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Assay Detail

CHEMBL769406

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

Binding
Inhibition of HIV-1 protease
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

Application of the three-dimensional structures of protein target molecules in structure-based drug design.
Greer J, Erickson JW, Baldwin JJ, Varney MD.
J Med Chem (1994) 37 : 1035 -1054
PubMed 8164249 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 7.89 9.66

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL48565 1 9.66
CHEMBL289846 1 9.66
CHEMBL300968 1 9.42
CHEMBL307193 1 8.52
CHEMBL3143979 1 8.00
CHEMBL2311105 1 7.92
CHEMBL275554 1 7.92
CHEMBL9726 1 7.40
CHEMBL9618 1 6.55
CHEMBL3351009 1 6.23
CHEMBL9409 1 5.52
CHEMBL9417 1 -
CHEMBL9735 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL48565 IC50 = 0.22 nM 9.66
CHEMBL289846 IC50 = 0.22 nM 9.66
CHEMBL300968 IC50 = 0.38 nM 9.42
CHEMBL307193 IC50 = 3.0 nM 8.52
CHEMBL3143979 IC50 = 10.0 nM 8.00
CHEMBL2311105 IC50 = 12.0 nM 7.92
CHEMBL275554 IC50 = 12.0 nM 7.92
CHEMBL9726 IC50 = 40.0 nM 7.40
CHEMBL9618 IC50 = 280.0 nM 6.55
CHEMBL3351009 IC50 = 590.0 nM 6.23
CHEMBL9409 IC50 = 3000.0 nM 5.52
CHEMBL9417 IC50 > 10000.0 nM -
CHEMBL9735 IC50 > 10000.0 nM -