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Assay Detail

CHEMBL769255

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

Binding
Inhibitory activity against recombinant HIV-1 Protease
10
Total Activities
10
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

Structure-based, C2 symmetric inhibitors of HIV protease.
Kempf DJ, Norbeck DW, Codacovi L, Wang XC, Kohlbrenner WE, Wideburg NE, Paul DA, Knigge MF, Vasavanonda S, Craig-Kennard A.
J Med Chem (1990) 33 : 2687 -2689
PubMed 2213822 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 8.04 9.66

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL83462 1 9.66
CHEMBL430891 1 8.52
CHEMBL90174 1 8.31
CHEMBL88255 1 8.00
CHEMBL275554 1 7.92
CHEMBL2311105 1 7.92
CHEMBL9618 1 7.40
CHEMBL9726 1 6.55
CHEMBL9735 1 -
CHEMBL88254 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL83462 IC50 = 0.22 nM 9.66
CHEMBL430891 IC50 = 3.0 nM 8.52
CHEMBL90174 IC50 = 4.9 nM 8.31
CHEMBL88255 IC50 = 10.0 nM 8.00
CHEMBL275554 IC50 = 12.0 nM 7.92
CHEMBL2311105 IC50 = 12.0 nM 7.92
CHEMBL9618 IC50 = 40.0 nM 7.40
CHEMBL9726 IC50 = 280.0 nM 6.55
CHEMBL9735 IC50 > 10000.0 nM -
CHEMBL88254 IC50 > 100.0 nM -