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Assay Detail

CHEMBL3606515

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

Functional
Antiviral activity against HIV1 LAI infected in human MT2 cells
13
Total Activities
13
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

Design of HIV-1 Protease Inhibitors with Amino-bis-tetrahydrofuran Derivatives as P2-Ligands to Enhance Backbone-Binding Interactions: Synthesis, Biological Evaluation, and Protein-Ligand X-ray Studies.
Ghosh AK, Martyr CD, Osswald HL, Sheri VR, Kassekert LA, Chen S, Agniswamy J, Wang YF, Hayashi H, Aoki M, Weber IT, Mitsuya H.
J Med Chem (2015) 58 : 6994 -7006
PubMed 26306007 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 7.99 9.47

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3605635 1 9.47
CHEMBL1323 DARUNAVIR 4.0 1 8.52
CHEMBL3605641 1 8.43
CHEMBL3605640 1 8.36
CHEMBL3605638 1 8.36
CHEMBL3605636 1 8.36
CHEMBL3605637 1 8.14
CHEMBL3605646 1 7.66
CHEMBL3605643 1 7.46
CHEMBL3605642 1 7.43
CHEMBL3605639 1 7.32
CHEMBL3605644 1 6.32
CHEMBL3605645 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3605635 IC50 = 0.34 nM 9.47
CHEMBL1323 DARUNAVIR IC50 = 3.0 nM 8.52
CHEMBL3605641 IC50 = 3.7 nM 8.43
CHEMBL3605640 IC50 = 4.4 nM 8.36
CHEMBL3605638 IC50 = 4.4 nM 8.36
CHEMBL3605636 IC50 = 4.4 nM 8.36
CHEMBL3605637 IC50 = 7.2 nM 8.14
CHEMBL3605646 IC50 = 22.0 nM 7.66
CHEMBL3605643 IC50 = 35.0 nM 7.46
CHEMBL3605642 IC50 = 37.0 nM 7.43
CHEMBL3605639 IC50 = 48.0 nM 7.32
CHEMBL3605644 IC50 = 480.0 nM 6.32
CHEMBL3605645 IC50 - -