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Assay Detail

CHEMBL4007134

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

Functional
Cytotoxicity against human U251 cells assessed as decrease in cell proliferation after 72 hrs by SRB assay
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type U-251
Confidence 1 — Organism
Curated By Autocuration

Target

U-251 (CHEMBL615022)
Type CELL-LINE
Organism Homo sapiens

Publication

Preliminary SAR on indole-3-carbinol and related fragments reveals a novel anticancer lead compound against resistant glioblastoma cells.
Sherer C, Tolaymat I, Rowther F, Warr T, Snape TJ.
Bioorg Med Chem Lett (2017) 27 : 1561 -1565
PubMed 28256372 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 12 3.44 4.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL391414 1 4.30
CHEMBL2349385 (2-PHENYL-1H-INDOL-3-YL)METHANOL 1 3.89
CHEMBL1904177 1 3.85
CHEMBL4084900 1 3.60
CHEMBL446452 ARUNDINE 3.0 1 3.55
CHEMBL155625 INDOLE-3-CARBINOL 2.0 1 3.41
CHEMBL1359077 1 3.22
CHEMBL226545 TRYPTOPHOL 1 2.91
CHEMBL3358210 1 2.91
CHEMBL1320312 1 2.75
CHEMBL75756 2-PHENYL-1H-INDOLE 1 -
CHEMBL15844 INDOLE 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL391414 EC50 = 50000.0 nM 4.30
CHEMBL2349385 (2-PHENYL-1H-INDOL-3-YL)METHANOL EC50 = 130000.0 nM 3.89
CHEMBL1904177 EC50 = 140000.0 nM 3.85
CHEMBL4084900 EC50 = 250000.0 nM 3.60
CHEMBL446452 ARUNDINE EC50 = 280000.0 nM 3.55
CHEMBL155625 INDOLE-3-CARBINOL EC50 = 390000.0 nM 3.41
CHEMBL1359077 EC50 = 600000.0 nM 3.22
CHEMBL226545 TRYPTOPHOL EC50 = 1220000.0 nM 2.91
CHEMBL3358210 EC50 = 1240000.0 nM 2.91
CHEMBL1320312 EC50 = 1760000.0 nM 2.75
CHEMBL75756 2-PHENYL-1H-INDOLE EC50 - -
CHEMBL15844 INDOLE EC50 - -