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Assay Detail

CHEMBL753039

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

Binding
Compound was evaluated for its ability to inhibit the NNRTI HIV-1 enzyme by 50% using enzyme assay
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Human immunodeficiency virus type 1 protease (CHEMBL243)
Type SINGLE PROTEIN
Organism Human immunodeficiency virus 1

Publication

Trifluoromethyl-containing 3-alkoxymethyl- and 3-aryloxymethyl-2-pyridinones are potent inhibitors of HIV-1 non-nucleoside reverse transcriptase.
Corbett JW, Kresge KJ, Pan S, Cordova BC, Klabe RM, Rodgers JD, Erickson-Viitanen SK.
Bioorg Med Chem Lett (2001) 11 : 309 -312
PubMed 11212098 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 7.51 7.51

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL283619 1 7.51

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL283619 IC50 = 31.0 nM 7.51