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Assay Detail

CHEMBL4132839

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

Binding
Inhibition of TS/AICARFTase/GARFTase in human KB cells assessed as reduction in cell proliferation in folate free medium after 72 hrs in presence of leucovorin by MTT assay
8
Total Activities
8
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 5 — Multiple protein complex / RNA
Curated By Intermediate

Publication

Novel 6-substituted benzoyl and non-benzoyl straight chain pyrrolo[2,3-d]pyrimidines as potential antitumor agents with multitargeted inhibition of TS, GARFTase and AICARFTase.
Xing R, Zhang H, Yuan J, Zhang K, Li L, Guo H, Zhao L, Zhang C, Li S, Gao T, Liu Y, Wang L.
Eur J Med Chem (2017) 139 : 531 -541
PubMed 28830032 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 8 8.08 10.11

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4177183 1 10.11
CHEMBL4162649 1 9.85
CHEMBL4170578 1 8.12
CHEMBL34259 METHOTREXATE 4.0 1 8.00
CHEMBL4174018 1 7.37
CHEMBL225072 PEMETREXED 4.0 1 7.16
CHEMBL4163732 1 7.04
CHEMBL4166099 1 6.97

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4177183 IC50 = 0.078 nM 10.11
CHEMBL4162649 IC50 = 0.14 nM 9.85
CHEMBL4170578 IC50 = 7.5 nM 8.12
CHEMBL34259 METHOTREXATE IC50 = 10.0 nM 8.00
CHEMBL4174018 IC50 = 43.0 nM 7.37
CHEMBL225072 PEMETREXED IC50 = 70.0 nM 7.16
CHEMBL4163732 IC50 = 92.0 nM 7.04
CHEMBL4166099 IC50 = 107.0 nM 6.97