BDBM509772 US11364246, Example 92.2::US20200361871A1, Example 92.1

SMILES CC(C)(NC(=O)c1cc(NC(=O)Cc2ccc(Cl)c(O)c2)ccn1)C#N

InChI Key InChIKey=SIPFQZLECWRUCV-UHFFFAOYSA-N

Data  3 EC50

  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 = 509772   

TargetAnoctamin-1(Human)
Tmem16A

US Patent
LigandPNGBDBM509772(US20200361871A1, Example 92.1 | US11364246, Exampl...)
Affinity DataEC50:  10nMAssay Description:Cell Culture and PreparationFisher rat thyroid (FRT) cells stably expressing human TMEM16A (TMEM16Aabc variant; Dr Luis Galietta, Insituto Giannina, ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/25/2022
Entry Details
US Patent

TargetAnoctamin-1(Human)
Tmem16A

US Patent
LigandPNGBDBM509772(US20200361871A1, Example 92.1 | US11364246, Exampl...)
Affinity DataEC50:  140nMAssay Description:Cell Culture and PreparationFisher rat thyroid (FRT) cells stably expressing human TMEM16A (TMEM16Aabc variant; Dr Luis Galietta, Insituto Giannina, ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/25/2022
Entry Details
US Patent

TargetAnoctamin-1(Human)
Tmem16A

US Patent
LigandPNGBDBM509772(US20200361871A1, Example 92.1 | US11364246, Exampl...)
Affinity DataEC50:  140nMAssay Description:Compound activity was quantified by measuring the increase in current upon compound addition and expressing this as a percentage increase of baseline...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/13/2022
Entry Details
US Patent