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

CHEMBL801175

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

Binding
Inhibition of HIV-1 Mutant HIV-1 RT enzymes containing the single amino acid substitution V179D
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Human immunodeficiency virus type 1 protease (CHEMBL243)
Type SINGLE PROTEIN
Organism Human immunodeficiency virus 1

Publication

Quinoxalinylethylpyridylthioureas (QXPTs) as potent non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors. Further SAR studies and identification of a novel orally bioavailable hydrazine-based antiviral agent.
Campiani G, Aiello F, Fabbrini M, Morelli E, Ramunno A, Armaroli S, Nacci V, Garofalo A, Greco G, Novellino E, Maga G, Spadari S, Bergamini A, Ventura L, Bongiovanni B, Capozzi M, Bolacchi F, Marini S, Coletta M, Guiso G, Caccia S.
J Med Chem (2001) 44 : 305 -315
PubMed 11462972 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 2 6.63 7.16

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL105976 1 7.16
CHEMBL317406 1 6.10

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL105976 Ki = 70.0 nM 7.16
CHEMBL317406 Ki = 800.0 nM 6.10