BDBM50619821 CHEMBL5411064

SMILES [#6]-[#6](-[#6])-[#6@@H]-1-[#6]-[#6@@H](-[#6@@H](-[#6])\[#6](-[#6]-1)=[#6]\[#6]=[#6]-1/[#6]-[#6@@H](-[#8])-[#6]-[#6@H](-[#8])-[#6]-1)-c1cccc(-[#8]-[#6]-[#6]C([#6])([#6])[#8])c1

InChI Key InChIKey=CFQMEDLIFWVAQL-UHFFFAOYSA-N

Data  2 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 2 hits for monomerid = 50619821   

TargetVitamin D3 receptor(Human)
Kanagawa University

Curated by ChEMBL
LigandPNGBDBM50619821(CHEMBL5411064)
Affinity DataEC50: >500nMAssay Description:Agonist activity at human Vitamin D receptor assessed as increase in gene transcriptional activity by luciferase reporter gene based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/15/2024
Entry Details
PubMed
TargetVitamin D3 receptor(Human)
Kanagawa University

Curated by ChEMBL
LigandPNGBDBM50619821(CHEMBL5411064)
Affinity DataEC50:  922nMAssay Description:Agonist activity at Vitamin D receptor (unknown origin) assessed as increase in fluorescein labeled TRAP220/DRIP-2 coactivator peptide requirement by...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/15/2024
Entry Details
PubMed