BDBM50606420 CHEMBL5184842

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)NCCC(=O)N[C@@H](CCCCNC(=O)CCC1=[N+]2C(C=C1)=Cc1c(C)cc(C)n1[B-]2(F)F)C(N)=O

InChI Key InChIKey=CXUZGQJWBLLFNP-UHFFFAOYSA-N

Data  2 Kd

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50606420   

TargetHistamine H1 receptor(Human)
University of Nottingham Biodiscovery Institute

Curated by ChEMBL
LigandPNGBDBM50606420(CHEMBL5184842)
Affinity DataKd:  1.29E+3nMAssay 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
LigandPNGBDBM50606420(CHEMBL5184842)
Affinity DataKd:  1.29E+3nMAssay 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