BDBM323438 3-(3-(2-Propylpentyloxy)Phenyl)Propan-1-Amine::US10188615, Example 2::US10639286, Example 2

SMILES CCCC(CCC)COc1cccc(CCCN)c1

InChI Key InChIKey=KQZPWHFGQRFKQO-UHFFFAOYSA-N

Data  4 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 4 hits for monomerid = 323438   

TargetRetinoid isomerohydrolase(Human)
Acucela

US Patent
LigandPNGBDBM323438(3-(3-(2-Propylpentyloxy)Phenyl)Propan-1-Amine | US...)
Affinity DataIC50: 55nMAssay Description:Isomerase inhibition reactions were performed essentially as described (Stecher et al., J. Biol. Chem. 274:8577-85 (1999); see also Golczak et al., P...More data for this Ligand-Target Pair
In DepthDetails
US Patent

TargetRetinoid isomerohydrolase(Bovine)
Acucela

US Patent
LigandPNGBDBM323438(3-(3-(2-Propylpentyloxy)Phenyl)Propan-1-Amine | US...)
Affinity DataIC50: 1.00E+3nMAssay Description:Isomerase inhibition reactions were performed essentially as described (Stecher et al., J. Biol. Chem. 274:8577-85 (1999); see also Golczak et al., P...More data for this Ligand-Target Pair
In DepthDetails
US Patent

TargetRetinaldehyde-binding protein 1(Bovine)
Acucela

US Patent
LigandPNGBDBM323438(3-(3-(2-Propylpentyloxy)Phenyl)Propan-1-Amine | US...)
Affinity DataIC50: 100nMAssay Description:Isomerase inhibition reactions were performed essentially as described (Stecher et al., J Biol. Chem. 274:8577-85 (1999).More data for this Ligand-Target Pair
In DepthDetails
US Patent

TargetRetinaldehyde-binding protein 1(Human)
Acucela

US Patent
LigandPNGBDBM323438(3-(3-(2-Propylpentyloxy)Phenyl)Propan-1-Amine | US...)
Affinity DataIC50: 55nMAssay Description:Isomerase inhibition reactions were performed essentially as described (Stecher et al., J Biol. Chem. 274:8577-85 (1999).More data for this Ligand-Target Pair
In DepthDetails
US Patent