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Assay Detail

CHEMBL2045979

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

Functional
Antiviral activity against HIV1 SF33 infected in human MT4 cells assessed as inhibition of viral p24 antigen production after 7 days by ELISA
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human immunodeficiency virus 1
Cell Type MT4
Confidence 1 — Organism
Curated By Autocuration

Target

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

Publication

Design, synthesis, and biological evaluation of 1-[(2-benzyloxyl/alkoxyl)methyl]-5-halo-6-aryluracils as potent HIV-1 non-nucleoside reverse transcriptase inhibitors with an improved drug resistance profile.
Wang X, Zhang J, Huang Y, Wang R, Zhang L, Qiao K, Li L, Liu C, Ouyang Y, Xu W, Zhang Z, Zhang L, Shao Y, Jiang S, Ma L, Liu J.
J Med Chem (2012) 55 : 2242 -2250
PubMed 22283377 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 13 7.20 8.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2041783 1 8.70
CHEMBL2041780 1 8.22
CHEMBL2041784 1 8.22
CHEMBL2041788 1 8.05
CHEMBL2041792 1 7.85
CHEMBL436546 1 7.66
CHEMBL2041782 1 7.35
CHEMBL57 NEVIRAPINE 4.0 1 7.17
CHEMBL2041791 1 6.46
CHEMBL2041781 1 6.27
CHEMBL2041789 1 6.21
CHEMBL2041787 1 5.76
CHEMBL2041785 1 5.68

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2041783 EC50 = 2.0 nM 8.70
CHEMBL2041780 EC50 = 6.0 nM 8.22
CHEMBL2041784 EC50 = 6.0 nM 8.22
CHEMBL2041788 EC50 = 9.0 nM 8.05
CHEMBL2041792 EC50 = 14.0 nM 7.85
CHEMBL436546 EC50 = 22.0 nM 7.66
CHEMBL2041782 EC50 = 45.0 nM 7.35
CHEMBL57 NEVIRAPINE EC50 = 68.0 nM 7.17
CHEMBL2041791 EC50 = 345.0 nM 6.46
CHEMBL2041781 EC50 = 537.0 nM 6.27
CHEMBL2041789 EC50 = 614.0 nM 6.21
CHEMBL2041787 EC50 = 1720.0 nM 5.76
CHEMBL2041785 EC50 = 2071.0 nM 5.68