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Cycloheximide, Tocris Bioscience™

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Quantity:
100mg
This item is not returnable. View return policy
66-81-9
C15H23NO4
281.35
MFCD00082346
YPHMISFOHDHNIV-FSZOTQKASA-N
cycloheximide, actidione, cycloheximide, naramycin a, kaken, actidion, actidone, hizarocin, naramycin, neocycloheximide
6197
CHEBI:27641
4-[(2R)-2-[(1S,3S,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]piperidine-2,6-dione
C[C@H]1C[C@H](C)C(=O)[C@@H](C1)[C@H](O)CC1CC(=O)NC(=O)C1
This item is not returnable. View return policy
66-81-9
C15H23NO4
281.35
MFCD00082346
YPHMISFOHDHNIV-FSZOTQKASA-N
cycloheximide, actidione, cycloheximide, naramycin a, kaken, actidion, actidone, hizarocin, naramycin, neocycloheximide
6197
CHEBI:27641
4-[(2R)-2-[(1S,3S,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]piperidine-2,6-dione
C[C@H]1C[C@H](C)C(=O)[C@@H](C1)[C@H](O)CC1CC(=O)NC(=O)C1

Description

Inhibitor of protein synthesis

Selective inhibitor of eukaryotic (over prokaryotic) protein synthesis, blocking tRNA binding and release from ribosomes. Induces apoptosis in a variety of transformed and normal cell lines, including T cells. Competitively inhibits the PPIase hFKBP12 (Ki = 3.4 μM). Also inhibits ferroptosis. Antifungal antibiotic. Exhibits anti-MERS-CoV activity in Vero cells in vitro (IC50 = 0.16 μM).
Quantity 100mg
Formula Weight 281.35
Percent Purity >97%
Chemical Name or Material Cycloheximide

Safety and Handling

Recommended Storage : Desiccate at Room Temperature