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BDBM50201079 CHEMBL3923652

SMILES: OC1CCCCCCCNc2ncc3c(cn(CCCC1)c3n2)C1CCOCC1

InChI Key: InChIKey=YXLDQBFWFZDCOF-UHFFFAOYSA-N

Data: 4 IC50  1 EC50

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 5 hits for monomerid = 50201079   
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 receptor UFO


(Homo sapiens (Human))
BDBM50201079
PNG
(CHEMBL3923652)
Show SMILES OC1CCCCCCCNc2ncc3c(cn(CCCC1)c3n2)C1CCOCC1
Show InChI InChI=1S/C23H36N4O2/c28-19-8-4-2-1-3-6-12-24-23-25-16-20-21(18-10-14-29-15-11-18)17-27(22(20)26-23)13-7-5-9-19/h16-19,28H,1-15H2,(H,24,25,26)
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KEGG

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PC cid
PC sid
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Article
PubMed
n/an/a 640n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of Axl (unknown origin) by microfluidic capillary electrophoresis assay


ACS Med Chem Lett 7: 1044-1049 (2016)


Article DOI: 10.1021/acsmedchemlett.6b00221
BindingDB Entry DOI: 10.7270/Q208679K
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Mer


(Homo sapiens (Human))
BDBM50201079
PNG
(CHEMBL3923652)
Show SMILES OC1CCCCCCCNc2ncc3c(cn(CCCC1)c3n2)C1CCOCC1
Show InChI InChI=1S/C23H36N4O2/c28-19-8-4-2-1-3-6-12-24-23-25-16-20-21(18-10-14-29-15-11-18)17-27(22(20)26-23)13-7-5-9-19/h16-19,28H,1-15H2,(H,24,25,26)
PDB
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Article
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n/an/a 94n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of MerTK (unknown origin) by microfluidic capillary electrophoresis assay


ACS Med Chem Lett 7: 1044-1049 (2016)


Article DOI: 10.1021/acsmedchemlett.6b00221
BindingDB Entry DOI: 10.7270/Q208679K
More data for this
Ligand-Target Pair
Receptor-type tyrosine-protein kinase FLT3


(Homo sapiens (Human))
BDBM50201079
PNG
(CHEMBL3923652)
Show SMILES OC1CCCCCCCNc2ncc3c(cn(CCCC1)c3n2)C1CCOCC1
Show InChI InChI=1S/C23H36N4O2/c28-19-8-4-2-1-3-6-12-24-23-25-16-20-21(18-10-14-29-15-11-18)17-27(22(20)26-23)13-7-5-9-19/h16-19,28H,1-15H2,(H,24,25,26)
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Article
PubMed
n/an/a 1.00E+3n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of Flt3 (unknown origin) by microfluidic capillary electrophoresis assay


ACS Med Chem Lett 7: 1044-1049 (2016)


Article DOI: 10.1021/acsmedchemlett.6b00221
BindingDB Entry DOI: 10.7270/Q208679K
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Mer


(Homo sapiens (Human))
BDBM50201079
PNG
(CHEMBL3923652)
Show SMILES OC1CCCCCCCNc2ncc3c(cn(CCCC1)c3n2)C1CCOCC1
Show InChI InChI=1S/C23H36N4O2/c28-19-8-4-2-1-3-6-12-24-23-25-16-20-21(18-10-14-29-15-11-18)17-27(22(20)26-23)13-7-5-9-19/h16-19,28H,1-15H2,(H,24,25,26)
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n/an/an/an/a>1.00E+3n/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of human MerTK kinase domain (1585 to 3000 residues) expressed in HEK293 cells co-expressing rat EGFR LBD assessed as inhibition of EGF-st...


ACS Med Chem Lett 7: 1044-1049 (2016)


Article DOI: 10.1021/acsmedchemlett.6b00221
BindingDB Entry DOI: 10.7270/Q208679K
More data for this
Ligand-Target Pair
Tyrosine-protein kinase receptor TYRO3


(Homo sapiens (Human))
BDBM50201079
PNG
(CHEMBL3923652)
Show SMILES OC1CCCCCCCNc2ncc3c(cn(CCCC1)c3n2)C1CCOCC1
Show InChI InChI=1S/C23H36N4O2/c28-19-8-4-2-1-3-6-12-24-23-25-16-20-21(18-10-14-29-15-11-18)17-27(22(20)26-23)13-7-5-9-19/h16-19,28H,1-15H2,(H,24,25,26)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.20E+3n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of Tyro3 (unknown origin) by microfluidic capillary electrophoresis assay


ACS Med Chem Lett 7: 1044-1049 (2016)


Article DOI: 10.1021/acsmedchemlett.6b00221
BindingDB Entry DOI: 10.7270/Q208679K
More data for this
Ligand-Target Pair