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Assay Detail

CHEMBL1655366

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Binding
Inhibition of Leishmania major PTR1
18
Total Activities
18
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Leishmania major
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Pteridine reductase 1 (CHEMBL6194)
Type SINGLE PROTEIN
Organism Leishmania major

Publication

Virtual screening identification of nonfolate compounds, including a CNS drug, as antiparasitic agents inhibiting pteridine reductase.
Ferrari S, Morandi F, Motiejunas D, Nerini E, Henrich S, Luciani R, Venturelli A, Lazzari S, Calò S, Gupta S, Hannaert V, Michels PA, Wade RC, Costi MP.
J Med Chem (2011) 54 : 211 -221
PubMed 21126022 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 18 4.36 4.66

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1650283 1 4.66
CHEMBL1650287 1 4.54
CHEMBL1650277 1 4.51
CHEMBL318275 1 4.40
CHEMBL744 RILUZOLE 4.0 1 4.30
CHEMBL1650288 1 4.05
CHEMBL1650465 1 4.03
CHEMBL432942 1 -
CHEMBL1413383 1 -
CHEMBL329785 1 -
CHEMBL1650466 1 -
CHEMBL1650282 1 -
CHEMBL1650274 1 -
CHEMBL595536 1 -
CHEMBL1650263 1 -
CHEMBL147741 3-FORMYLINDOLE 1 -
CHEMBL284348 DALFAMPRIDINE 4.0 1 -
CHEMBL1650237 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1650283 IC50 = 22000.0 nM 4.66
CHEMBL1650287 IC50 = 29000.0 nM 4.54
CHEMBL1650277 IC50 = 31000.0 nM 4.51
CHEMBL318275 IC50 = 40000.0 nM 4.40
CHEMBL744 RILUZOLE IC50 = 50000.0 nM 4.30
CHEMBL1650288 IC50 = 89000.0 nM 4.05
CHEMBL1650465 IC50 = 93000.0 nM 4.03
CHEMBL432942 IC50 = 212000.0 nM -
CHEMBL1413383 IC50 = 1000000.0 nM -
CHEMBL329785 IC50 = 1800000.0 nM -
CHEMBL1650466 IC50 = 116000.0 nM -
CHEMBL1650282 IC50 = 309000.0 nM -
CHEMBL1650274 IC50 = 2300000.0 nM -
CHEMBL595536 IC50 = 390000.0 nM -
CHEMBL1650263 IC50 = 1000000.0 nM -
CHEMBL147741 3-FORMYLINDOLE IC50 = 1100000.0 nM -
CHEMBL284348 DALFAMPRIDINE IC50 = 1900000.0 nM -
CHEMBL1650237 IC50 = 5600000.0 nM -