BDBM799592 4-(6-(6-(4-(methylsulfonyl)benzyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-(1-(trifluoromethyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile::US12583855, Example 84

SMILES CS(=O)(=O)c1ccc(CN2C3CC2CN(c2ccc(-c4cc(-c5cnn(C(F)(F)F)c5)cn5ncc(C#N)c45)cn2)C3)cc1

InChI Key InChIKey=ZYNNTPMVUWLNCL-UHFFFAOYSA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 799592   

TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
Shouyao Holdings (Beijing) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 799592BDBM799592(4-(6-(6-(4-(methylsulfonyl)benzyl)-3,6-diazabicycl...)
Affinity DataIC50: 0.309nMAssay Description:The compounds in this invention inhibited the enzymatic activity of RETWT with IC50 values determined by homogeneous time-resolved fluorescence (HTRF...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
8/3/2026
Entry Details
US Patent

TargetVascular endothelial growth factor receptor 2(Human)
Shouyao Holdings (Beijing) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 799592BDBM799592(4-(6-(6-(4-(methylsulfonyl)benzyl)-3,6-diazabicycl...)
Affinity DataIC50: 13.3nMAssay Description:The compounds in this invention inhibited the enzymatic activity of VEGFR2 with IC50 values determined by homogeneous time-resolved fluorescence (HTR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
8/3/2026
Entry Details
US Patent