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

CHEMBL873416

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

Binding
Inhibition of HIV protease at pH 6.4, 37 degree C
13
Total Activities
13
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

Hydroxyethylamine analogues of the p17/p24 substrate cleavage site are tight-binding inhibitors of HIV protease.
Rich DH, Green J, Toth MV, Marshall GR, Kent SB.
J Med Chem (1990) 33 : 1285 -1288
PubMed 2184237 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 13 6.72 9.22

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3143731 1 9.22
CHEMBL109500 1 9.18
CHEMBL2371768 1 7.75
CHEMBL2311136 1 7.68
CHEMBL3143736 1 7.68
CHEMBL3143738 1 7.16
CHEMBL3143739 1 6.38
CHEMBL2371777 1 6.11
CHEMBL52494 1 5.97
CHEMBL417012 1 5.58
CHEMBL3143737 1 5.34
CHEMBL2371769 1 4.89
CHEMBL49026 1 4.41

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3143731 Ki = 0.6 nM 9.22
CHEMBL109500 Ki = 0.66 nM 9.18
CHEMBL2371768 Ki = 18.0 nM 7.75
CHEMBL2311136 Ki = 21.0 nM 7.68
CHEMBL3143736 Ki = 21.0 nM 7.68
CHEMBL3143738 Ki = 70.0 nM 7.16
CHEMBL3143739 Ki = 420.0 nM 6.38
CHEMBL2371777 Ki = 780.0 nM 6.11
CHEMBL52494 Ki = 1060.0 nM 5.97
CHEMBL417012 Ki = 2640.0 nM 5.58
CHEMBL3143737 Ki = 4520.0 nM 5.34
CHEMBL2371769 Ki = 13000.0 nM 4.89
CHEMBL49026 Ki = 39000.0 nM 4.41