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Assay Detail

CHEMBL711462

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Functional
Compound was evaluated for the inhibition of HIV-1 induced CPE (HTLV-III B strain ) replication in MT-4 cells
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type MT4
Confidence 1 — Organism
Curated By Intermediate

Target

MT4 (CHEMBL388)
Type CELL-LINE
Organism Homo sapiens

Publication

Thiadiazole derivatives: highly potent and specific HIV-1 reverse transcriptase inhibitors.
Hanasaki Y, Watanabe H, Katsuura K, Takayama H, Shirakawa S, Yamaguchi K, Sakai S, Ijichi K, Fujiwara M, Konno K.
J Med Chem (1995) 38 : 2038 -2040
PubMed 7540208 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 12 7.12 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL129 ZIDOVUDINE 4.0 1 8.40
CHEMBL37624 LOVIRIDE 2.0 1 8.22
CHEMBL60314 1 7.89
CHEMBL62905 1 7.41
CHEMBL62196 1 7.41
CHEMBL57 NEVIRAPINE 4.0 1 7.14
CHEMBL64381 1 7.00
CHEMBL62238 1 6.62
CHEMBL292028 1 6.50
CHEMBL294325 1 4.64
CHEMBL62690 1 -
CHEMBL292265 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL129 ZIDOVUDINE EC50 = 4.0 nM 8.40
CHEMBL37624 LOVIRIDE EC50 = 6.0 nM 8.22
CHEMBL60314 EC50 = 13.0 nM 7.89
CHEMBL62905 EC50 = 39.0 nM 7.41
CHEMBL62196 EC50 = 39.0 nM 7.41
CHEMBL57 NEVIRAPINE EC50 = 73.0 nM 7.14
CHEMBL64381 EC50 = 100.0 nM 7.00
CHEMBL62238 EC50 = 240.0 nM 6.62
CHEMBL292028 EC50 = 320.0 nM 6.50
CHEMBL294325 EC50 = 23000.0 nM 4.64
CHEMBL62690 EC50 > 560000.0 nM -
CHEMBL292265 EC50 > 535000.0 nM -