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Assay Detail

CHEMBL713410

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

Functional
Concentration required to inhibit HIV-1 induced cytopathicity in MT-4 cells by 50%
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

MT4 (CHEMBL388)
Type CELL-LINE
Organism Homo sapiens

Publication

TSAO analogues. Stereospecific synthesis and anti-HIV-1 activity of 1-[2',5'-bis-O-(tert-butyldimethylsilyl)-beta-D-ribofuranosyl]-3'-spiro -5''- (4''-amino-1'',2''-oxathiole 2'',2''-dioxide) pyrimidine and pyrimidine-modified nucleosides.
Pérez-Pérez MJ, San-Félix A, Balzarini J, De Clercq E, Camarasa MJ.
J Med Chem (1992) 35 : 2988 -2995
PubMed 1501224 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 15 6.78 7.23

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL211582 1 7.23
CHEMBL2115411 1 7.22
CHEMBL3142769 1 7.18
CHEMBL46961 1 7.12
CHEMBL3142770 1 6.91
CHEMBL3142761 1 6.90
CHEMBL57 NEVIRAPINE 4.0 1 6.89
CHEMBL2115239 1 6.69
CHEMBL3142758 1 6.63
CHEMBL3142768 1 6.42
CHEMBL3142760 1 6.21
CHEMBL3142762 1 6.00
CHEMBL3142771 1 -
CHEMBL3142759 1 -
CHEMBL3142643 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL211582 EC50 = 59.0 nM 7.23
CHEMBL2115411 EC50 = 60.0 nM 7.22
CHEMBL3142769 EC50 = 66.0 nM 7.18
CHEMBL46961 EC50 = 76.0 nM 7.12
CHEMBL3142770 EC50 = 123.0 nM 6.91
CHEMBL3142761 EC50 = 127.0 nM 6.90
CHEMBL57 NEVIRAPINE EC50 = 128.0 nM 6.89
CHEMBL2115239 EC50 = 206.0 nM 6.69
CHEMBL3142758 EC50 = 233.0 nM 6.63
CHEMBL3142768 EC50 = 377.0 nM 6.42
CHEMBL3142760 EC50 = 615.0 nM 6.21
CHEMBL3142762 EC50 = 1000.0 nM 6.00
CHEMBL3142771 EC50 > 15000.0 nM -
CHEMBL3142759 EC50 > 200000.0 nM -
CHEMBL3142643 EC50 > 80000.0 nM -