Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL800662

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

Binding
Inhibition of Reverse transcriptase (Wild Type) with poly(rA)600:oligo(dT)10 template primer
13
Total Activities
13
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 Expert

Target

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

Publication

Synthesis and structure-activity relationships of the (alkylamino)piperidine-containing BHAP class of non-nucleoside reverse transcriptase inhibitors: effect of 3-alkylpyridine ring substitution.
Genin MJ, Poel TJ, May PD, Kopta LA, Yagi Y, Olmsted RA, Friis JM, Voorman RL, Adams WJ, Thomas RC, Romero DL.
J Med Chem (1999) 42 : 4140 -4149
PubMed 10514284 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 6.65 7.21

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL336635 1 7.21
CHEMBL336807 1 7.01
CHEMBL132770 1 6.89
CHEMBL132491 1 6.85
CHEMBL134106 1 6.85
CHEMBL331330 1 6.60
CHEMBL130177 1 6.60
CHEMBL593 DELAVIRDINE 4.0 1 6.58
CHEMBL132883 1 6.57
CHEMBL336318 1 6.39
CHEMBL127283 1 6.37
CHEMBL124338 1 6.30
CHEMBL133469 1 6.29

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL336635 IC50 = 61.0 nM 7.21
CHEMBL336807 IC50 = 98.0 nM 7.01
CHEMBL132770 IC50 = 130.0 nM 6.89
CHEMBL132491 IC50 = 140.0 nM 6.85
CHEMBL134106 IC50 = 140.0 nM 6.85
CHEMBL331330 IC50 = 250.0 nM 6.60
CHEMBL130177 IC50 = 250.0 nM 6.60
CHEMBL593 DELAVIRDINE IC50 = 260.0 nM 6.58
CHEMBL132883 IC50 = 270.0 nM 6.57
CHEMBL336318 IC50 = 410.0 nM 6.39
CHEMBL127283 IC50 = 430.0 nM 6.37
CHEMBL124338 IC50 = 500.0 nM 6.30
CHEMBL133469 IC50 = 510.0 nM 6.29