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BDBM50263513 CHEMBL477172::N-(2-chloro-6-methylphenyl)-1-(6-(4-(morpholinomethyl)pyridin-2-ylamino)pyrimidin-4-yl)-1H-benzo[d]imidazol-2-amine

SMILES: Cc1cccc(Cl)c1Nc1nc2ccccc2n1-c1cc(Nc2cc(CN3CCOCC3)ccn2)ncn1

InChI Key: InChIKey=KNPRFHFPAKZBIG-UHFFFAOYSA-N

Data: 2 IC50

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 2 hits for monomerid = 50263513   
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
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50263513
PNG
(CHEMBL477172 | N-(2-chloro-6-methylphenyl)-1-(6-(4...)
Show SMILES Cc1cccc(Cl)c1Nc1nc2ccccc2n1-c1cc(Nc2cc(CN3CCOCC3)ccn2)ncn1
Show InChI InChI=1S/C28H27ClN8O/c1-19-5-4-6-21(29)27(19)35-28-33-22-7-2-3-8-23(22)37(28)26-16-25(31-18-32-26)34-24-15-20(9-10-30-24)17-36-11-13-38-14-12-36/h2-10,15-16,18H,11-14,17H2,1H3,(H,33,35)(H,30,31,32,34)
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 17n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of TEL fused Lck (unknown origin)-mediated proliferation of TEL-Lck transformed mouse BA/F3 cells after 48 hrs by bright-glo luciferase as...


Bioorg Med Chem Lett 18: 5618-21 (2008)


Article DOI: 10.1016/j.bmcl.2008.08.104
BindingDB Entry DOI: 10.7270/Q2DN44WQ
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50263513
PNG
(CHEMBL477172 | N-(2-chloro-6-methylphenyl)-1-(6-(4...)
Show SMILES Cc1cccc(Cl)c1Nc1nc2ccccc2n1-c1cc(Nc2cc(CN3CCOCC3)ccn2)ncn1
Show InChI InChI=1S/C28H27ClN8O/c1-19-5-4-6-21(29)27(19)35-28-33-22-7-2-3-8-23(22)37(28)26-16-25(31-18-32-26)34-24-15-20(9-10-30-24)17-36-11-13-38-14-12-36/h2-10,15-16,18H,11-14,17H2,1H3,(H,33,35)(H,30,31,32,34)
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 14n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Lck by lance assay


Bioorg Med Chem Lett 18: 5618-21 (2008)


Article DOI: 10.1016/j.bmcl.2008.08.104
BindingDB Entry DOI: 10.7270/Q2DN44WQ
More data for this
Ligand-Target Pair