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Assay Detail

CHEMBL4390131

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

Binding
Inhibition of Pneumocystis jirovecii DHFR expressed in Escherichia coli Rosetta-gami B (DE3) assessed as reduction in consumption of NADPH using 18 uM DHFA as substrate
9
Total Activities
9
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Pneumocystis jirovecii
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Development of substituted pyrido[3,2-d]pyrimidines as potent and selective dihydrofolate reductase inhibitors for pneumocystis pneumonia infection.
Shah K, Queener S, Cody V, Pace J, Gangjee A.
Bioorg Med Chem Lett (2019) 29 : 1874 -1880
PubMed 31176699 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 9 6.95 8.80

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL7492 PIRITREXIM 2.0 1 8.80
CHEMBL119 TRIMETREXATE 4.0 1 8.68
CHEMBL22 TRIMETHOPRIM 4.0 1 6.92
CHEMBL2382323 1 6.60
CHEMBL2382314 1 6.52
CHEMBL2382315 1 6.40
CHEMBL2382321 1 6.40
CHEMBL2382319 1 6.21
CHEMBL2382325 1 6.06

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL7492 PIRITREXIM IC50 = 1.6 nM 8.80
CHEMBL119 TRIMETREXATE IC50 = 2.1 nM 8.68
CHEMBL22 TRIMETHOPRIM IC50 = 120.0 nM 6.92
CHEMBL2382323 IC50 = 250.0 nM 6.60
CHEMBL2382314 IC50 = 300.0 nM 6.52
CHEMBL2382315 IC50 = 400.0 nM 6.40
CHEMBL2382321 IC50 = 400.0 nM 6.40
CHEMBL2382319 IC50 = 620.0 nM 6.21
CHEMBL2382325 IC50 = 870.0 nM 6.06