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Assay Detail

CHEMBL4765820

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

Functional
Antiproliferative activity against human HT-29 cells assessed as cell growth inhibition incubated for 72 hrs by MTS assay
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type HT-29
Confidence 1 — Organism
Curated By Autocuration

Target

HT-29 (CHEMBL384)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis and Biological Evaluation of N-[2-(4-Hydroxyphenylamino)-pyridin-3-yl]-4-methoxy-benzenesulfonamide (ABT-751) Tricyclic Analogues as Antimitotic and Antivascular Agents with Potent in Vivo Antitumor Activity.
Segaoula Z,Leclercq J,Verones V,Flouquet N,Lecoeur M,Ach L,Renault N,Barczyk A,Melnyk P,Berthelot P,Thuru X,Lebegue N
J Med Chem (2016) 59 : 8422 -8440
PubMed 27538123 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 6.17 8.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4794337 1 8.00
CHEMBL4785331 1 7.38
CHEMBL4777687 1 6.80
CHEMBL4779335 1 6.70
CHEMBL20684 ABT-751 2.0 1 6.68
CHEMBL4789264 1 6.12
CHEMBL4778834 1 5.39
CHEMBL4799616 1 5.33
CHEMBL4776691 1 5.24
CHEMBL4784977 1 5.11
CHEMBL4792371 1 5.11

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4794337 IC50 = 10.0 nM 8.00
CHEMBL4785331 IC50 = 42.0 nM 7.38
CHEMBL4777687 IC50 = 160.0 nM 6.80
CHEMBL4779335 IC50 = 200.0 nM 6.70
CHEMBL20684 ABT-751 IC50 = 210.0 nM 6.68
CHEMBL4789264 IC50 = 766.0 nM 6.12
CHEMBL4778834 IC50 = 4050.0 nM 5.39
CHEMBL4799616 IC50 = 4730.0 nM 5.33
CHEMBL4776691 IC50 = 5730.0 nM 5.24
CHEMBL4784977 IC50 = 7770.0 nM 5.11
CHEMBL4792371 IC50 = 7780.0 nM 5.11