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Assay Detail

CHEMBL709608

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

Functional
Tested in vitro for anticancer activity against LNCaP cells
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type LNCaP
Confidence 1 — Organism
Curated By Expert

Target

LNCaP (CHEMBL612518)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis and biological evaluation of 2',3'-didehydro-2',3'- dideoxy-5-fluorocytidine (D4FC) analogues: discovery of carbocyclic nucleoside triphosphates with potent inhibitory activity against HIV-1 reverse transcriptase.
Shi J, McAtee JJ, Schlueter Wirtz S, Tharnish P, Juodawlkis A, Liotta DC, Schinazi RF.
J Med Chem (1999) 42 : 859 -867
PubMed 10072683 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 4.53 5.92

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL123292 CYCLOHEXIMIDE 2.0 1 5.92
CHEMBL38700 ELVUCITABINE 2.0 1 4.26
CHEMBL169267 1 4.24
CHEMBL355426 1 4.17
CHEMBL2368322 1 4.07
CHEMBL2368321 1 -
CHEMBL354904 1 -
CHEMBL185 FLUOROURACIL 4.0 1 -
CHEMBL355081 1 -
CHEMBL366529 1 -
CHEMBL169434 1 -
CHEMBL169277 1 -
CHEMBL171286 1 -
CHEMBL109831 DEXELVUCITABINE 2.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL123292 CYCLOHEXIMIDE IC50 = 1200.0 nM 5.92
CHEMBL38700 ELVUCITABINE IC50 = 55200.0 nM 4.26
CHEMBL169267 IC50 = 57200.0 nM 4.24
CHEMBL355426 IC50 = 67800.0 nM 4.17
CHEMBL2368322 IC50 = 85800.0 nM 4.07
CHEMBL2368321 IC50 > 100000.0 nM -
CHEMBL354904 IC50 > 100000.0 nM -
CHEMBL185 FLUOROURACIL IC50 > 100000.0 nM -
CHEMBL355081 IC50 > 100000.0 nM -
CHEMBL366529 IC50 > 100000.0 nM -
CHEMBL169434 IC50 > 100000.0 nM -
CHEMBL169277 IC50 > 100000.0 nM -
CHEMBL171286 IC50 > 100000.0 nM -
CHEMBL109831 DEXELVUCITABINE IC50 > 100000.0 nM -