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Assay Detail

CHEMBL689316

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

Binding
In vitro inhibition of HIV-1 protease.
18
Total Activities
18
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Expert

Target

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

Publication

Synthesis and pharmacokinetics of potent carbamate HIV-1 protease inhibitors containing novel high affinity hydroxyethylamine isosteres
Hornback WJ, Munroe JE, Shepherd TA, Hatch SD, Muesing MA, Wiskerchen M, Colacino JM, Baxter AJ, Su KS, Campanale KM
Bioorg Med Chem Lett (1995) 5 : 2891 -2896
· DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 18 8.82 9.59

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL95546 1 9.59
CHEMBL99336 1 9.55
CHEMBL321949 1 9.40
CHEMBL97585 1 9.38
CHEMBL99214 1 9.12
CHEMBL316717 1 9.02
CHEMBL114 SAQUINAVIR 4.0 1 9.00
CHEMBL316718 1 8.89
CHEMBL318129 1 8.85
CHEMBL100048 1 8.77
CHEMBL316608 1 8.70
CHEMBL100271 1 8.59
CHEMBL321778 1 8.59
CHEMBL318894 1 8.52
CHEMBL18067 1 8.37
CHEMBL320602 1 8.28
CHEMBL261340 1 8.09
CHEMBL277801 1 8.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL95546 IC50 = 0.26 nM 9.59
CHEMBL99336 IC50 = 0.28 nM 9.55
CHEMBL321949 IC50 = 0.4 nM 9.40
CHEMBL97585 IC50 = 0.42 nM 9.38
CHEMBL99214 IC50 = 0.75 nM 9.12
CHEMBL316717 IC50 = 0.95 nM 9.02
CHEMBL114 SAQUINAVIR IC50 = 1.0 nM 9.00
CHEMBL316718 IC50 = 1.3 nM 8.89
CHEMBL318129 IC50 = 1.4 nM 8.85
CHEMBL100048 IC50 = 1.7 nM 8.77
CHEMBL316608 IC50 = 2.0 nM 8.70
CHEMBL100271 IC50 = 2.6 nM 8.59
CHEMBL321778 IC50 = 2.6 nM 8.59
CHEMBL318894 IC50 = 3.0 nM 8.52
CHEMBL18067 IC50 = 4.3 nM 8.37
CHEMBL320602 IC50 = 5.2 nM 8.28
CHEMBL261340 IC50 = 8.1 nM 8.09
CHEMBL277801 IC50 = 10.0 nM 8.00