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Assay Detail

CHEMBL5385443

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

Binding
Inhibition of HIV-1 reverse transcriptase RT52A mutant using ABTS as substrate preincubated with compound for 1 hr followed by template-primer addition for 1 hr and measured 20 mins after substrate addition by absorbance based Roche colorimetric assay
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Human immunodeficiency virus 1
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Human immunodeficiency virus type 1 reverse transcriptase (CHEMBL247)
Type SINGLE PROTEIN
Organism Human immunodeficiency virus 1

Publication

Halo Library, a Tool for Rapid Identification of Ligand Binding Sites on Proteins Using Crystallographic Fragment Screening.
Chopra A, Bauman JD, Ruiz FX, Arnold E.
J Med Chem (2023) 66 : 6013 -6024
PubMed 37115705 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 2.63 2.68

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5413115 1 2.68
CHEMBL452901 1 2.68
CHEMBL23507 5-FLUOROINDOLE-2-CARBOXYLIC ACID 1 2.54

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5413115 IC50 = 2100000.0 nM 2.68
CHEMBL452901 IC50 = 2100000.0 nM 2.68
CHEMBL23507 5-FLUOROINDOLE-2-CARBOXYLIC ACID IC50 = 2900000.0 nM 2.54