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Assay Detail

CHEMBL3626326

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

Functional
Antiviral activity against HIV1 RF infected in CEM-SS cells assessed as inhibition of virus-induced cytopathic effect by MTS assay
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human immunodeficiency virus 1
Cell Type CEM-SS
Confidence 1 — Organism
Curated By Autocuration

Target

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

Publication

Novel anti-HIV-1 NNRTIs based on a pyrazolo[4,3-d]isoxazole backbone scaffold: design, synthesis and insights into the molecular basis of action
Gomha SM, Badrey MG, Abdalla MM, Arafa RK
Medchemcomm (2014) 5 : 1685 -1692
· DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 13 9.35 9.60

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3621609 1 9.60
CHEMBL3621605 1 9.60
CHEMBL3621607 1 9.47
CHEMBL3621608 1 9.46
CHEMBL3621606 1 9.44
CHEMBL3621613 1 9.37
CHEMBL3621612 1 9.36
CHEMBL3621611 1 9.34
CHEMBL3621610 1 9.33
CHEMBL3621604 1 9.27
CHEMBL3621614 1 9.17
CHEMBL3621603 1 9.11
CHEMBL223228 EFAVIRENZ 4.0 1 9.04

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3621609 EC50 = 0.25 nM 9.60
CHEMBL3621605 EC50 = 0.25 nM 9.60
CHEMBL3621607 EC50 = 0.34 nM 9.47
CHEMBL3621608 EC50 = 0.35 nM 9.46
CHEMBL3621606 EC50 = 0.36 nM 9.44
CHEMBL3621613 EC50 = 0.43 nM 9.37
CHEMBL3621612 EC50 = 0.44 nM 9.36
CHEMBL3621611 EC50 = 0.46 nM 9.34
CHEMBL3621610 EC50 = 0.47 nM 9.33
CHEMBL3621604 EC50 = 0.54 nM 9.27
CHEMBL3621614 EC50 = 0.67 nM 9.17
CHEMBL3621603 EC50 = 0.78 nM 9.11
CHEMBL223228 EFAVIRENZ EC50 = 0.92 nM 9.04