
Cycloheximide
Cycloheximide is a dicarboximide that is 4-(2-hydroxyethyl)piperidine-2,6-dione in which one of the hydrogens attached to the carbon bearing the hydroxy group is replaced by a 3,5-dimethyl-2-oxocyclohexyl group. It is an antibiotic produced by the bacterium Streptomyces griseus. It has a role as an anticoronaviral agent, a ferroptosis inhibitor, a protein synthesis inhibitor, a neuroprotective agent and a bacterial metabolite. It is a dicarboximide, a secondary alcohol, a cyclic ketone, a member of piperidones, a piperidine antibiotic and an antibiotic fungicide. It is functionally related to a piperidine-2,6-dione. — ChEBI
- IUPAC name
- 4-[(2R)-2-[(1S,3S,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]piperidine-2,6-dione
- Molecular formula
- C15H23NO4
- Molecular weight
- 281.35 g/mol
- Exact mass
- 281.16270821 Da
- XLogP3
- 0.5
- Topological polar surface area
- 83.5 Ų
- Hydrogen-bond donors
- 2
- Hydrogen-bond acceptors
- 4
- Covalent units
- 1
- Defined stereocentres
- 4
Also known as
16 more reported names
External database identifiers
- ChEBI:CHEBI:27641
- ChEMBL:CHEMBL123292
- EPA DTXSID:DTXSID6024882
- PubMed:41789448
- PubMed:40250488
- PubMed:39954839
- PubMed:39880321
- PubMed:39580082
- PubMed:39461407
- PubMed:39431643
- PubMed:39241941
- PubMed:39089414
- PubMed:38960301
- PubMed:37414201
- PubMed:37302538
Retrieved from NIH PubChem on 2026-09-02 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.