null

SMILES CCN1CCN(CC1)c1ccc(Nc2cc(ncn2)N(C)C(=O)Nc2c(Cl)c(OC)cc(OC)c2Cl)c(NC(=O)C=C)c1

InChI Key InChIKey=MBWRLLRCTIYXDW-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 249396   

TargetFibroblast growth factor receptor 2(Homo sapiens (Human))
EISAI R&D MANAGEMENT CO., LTD.

US Patent
LigandPNGBDBM249396(US10537571, Compound 108 | US10562888, Compound 10...)copy SMILEScopy InChI
Affinity DataIC50: 1.98E+3nMpH: 7.5 T: 2°CAssay Description:Compounds were profiled for FGFR inhibition activity at Reaction Biology Corporation (Malvern, Pa.) with their Kinase HotSpot assay. See, Anastassiad...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2K07351US Patent
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))
EISAI R&D MANAGEMENT CO., LTD.

US Patent
LigandPNGBDBM249396(US10537571, Compound 108 | US10562888, Compound 10...)copy SMILEScopy InChI
Affinity DataIC50: 1.98E+3nMAssay Description:Recombinant FGFR1 (2.5 nM), FGFR2 (1 nM), FGFR3 (5 nM), or FGFR4 (12 nM) (Invitrogen™) was prepared as a mixture with substrate KKKSPGEYVNIEFG (...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2542QPZUS Patent
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))
EISAI R&D MANAGEMENT CO., LTD.

US Patent
LigandPNGBDBM249396(US10537571, Compound 108 | US10562888, Compound 10...)copy SMILEScopy InChI
Affinity DataIC50: 1.98E+3nMAssay Description:Recombinant FGFR1 (2.5 nM), FGFR2 (1 nM), FGFR3 (5 nM), or FGFR4 (12 nM) was prepared as a mixture with substrate KKKSPGEYVNIEFG (SEQ ID NO:1) (20 &#...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JH3PKSUS Patent
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))
EISAI R&D MANAGEMENT CO., LTD.

US Patent
LigandPNGBDBM249396(US10537571, Compound 108 | US10562888, Compound 10...)copy SMILEScopy InChI
Affinity DataIC50: 1.98E+3nMAssay Description:Recombinant FGFR1 (2.5 nM), FGFR2 (1 nM), FGFR3 (5 nM), or FGFR4 (12 nM) was prepared as a mixture with substrate KKKSPGEYVNIEFG (SEQ ID NO:1) (20 μ...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q289188GUS Patent
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))
EISAI R&D MANAGEMENT CO., LTD.

US Patent
LigandPNGBDBM249396(US10537571, Compound 108 | US10562888, Compound 10...)copy SMILEScopy InChI
Affinity DataIC50: 579nMAssay Description:The experimental procedure is briefly described as follows: the test compound was first dissolved in DMSO to prepare a stock solution, and then gradi...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25M68RTUS Patent
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))
EISAI R&D MANAGEMENT CO., LTD.

US Patent
LigandPNGBDBM249396(US10537571, Compound 108 | US10562888, Compound 10...)copy SMILEScopy InChI
Affinity DataIC50: 1.29E+3nMAssay Description:Inhibition of human FGFR2 using Poly [E,Y] 4:1 substrate pre-incubated for 15 to 60 mins followed by ATP and [gamma33P]-ATP additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9GHPPubMed
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))
EISAI R&D MANAGEMENT CO., LTD.

US Patent
LigandPNGBDBM249396(US10537571, Compound 108 | US10562888, Compound 10...)copy SMILEScopy InChI
Affinity DataIC50: 1.98E+3nMAssay Description:Recombinant FGFR1 (2.5 nM), FGFR2 (1 nM), FGFR3 (5 nM), or FGFR4 (12 nM) (Invitrogen™) was prepared as a mixture with substrate KKKSPGEYVNIEFG (SEQ I...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PN98QHUS Patent
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))
EISAI R&D MANAGEMENT CO., LTD.

US Patent
LigandPNGBDBM249396(US10537571, Compound 108 | US10562888, Compound 10...)copy SMILEScopy InChI
Affinity DataIC50: 579nMAssay Description:The following method was used to determine the inhibition degree of the kinase activity of recombinant human FGFR protein by the compounds of the pre...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Z322RSUS Patent
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))
EISAI R&D MANAGEMENT CO., LTD.

US Patent
LigandPNGBDBM249396(US10537571, Compound 108 | US10562888, Compound 10...)copy SMILEScopy InChI
Affinity DataIC50: 1.29E+3nMAssay Description:Inhibition of FGFR2 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z60SWJPubMed
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))
EISAI R&D MANAGEMENT CO., LTD.

US Patent
LigandPNGBDBM249396(US10537571, Compound 108 | US10562888, Compound 10...)copy SMILEScopy InChI
Affinity DataIC50: 1.20nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ43WXPubMed