null

SMILES CC(C)(C)OC(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NNC(=O)OCC(=O)N1CCCc2ccccc12

InChI Key InChIKey=MITOFRSPGLYHSJ-QFIPXVFZSA-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 4 hits for monomerid = 51395   

TargetProcathepsin L(Homo sapiens (Human))
PCMD

Curated by PubChem BioAssay
LigandPNGBDBM51395(CHEMBL263634 | N-[(2S)-1-[[[2-(3,4-dihydro-2H-quin...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Screening Center: Penn Center for Molecular Discovery Center Affiliation: University of Pennsylvania Network: Molecular Library Screening Center Netw...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BG2MD4PCBioAssay
TargetProcathepsin L(Homo sapiens (Human))
PCMD

Curated by PubChem BioAssay
LigandPNGBDBM51395(CHEMBL263634 | N-[(2S)-1-[[[2-(3,4-dihydro-2H-quin...)copy SMILEScopy InChI
Affinity DataIC50: 6.90E+3nMAssay Description:pA2 for NK2 receptor of rabbit pulmonary arteryMore data for this Ligand-Target Pair
In DepthDetails
TargetProcathepsin L(Homo sapiens (Human))
PCMD

Curated by PubChem BioAssay
LigandPNGBDBM51395(CHEMBL263634 | N-[(2S)-1-[[[2-(3,4-dihydro-2H-quin...)copy SMILEScopy InChI
Affinity DataIC50: 6.90nMMore data for this Ligand-Target Pair
In DepthDetails
TargetProcathepsin L(Homo sapiens (Human))
PCMD

Curated by PubChem BioAssay
LigandPNGBDBM51395(CHEMBL263634 | N-[(2S)-1-[[[2-(3,4-dihydro-2H-quin...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibition of human cathepsin LMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29Z95SVPubMed