Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL830309

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

Binding
Inhibitory activity against human immunodeficiency virus 1 protease
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Human immunodeficiency virus 1
Confidence 9 — Direct single protein target
Curated By Expert

Target

Human immunodeficiency virus type 1 protease (CHEMBL243)
Type SINGLE PROTEIN
Organism Human immunodeficiency virus 1

Publication

Structure-based design: synthesis and biological evaluation of a series of novel cycloamide-derived HIV-1 protease inhibitors.
Ghosh AK, Swanson LM, Cho H, Leshchenko S, Hussain KA, Kay S, Walters DE, Koh Y, Mitsuya H.
J Med Chem (2005) 48 : 3576 -3585
PubMed 15887965 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 11 8.53 10.82

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1323 DARUNAVIR 4.0 1 10.82
CHEMBL195791 1 9.15
CHEMBL191880 1 9.00
CHEMBL426812 1 8.70
CHEMBL195666 1 8.70
CHEMBL364086 1 8.70
CHEMBL192190 1 8.52
CHEMBL372224 1 8.05
CHEMBL194770 1 7.92
CHEMBL191830 1 7.70
CHEMBL372010 1 6.57

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1323 DARUNAVIR Ki = 0.015 nM 10.82
CHEMBL195791 Ki = 0.7 nM 9.15
CHEMBL191880 Ki = 1.0 nM 9.00
CHEMBL426812 Ki = 2.0 nM 8.70
CHEMBL195666 Ki = 2.0 nM 8.70
CHEMBL364086 Ki = 2.0 nM 8.70
CHEMBL192190 Ki = 3.0 nM 8.52
CHEMBL372224 Ki = 9.0 nM 8.05
CHEMBL194770 Ki = 12.0 nM 7.92
CHEMBL191830 Ki = 20.0 nM 7.70
CHEMBL372010 Ki = 270.0 nM 6.57