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Assay Detail

CHEMBL923236

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

Functional
Cytotoxicity against human XF498 cells after 3 days by SRB assay
16
Total Activities
16
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type XF498
Confidence 1 — Organism
Curated By Autocuration

Target

XF498 (CHEMBL613533)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis of 1-/2-substituted-[1,2,3]triazolo[4,5-g]phthalazine-4,9-diones and evaluation of their cytotoxicity and topoisomerase II inhibition.
Kim JS, Rhee HK, Park HJ, Lee SK, Lee CO, Park Choo HY.
Bioorg Med Chem (2008) 16 : 4545 -4550
PubMed 18321715 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 16 7.32 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL259989 1 8.40
CHEMBL261342 1 7.85
CHEMBL261876 1 7.77
CHEMBL261330 1 7.75
CHEMBL261294 1 7.72
CHEMBL260223 1 7.72
CHEMBL406853 1 7.47
CHEMBL259778 1 7.46
CHEMBL53463 DOXORUBICIN 4.0 1 7.36
CHEMBL260224 1 7.31
CHEMBL258925 1 7.07
CHEMBL259225 1 6.93
CHEMBL261341 1 6.85
CHEMBL260541 1 6.74
CHEMBL44657 ETOPOSIDE 4.0 1 5.46
CHEMBL259990 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL259989 IC50 = 4.0 nM 8.40
CHEMBL261342 IC50 = 14.0 nM 7.85
CHEMBL261876 IC50 = 17.0 nM 7.77
CHEMBL261330 IC50 = 18.0 nM 7.75
CHEMBL261294 IC50 = 19.0 nM 7.72
CHEMBL260223 IC50 = 19.0 nM 7.72
CHEMBL406853 IC50 = 34.0 nM 7.47
CHEMBL259778 IC50 = 35.0 nM 7.46
CHEMBL53463 DOXORUBICIN IC50 = 44.0 nM 7.36
CHEMBL260224 IC50 = 49.0 nM 7.31
CHEMBL258925 IC50 = 85.0 nM 7.07
CHEMBL259225 IC50 = 118.0 nM 6.93
CHEMBL261341 IC50 = 140.0 nM 6.85
CHEMBL260541 IC50 = 181.0 nM 6.74
CHEMBL44657 ETOPOSIDE IC50 = 3480.0 nM 5.46
CHEMBL259990 IC50 > 10000.0 nM -