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Assay Detail

CHEMBL835019

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

Functional
Concentration required for 50% protection of infected MT-4 cells from wtIIIB-HIV-1-induced cytopathogenicity was determined by the MTT method
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type MT4
Confidence 1 — Organism
Curated By Intermediate

Target

MT4 (CHEMBL388)
Type CELL-LINE
Organism Homo sapiens

Publication

Docking and 3-D QSAR studies on indolyl aryl sulfones. Binding mode exploration at the HIV-1 reverse transcriptase non-nucleoside binding site and design of highly active N-(2-hydroxyethyl)carboxamide and N-(2-hydroxyethyl)carbohydrazide derivatives.
Ragno R, Artico M, De Martino G, La Regina G, Coluccia A, Di Pasquali A, Silvestri R.
J Med Chem (2005) 48 : 213 -223
PubMed 15634015 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 14 6.33 9.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL366702 1 9.00
CHEMBL176239 1 9.00
CHEMBL366914 1 8.00
CHEMBL180522 1 8.00
CHEMBL180330 1 6.89
CHEMBL148987 1 6.00
CHEMBL179469 1 5.64
CHEMBL357793 1 5.40
CHEMBL342760 1 5.30
CHEMBL151377 1 5.22
CHEMBL149104 1 4.96
CHEMBL359306 1 4.80
CHEMBL355999 1 4.13
CHEMBL151810 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL366702 EC50 = 1.0 nM 9.00
CHEMBL176239 EC50 = 1.0 nM 9.00
CHEMBL366914 EC50 = 10.0 nM 8.00
CHEMBL180522 EC50 = 10.0 nM 8.00
CHEMBL180330 EC50 = 128.82 nM 6.89
CHEMBL148987 EC50 = 1000.0 nM 6.00
CHEMBL179469 EC50 = 2290.87 nM 5.64
CHEMBL357793 EC50 = 3981.07 nM 5.40
CHEMBL342760 EC50 = 5011.87 nM 5.30
CHEMBL151377 EC50 = 6025.6 nM 5.22
CHEMBL149104 EC50 = 10964.78 nM 4.96
CHEMBL359306 EC50 = 15848.93 nM 4.80
CHEMBL355999 EC50 = 74131.02 nM 4.13
CHEMBL151810 EC50 = 151356.12 nM -