null

SMILES Nc1ncc(cc1C(=O)N[C@H]1CC[C@H](O)CC1)-c1ccc(cc1)[C@]12C[C@H]1CN(CCN1CCOCC1)C2

InChI Key InChIKey=JFDSOYMKCLUKEJ-VVEDBRRQSA-N

  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 2 hits for monomerid = 451781   

TargetTGF-beta receptor type-1 [162-503](Homo sapiens (Human))
Novartis AG

US Patent
LigandPNGBDBM451781(US10710980, Example 13 | US10947218, Example 13)copy SMILEScopy InChI
Affinity DataIC50: 3.10E+3nMAssay Description:In the applied method, this separation takes place inside a chip that contains a complex capillary system for simultaneous analysis of 12 samples (“1...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DF6V81US Patent
TargetTGF-beta receptor type-1 [162-503](Homo sapiens (Human))
Novartis AG

US Patent
LigandPNGBDBM451781(US10710980, Example 13 | US10947218, Example 13)copy SMILEScopy InChI
Affinity DataIC50: 3.10E+3nMAssay Description:A kinase selectivity panel which measures substrate peptide phosphorylation was set-up for wild-type ALK2 (aa172-499), ALK2 FOP mutant (aa172-499 R20...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24F1TVVUS Patent