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Assay Detail

CHEMBL4733474

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

Functional
Inhibition of erastin-induced ferroptosis in human HT-1080 cells assessed as cell viability incubated for 48 hrs by MTT assay
98
Total Activities
98
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type HT-1080
Confidence 1 — Organism
Curated By Autocuration

Target

HT-1080 (CHEMBL614580)
Type CELL-LINE
Organism Homo sapiens

Publication

Structure-activity relationship studies of phenothiazine derivatives as a new class of ferroptosis inhibitors together with the therapeutic effect in an ischemic stroke model.
Yang W,Liu X,Song C,Ji S,Yang J,Liu Y,You J,Zhang J,Huang S,Cheng W,Shao Z,Li L,Yang S
Eur J Med Chem (2021) 209 : 112842 -112842
PubMed 33065375 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 98 7.41 9.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4754158 1 9.30
CHEMBL4748592 1 8.40
CHEMBL4747920 1 8.30
CHEMBL4750813 1 8.30
CHEMBL4743554 1 8.30
CHEMBL4793040 1 8.30
CHEMBL4750992 1 8.30
CHEMBL4760962 1 8.22
CHEMBL4791794 1 8.22
CHEMBL4752574 1 8.22
CHEMBL4750463 1 8.22
CHEMBL4788181 1 8.22
CHEMBL4746877 1 8.15
CHEMBL4782284 1 8.05
CHEMBL4760238 1 8.05
CHEMBL4792206 1 7.92
CHEMBL4782741 1 7.89
CHEMBL4744355 1 7.89
CHEMBL4749286 1 7.89
CHEMBL4761414 1 7.85
CHEMBL4785795 1 7.85
CHEMBL4798733 1 7.85
CHEMBL4741152 1 7.82
CHEMBL4748182 1 7.82
CHEMBL4746229 1 7.80
CHEMBL4744457 1 7.80
CHEMBL4783979 1 7.77
CHEMBL4784854 1 7.77
CHEMBL4795684 1 7.77
CHEMBL4784301 1 7.77

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4754158 EC50 = 0.5 nM 9.30
CHEMBL4748592 EC50 = 4.0 nM 8.40
CHEMBL4750813 EC50 = 5.0 nM 8.30
CHEMBL4743554 EC50 = 5.0 nM 8.30
CHEMBL4793040 EC50 = 5.0 nM 8.30
CHEMBL4750992 EC50 = 5.0 nM 8.30
CHEMBL4747920 EC50 = 5.0 nM 8.30
CHEMBL4760962 EC50 = 6.0 nM 8.22
CHEMBL4791794 EC50 = 6.0 nM 8.22
CHEMBL4752574 EC50 = 6.0 nM 8.22
CHEMBL4750463 EC50 = 6.0 nM 8.22
CHEMBL4788181 EC50 = 6.0 nM 8.22
CHEMBL4746877 EC50 = 7.0 nM 8.15
CHEMBL4782284 EC50 = 9.0 nM 8.05
CHEMBL4760238 EC50 = 9.0 nM 8.05
CHEMBL4792206 EC50 = 12.0 nM 7.92
CHEMBL4782741 EC50 = 13.0 nM 7.89
CHEMBL4744355 EC50 = 13.0 nM 7.89
CHEMBL4749286 EC50 = 13.0 nM 7.89
CHEMBL4761414 EC50 = 14.0 nM 7.85
CHEMBL4785795 EC50 = 14.0 nM 7.85
CHEMBL4798733 EC50 = 14.0 nM 7.85
CHEMBL4741152 EC50 = 15.0 nM 7.82
CHEMBL4748182 EC50 = 15.0 nM 7.82
CHEMBL4744457 EC50 = 16.0 nM 7.80
CHEMBL4746229 EC50 = 16.0 nM 7.80
CHEMBL4783979 EC50 = 17.0 nM 7.77
CHEMBL4784854 EC50 = 17.0 nM 7.77
CHEMBL4795684 EC50 = 17.0 nM 7.77
CHEMBL4784301 EC50 = 17.0 nM 7.77
CHEMBL4753513 EC50 = 17.0 nM 7.77
CHEMBL4751246 EC50 = 17.0 nM 7.77
CHEMBL4748738 EC50 = 17.0 nM 7.77
CHEMBL4785550 EC50 = 18.0 nM 7.75
CHEMBL4745484 EC50 = 18.0 nM 7.75
CHEMBL4796151 EC50 = 19.0 nM 7.72
CHEMBL4778775 EC50 = 19.0 nM 7.72
CHEMBL4790196 EC50 = 20.0 nM 7.70
CHEMBL4784394 EC50 = 21.0 nM 7.68
CHEMBL4798099 EC50 = 21.0 nM 7.68
CHEMBL4745443 EC50 = 22.0 nM 7.66
CHEMBL4753462 EC50 = 22.0 nM 7.66
CHEMBL4762750 EC50 = 24.0 nM 7.62
CHEMBL4778927 EC50 = 25.0 nM 7.60
CHEMBL4763148 EC50 = 25.0 nM 7.60
CHEMBL4749099 EC50 = 25.0 nM 7.60
CHEMBL4745943 EC50 = 28.0 nM 7.55
CHEMBL4759402 EC50 = 30.0 nM 7.52
CHEMBL4797413 EC50 = 30.0 nM 7.52
CHEMBL4785745 EC50 = 32.0 nM 7.50