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Assay Detail

CHEMBL1805149

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Binding
Inhibition of HIV1 reverse transcriptase L100I mutant
8
Total Activities
8
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Human immunodeficiency virus 1
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Human immunodeficiency virus type 1 reverse transcriptase (CHEMBL247)
Type SINGLE PROTEIN
Organism Human immunodeficiency virus 1

Publication

Enantioselective binding of second generation pyrrolobenzoxazepinones to the catalytic ternary complex of HIV-1 RT wild-type and L100I and K103N drug resistant mutants.
Butini S, Gemma S, Brindisi M, Borrelli G, Fiorini I, Samuele A, Karytinos A, Facchini M, Lossani A, Zanoli S, Campiani G, Novellino E, Focher F, Maga G.
Bioorg Med Chem Lett (2011) 21 : 3935 -3938
PubMed 21636271 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 8 6.09 6.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL223769 1 6.70
CHEMBL225004 1 6.60
CHEMBL1688496 1 6.00
CHEMBL57 NEVIRAPINE 4.0 1 5.05
CHEMBL1688513 1 -
CHEMBL1688575 1 -
CHEMBL1688505 1 -
CHEMBL1688504 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL223769 IC50 = 200.0 nM 6.70
CHEMBL225004 IC50 = 250.0 nM 6.60
CHEMBL1688496 IC50 = 990.0 nM 6.00
CHEMBL57 NEVIRAPINE IC50 = 9000.0 nM 5.05
CHEMBL1688513 IC50 > 400000.0 nM -
CHEMBL1688575 IC50 > 400000.0 nM -
CHEMBL1688505 IC50 > 400000.0 nM -
CHEMBL1688504 IC50 > 400000.0 nM -