BDBM50606458 CHEMBL5193095

SMILES CC(C)[C@H](NC(=O)CCN1CCC(CC1)Oc1ccccc1Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](Cc1ccccc1)C(N)=O

InChI Key InChIKey=OIZCCSOKPCEDQA-UHFFFAOYSA-N

Data  2 KI

  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 = 50606458   

TargetHistamine H1 receptor(Human)
University of Nottingham Biodiscovery Institute

Curated by ChEMBL
LigandPNGBDBM50606458(CHEMBL5193095)
Affinity DataKi:  89nMAssay Description:Displacement of fluorophore-labeled mepyramine from Nluc-tagged human H1R expressed in HEK293T cells incubated for 2 hrs by NanoBRET competition bind...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/26/2023
Entry Details
PubMed
TargetHistamine H1 receptor(Human)
University of Nottingham Biodiscovery Institute

Curated by ChEMBL
LigandPNGBDBM50606458(CHEMBL5193095)
Affinity DataKi:  89nMAssay Description:Displacement of fluorophore-labeled mepyramine from Nluc-tagged human H1R expressed in HEK293T cells incubated for 2 hrs by NanoBRET competition bind...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/26/2023
Entry Details
PubMed