null

SMILES [H][C@@]12CCCN1C(=O)[C@@H](N)CSSC[C@H](NC(=O)[C@H](Cc1c[nH]c3ccccc13)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CC1CCN(CC1)C(N)=N)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](C)NC2=O)C(O)=O

InChI Key InChIKey=OHKHDWZCCRSLRV-GAHVENFSSA-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 2 hits for monomerid = 50499238   

TargetPlasminogen(Mus musculus)
Aarhus University

Curated by ChEMBL
LigandPNGBDBM50499238(CHEMBL3735263)copy SMILEScopy InChI
Affinity DataKi:  3.67E+3nMAssay Description:Inhibition of mouse plasmin after 15 mins using H-D-Ile-Pro-Arg-p-nitroanilide as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8JH7PubMed
TargetPlasminogen(Homo sapiens (Human))
Aarhus University

Curated by ChEMBL
LigandPNGBDBM50499238(CHEMBL3735263)copy SMILEScopy InChI
Affinity DataKi:  9.80E+3nMAssay Description:Inhibition of human plasmin after 15 mins using H-D-Ile-Pro-Arg-p-nitroanilide as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8JH7PubMed