Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL1680109

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition of PI3Kalpha-mediated Akt phosphorylation at Ser473 in human A2780 cells after 1 hr
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type A2780
Confidence 9 — Direct single protein target
Curated By Autocuration

Publication

Synthesis and in Vitro and in Vivo Evaluation of Phosphoinositide-3-kinase Inhibitors.
Burger MT, Knapp M, Wagman A, Ni ZJ, Hendrickson T, Atallah G, Zhang Y, Frazier K, Verhagen J, Pfister K, Ng S, Smith A, Bartulis S, Merrit H, Weismann M, Xin X, Haznedar J, Voliva CF, Iwanowicz E, Pecchi S.
ACS Med Chem Lett (2011) 2 : 34 -38
PubMed 24900252 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 13 6.71 8.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1672327 1 8.00
CHEMBL1672323 1 7.40
CHEMBL1672328 1 7.05
CHEMBL1672324 1 6.96
CHEMBL1672326 1 6.96
CHEMBL1672331 1 6.89
CHEMBL1672330 1 6.66
CHEMBL1672316 1 6.51
CHEMBL1672314 1 6.43
CHEMBL1672319 1 6.41
CHEMBL1672321 1 6.35
CHEMBL1672315 1 6.19
CHEMBL1672320 1 5.48

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1672327 EC50 = 10.0 nM 8.00
CHEMBL1672323 EC50 = 40.0 nM 7.40
CHEMBL1672328 EC50 = 90.0 nM 7.05
CHEMBL1672324 EC50 = 110.0 nM 6.96
CHEMBL1672326 EC50 = 110.0 nM 6.96
CHEMBL1672331 EC50 = 130.0 nM 6.89
CHEMBL1672330 EC50 = 220.0 nM 6.66
CHEMBL1672316 EC50 = 310.0 nM 6.51
CHEMBL1672314 EC50 = 370.0 nM 6.43
CHEMBL1672319 EC50 = 390.0 nM 6.41
CHEMBL1672321 EC50 = 450.0 nM 6.35
CHEMBL1672315 EC50 = 650.0 nM 6.19
CHEMBL1672320 EC50 = 3300.0 nM 5.48