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Assay Detail

CHEMBL1659965

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

Functional
Antiviral activity against HIV1 expressing protease L10I/L24I/M46I/V82I/I84V mutant infected in human MT4 cells selected after 50 passages of GRL-216 by MTT 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 MT4
Confidence 1 — Organism
Curated By Autocuration

Target

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

Publication

Novel protease inhibitors (PIs) containing macrocyclic components and 3(R),3a(S),6a(R)-bis-tetrahydrofuranylurethane that are potent against multi-PI-resistant HIV-1 variants in vitro.
Tojo Y, Koh Y, Amano M, Aoki M, Das D, Kulkarni S, Anderson DD, Ghosh AK, Mitsuya H.
Antimicrob Agents Chemother (2010) 54 : 3460 -3470
PubMed 20439612 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 10 7.06 8.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1323 DARUNAVIR 4.0 1 8.05
CHEMBL1163 ATAZANAVIR 4.0 1 7.85
CHEMBL222559 TIPRANAVIR 4.0 1 7.54
CHEMBL571882 1 7.03
CHEMBL584 NELFINAVIR 4.0 1 6.89
CHEMBL729 LOPINAVIR 4.0 1 6.72
CHEMBL577560 1 6.72
CHEMBL1650599 1 6.62
CHEMBL116 AMPRENAVIR 4.0 1 6.58
CHEMBL571982 1 6.58

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1323 DARUNAVIR EC50 = 9.0 nM 8.05
CHEMBL1163 ATAZANAVIR EC50 = 14.0 nM 7.85
CHEMBL222559 TIPRANAVIR EC50 = 29.0 nM 7.54
CHEMBL571882 EC50 = 94.0 nM 7.03
CHEMBL584 NELFINAVIR EC50 = 130.0 nM 6.89
CHEMBL729 LOPINAVIR EC50 = 190.0 nM 6.72
CHEMBL577560 EC50 = 190.0 nM 6.72
CHEMBL1650599 EC50 = 240.0 nM 6.62
CHEMBL116 AMPRENAVIR EC50 = 260.0 nM 6.58
CHEMBL571982 EC50 = 260.0 nM 6.58