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Assay Detail

CHEMBL764269

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Binding
Inhibition of HIV-1 protease
12
Total Activities
12
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

An orally bioavailable pyrrolinone inhibitor of HIV-1 protease: computational analysis and X-ray crystal structure of the enzyme complex.
Smith AB, Hirschmann R, Pasternak A, Yao W, Sprengeler PA, Holloway MK, Kuo LC, Chen Z, Darke PL, Schleif WA.
J Med Chem (1997) 40 : 2440 -2444
PubMed 9258349 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 8.61 10.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2062160 1 10.52
CHEMBL298316 1 9.80
CHEMBL296115 1 9.52
CHEMBL5483011 INDINAVIR 3.0 1 9.44
CHEMBL289195 1 9.22
CHEMBL293808 1 8.70
CHEMBL430445 1 8.22
CHEMBL108960 1 8.15
CHEMBL70140 1 8.00
CHEMBL291974 1 7.92
CHEMBL2062145 1 7.07
CHEMBL606565 1 6.73

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2062160 IC50 = 0.03 nM 10.52
CHEMBL298316 IC50 = 0.16 nM 9.80
CHEMBL296115 IC50 = 0.3 nM 9.52
CHEMBL5483011 INDINAVIR IC50 = 0.36 nM 9.44
CHEMBL289195 IC50 = 0.6 nM 9.22
CHEMBL293808 IC50 = 2.0 nM 8.70
CHEMBL430445 IC50 = 6.0 nM 8.22
CHEMBL108960 IC50 = 7.0 nM 8.15
CHEMBL70140 IC50 = 10.0 nM 8.00
CHEMBL291974 IC50 = 11.9 nM 7.92
CHEMBL2062145 IC50 = 86.0 nM 7.07
CHEMBL606565 IC50 = 186.0 nM 6.73