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Assay Detail

CHEMBL798924

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

Binding
Inhibition of recombinant reverse transcriptase (RT) in cell-free Quan-T-RT assay system
14
Total Activities
14
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

N'-[2-(2-thiophene)ethyl]-N'-[2-(5-bromopyridyl)] thiourea as a potent inhibitor of NNI-resistant and multidrug-resistant human immunodeficiency virus-1.
Uckun FM, Pendergrass S, Maher D, Zhu D, Tuel-Ahlgren L, Mao C, Venkatachalam TK.
Bioorg Med Chem Lett (1999) 9 : 3411 -3416
PubMed 10617082 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 5.85 6.22

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL39999 TROVIRDINE 2.0 1 6.22
CHEMBL69952 1 6.22
CHEMBL114559 1 6.16
CHEMBL116474 1 6.10
CHEMBL35033 EMIVIRINE 2.0 1 6.10
CHEMBL116350 1 6.05
CHEMBL114598 1 5.92
CHEMBL593 DELAVIRDINE 4.0 1 5.82
CHEMBL432812 1 5.31
CHEMBL57 NEVIRAPINE 4.0 1 4.64
CHEMBL117524 1 -
CHEMBL114652 1 -
CHEMBL117182 1 -
CHEMBL129 ZIDOVUDINE 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL39999 TROVIRDINE IC50 = 600.0 nM 6.22
CHEMBL69952 IC50 = 600.0 nM 6.22
CHEMBL114559 IC50 = 700.0 nM 6.16
CHEMBL116474 IC50 = 800.0 nM 6.10
CHEMBL35033 EMIVIRINE IC50 = 800.0 nM 6.10
CHEMBL116350 IC50 = 900.0 nM 6.05
CHEMBL114598 IC50 = 1200.0 nM 5.92
CHEMBL593 DELAVIRDINE IC50 = 1500.0 nM 5.82
CHEMBL432812 IC50 = 4900.0 nM 5.31
CHEMBL57 NEVIRAPINE IC50 = 23000.0 nM 4.64
CHEMBL117524 IC50 > 100000.0 nM -
CHEMBL114652 IC50 > 100000.0 nM -
CHEMBL117182 IC50 > 100000.0 nM -
CHEMBL129 ZIDOVUDINE IC50 > 100000.0 nM -