BDBM50521071 CHEMBL2093209::TDR77394

SMILES COc1cccc(c1)C(=O)Nc1nnc(o1)-c1ccc2CCCCc2c1

InChI Key InChIKey=RTFQJIKRVGJSHN-UHFFFAOYSA-N

Data  2 IC50

  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 = 50521071   

TargetAdenylate cyclase type 8(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50521071(CHEMBL2093209 | TDR77394)
Affinity DataIC50:  5.30E+3nMAssay Description:Inhibition of human AC8 expressed in HEK293 cells assessed as decrease in A23187-stimulated cAMP accumulation preincubated for 30 mins followed by A2...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenylate cyclase type 1(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50521071(CHEMBL2093209 | TDR77394)
Affinity DataIC50:  3.10E+3nMAssay Description:Inhibition of human AC1 expressed in HEK293 cells assessed as decrease in A23187-stimulated cAMP accumulation preincubated for 30 mins followed by A2...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed