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Assay Detail

CHEMBL4370283

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Functional
Antiproliferative activity against human A549 cells after 72 hrs by MTT assay
11
Total Activities
11
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

Design, Synthesis, and Biological Evaluation of 6-Substituted Thieno[3,2- d]pyrimidine Analogues as Dual Epidermal Growth Factor Receptor Kinase and Microtubule Inhibitors.
Romagnoli R, Prencipe F, Oliva P, Baraldi S, Baraldi PG, Schiaffino Ortega S, Chayah M, Kimatrai Salvador M, Lopez-Cara LC, Brancale A, Ferla S, Hamel E, Ronca R, Bortolozzi R, Mariotto E, Mattiuzzo E, Viola G.
J Med Chem (2019) 62 : 1274 -1290
PubMed 30633509 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 6.02 7.72

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4569885 1 7.72
CHEMBL67 COMBRETASTATIN A4 -1.0 1 6.75
CHEMBL4546122 1 6.37
CHEMBL4572443 1 6.28
CHEMBL4552482 1 6.22
CHEMBL4473768 1 6.11
CHEMBL4473422 1 5.96
CHEMBL4541014 1 5.64
CHEMBL4460381 1 5.29
CHEMBL4520163 1 5.06
CHEMBL4475082 1 4.87

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4569885 IC50 = 19.0 nM 7.72
CHEMBL67 COMBRETASTATIN A4 IC50 = 180.0 nM 6.75
CHEMBL4546122 IC50 = 430.0 nM 6.37
CHEMBL4572443 IC50 = 530.0 nM 6.28
CHEMBL4552482 IC50 = 600.0 nM 6.22
CHEMBL4473768 IC50 = 770.0 nM 6.11
CHEMBL4473422 IC50 = 1100.0 nM 5.96
CHEMBL4541014 IC50 = 2300.0 nM 5.64
CHEMBL4460381 IC50 = 5100.0 nM 5.29
CHEMBL4520163 IC50 = 8800.0 nM 5.06
CHEMBL4475082 IC50 = 13500.0 nM 4.87