null

SMILES CSCC[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CNC(C)=O)C(=O)NCc1cn(nn1)[C@@H](C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@H](C)C(=O)N[C@H](CCCNC(N)=N)C(N)=O

InChI Key InChIKey=IVXVAQIIVMKYGT-FBTQSVADSA-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 = 50464763   

TargetCathepsin K(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464763(CHEMBL4292973)copy SMILEScopy InChI
Affinity DataKi:  1.00E+4nMAssay Description:Reversible competitive inhibition of human cathepsin K using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetCathepsin S(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464763(CHEMBL4292973)copy SMILEScopy InChI
Affinity DataKi:  1.50E+4nMAssay Description:Reversible competitive inhibition of human cathepsin S using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity at ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetProcathepsin L(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464763(CHEMBL4292973)copy SMILEScopy InChI
Affinity DataKi:  3.00E+4nMAssay Description:Reversible competitive inhibition of human cathepsin L using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetCathepsin S(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464763(CHEMBL4292973)copy SMILEScopy InChI
Affinity DataKi:  4.20E+4nMAssay Description:Reversible competitive inhibition of human cathepsin S using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity at ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed