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Assay Detail

CHEMBL5380296

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

Functional
Antiproliferative activity against human SR cells assessed as inhibition of cell growth incubated for 2 to 4 hrs by MTT assay
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type SR
Confidence 1 — Organism
Curated By Autocuration

Target

SR (CHEMBL614300)
Type CELL-LINE
Organism Homo sapiens

Publication

Design, synthesis and biological evaluation of novel morpholinopyrimidine-5-carbonitrile derivatives as dual PI3K/mTOR inhibitors.
Rady GS, El Deeb MA, Sarg MTM, Taher AT, Helwa AA.
RSC Med Chem (2024) 15 : 733 -752
PubMed 38389871 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 6.22 7.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5432408 1 7.05
CHEMBL5437417 1 7.00
CHEMBL5436786 1 6.46
CHEMBL53463 DOXORUBICIN 4.0 1 6.23
CHEMBL5413498 1 6.11
CHEMBL388978 STAUROSPORINE 1 5.58
CHEMBL185 FLUOROURACIL 4.0 1 5.13

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5432408 IC50 = 90.0 nM 7.05
CHEMBL5437417 IC50 = 100.0 nM 7.00
CHEMBL5436786 IC50 = 350.0 nM 6.46
CHEMBL53463 DOXORUBICIN IC50 = 590.0 nM 6.23
CHEMBL5413498 IC50 = 770.0 nM 6.11
CHEMBL388978 STAUROSPORINE IC50 = 2620.0 nM 5.58
CHEMBL185 FLUOROURACIL IC50 = 7380.0 nM 5.13