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Assay Detail

CHEMBL799136

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

Binding
The compound was evaluated for the inhibition of HIV-1 reverse transcriptase
9
Total Activities
9
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 reverse transcriptase (CHEMBL247)
Type SINGLE PROTEIN
Organism Human immunodeficiency virus 1

Publication

Novel 2,2-dioxide-4,4-disubstituted-1,3-H-2,1,3-benzothiadiazines as non-nucleoside reverse transcriptase inhibitors.
Corbett JW, Gearhart LA, Ko SS, Rodgers JD, Cordova BC, Klabe RM, Erickson-Viitanen SK.
Bioorg Med Chem Lett (2000) 10 : 193 -195
PubMed 10673109 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 9 6.17 7.75

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL57995 1 7.75
CHEMBL283619 1 7.51
CHEMBL223228 EFAVIRENZ 4.0 1 7.33
CHEMBL58596 1 6.86
CHEMBL929 DELAVIRDINE MESYLATE 4.0 1 6.38
CHEMBL58865 1 5.33
CHEMBL57 NEVIRAPINE 4.0 1 5.31
CHEMBL299935 1 4.61
CHEMBL58552 1 4.45

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL57995 IC50 = 18.0 nM 7.75
CHEMBL283619 IC50 = 31.0 nM 7.51
CHEMBL223228 EFAVIRENZ IC50 = 47.0 nM 7.33
CHEMBL58596 IC50 = 137.0 nM 6.86
CHEMBL929 DELAVIRDINE MESYLATE IC50 = 422.0 nM 6.38
CHEMBL58865 IC50 = 4627.0 nM 5.33
CHEMBL57 NEVIRAPINE IC50 = 4848.0 nM 5.31
CHEMBL299935 IC50 = 24667.0 nM 4.61
CHEMBL58552 IC50 = 35870.0 nM 4.45