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Assay Detail

CHEMBL4329973

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

Binding
Inhibition of Plasmodium falciparum V1/S DHFR IRNL haplotype N51I/C59R/S108N/I164L quadruple mutant
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Plasmodium falciparum
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Hybrid Inhibitors of Malarial Dihydrofolate Reductase with Dual Binding Modes That Can Forestall Resistance.
Tarnchompoo B, Chitnumsub P, Jaruwat A, Shaw PJ, Vanichtanankul J, Poen S, Rattanajak R, Wongsombat C, Tonsomboon A, Decharuangsilp S, Anukunwithaya T, Arwon U, Kamchonwongpaisan S, Yuthavong Y.
ACS Med Chem Lett (2018) 9 : 1235 -1240
PubMed 30613332 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 3 7.71 8.48

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL278847 1 8.48
CHEMBL3819601 1 8.25
CHEMBL36 PYRIMETHAMINE 4.0 1 6.41

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL278847 Ki = 3.3 nM 8.48
CHEMBL3819601 Ki = 5.59 nM 8.25
CHEMBL36 PYRIMETHAMINE Ki = 390.0 nM 6.41