null

SMILES CCCCS(=O)(=O)NC(=O)[C@H](NC(=O)[C@@H](Cc1ccc(cc1)-c1ccno1)N(C)C(=O)c1cc(C)cc(C)c1)C(C)C

InChI Key InChIKey=IFLIQLQVUMXNFU-IXCJQBJRSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50071447   

TargetEndothelin receptor type B(Homo sapiens (Human))
Takarazuka Research Institute

Curated by ChEMBL
LigandPNGBDBM50071447(CHEMBL310919 | N-[(R)-1-[(R)-1-(Butane-1-sulfonyla...)copy SMILEScopy InChI
Affinity DataKi:  24nMAssay Description:Compound was tested for the binding affinity against Endothelin B receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M3609PubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Takarazuka Research Institute

Curated by ChEMBL
LigandPNGBDBM50071447(CHEMBL310919 | N-[(R)-1-[(R)-1-(Butane-1-sulfonyla...)copy SMILEScopy InChI
Affinity DataKi:  850nMAssay Description:Compound was tested for the binding affinity against Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M3609PubMed