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Assay Detail

CHEMBL677015

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

Functional
Inhibitory activity against GC3/M TK- human adreno carcinoma cell lines.
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type GC3/MTK-
Confidence 1 — Organism
Curated By Intermediate

Target

GC3/MTK- (CHEMBL614157)
Type CELL-LINE
Organism Homo sapiens

Publication

Structure-based design of substituted diphenyl sulfones and sulfoxides as lipophilic inhibitors of thymidylate synthase.
Jones TR, Webber SE, Varney MD, Reddy MR, Lewis KK, Kathardekar V, Mazdiyasni H, Deal J, Nguyen D, Welsh KM, Webber S, Johnston A, Matthews DA, Smith WW, Janson CA, Bacquet RJ, Howland EF, Booth CL, Herrmann SM, Ward RW, White J, Bartlett CA, Morse CA.
J Med Chem (1997) 40 : 677 -683
PubMed 9057854 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 5.47 5.99

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL417222 1 5.99
CHEMBL159213 1 5.92
CHEMBL158542 1 5.55
CHEMBL162076 1 5.52
CHEMBL161450 1 5.48
CHEMBL159364 1 5.47
CHEMBL160215 1 5.42
CHEMBL162754 1 5.41
CHEMBL159209 1 5.40
CHEMBL161025 1 5.38
CHEMBL161685 1 5.37
CHEMBL291548 1 5.12
CHEMBL157702 1 5.04
CHEMBL159144 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL417222 IC50 = 1030.0 nM 5.99
CHEMBL159213 IC50 = 1200.0 nM 5.92
CHEMBL158542 IC50 = 2800.0 nM 5.55
CHEMBL162076 IC50 = 3000.0 nM 5.52
CHEMBL161450 IC50 = 3300.0 nM 5.48
CHEMBL159364 IC50 = 3400.0 nM 5.47
CHEMBL160215 IC50 = 3800.0 nM 5.42
CHEMBL162754 IC50 = 3900.0 nM 5.41
CHEMBL159209 IC50 = 4000.0 nM 5.40
CHEMBL161025 IC50 = 4200.0 nM 5.38
CHEMBL161685 IC50 = 4300.0 nM 5.37
CHEMBL291548 IC50 = 7500.0 nM 5.12
CHEMBL157702 IC50 = 9100.0 nM 5.04
CHEMBL159144 IC50 > 5000.0 nM -