BDBM50607674 CHEMBL5220347::US20240239774, Example 123

SMILES Cn1cc(Cc2ccccc2OCCN2CC3(COC3)C2)c(n1)-c1cc(Cl)nc(N)n1

InChI Key InChIKey=UCAQZKORNBZGSL-UHFFFAOYSA-N

Data  3 IC50

  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 3 hits for monomerid = 50607674   

TargetAdenylate cyclase type 10(Human)
Cornell University

US Patent
LigandPNGBDBM50607674(CHEMBL5220347 | US20240239774, Example 123)
Affinity DataIC50: 5nMAssay Description:Assays for sAC activity using purified protein were performed in 100 ul reactions containing 4 mM MgCl2, 2 mM CaCl2, 1 mM ATP, 40 mM NaHCO3, 50 mM Tr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/30/2024
Entry Details
US Patent

TargetAdenylate cyclase type 10(Human)
Cornell University

US Patent
LigandPNGBDBM50607674(CHEMBL5220347 | US20240239774, Example 123)
Affinity DataIC50: 7.10nMAssay Description:Assays for sAC activity using purified protein were performed in 100 ul reactions containing 4 mM MgCl2, 2 mM CaCl2, 1 mM ATP, 40 mM NaHCO3, 50 mM Tr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/30/2024
Entry Details
US Patent

TargetAdenylate cyclase type 10(Human)
Cornell University

US Patent
LigandPNGBDBM50607674(CHEMBL5220347 | US20240239774, Example 123)
Affinity DataIC50: 7.80nMAssay Description:Inhibition of human ADCY10 assessed as cAMP accumulation preincubated for 15 mins followed by substrate addition using alpha-32P labelled ATP as subs...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/26/2023
Entry Details
PubMed