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Assay Detail

CHEMBL702645

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

Functional
Concentration required to inhibit the growth of paclitaxel-sensitive human epidermoid carcinoma cells KB-31 by 50 percent (72 hr exposure)
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type KB 3-1
Confidence 1 — Organism
Curated By Intermediate

Target

KB 3-1 (CHEMBL614590)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis and biological evaluation of highly potent analogues of epothilones B and D.
Altmann KH, Bold G, Caravatti G, Flörsheimer A, Guagnano V, Wartmann M.
Bioorg Med Chem Lett (2000) 10 : 2765 -2768
PubMed 11133086 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 9.40 9.96

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2373443 1 9.96
CHEMBL92925 1 9.89
CHEMBL96115 1 9.89
CHEMBL328208 1 9.85
CHEMBL94657 PATUPILONE 3.0 1 9.72
CHEMBL95328 1 9.68
CHEMBL94599 1 9.52
CHEMBL92285 1 9.35
CHEMBL93904 1 9.34
CHEMBL328224 1 9.23
CHEMBL329993 EPOTHILONE A 1 8.67
CHEMBL96172 EPOTHILONE D 2.0 1 8.57
CHEMBL428647 PACLITAXEL 4.0 1 8.54

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2373443 IC50 = 0.11 nM 9.96
CHEMBL92925 IC50 = 0.13 nM 9.89
CHEMBL96115 IC50 = 0.13 nM 9.89
CHEMBL328208 IC50 = 0.14 nM 9.85
CHEMBL94657 PATUPILONE IC50 = 0.19 nM 9.72
CHEMBL95328 IC50 = 0.21 nM 9.68
CHEMBL94599 IC50 = 0.3 nM 9.52
CHEMBL92285 IC50 = 0.45 nM 9.35
CHEMBL93904 IC50 = 0.46 nM 9.34
CHEMBL328224 IC50 = 0.59 nM 9.23
CHEMBL329993 EPOTHILONE A IC50 = 2.15 nM 8.67
CHEMBL96172 EPOTHILONE D IC50 = 2.7 nM 8.57
CHEMBL428647 PACLITAXEL IC50 = 2.92 nM 8.54