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BDBM50193112 CHEMBL3966536

SMILES: Cl.CNCCOc1ccc(cc1)-c1sc2nc(nc(NN3C(=O)C=C(C)C3=O)c2c1C)-c1cccs1

InChI Key: InChIKey=HMQJWZRTKGHVMP-UHFFFAOYSA-N

Data: 4 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 4 hits for monomerid = 50193112   
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 ABL1


(Homo sapiens (Human))
BDBM50193112
PNG
(CHEMBL3966536)
Show SMILES Cl.CNCCOc1ccc(cc1)-c1sc2nc(nc(NN3C(=O)C=C(C)C3=O)c2c1C)-c1cccs1 |t:23|
Show InChI InChI=1S/C25H23N5O3S2.ClH/c1-14-13-19(31)30(25(14)32)29-23-20-15(2)21(16-6-8-17(9-7-16)33-11-10-26-3)35-24(20)28-22(27-23)18-5-4-12-34-18;/h4-9,12-13,26H,10-11H2,1-3H3,(H,27,28,29);1H
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UniChem
Article
PubMed
n/an/a 2.88E+3n/an/an/an/an/an/a



Yonsei University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human ABL1 expressed in insect cells preincubated for 15 mins followed by poly(Glu:Tyr) substrate addition for 30 mins in p...


Eur J Med Chem 120: 74-85 (2016)


Article DOI: 10.1016/j.ejmech.2016.05.022
BindingDB Entry DOI: 10.7270/Q2BG2QX3
More data for this
Ligand-Target Pair
Tyrosine-protein kinase receptor FLT3


(Homo sapiens (Human))
BDBM50193112
PNG
(CHEMBL3966536)
Show SMILES Cl.CNCCOc1ccc(cc1)-c1sc2nc(nc(NN3C(=O)C=C(C)C3=O)c2c1C)-c1cccs1 |t:23|
Show InChI InChI=1S/C25H23N5O3S2.ClH/c1-14-13-19(31)30(25(14)32)29-23-20-15(2)21(16-6-8-17(9-7-16)33-11-10-26-3)35-24(20)28-22(27-23)18-5-4-12-34-18;/h4-9,12-13,26H,10-11H2,1-3H3,(H,27,28,29);1H
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UniChem
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n/an/a 11n/an/an/an/an/an/a



Yonsei University

Curated by ChEMBL




Bioorg Med Chem Lett 27: 496-500 (2017)


BindingDB Entry DOI: 10.7270/Q2SF2ZFD
More data for this
Ligand-Target Pair
Angiopoietin-1 receptor


(Homo sapiens (Human))
BDBM50193112
PNG
(CHEMBL3966536)
Show SMILES Cl.CNCCOc1ccc(cc1)-c1sc2nc(nc(NN3C(=O)C=C(C)C3=O)c2c1C)-c1cccs1 |t:23|
Show InChI InChI=1S/C25H23N5O3S2.ClH/c1-14-13-19(31)30(25(14)32)29-23-20-15(2)21(16-6-8-17(9-7-16)33-11-10-26-3)35-24(20)28-22(27-23)18-5-4-12-34-18;/h4-9,12-13,26H,10-11H2,1-3H3,(H,27,28,29);1H
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UniProtKB/SwissProt

B.MOAD
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antibodypedia
GoogleScholar
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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 9.75E+3n/an/an/an/an/an/a



Yonsei University

Curated by ChEMBL


Assay Description
Inhibition of human TIE2 preincubated for 15 mins followed by substrate addition measured after 30 mins in presence of [gamma-32P]ATP by TR-FRET assa...


Eur J Med Chem 120: 74-85 (2016)


Article DOI: 10.1016/j.ejmech.2016.05.022
BindingDB Entry DOI: 10.7270/Q2BG2QX3
More data for this
Ligand-Target Pair
Tyrosine-protein kinase receptor FLT3


(Homo sapiens (Human))
BDBM50193112
PNG
(CHEMBL3966536)
Show SMILES Cl.CNCCOc1ccc(cc1)-c1sc2nc(nc(NN3C(=O)C=C(C)C3=O)c2c1C)-c1cccs1 |t:23|
Show InChI InChI=1S/C25H23N5O3S2.ClH/c1-14-13-19(31)30(25(14)32)29-23-20-15(2)21(16-6-8-17(9-7-16)33-11-10-26-3)35-24(20)28-22(27-23)18-5-4-12-34-18;/h4-9,12-13,26H,10-11H2,1-3H3,(H,27,28,29);1H
PDB
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KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
MMDB
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 8n/an/an/an/an/an/a



Yonsei University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human FLT3 expressed in insect Sf21 cells preincubated for 15 mins followed by poly(Glu:Tyr) substrate addition for 30 mins...


Eur J Med Chem 120: 74-85 (2016)


Article DOI: 10.1016/j.ejmech.2016.05.022
BindingDB Entry DOI: 10.7270/Q2BG2QX3
More data for this
Ligand-Target Pair