null

SMILES O[C@H]1CCN(CC(=C)c2ccc3[C@@H](CCCc3c2)NC(=O)C[C@@H](NS(=O)(=O)c2cccc(c2)C(F)(F)F)c2ccccc2)C1

InChI Key InChIKey=SUTWITAROAZMMF-LXLYTFERSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50322859   

TargetB1 bradykinin receptor(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50322859((R)-N-((R)-6-(3-((S)-3-hydroxypyrrolidin-1-yl)prop...)copy SMILEScopy InChI
Affinity DataKi:  3.5nMAssay Description:Displacement of [3H]Lys-desArg9-BK from human bradykinin B1 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25Q4W88PubMed
TargetB1 bradykinin receptor(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50322859((R)-N-((R)-6-(3-((S)-3-hydroxypyrrolidin-1-yl)prop...)copy SMILEScopy InChI
Affinity DataIC50: 3.90nMAssay Description:Antagonist activity at human bradykinin B1 receptor assessed as inhibition of Lys-desArg9-BK-induced calcium fluxMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25Q4W88PubMed