BDBM103358 US8552202, Compound 9

SMILES Cl[C@H]1CN([C@H]2[C@@H]1OCC2=O)C(=O)[C@@H](NC(=O)c1cccc(c1)-n1cnnn1)C1CCCCC1

InChI Key InChIKey=OGRMAGULSQOTTD-IJXRJRJASA-N

Data  5 KI

  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 5 hits for monomerid = 103358   

TargetCathepsin S(Homo sapiens (Human))
Amura Therapeutics

US Patent
LigandPNGBDBM103358(US8552202, Compound 9)
Affinity DataKi:  3.60nMAssay Description:In vitro inhibition assay using cathepsin.More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCathepsin K(Homo sapiens (Human))
Amura Therapeutics

US Patent
LigandPNGBDBM103358(US8552202, Compound 9)
Affinity DataKi:  27nMAssay Description:In vitro inhibition assay using cathepsin.More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCathepsin L2(Homo sapiens (Human))
Amura Therapeutics

US Patent
LigandPNGBDBM103358(US8552202, Compound 9)
Affinity DataKi:  240nMAssay Description:In vitro inhibition assay using cathepsin.More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCathepsin B(Homo sapiens (Human))
Amura Therapeutics

US Patent
LigandPNGBDBM103358(US8552202, Compound 9)
Affinity DataKi:  650nMAssay Description:In vitro inhibition assay using cathepsin.More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetProcathepsin L(Homo sapiens (Human))
Amura Therapeutics

US Patent
LigandPNGBDBM103358(US8552202, Compound 9)
Affinity DataKi: >1.20E+3nMAssay Description:In vitro inhibition assay using cathepsin.More data for this Ligand-Target Pair
In DepthDetails US Patent