BDBM376953 US10329300, Example 41::US11696917, Example 41::US9920060, 41

SMILES CN(C)C(=O)Cc1ccnc2c(NC(=O)c3nn([C@@H]4CCCN(C4)C(=O)C=C)c4ncnc(N)c34)cccc12

InChI Key InChIKey=CVSYFRKEXSTWBC-QGZVFWFLSA-N

Data  3 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 3 hits for monomerid = 376953   

TargetReceptor tyrosine-protein kinase erbB-2(Homo sapiens (Human))
Taiho Pharmaceutical

US Patent
LigandPNGBDBM376953(US10329300, Example 41 | US11696917, Example 41 | ...)
Affinity DataIC50:  18nMAssay Description:For setting the conditions for the method for measuring the in vitro inhibitory activity of a compound against HER2-phosphorylating activity, Profile...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetReceptor tyrosine-protein kinase erbB-2(Homo sapiens (Human))
Taiho Pharmaceutical

US Patent
LigandPNGBDBM376953(US10329300, Example 41 | US11696917, Example 41 | ...)
Affinity DataIC50:  18nMAssay Description:For setting the conditions for the method for measuring the in vitro inhibitory activity of a compound against HER2-phosphorylating activity, Profile...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetReceptor tyrosine-protein kinase erbB-2(Homo sapiens (Human))
Taiho Pharmaceutical

US Patent
LigandPNGBDBM376953(US10329300, Example 41 | US11696917, Example 41 | ...)
Affinity DataIC50:  18nMAssay Description:For the inhibitory activity measurement of each compound, the compound of the present invention or staurosporine was first serially diluted with dime...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent