null

SMILES O=C(NCC#N)C(Cc1cccc(c1)-c1nnco1)NC(=O)c1ccccc1

InChI Key InChIKey=ZRKTXOUQLJMAQT-UHFFFAOYSA-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 5 hits for monomerid = 50414635   

TargetProcathepsin L(Homo sapiens (Human))
AstraZeneca

Curated by ChEMBL
LigandPNGBDBM50414635(CHEMBL564626)copy SMILEScopy InChI
Affinity DataIC50: 501nMAssay Description:Inhibition of cathepsin L assessed as inhibition of fluorogenic substrate cleavageMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N017S3PubMed
TargetCathepsin B(Homo sapiens (Human))
AstraZeneca

Curated by ChEMBL
LigandPNGBDBM50414635(CHEMBL564626)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human liver cathepsin B assessed as inhibition of fluorogenic substrate cleavageMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N017S3PubMed
TargetCathepsin S(Homo sapiens (Human))
AstraZeneca

Curated by ChEMBL
LigandPNGBDBM50414635(CHEMBL564626)copy SMILEScopy InChI
Affinity DataIC50: 19.9nMAssay Description:Inhibition of cathepsin S assessed as inhibition of fluorogenic substrate cleavageMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N017S3PubMed
TargetCathepsin L2(Homo sapiens (Human))
AstraZeneca

Curated by ChEMBL
LigandPNGBDBM50414635(CHEMBL564626)copy SMILEScopy InChI
Affinity DataIC50: 158nMAssay Description:Inhibition of cathepsin L2 assessed as inhibition of fluorogenic substrate cleavageMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N017S3PubMed
TargetCathepsin K(Homo sapiens (Human))
AstraZeneca

Curated by ChEMBL
LigandPNGBDBM50414635(CHEMBL564626)copy SMILEScopy InChI
Affinity DataIC50: 1.26E+3nMAssay Description:Inhibition of cathepsin K assessed as inhibition of fluorogenic substrate cleavageMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N017S3PubMed