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Assay Detail

CHEMBL654553

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

Functional
Concentration of compound required to inhibit 50% of viral replication of human immunodeficiency virus in CEM-F cells
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type CCRF-CEM
Confidence 1 — Organism
Curated By Intermediate

Target

CCRF-CEM (CHEMBL382)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis and antiviral activity of several 2,5'-anhydro analogues of 3'-azido-3'-deoxythymidine, 3'-azido-2',3'-dideoxyuridine, 3'-azido-2',3'-dideoxy-5-halouridines, and 3'-deoxythymidine against human immunodeficiency virus and Rauscher-murine leukemia virus.
Lin TS, Shen ZY, August EM, Brankovan V, Yang H, Ghazzouli I, Prusoff WH.
J Med Chem (1989) 32 : 1891 -1895
PubMed 2754712 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 5.35 7.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL129 ZIDOVUDINE 4.0 1 7.00
CHEMBL444314 1 6.42
CHEMBL1794993 1 6.25
CHEMBL591804 NAVURIDINE 2.0 1 5.56
CHEMBL1794992 1 5.30
CHEMBL1791024 1 5.06
CHEMBL1794990 1 4.92
CHEMBL1791030 1 4.90
CHEMBL1794994 1 4.57
CHEMBL1794991 1 4.55
CHEMBL443742 1 4.32

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL129 ZIDOVUDINE IC50 = 100.0 nM 7.00
CHEMBL444314 IC50 = 380.0 nM 6.42
CHEMBL1794993 IC50 = 560.0 nM 6.25
CHEMBL591804 NAVURIDINE IC50 = 2760.0 nM 5.56
CHEMBL1794992 IC50 = 4950.0 nM 5.30
CHEMBL1791024 IC50 = 8730.0 nM 5.06
CHEMBL1794990 IC50 = 12000.0 nM 4.92
CHEMBL1791030 IC50 = 12600.0 nM 4.90
CHEMBL1794994 IC50 = 27100.0 nM 4.57
CHEMBL1794991 IC50 = 28000.0 nM 4.55
CHEMBL443742 IC50 = 48000.0 nM 4.32