Cycloheximide 0.2μM R00 exp15

Translation elongation inhibitor, binds 60S ribosomal subunit

  • Class / Subclass 1: Proteostasis / Translation Inhibitor
  • Class / Subclass 2: Environmental Stresses / Toxin

Compound References

  • PubChem Name: Cycloheximide
  • Synonyms: Naramycin A; Actidione; CHX
  • CAS #: 66-81-9
  • PubChem CID: 6197
  • IUPAC: 4-[(2R)-2-[(1S,3S,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]piperidine-2,6-dione
  • INCHI Name: InChI=1S/C15H23NO4/c1-8-3-9(2)15(20)11(4-8)12(17)5-10-6-13(18)16-14(19)7-10/h8-12,17H,3-7H2,1-2H3,(H,16,18,19)/t8-,9-,11-,12+/m0/s1
  • INCHI Key: YPHMISFOHDHNIV-FSZOTQKASA-N
  • Molecular Weight: 281.35
  • Canonical SMILES: CC1CC(C(=O)C(C1)C(CC2CC(=O)NC(=O)C2)O)C
  • Isomeric SMILES: C[C@H]1C[C@@H](C(=O)[C@@H](C1)[C@@H](CC2CC(=O)NC(=O)C2)O)C
  • Molecular Formula: C15H23NO4

Compound Supplier

  • Supplier Name: Sigma-Aldrich
  • Catalog #: C7698
  • Lot #: MKBR7146V

Compound Characterization

  • HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C15H23NO4 282.16998; found 282.17004

Dose Response Curve

  • Platform ID: Cycloheximide
  • Min: 3.7773; Max: 80.9065





IC Concentration (µM)
IC10 N/A
IC20 0.1270
IC30 0.3675
IC40 0.8782
IC50 1.9535
IC60 N/A
IC70 N/A
IC80 N/A
IC90 N/A


  • Round: 00
  • Dose: 200nM
  • Days of incubation: 8
  • Doublings: 5.6
  • Numbers of reads: 9929747
Sensitive/Resistant hits (FDR<0.05)CRANKSScore PlotTop 30 GenesScreen SimilarityTop 30 Sensitive GO termsTop 30 Resistant GO terms
3/0ScoresViewViewViewViewView

  • Last modified: 2026/01/15 21:36
  • by 127.0.0.1