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Assay Detail

CHEMBL4705549

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

Functional
Antiviral activity against HIV2 ROD infected in human CEM/0 cells assessed as inhibition of virus-induced syncytia cell formation measured after 4 to 5 days by microscopic analysis
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human immunodeficiency virus 1
Cell Type CEM/0
Confidence 1 — Organism
Curated By Autocuration

Target

Human immunodeficiency virus 1 (CHEMBL378)
Type ORGANISM
Organism Human immunodeficiency virus 1

Publication

γ-Ketobenzyl-Modified Nucleoside Triphosphate Prodrugs as Potential Antivirals.
Nack T,Dinis de Oliveira T,Weber S,Schols D,Balzarini J,Meier C
J Med Chem (2020) 63 : 13745 -13761
PubMed 33186038 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 11 6.16 7.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4791857 1 7.00
CHEMBL991 STAVUDINE 4.0 1 6.66
CHEMBL485652 STAVUDINE TRIPHOSPHATE -1.0 1 6.40
CHEMBL4792961 1 6.22
CHEMBL4754622 1 6.21
CHEMBL4757045 1 6.11
CHEMBL4751622 1 6.08
CHEMBL4785596 1 5.96
CHEMBL4790264 1 5.92
CHEMBL4797903 1 5.06
CHEMBL4779618 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4791857 EC50 = 100.0 nM 7.00
CHEMBL991 STAVUDINE EC50 = 220.0 nM 6.66
CHEMBL485652 STAVUDINE TRIPHOSPHATE EC50 = 400.0 nM 6.40
CHEMBL4792961 EC50 = 600.0 nM 6.22
CHEMBL4754622 EC50 = 620.0 nM 6.21
CHEMBL4757045 EC50 = 780.0 nM 6.11
CHEMBL4751622 EC50 = 830.0 nM 6.08
CHEMBL4785596 EC50 = 1100.0 nM 5.96
CHEMBL4790264 EC50 = 1200.0 nM 5.92
CHEMBL4797903 EC50 = 8800.0 nM 5.06
CHEMBL4779618 EC50 > 10000.0 nM -