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Assay Detail

CHEMBL695386

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

Functional
The compound was tested for inhibition against HIV-III B from C8 166 cell lines
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism human immunodeficiency virus type 3b
Cell Type C8116
Confidence 1 — Organism
Curated By Intermediate

Target

Human immunodeficiency virus 3 (CHEMBL612359)
Type ORGANISM
Organism Human immunodeficiency virus 3

Publication

Pyrrolobenzoxazepinone derivatives as non-nucleoside HIV-1 RT inhibitors: further structure-activity relationship studies and identification of more potent broad-spectrum HIV-1 RT inhibitors with antiviral activity.
Campiani G, Morelli E, Fabbrini M, Nacci V, Greco G, Novellino E, Ramunno A, Maga G, Spadari S, Caliendo G, Bergamini A, Faggioli E, Uccella I, Bolacchi F, Marini S, Coletta M, Nacca A, Caccia S.
J Med Chem (1999) 42 : 4462 -4470
PubMed 10543890 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 2 9.70 10.48

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL140665 1 10.48
CHEMBL138969 1 8.92

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL140665 EC50 = 0.033 nM 10.48
CHEMBL138969 EC50 = 1.2 nM 8.92