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Assay Detail

CHEMBL3373087

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

Functional
Cytotoxicity against human A549 cells assessed as growth inhibition after 48 hrs by MTT method
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type A549
Confidence 1 — Organism
Curated By Autocuration

Target

A549 (CHEMBL392)
Type CELL-LINE
Organism Homo sapiens

Publication

New pyrrole derivatives with potent tubulin polymerization inhibiting activity as anticancer agents including hedgehog-dependent cancer.
La Regina G, Bai R, Coluccia A, Famiglini V, Pelliccia S, Passacantilli S, Mazzoccoli C, Ruggieri V, Sisinni L, Bolognesi A, Rensen WM, Miele A, Nalli M, Alfonsi R, Di Marcotullio L, Gulino A, Brancale A, Novellino E, Dondio G, Vultaggio S, Varasi M, Mercurio C, Hamel E, Lavia P, Silvestri R.
J Med Chem (2014) 57 : 6531 -6552
PubMed 25025991 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 6.55 8.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3318100 1 8.00
CHEMBL3318115 1 7.10
CHEMBL3318085 1 6.70
CHEMBL3318113 1 6.00
CHEMBL3318125 1 6.00
CHEMBL3318114 1 5.52
CHEMBL3318123 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3318100 IC50 = 10.0 nM 8.00
CHEMBL3318115 IC50 = 80.0 nM 7.10
CHEMBL3318085 IC50 = 200.0 nM 6.70
CHEMBL3318113 IC50 = 1000.0 nM 6.00
CHEMBL3318125 IC50 = 1000.0 nM 6.00
CHEMBL3318114 IC50 = 3000.0 nM 5.52
CHEMBL3318123 IC50 > 10000.0 nM -