BDBM50606429 CHEMBL5175488

SMILES C[C@@H](NC(=O)CCN1CCC(CC1)Oc1ccccc1Cc1ccccc1)C(=O)N[C@H](C)C(=O)N[C@H](C)C(=O)NCCNC(=O)CCCCCNC(=O)COc1ccc(\C=C\C2=[N+]3C(C=C2)=Cc2ccc(-c4cccs4)n2[B-]3(F)F)cc1

InChI Key InChIKey=CSVVEXGAAAWMNF-UHFFFAOYSA-N

Data  1 KI  1 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 = 50606429   

TargetHistamine H1 receptor(Human)
University of Nottingham Biodiscovery Institute

Curated by ChEMBL
LigandPNGBDBM50606429(CHEMBL5175488)
Affinity DataKi:  4nMAssay Description:Displacement of [3H]mepyramine from human H1R expressed in HEK293T cells by radioligand competition binding assayMore 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
LigandPNGBDBM50606429(CHEMBL5175488)
Affinity DataKd:  7.90nMAssay Description:Binding affinity to NLuc-tagged human H1R expressed in HEK293T cells incubated for 1 hr using furimazine as substrate measured after 5 mins by NanoBR...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/26/2023
Entry Details
PubMed