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BDBM50265639 3-{5-[(3S)-3-(Dimethylamino)pyrrolidinyl]benzimidazol-2-yl}-4-aminohydroquinolin-2-one::CHEMBL496150

SMILES: CN(C)[C@H]1CCN(C1)c1ccc2nc([nH]c2c1)-c1c(N)c2ccccc2[nH]c1=O

InChI Key: InChIKey=LYWLFOKRWJGIJX-AWEZNQCLSA-N

Data: 3 IC50

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   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50265639   
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
Platelet-derived growth factor receptor beta


(Homo sapiens (Human))
BDBM50265639
PNG
(3-{5-[(3S)-3-(Dimethylamino)pyrrolidinyl]benzimida...)
Show SMILES CN(C)[C@H]1CCN(C1)c1ccc2nc([nH]c2c1)-c1c(N)c2ccccc2[nH]c1=O |r|
Show InChI InChI=1S/C22H24N6O/c1-27(2)14-9-10-28(12-14)13-7-8-17-18(11-13)25-21(24-17)19-20(23)15-5-3-4-6-16(15)26-22(19)29/h3-8,11,14H,9-10,12H2,1-2H3,(H,24,25)(H3,23,26,29)/t14-/m0/s1
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PC cid
PC sid
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Article
PubMed
n/an/a 4n/an/an/an/an/an/a



Novartis Institutes for Biomedical Research

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDGFRbeta


J Med Chem 52: 278-92 (2009)


Article DOI: 10.1021/jm800790t
BindingDB Entry DOI: 10.7270/Q2TD9X7X
More data for this
Ligand-Target Pair
Fibroblast growth factor receptor 1


(Homo sapiens (Human))
BDBM50265639
PNG
(3-{5-[(3S)-3-(Dimethylamino)pyrrolidinyl]benzimida...)
Show SMILES CN(C)[C@H]1CCN(C1)c1ccc2nc([nH]c2c1)-c1c(N)c2ccccc2[nH]c1=O |r|
Show InChI InChI=1S/C22H24N6O/c1-27(2)14-9-10-28(12-14)13-7-8-17-18(11-13)25-21(24-17)19-20(23)15-5-3-4-6-16(15)26-22(19)29/h3-8,11,14H,9-10,12H2,1-2H3,(H,24,25)(H3,23,26,29)/t14-/m0/s1
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PC sid
UniChem

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Article
PubMed
n/an/a 20n/an/an/an/an/an/a



Novartis Institutes for Biomedical Research

Curated by ChEMBL


Assay Description
Inhibition of human recombinant FGFR1


J Med Chem 52: 278-92 (2009)


Article DOI: 10.1021/jm800790t
BindingDB Entry DOI: 10.7270/Q2TD9X7X
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50265639
PNG
(3-{5-[(3S)-3-(Dimethylamino)pyrrolidinyl]benzimida...)
Show SMILES CN(C)[C@H]1CCN(C1)c1ccc2nc([nH]c2c1)-c1c(N)c2ccccc2[nH]c1=O |r|
Show InChI InChI=1S/C22H24N6O/c1-27(2)14-9-10-28(12-14)13-7-8-17-18(11-13)25-21(24-17)19-20(23)15-5-3-4-6-16(15)26-22(19)29/h3-8,11,14H,9-10,12H2,1-2H3,(H,24,25)(H3,23,26,29)/t14-/m0/s1
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 60n/an/an/an/an/an/a



Novartis Institutes for Biomedical Research

Curated by ChEMBL


Assay Description
Inhibition of human recombinant VEGFR2


J Med Chem 52: 278-92 (2009)


Article DOI: 10.1021/jm800790t
BindingDB Entry DOI: 10.7270/Q2TD9X7X
More data for this
Ligand-Target Pair