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1 similar compounds to monomer 50384599

Compile data set for download or QSAR
Wt: 337.4
BDBM50384580

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50384580   
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 Mer


(Homo sapiens (Human))
BDBM50384580
PNG
(CHEMBL2036789 | US9744172, Compound UNC00000490A)
Show SMILES CNc1ncc2c(nn(CC3CCC(N)CC3)c2n1)-c1cccnc1
Show InChI InChI=1S/C18H23N7/c1-20-18-22-10-15-16(13-3-2-8-21-9-13)24-25(17(15)23-18)11-12-4-6-14(19)7-5-12/h2-3,8-10,12,14H,4-7,11,19H2,1H3,(H,20,22,23)
PDB
MMDB

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PC cid
PC sid
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Article
PubMed
n/an/a 530n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of Mer expressed in Escherichia coli BL21 (DE3) cells using EFPIYDFLPAKKK-CONH2 as substrate after 180 mins by microfluid capillary electr...


ACS Med Chem Lett 3: 129-134 (2012)


Article DOI: 10.1021/ml200239k
BindingDB Entry DOI: 10.7270/Q2F76DMC
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Mer


(Homo sapiens (Human))
BDBM50384580
PNG
(CHEMBL2036789 | US9744172, Compound UNC00000490A)
Show SMILES CNc1ncc2c(nn(CC3CCC(N)CC3)c2n1)-c1cccnc1
Show InChI InChI=1S/C18H23N7/c1-20-18-22-10-15-16(13-3-2-8-21-9-13)24-25(17(15)23-18)11-12-4-6-14(19)7-5-12/h2-3,8-10,12,14H,4-7,11,19H2,1H3,(H,20,22,23)
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US Patent
n/an/a 550n/an/an/an/an/an/a



The University of North Carolina at Chapel Hill

US Patent


Assay Description
The ectopic expression of Mer receptor tyrosine kinase (Mer) has been identified as a tumor cell survival gene product in Acute Lymphoblastic Leukemi...


US Patent US9744172 (2017)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase receptor TYRO3


(Homo sapiens (Human))
BDBM50384580
PNG
(CHEMBL2036789 | US9744172, Compound UNC00000490A)
Show SMILES CNc1ncc2c(nn(CC3CCC(N)CC3)c2n1)-c1cccnc1
Show InChI InChI=1S/C18H23N7/c1-20-18-22-10-15-16(13-3-2-8-21-9-13)24-25(17(15)23-18)11-12-4-6-14(19)7-5-12/h2-3,8-10,12,14H,4-7,11,19H2,1H3,(H,20,22,23)
PDB
MMDB

KEGG

UniProtKB/SwissProt

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DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 5.40E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of Tyro3 using EFPIYDFLPAKKK-CONH2 as substrate after 180 mins by microfluid capillary electrophoresis assay


ACS Med Chem Lett 3: 129-134 (2012)


Article DOI: 10.1021/ml200239k
BindingDB Entry DOI: 10.7270/Q2F76DMC
More data for this
Ligand-Target Pair
Tyrosine-protein kinase receptor UFO


(Homo sapiens (Human))
BDBM50384580
PNG
(CHEMBL2036789 | US9744172, Compound UNC00000490A)
Show SMILES CNc1ncc2c(nn(CC3CCC(N)CC3)c2n1)-c1cccnc1
Show InChI InChI=1S/C18H23N7/c1-20-18-22-10-15-16(13-3-2-8-21-9-13)24-25(17(15)23-18)11-12-4-6-14(19)7-5-12/h2-3,8-10,12,14H,4-7,11,19H2,1H3,(H,20,22,23)
PDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 750n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of Axl using KKKKEEIYFFF-CONH2 as substrate after 180 mins by microfluid capillary electrophoresis assay


ACS Med Chem Lett 3: 129-134 (2012)


Article DOI: 10.1021/ml200239k
BindingDB Entry DOI: 10.7270/Q2F76DMC
More data for this
Ligand-Target Pair