null

SMILES NC1(CCC1)c1ccc(cc1)-c1nc2ccn3c(n[nH]c3=O)c2cc1-c1ccccc1

InChI Key InChIKey=ULDXWLCXEDXJGE-UHFFFAOYSA-N

  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 3 hits for monomerid = 50313650   

TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313650(8-(4-(1-aminocyclobutyl)phenyl)-9-phenyl-[1,2,4]tr...)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Inhibition of Akt1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VD6ZK0PubMed
TargetRAC-beta serine/threonine-protein kinase(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313650(8-(4-(1-aminocyclobutyl)phenyl)-9-phenyl-[1,2,4]tr...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Inhibition of Akt2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VD6ZK0PubMed
TargetRAC-gamma serine/threonine-protein kinase(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313650(8-(4-(1-aminocyclobutyl)phenyl)-9-phenyl-[1,2,4]tr...)copy SMILEScopy InChI
Affinity DataIC50: 65nMAssay Description:Inhibition of Akt3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VD6ZK0PubMed