Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL712255

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

Functional
Compound was evaluated for its antiviral inhibition in MT-4 cell culture
12
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type MT4
Confidence 1 — Organism
Curated By Intermediate

Target

MT4 (CHEMBL388)
Type CELL-LINE
Organism Homo sapiens

Publication

Novel inhibitors of HIV protease: design, synthesis and biological evaluation of picomolar inhibitors containing cyclic P1/P2 scaffolds.
Spaltenstein A, Almond MR, Bock WJ, Cleary DG, Furfine ES, Hazen RJ, Kazmierski WM, Salituro FG, Tung RD, Wright LL.
Bioorg Med Chem Lett (2000) 10 : 1159 -1162
PubMed 10866371 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 6.80 7.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL114 SAQUINAVIR 4.0 1 7.70
CHEMBL5483011 INDINAVIR 3.0 1 7.40
CHEMBL584 NELFINAVIR 4.0 1 7.30
CHEMBL116 AMPRENAVIR 4.0 1 7.00
CHEMBL163 RITONAVIR 4.0 1 6.68
CHEMBL279869 1 6.52
CHEMBL263072 2 6.52
CHEMBL262204 1 6.52
CHEMBL278928 1 5.82
CHEMBL279397 1 -
CHEMBL16167 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL114 SAQUINAVIR IC50 = 20.0 nM 7.70
CHEMBL5483011 INDINAVIR IC50 = 40.0 nM 7.40
CHEMBL584 NELFINAVIR IC50 = 50.0 nM 7.30
CHEMBL116 AMPRENAVIR IC50 = 100.0 nM 7.00
CHEMBL163 RITONAVIR IC50 = 210.0 nM 6.68
CHEMBL279869 IC50 = 300.0 nM 6.52
CHEMBL263072 IC50 = 300.0 nM 6.52
CHEMBL263072 IC50 = 300.0 nM 6.52
CHEMBL262204 IC50 = 300.0 nM 6.52
CHEMBL278928 IC50 = 1500.0 nM 5.82
CHEMBL279397 IC50 > 50000.0 nM -
CHEMBL16167 IC50 > 50000.0 nM -