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Assay Detail

CHEMBL1024276

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Binding
Inhibition of HIV1 reverse transcriptase after 1 hr by ELISA
16
Total Activities
16
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Human immunodeficiency virus 1
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Human immunodeficiency virus type 1 reverse transcriptase (CHEMBL247)
Type SINGLE PROTEIN
Organism Human immunodeficiency virus 1

Publication

Design, microwave-assisted synthesis and HIV-RT inhibitory activity of 2-(2,6-dihalophenyl)-3-(4,6-dimethyl-5-(un)substituted-pyrimidin-2-yl)thiazolidin-4-ones.
Chen H, Bai J, Jiao L, Guo Z, Yin Q, Li X.
Bioorg Med Chem (2009) 17 : 3980 -3986
PubMed 19411176 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 16 5.69 6.64

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL487954 1 6.64
CHEMBL522748 1 6.58
CHEMBL390110 1 6.42
CHEMBL496888 1 6.11
CHEMBL390956 1 6.08
CHEMBL518929 1 6.07
CHEMBL463594 1 5.99
CHEMBL518536 1 5.91
CHEMBL520199 1 5.82
CHEMBL487140 1 5.70
CHEMBL486939 1 5.54
CHEMBL497056 1 5.37
CHEMBL517008 1 5.01
CHEMBL486937 1 4.80
CHEMBL486938 1 4.79
CHEMBL463593 1 4.13

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL487954 IC50 = 230.0 nM 6.64
CHEMBL522748 IC50 = 260.0 nM 6.58
CHEMBL390110 IC50 = 380.0 nM 6.42
CHEMBL496888 IC50 = 770.0 nM 6.11
CHEMBL390956 IC50 = 830.0 nM 6.08
CHEMBL518929 IC50 = 850.0 nM 6.07
CHEMBL463594 IC50 = 1020.0 nM 5.99
CHEMBL518536 IC50 = 1220.0 nM 5.91
CHEMBL520199 IC50 = 1520.0 nM 5.82
CHEMBL487140 IC50 = 2010.0 nM 5.70
CHEMBL486939 IC50 = 2920.0 nM 5.54
CHEMBL497056 IC50 = 4290.0 nM 5.37
CHEMBL517008 IC50 = 9820.0 nM 5.01
CHEMBL486937 IC50 = 15960.0 nM 4.80
CHEMBL486938 IC50 = 16150.0 nM 4.79
CHEMBL463593 IC50 = 74390.0 nM 4.13