BDBM50606425 CHEMBL5208169

SMILES C[C@H](NC(=O)[C@H](C)NC(=O)[C@H](Cc1ccccc1)NC(=O)CCN1CCC(CC1)Oc1ccccc1Cc1ccccc1)C(=O)NCCC(=O)N[C@@H](CCCCNC(=O)CCC1=[N+]2C(C=C1)=Cc1ccc(-c3cccs3)n1[B-]2(F)F)C(N)=O

InChI Key InChIKey=DGFHCELJLORPDV-UHFFFAOYSA-N

Data  2 Kd

  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 = 50606425   

TargetHistamine H1 receptor(Human)
University of Nottingham Biodiscovery Institute

Curated by ChEMBL
LigandPNGBDBM50606425(CHEMBL5208169)
Affinity DataKd:  724nMAssay Description:Binding affinity to NLuc-tagged human H1R expressed in HEK293T cells using NanoGlo as substrate preincubated for 2 hrs followed by substrate addition...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
LigandPNGBDBM50606425(CHEMBL5208169)
Affinity DataKd:  724nMAssay Description:Binding affinity to NLuc-tagged human H1R expressed in HEK293T cells using NanoGlo as substrate preincubated for 2 hrs followed by substrate addition...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/26/2023
Entry Details
PubMed