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Assay Detail

CHEMBL1049688

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

Functional
Antiproliferative activity against human IGROV1 cells assessed as growth inhibition after 72 hrs by Coulter counting analysis
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

IGROV-1 (CHEMBL613984)
Type CELL-LINE
Organism Homo sapiens

Publication

Histone deacetylase and microtubules as targets for the synthesis of releasable conjugate compounds.
Passarella D, Comi D, Vanossi A, Paganini G, Colombo F, Ferrante L, Zuco V, Danieli B, Zunino F.
Bioorg Med Chem Lett (2009) 19 : 6358 -6363
PubMed 19833515 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 6.83 7.92

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL18981 THIOCOLCHICINE 1 7.92
CHEMBL566629 1 7.75
CHEMBL567988 1 7.72
CHEMBL298240 1 7.64
CHEMBL570142 1 7.30
CHEMBL428647 PACLITAXEL 4.0 1 7.22
CHEMBL572365 1 7.11
CHEMBL305522 CEPHALOMANNINE 1 6.52
CHEMBL566831 1 6.32
CHEMBL568139 1 6.28
CHEMBL587393 1 6.14
CHEMBL577096 1 6.13
CHEMBL566673 1 4.72

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL18981 THIOCOLCHICINE IC50 = 12.0 nM 7.92
CHEMBL566629 IC50 = 18.0 nM 7.75
CHEMBL567988 IC50 = 19.0 nM 7.72
CHEMBL298240 IC50 = 23.0 nM 7.64
CHEMBL570142 IC50 = 50.0 nM 7.30
CHEMBL428647 PACLITAXEL IC50 = 60.0 nM 7.22
CHEMBL572365 IC50 = 78.0 nM 7.11
CHEMBL305522 CEPHALOMANNINE IC50 = 300.0 nM 6.52
CHEMBL566831 IC50 = 480.0 nM 6.32
CHEMBL568139 IC50 = 530.0 nM 6.28
CHEMBL587393 IC50 = 720.0 nM 6.14
CHEMBL577096 IC50 = 740.0 nM 6.13
CHEMBL566673 IC50 = 19100.0 nM 4.72