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Assay Detail

CHEMBL769053

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Binding
Inhibition of HIV-1 protease
14
Total Activities
14
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

3-Tetrahydrofuran and pyran urethanes as high-affinity P2-ligands for HIV-1 protease inhibitors.
Ghosh AK, Thompson WJ, McKee SP, Duong TT, Lyle TA, Chen JC, Darke PL, Zugay JA, Emini EA, Schleif WA.
J Med Chem (1993) 36 : 292 -294
PubMed 8423600 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 7.81 10.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL319092 1 10.52
CHEMBL296115 1 9.52
CHEMBL101560 1 9.48
CHEMBL98885 1 8.91
CHEMBL99600 1 7.31
CHEMBL18389 1 6.80
CHEMBL321571 1 6.51
CHEMBL330615 1 6.50
CHEMBL327277 1 6.41
CHEMBL99213 1 6.16
CHEMBL319408 1 -
CHEMBL82338 1 -
CHEMBL319792 1 -
CHEMBL430469 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL319092 IC50 = 0.03 nM 10.52
CHEMBL296115 IC50 = 0.3 nM 9.52
CHEMBL101560 IC50 = 0.33 nM 9.48
CHEMBL98885 IC50 = 1.22 nM 8.91
CHEMBL99600 IC50 = 48.9 nM 7.31
CHEMBL18389 IC50 = 160.0 nM 6.80
CHEMBL321571 IC50 = 308.0 nM 6.51
CHEMBL330615 IC50 = 314.0 nM 6.50
CHEMBL327277 IC50 = 392.0 nM 6.41
CHEMBL99213 IC50 = 694.0 nM 6.16
CHEMBL319408 IC50 < 0.03 nM -
CHEMBL82338 IC50 > 3000.0 nM -
CHEMBL319792 IC50 < 0.03 nM -
CHEMBL430469 IC50 < 0.03 nM -