BDBM50331629 5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarbamoyl)-2-methylphenyl)-1H-pyrazole-4-carboxamide::CHEMBL1290746

SMILES Cc1ccc(cc1NC(=O)c1cnn(c1N)-c1ccccc1F)C(=O)Nc1ccon1

InChI Key InChIKey=HFTDLOVSQHYBFJ-UHFFFAOYSA-N

Data  24 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 24 hits for monomerid = 50331629   

TargetProtein kinase C alpha type(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >4.00E+4nMAssay Description:Inhibition of PKCalphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C19(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50:  2.30E+4nMAssay Description:Inhibition of CYP2C19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of KDRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >1.50E+4nMAssay Description:Inhibition of BtkMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMAP kinase-activated protein kinase 2(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of MK2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ITK/TSK(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of ItkMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of STAT3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of FGFR1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase SYK(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of SykMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of IGF-1RMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK3(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of Jak3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50:  7.00E+3nMAssay Description:Inhibition of LckMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNon-receptor tyrosine-protein kinase TYK2(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of Tyk2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase PLK1(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >1.50E+4nMAssay Description:Inhibition of PLK1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDiacylglycerol O-acyltransferase 1(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >2.00E+4nMAssay Description:Inhibition of DGATMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C beta type(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >4.00E+4nMAssay Description:Inhibition of PKAbetaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C delta type(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >4.00E+4nMAssay Description:Inhibition of PKCdeltaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C zeta type(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >2.00E+4nMAssay Description:Inhibition of PKCzetaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 1A2(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >1.30E+4nMAssay Description:Inhibition of CYP1A2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >1.60E+5nMAssay Description:Inhibition of human ERG by flux assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >1.30E+4nMAssay Description:Inhibition of CYP3A4More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50: >1.30E+4nMAssay Description:Inhibition of CYP2D6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50:  2.30E+4nMAssay Description:Inhibition of CYP2C9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
Bristol-Myers Squibb Research And Development

Curated by ChEMBL
LigandPNGBDBM50331629(5-amino-1-(2-fluorophenyl)-N-(5-(isoxazol-3-ylcarb...)
Affinity DataIC50:  2nMAssay Description:Inhibition of human recombinant p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed