BDBM50271157 CHEMBL4127012

SMILES CN(C)C(=O)c1cc([C@@H]2CCCN2c2cc(F)cc(F)c2)c2nc(cnc2c1)N1CCOCC1

InChI Key InChIKey=PNYSVXYTVOTZHS-UHFFFAOYSA-N

Data  2 IC50  5 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 7 hits for monomerid = 50271157   

TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform(Human)
Therachem Research Medilab (India)

Curated by ChEMBL
LigandPNGBDBM50271157(CHEMBL4127012)
Affinity DataKd:  1.09E+3nMAssay Description:Binding affinity to wild-type human PIK3Cbeta (P118 to S1070 residues) expressed in mammalian expression system by KINOMEScan assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Human)
Therachem Research Medilab (India)

Curated by ChEMBL
LigandPNGBDBM50271157(CHEMBL4127012)
Affinity DataKd: >3.02E+4nMAssay Description:Binding affinity to wild-type human PIK3Cgamma (S144 to A1102 residues) expressed in mammalian expression system by KINOMEScan assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine/threonine-protein kinase mTOR(Human)
Therachem Research Medilab (India)

Curated by ChEMBL
LigandPNGBDBM50271157(CHEMBL4127012)
Affinity DataKd: >3.02E+4nMAssay Description:Binding affinity to wild-type human MTOR (L1382 to W2549 residues) expressed in mammalian expression system by KINOMEScan assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform(Human)
Therachem Research Medilab (India)

Curated by ChEMBL
LigandPNGBDBM50271157(CHEMBL4127012)
Affinity DataIC50: 513nMAssay Description:Inhibition of PI3Kbeta in human PC3 cells assessed as reduction in AKT phosphorylation at S473 residue measured after 60 mins by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Therachem Research Medilab (India)

Curated by ChEMBL
LigandPNGBDBM50271157(CHEMBL4127012)
Affinity DataKd:  1.64E+4nMAssay Description:Binding affinity to wild-type human PIK3Cdelta (R108 to Q1044 residues) expressed in mammalian expression system by KINOMEScan assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform(Human)
Therachem Research Medilab (India)

Curated by ChEMBL
LigandPNGBDBM50271157(CHEMBL4127012)
Affinity DataIC50: 513nMAssay Description:Inhibition of PI3Kbeta in human PC3 cells assessed as reduction in AKT phosphorylation at Thr308 residue measured after 60 mins by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Human)
Therachem Research Medilab (India)

Curated by ChEMBL
LigandPNGBDBM50271157(CHEMBL4127012)
Affinity DataKd:  1.23E+4nMAssay Description:Binding affinity to wild-type human PIK3Calpha (R108 to N1068 residues) expressed in mammalian expression system by KINOMEScan assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed