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Assay Detail

CHEMBL981940

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

Binding
Inhibition of HIV protease
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Human immunodeficiency virus
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

2-Pyridyl P1'-substituted symmetry-based human immunodeficiency virus protease inhibitors (A-792611 and A-790742) with potential for convenient dosing and reduced side effects.
Degoey DA, Grampovnik DJ, Flentge CA, Flosi WJ, Chen HJ, Yeung CM, Randolph JT, Klein LL, Dekhtyar T, Colletti L, Marsh KC, Stoll V, Mamo M, Morfitt DC, Nguyen B, Schmidt JM, Swanson SJ, Mo H, Kati WM, Molla A, Kempf DJ.
J Med Chem (2009) 52 : 2571 -2586
PubMed 19323562 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 2 10.84 10.85

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL470508 1 10.85
CHEMBL507731 1 10.82

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL470508 Ki = 0.014 nM 10.85
CHEMBL507731 Ki = 0.015 nM 10.82