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BDBM50189601 (E)-3-(4-methoxyphenylimino)indolin-2-one::(E/Z)-3-(4-methoxyphenylimino)indolin-2-one::CHEMBL378695

SMILES: COc1ccc(cc1)\N=C1\C(=O)Nc2ccccc12

InChI Key: InChIKey=PXSATUQXASGWQE-UHFFFAOYSA-N

Data: 1 KI  3 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50189601   
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
Galanin receptor 3


(Homo sapiens (Human))
BDBM50189601
PNG
((E)-3-(4-methoxyphenylimino)indolin-2-one | (E/Z)-...)
Show SMILES COc1ccc(cc1)\N=C1\C(=O)Nc2ccccc12
Show InChI InChI=1S/C15H12N2O2/c1-19-11-8-6-10(7-9-11)16-14-12-4-2-3-5-13(12)17-15(14)18/h2-9H,1H3,(H,16,17,18)
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>1.00E+4n/an/an/an/an/an/an/an/a



Lundbeck Research USA, Inc.

Curated by ChEMBL


Assay Description
Displacement of [125I]galanin from human GAL3


J Med Chem 49: 3757-8 (2006)


Article DOI: 10.1021/jm060001n
BindingDB Entry DOI: 10.7270/Q2T72H2B
More data for this
Ligand-Target Pair
Leucine-rich repeat serine/threonine-protein kinase 2 (LRRK2)


(Homo sapiens (Human))
BDBM50189601
PNG
((E)-3-(4-methoxyphenylimino)indolin-2-one | (E/Z)-...)
Show SMILES COc1ccc(cc1)\N=C1\C(=O)Nc2ccccc12
Show InChI InChI=1S/C15H12N2O2/c1-19-11-8-6-10(7-9-11)16-14-12-4-2-3-5-13(12)17-15(14)18/h2-9H,1H3,(H,16,17,18)
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PubMed
n/an/a 2.17E+3n/an/an/an/an/an/a



Centro de Investigaciones Biol�gicas-CSIC

Curated by ChEMBL


Assay Description
Inhibition of recombinant catalytic human GST-tagged LLRK2 (970 to 2527 residues) expressed in baculovirus expression system using LRRKtide as substr...


Eur J Med Chem 138: 328-342 (2017)


Article DOI: 10.1016/j.ejmech.2017.06.060
BindingDB Entry DOI: 10.7270/Q2V40XTP
More data for this
Ligand-Target Pair
Leucine-rich repeat serine/threonine-protein kinase 2 (LRRK2)


(Homo sapiens (Human))
BDBM50189601
PNG
((E)-3-(4-methoxyphenylimino)indolin-2-one | (E/Z)-...)
Show SMILES COc1ccc(cc1)\N=C1\C(=O)Nc2ccccc12
Show InChI InChI=1S/C15H12N2O2/c1-19-11-8-6-10(7-9-11)16-14-12-4-2-3-5-13(12)17-15(14)18/h2-9H,1H3,(H,16,17,18)
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n/an/a 2.33E+3n/an/an/an/an/an/a



Centro de Investigaciones Biol�gicas-CSIC

Curated by ChEMBL


Assay Description
Inhibition of recombinant catalytic human GST-tagged LLRK2 G2019S mutant (970 to 2527 residues) expressed in baculovirus expression system using LRRK...


Eur J Med Chem 138: 328-342 (2017)


Article DOI: 10.1016/j.ejmech.2017.06.060
BindingDB Entry DOI: 10.7270/Q2V40XTP
More data for this
Ligand-Target Pair
Transthyretin


(Homo sapiens (Human))
BDBM50189601
PNG
((E)-3-(4-methoxyphenylimino)indolin-2-one | (E/Z)-...)
Show SMILES COc1ccc(cc1)\N=C1\C(=O)Nc2ccccc12
Show InChI InChI=1S/C15H12N2O2/c1-19-11-8-6-10(7-9-11)16-14-12-4-2-3-5-13(12)17-15(14)18/h2-9H,1H3,(H,16,17,18)
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n/an/a 8.10E+3n/an/an/an/an/an/a



Universitat de Barcelona

Curated by ChEMBL


Assay Description
Inhibition of TTR mediated fibrillogenesis assessed as acid-induced protein aggregation turbidity after 1.5 hrs by turbidimetric assay


Bioorg Med Chem Lett 19: 5270-3 (2009)


Article DOI: 10.1016/j.bmcl.2009.03.004
BindingDB Entry DOI: 10.7270/Q2SF2W7W
More data for this
Ligand-Target Pair