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Assay Detail

CHEMBL655349

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Functional
Effective concentration required to achieve 50% inhibition of HIV-1 181C (nevirapine-resistant HIV-1) multiplication in CEM-SS cells.
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type CEM-SS
Confidence 1 — Organism
Curated By Intermediate

Target

CEM-SS (CHEMBL614548)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis and evaluation of "AZT-HEPT", "AZT-pyridinone", and "ddC-HEPT" conjugates as inhibitors of HIV reverse transcriptase.
Pontikis R, Dollé V, Guillaumel J, Dechaux E, Note R, Nguyen CH, Legraverend M, Bisagni E, Aubertin AM, Grierson DS, Monneret C.
J Med Chem (2000) 43 : 1927 -1939
PubMed 10821705 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 7 5.46 6.28

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL20610 1 6.28
CHEMBL58914 1 4.64
CHEMBL57161 1 -
CHEMBL58213 1 -
CHEMBL853 ZALCITABINE 4.0 1 -
CHEMBL440482 1 -
CHEMBL129 ZIDOVUDINE 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL20610 EC50 = 530.0 nM 6.28
CHEMBL58914 EC50 = 23000.0 nM 4.64
CHEMBL57161 EC50 > 50000.0 nM -
CHEMBL58213 EC50 > 33000.0 nM -
CHEMBL853 ZALCITABINE EC50 > 33000.0 nM -
CHEMBL440482 EC50 > 25000.0 nM -
CHEMBL129 ZIDOVUDINE EC50 = - nM -