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Assay Detail

CHEMBL804071

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

Binding
Inhibition of HIV-1 RT using rC-dG as template
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

5-chloro-3-(phenylsulfonyl)indole-2-carboxamide: a novel, non-nucleoside inhibitor of HIV-1 reverse transcriptase.
Williams TM, Ciccarone TM, MacTough SC, Rooney CS, Balani SK, Condra JH, Emini EA, Goldman ME, Greenlee WJ, Kauffman LR.
J Med Chem (1993) 36 : 1291 -1294
PubMed 7683725 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 6.63 8.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL283950 L-737126 1 8.52
CHEMBL286759 1 7.85
CHEMBL23456 1 7.66
CHEMBL23401 1 7.64
CHEMBL268871 L-697661 1 7.44
CHEMBL280551 1 7.20
CHEMBL57 NEVIRAPINE 4.0 1 7.00
CHEMBL285799 1 6.95
CHEMBL24273 1 6.81
CHEMBL293498 1 6.51
CHEMBL286378 1 6.13
CHEMBL280527 ATEVIRDINE MESYLATE 2.0 1 5.88
CHEMBL286404 1 5.60
CHEMBL24214 1 4.14
CHEMBL23678 1 4.06

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL283950 L-737126 IC50 = 3.0 nM 8.52
CHEMBL286759 IC50 = 14.0 nM 7.85
CHEMBL23456 IC50 = 22.0 nM 7.66
CHEMBL23401 IC50 = 23.0 nM 7.64
CHEMBL268871 L-697661 IC50 = 36.0 nM 7.44
CHEMBL280551 IC50 = 63.0 nM 7.20
CHEMBL57 NEVIRAPINE IC50 = 101.0 nM 7.00
CHEMBL285799 IC50 = 112.0 nM 6.95
CHEMBL24273 IC50 = 156.0 nM 6.81
CHEMBL293498 IC50 = 311.0 nM 6.51
CHEMBL286378 IC50 = 746.0 nM 6.13
CHEMBL280527 ATEVIRDINE MESYLATE IC50 = 1320.0 nM 5.88
CHEMBL286404 IC50 = 2500.0 nM 5.60
CHEMBL24214 IC50 = 72800.0 nM 4.14
CHEMBL23678 IC50 = 87600.0 nM 4.06