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Assay Detail

CHEMBL757713

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

Functional
Inhibit the replication of the HIV-1 strain HTLV111B in human peripheral blood mononuclear cell
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

ADMET (CHEMBL612558)
Type ADMET

Publication

Stereochemistry of halopyridyl and thiazolyl thiourea compounds is a major determinant of their potency as nonnucleoside inhibitors of HIV-1 reverse transcriptase.
Venkatachalam TK, Sudbeck EA, Mao C, Uckun FM.
Bioorg Med Chem Lett (2000) 10 : 2071 -2074
PubMed 10999473 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 8.04 9.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL417737 1 9.00
CHEMBL39999 TROVIRDINE 2.0 1 8.15
CHEMBL593 DELAVIRDINE 4.0 1 8.05
CHEMBL292339 1 8.00
CHEMBL432526 1 8.00
CHEMBL302866 1 7.60
CHEMBL57 NEVIRAPINE 4.0 1 7.47
CHEMBL416876 1 -
CHEMBL291886 1 -
CHEMBL305150 1 -
CHEMBL434213 1 -
CHEMBL63222 1 -
CHEMBL65242 1 -
CHEMBL295585 1 -
CHEMBL304914 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL417737 IC50 = 1.0 nM 9.00
CHEMBL39999 TROVIRDINE IC50 = 7.0 nM 8.15
CHEMBL593 DELAVIRDINE IC50 = 9.0 nM 8.05
CHEMBL292339 IC50 = 10.0 nM 8.00
CHEMBL432526 IC50 = 10.0 nM 8.00
CHEMBL302866 IC50 = 25.0 nM 7.60
CHEMBL57 NEVIRAPINE IC50 = 34.0 nM 7.47
CHEMBL416876 IC50 > 1000.0 nM -
CHEMBL291886 IC50 - nM -
CHEMBL305150 IC50 > 1000.0 nM -
CHEMBL434213 IC50 > 1000.0 nM -
CHEMBL63222 IC50 > 1000.0 nM -
CHEMBL65242 IC50 > 1000.0 nM -
CHEMBL295585 IC50 < 1.0 nM -
CHEMBL304914 IC50 > 1000.0 nM -