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Assay Detail

CHEMBL1820935

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

Functional
Antiviral activity against wild type HIV1 LAI-3B infected in human C8166 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human immunodeficiency virus 1
Cell Type C8166
Confidence 1 — Organism
Curated By Autocuration

Target

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

Publication

Synthesis and biological evaluation of HQCAs with aryl or benzyl substituents on N-1 position as potential HIV-1 integrase inhibitors.
He QQ, Zhang X, Wu HQ, Gu SX, Ma XD, Yang LM, Zheng YT, Chen FE.
Bioorg Med Chem (2011) 19 : 5553 -5558
PubMed 21862337 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 15 5.58 9.68

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL204656 ELVITEGRAVIR 4.0 1 9.68
CHEMBL1818956 1 6.89
CHEMBL1818949 1 5.50
CHEMBL1818952 1 5.49
CHEMBL1818945 1 5.45
CHEMBL1818953 1 5.31
CHEMBL1818950 1 5.26
CHEMBL1818955 1 5.24
CHEMBL1818951 1 5.19
CHEMBL1818947 1 5.15
CHEMBL1818954 1 5.03
CHEMBL1818944 1 4.69
CHEMBL1818948 1 4.68
CHEMBL1818946 1 4.60
CHEMBL1818943 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL204656 ELVITEGRAVIR EC50 = 0.21 nM 9.68
CHEMBL1818956 EC50 = 130.0 nM 6.89
CHEMBL1818949 EC50 = 3170.0 nM 5.50
CHEMBL1818952 EC50 = 3270.0 nM 5.49
CHEMBL1818945 EC50 = 3580.0 nM 5.45
CHEMBL1818953 EC50 = 4930.0 nM 5.31
CHEMBL1818950 EC50 = 5550.0 nM 5.26
CHEMBL1818955 EC50 = 5740.0 nM 5.24
CHEMBL1818951 EC50 = 6460.0 nM 5.19
CHEMBL1818947 EC50 = 7120.0 nM 5.15
CHEMBL1818954 EC50 = 9340.0 nM 5.03
CHEMBL1818944 EC50 = 20480.0 nM 4.69
CHEMBL1818948 EC50 = 20870.0 nM 4.68
CHEMBL1818946 EC50 = 24930.0 nM 4.60
CHEMBL1818943 EC50 = 307570.0 nM -