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1 similar compounds to monomer 22449

Compile data set for download or QSAR
Wt: 430.8
BDBM50166155

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50166155   
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 17B (STK17B)


(Homo sapiens (Human))
BDBM50166155
PNG
(CHEMBL3797619)
Show SMILES O\N=C1\C(\Nc2ccccc\12)=C1\C(=O)Nc2ccc(NC(=O)c3ccc(Cl)cc3)cc12
Show InChI InChI=1S/C23H15ClN4O3/c24-13-7-5-12(6-8-13)22(29)25-14-9-10-18-16(11-14)19(23(30)27-18)21-20(28-31)15-3-1-2-4-17(15)26-21/h1-11,26,31H,(H,25,29)(H,27,30)/b21-19-,28-20+
PDB

UniProtKB/SwissProt

GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 3.20E+3n/an/an/an/an/an/a



Korea Research Institute of Chemical Technology

Curated by ChEMBL


Assay Description
Inhibition of DRAK2 (unknown origin) using MRLC3 peptide as substrate incubated for 2 hrs by ADP-Glo kinase assay


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))
BDBM50166155
PNG
(CHEMBL3797619)
Show SMILES O\N=C1\C(\Nc2ccccc\12)=C1\C(=O)Nc2ccc(NC(=O)c3ccc(Cl)cc3)cc12
Show InChI InChI=1S/C23H15ClN4O3/c24-13-7-5-12(6-8-13)22(29)25-14-9-10-18-16(11-14)19(23(30)27-18)21-20(28-31)15-3-1-2-4-17(15)26-21/h1-11,26,31H,(H,25,29)(H,27,30)/b21-19-,28-20+
KEGG

UniProtKB/SwissProt

GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 3.00E+3n/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