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Assay Detail

CHEMBL691402

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Binding
Binding affinity for HIV -1 Protease
11
Total Activities
11
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

Unsymmetrical cyclic ureas as HIV-1 protease inhibitors: novel biaryl indazoles as P2/P2' substituents.
Patel M, Rodgers JD, McHugh RJ, Johnson BL, Cordova BC, Klabe RM, Bacheler LT, Erickson-Viitanen S, Ko SS.
Bioorg Med Chem Lett (1999) 9 : 3217 -3220
PubMed 10576691 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 11 9.76 10.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL82422 1 10.52
CHEMBL107817 1 10.24
CHEMBL109377 1 10.05
CHEMBL323043 1 9.89
CHEMBL108498 1 9.74
CHEMBL321669 1 9.62
CHEMBL323449 1 9.60
CHEMBL108932 1 9.59
CHEMBL322991 1 9.52
CHEMBL163 RITONAVIR 4.0 1 9.43
CHEMBL107648 1 9.21

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL82422 Ki = 0.03 nM 10.52
CHEMBL107817 Ki = 0.058 nM 10.24
CHEMBL109377 Ki = 0.09 nM 10.05
CHEMBL323043 Ki = 0.13 nM 9.89
CHEMBL108498 Ki = 0.18 nM 9.74
CHEMBL321669 Ki = 0.24 nM 9.62
CHEMBL323449 Ki = 0.25 nM 9.60
CHEMBL108932 Ki = 0.26 nM 9.59
CHEMBL322991 Ki = 0.3 nM 9.52
CHEMBL163 RITONAVIR Ki = 0.37 nM 9.43
CHEMBL107648 Ki = 0.61 nM 9.21