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Assay Detail

CHEMBL1930892

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

Functional
Cytotoxicity against human K562 cells after 72 hrs by sulforhodamine B and MTT assay
8
Total Activities
8
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type K562
Confidence 1 — Organism
Curated By Autocuration

Target

K562 (CHEMBL385)
Type CELL-LINE
Organism Homo sapiens

Publication

Design, synthesis and biological evaluation of novel glycosylated diphyllin derivatives as topoisomerase II inhibitors.
Shi DK, Zhang W, Ding N, Li M, Li YX.
Eur J Med Chem (2012) 47 : 424 -431
PubMed 22119124 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 8 6.01 7.36

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1929104 1 7.36
CHEMBL53463 DOXORUBICIN 4.0 1 6.37
CHEMBL505932 1 6.09
CHEMBL458904 PATENTIFLORIN A 1 5.84
CHEMBL221190 DIPHYLLIN 1 5.78
CHEMBL1929098 1 5.36
CHEMBL44657 ETOPOSIDE 4.0 1 5.29
CHEMBL90555 VINCRISTINE 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1929104 IC50 = 44.0 nM 7.36
CHEMBL53463 DOXORUBICIN IC50 = 430.0 nM 6.37
CHEMBL505932 IC50 = 808.0 nM 6.09
CHEMBL458904 PATENTIFLORIN A IC50 = 1430.0 nM 5.84
CHEMBL221190 DIPHYLLIN IC50 = 1670.0 nM 5.78
CHEMBL1929098 IC50 = 4402.0 nM 5.36
CHEMBL44657 ETOPOSIDE IC50 = 5160.0 nM 5.29
CHEMBL90555 VINCRISTINE IC50 - -