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Assay Detail

CHEMBL1827430

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

Functional
Antiviral activity against HIV1 3B infected in human MT-2 cells assessed as reduction in virus-induced cytopathic effect after 5 days by luminescence assay
10
Total Activities
10
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human immunodeficiency virus 1
Cell Type MT2
Confidence 1 — Organism
Curated By Autocuration

Target

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

Publication

A novel and efficient one-pot synthesis of symmetrical diamide (bis-amidate) prodrugs of acyclic nucleoside phosphonates and evaluation of their biological activities.
Jansa P, Baszczyňski O, Dračínský M, Votruba I, Zídek Z, Bahador G, Stepan G, Cihlar T, Mackman R, Holý A, Janeba Z.
Eur J Med Chem (2011) 46 : 3748 -3754
PubMed 21664011 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 10 5.68 6.54

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1823515 1 6.54
CHEMBL1823512 1 6.27
CHEMBL482690 1 6.03
CHEMBL1823511 1 6.03
CHEMBL1823516 1 5.95
CHEMBL1823513 1 5.26
CHEMBL2021513 1 5.15
CHEMBL1823514 1 4.97
CHEMBL1766195 1 4.88
CHEMBL1823510 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1823515 EC50 = 290.0 nM 6.54
CHEMBL1823512 EC50 = 540.0 nM 6.27
CHEMBL482690 EC50 = 940.0 nM 6.03
CHEMBL1823511 EC50 = 930.0 nM 6.03
CHEMBL1823516 EC50 = 1130.0 nM 5.95
CHEMBL1823513 EC50 = 5510.0 nM 5.26
CHEMBL2021513 EC50 = 7040.0 nM 5.15
CHEMBL1823514 EC50 = 10730.0 nM 4.97
CHEMBL1766195 EC50 = 13250.0 nM 4.88
CHEMBL1823510 EC50 > 85300.0 nM -