BDBM50595354 CHEMBL5186371

SMILES CCC[C@@H]1NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)CN(CCO)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C1=O)C(C)C

InChI Key InChIKey=IMPFFOZMRCAQQK-UHFFFAOYSA-N

Data  1 EC50

  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 1 hit for monomerid = 50595354   

TargetPotassium voltage-gated channel subfamily H member 2(Human)
Gwangju Insitute of Science and Technology (Gist)

Curated by ChEMBL
LigandPNGBDBM50595354(CHEMBL5186371)
Affinity DataEC50: >1.00E+4nMAssay Description:Inhibition of hERG incubated for 2 hrs by fluorescence polarization based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/21/2023
Entry Details
PubMed