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Assay Detail

CHEMBL872963

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Functional
Inhibitory concentration to reduce cell number to 50% in a panel of cultured, wild type human Jurkat leukemia (JL C) cells.
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Publication

Structure-activity relationships for pyrido-, imidazo-, pyrazolo-, pyrazino-, and pyrrolophenazinecarboxamides as topoisomerase-targeted anticancer agents.
Gamage SA, Spicer JA, Rewcastle GW, Milton J, Sohal S, Dangerfield W, Mistry P, Vicker N, Charlton PA, Denny WA.
J Med Chem (2002) 45 : 740 -743
PubMed 11806725 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 7.07 8.02

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL53463 DOXORUBICIN 4.0 1 8.02
CHEMBL349474 1 7.77
CHEMBL433703 1 7.68
CHEMBL162885 1 7.55
CHEMBL162739 1 7.36
CHEMBL355827 1 7.13
CHEMBL163525 1 7.10
CHEMBL162112 1 7.03
CHEMBL162987 1 7.01
CHEMBL351244 1 6.80
CHEMBL163577 1 6.78
CHEMBL353127 1 6.71
CHEMBL163072 1 6.50
CHEMBL164407 1 5.60

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL53463 DOXORUBICIN IC50 = 9.6 nM 8.02
CHEMBL349474 IC50 = 17.0 nM 7.77
CHEMBL433703 IC50 = 21.0 nM 7.68
CHEMBL162885 IC50 = 28.0 nM 7.55
CHEMBL162739 IC50 = 44.0 nM 7.36
CHEMBL355827 IC50 = 74.0 nM 7.13
CHEMBL163525 IC50 = 79.0 nM 7.10
CHEMBL162112 IC50 = 93.0 nM 7.03
CHEMBL162987 IC50 = 98.0 nM 7.01
CHEMBL351244 IC50 = 159.0 nM 6.80
CHEMBL163577 IC50 = 165.0 nM 6.78
CHEMBL353127 IC50 = 194.0 nM 6.71
CHEMBL163072 IC50 = 317.0 nM 6.50
CHEMBL164407 IC50 = 2500.0 nM 5.60