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

CHEMBL889372

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

Functional
Antiviral activity against ritonavir and nelfinavir-resistant HIV1 NL432
8
Total Activities
8
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human immunodeficiency virus 1
Confidence 1 — Organism
Curated By Intermediate

Target

Human immunodeficiency virus 1 (CHEMBL378)
Type ORGANISM
Organism Human immunodeficiency virus 1

Publication

Synthesis and antiviral property of allophenylnorstatine-based HIV protease inhibitors incorporating D-cysteine derivatives as P2/P3 moieties.
Ami E, Nakahara K, Sato A, Nguyen JT, Hidaka K, Hamada Y, Nakatani S, Kimura T, Hayashi Y, Kiso Y.
Bioorg Med Chem Lett (2007) 17 : 4213 -4217
PubMed 17537628 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 8 7.47 7.89

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL396465 1 7.89
CHEMBL230484 1 7.85
CHEMBL414775 1 7.64
CHEMBL396462 1 7.64
CHEMBL396334 1 7.50
CHEMBL414959 1 7.28
CHEMBL584 NELFINAVIR 4.0 1 7.17
CHEMBL163 RITONAVIR 4.0 1 6.79

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL396465 EC50 = 13.0 nM 7.89
CHEMBL230484 EC50 = 14.0 nM 7.85
CHEMBL414775 EC50 = 23.0 nM 7.64
CHEMBL396462 EC50 = 23.0 nM 7.64
CHEMBL396334 EC50 = 32.0 nM 7.50
CHEMBL414959 EC50 = 52.0 nM 7.28
CHEMBL584 NELFINAVIR EC50 = 67.0 nM 7.17
CHEMBL163 RITONAVIR EC50 = 162.0 nM 6.79