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Assay Detail

CHEMBL713512

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

Functional
Effective concentration required to achieve 50% protection of MT-4 cells against the cytopathic effect of HIV-1.
18
Total Activities
18
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human immunodeficiency virus 1
Cell Type MT4
Confidence 1 — Organism
Curated By Expert

Target

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

Publication

Synthesis and anti-HIV-1 activity of 4,5,6,7-tetrahydro-5-methylimidazo [4,5,1-jk][1,4]benzodiazepin-2(1H)-one (TIBO) derivatives. 3.
Breslin HJ, Kukla MJ, Ludovici DW, Mohrbacher R, Ho W, Miranda M, Rodgers JD, Hitchens TK, Leo G, Gauthier DA.
J Med Chem (1995) 38 : 771 -793
PubMed 7877143 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 18 6.23 7.64

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL304294 1 7.64
CHEMBL163664 1 7.58
CHEMBL352774 1 7.47
CHEMBL349271 1 7.22
CHEMBL65881 1 7.11
CHEMBL307994 1 6.80
CHEMBL354277 1 6.17
CHEMBL350982 1 5.94
CHEMBL68933 1 4.87
CHEMBL66043 1 4.84
CHEMBL348749 1 4.64
CHEMBL68175 1 4.49
CHEMBL351008 1 -
CHEMBL164708 1 -
CHEMBL167899 1 -
CHEMBL353000 1 -
CHEMBL349912 1 -
CHEMBL354789 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL304294 IC50 = 23.0 nM 7.64
CHEMBL163664 IC50 = 26.0 nM 7.58
CHEMBL352774 IC50 = 34.0 nM 7.47
CHEMBL349271 IC50 = 60.0 nM 7.22
CHEMBL65881 IC50 = 78.0 nM 7.11
CHEMBL307994 IC50 = 160.0 nM 6.80
CHEMBL354277 IC50 = 670.0 nM 6.17
CHEMBL350982 IC50 = 1150.0 nM 5.94
CHEMBL68933 IC50 = 13400.0 nM 4.87
CHEMBL66043 IC50 = 14300.0 nM 4.84
CHEMBL348749 IC50 = 23100.0 nM 4.64
CHEMBL68175 IC50 = 32100.0 nM 4.49
CHEMBL351008 IC50 > 10000.0 nM -
CHEMBL164708 IC50 > 250000.0 nM -
CHEMBL167899 IC50 > 250000.0 nM -
CHEMBL353000 IC50 > 250000.0 nM -
CHEMBL349912 IC50 > 250000.0 nM -
CHEMBL354789 IC50 > 250000.0 nM -