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Assay Detail

CHEMBL656060

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

Functional
Compound was tested for the inhibition of human CCRF-CEM leukemia cell growth
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type CCRF-CEM
Confidence 1 — Organism
Curated By Intermediate

Target

CCRF-CEM (CHEMBL382)
Type CELL-LINE
Organism Homo sapiens

Publication

Design and synthesis of novel 6,7-imidazotetrahydroquinoline inhibitors of thymidylate synthase using iterative protein crystal structure analysis.
Reich SH, Fuhry MA, Nguyen D, Pino MJ, Welsh KM, Webber S, Janson CA, Jordan SR, Matthews DA, Smith WW.
J Med Chem (1992) 35 : 847 -858
PubMed 1548676 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 5.29 6.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL171057 1 6.05
CHEMBL352620 1 5.75
CHEMBL56662 1 5.66
CHEMBL169726 1 5.48
CHEMBL301256 1 5.41
CHEMBL168524 1 5.40
CHEMBL171314 1 5.29
CHEMBL169727 1 5.10
CHEMBL353700 1 4.96
CHEMBL169921 1 4.66
CHEMBL169411 1 4.40
CHEMBL353813 1 -
CHEMBL172176 1 -
CHEMBL353191 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL171057 IC50 = 900.0 nM 6.05
CHEMBL352620 IC50 = 1800.0 nM 5.75
CHEMBL56662 IC50 = 2200.0 nM 5.66
CHEMBL169726 IC50 = 3300.0 nM 5.48
CHEMBL301256 IC50 = 3900.0 nM 5.41
CHEMBL168524 IC50 = 4000.0 nM 5.40
CHEMBL171314 IC50 = 5100.0 nM 5.29
CHEMBL169727 IC50 = 8000.0 nM 5.10
CHEMBL353700 IC50 = 11000.0 nM 4.96
CHEMBL169921 IC50 = 22000.0 nM 4.66
CHEMBL169411 IC50 = 40000.0 nM 4.40
CHEMBL353813 IC50 > 5000.0 nM -
CHEMBL172176 IC50 > 10000.0 nM -
CHEMBL353191 IC50 > 10000.0 nM -