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Assay Detail

CHEMBL3106434

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

Functional
Cytotoxicity against human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTitre-Blue fluorescence assay in presence of folic acid
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

KB (CHEMBL398)
Type CELL-LINE
Organism Homo sapiens

Publication

Discovery of 5-substituted pyrrolo[2,3-d]pyrimidine antifolates as dual-acting inhibitors of glycinamide ribonucleotide formyltransferase and 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase in de novo purine nucleotide biosynthesis: implications of inhibiting 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase to ampk activation and antitumor activity.
Mitchell-Ryan S, Wang Y, Raghavan S, Ravindra MP, Hales E, Orr S, Cherian C, Hou Z, Matherly LH, Gangjee A.
J Med Chem (2013) 56 : 10016 -10032
PubMed 24256410 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 6.16 6.27

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL374172 1 6.27
CHEMBL3104645 1 6.16
CHEMBL225072 PEMETREXED 4.0 1 6.16
CHEMBL2426246 1 6.05
CHEMBL3105240 1 -
CHEMBL2426247 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL374172 IC50 = 533.0 nM 6.27
CHEMBL3104645 IC50 = 700.0 nM 6.16
CHEMBL225072 PEMETREXED IC50 = 690.0 nM 6.16
CHEMBL2426246 IC50 = 898.0 nM 6.05
CHEMBL3105240 IC50 > 1000.0 nM -
CHEMBL2426247 IC50 > 1000.0 nM -