1S/C13H15Cl2N5/c14-9-2-4-10(5-3-9)19-13-18-8-11(15)12(20-13)17-7-1-6-16/h2-5,8H,1,6-7,16H2,(H2,17,18,19,20)
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KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50111572
PNG
(CHEMBL3605057)
Show SMILES O=C(NCCCNc1nc(Nc2cccc(CN3CCOCC3)c2)ncc1C1CC1)C1CCC1
Show InChI InChI=1S/C26H36N6O2/c33-25(21-5-2-6-21)28-11-3-10-27-24-23(20-8-9-20)17-29-26(31-24)30-22-7-1-4-19(16-22)18-32-12-14-34-15-13-32/h1,4,7,16-17,20-21H,2-3,5-6,8-15,18H2,(H,28,33)(H2,27,29,30,31)
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n/an/a 43n/an/an/an/an/an/a


TBA

Assay Description
Displacement of tracer K9 from NLuc fused DRAK1 (unknown origin) expressed in HEK293 cells by NanoBRET assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00440
BindingDB Entry DOI: 10.7270/Q27S7SND
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441864
PNG
(US10647686, Example (11))
Show SMILES CCc1ccc(Nc2ncc(Cl)c(NCCCN)n2)cc1
Show InChI InChI=1S/C15H20ClN5/c1-2-11-4-6-12(7-5-11)20-15-19-10-13(16)14(21-15)18-9-3-8-17/h4-7,10H,2-3,8-9,17H2,1H3,(H2,18,19,20,21)
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US Patent
n/an/a 44n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441897
PNG
(US10647686, Example (40) | US10647686, Example 40)
Show SMILES NCCCCNc1nc(Nc2ccc(Cl)cc2)ncc1Cl
Show InChI InChI=1S/C14H17Cl2N5/c15-10-3-5-11(6-4-10)20-14-19-9-12(16)13(21-14)18-8-2-1-7-17/h3-6,9H,1-2,7-8,17H2,(H2,18,19,20,21)
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US Patent
n/an/a 47n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM441897
PNG
(US10647686, Example (40) | US10647686, Example 40)
Show SMILES NCCCCNc1nc(Nc2ccc(Cl)cc2)ncc1Cl
Show InChI InChI=1S/C14H17Cl2N5/c15-10-3-5-11(6-4-10)20-14-19-9-12(16)13(21-14)18-8-2-1-7-17/h3-6,9H,1-2,7-8,17H2,(H2,18,19,20,21)
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n/an/a 47n/an/an/an/an/an/a



KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY

US Patent


Assay Description
To measure the DRAK1 and DRAK2 activity, the substrate MRCL3 peptide and ATP were mixed with the enzymes. After an appropriate period of time, the re...


US Patent US10647686 (2020)


BindingDB Entry DOI: 10.7270/Q2MS3WSB
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50606012
PNG
(CHEMBL5087558)
Show SMILES CC(C)(C)NC(=O)c1ccc-2cc1OCCOCCNc1ccn3ncc-2c3n1
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n/an/a 49n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00173
BindingDB Entry DOI: 10.7270/Q2NC6587
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Serine/threonine-protein kinase 17A


(Homo sapiens (Human))
BDBM50166121
PNG
(CHEMBL3797480)
Show SMILES CCCCC(=O)Nc1ccc2NC(=O)\C(=C3/Nc4ccccc4/C/3=N\O)c2c1
Show InChI InChI=1S/C21H20N4O3/c1-2-3-8-17(26)22-12-9-10-16-14(11-12)18(21(27)24-16)20-19(25-28)13-6-4-5-7-15(13)23-20/h4-7,9-11,23,28H,2-3,8H2,1H3,(H,22,26)(H,24,27)/b20-18-,25-19+
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n/an/a 51n/an/an/an/an/an/a



Korea Research Institute of Chemical Technology

Curated by ChEMBL


Assay Description
Inhibition of DRAK1 (unknown origin)


Bioorg Med Chem Lett 26: 2719-23 (2016)


Article DOI: 10.1016/j.bmcl.2016.03.111
BindingDB Entry DOI: 10.7270/Q2N29ZTZ
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase 17A


(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 54n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00173
BindingDB Entry DOI: 10.7270/Q2NC6587
More data for this
Ligand-Target Pair
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