Acetoxycycloheximide
Names
IUPAC name
(1R,3S,5S)-3-[(1R)-2-(2,6-Dioxo-4-piperidinyl)-1-hydroxyethyl]-1,5-dimethyl-4-oxocyclohexyl acetate
Other names
Acetyloxycycloheximide
E-73
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C17H25NO6/c1-9-7-17(3,24-10(2)19)8-12(16(9)23)13(20)4-11-5-14(21)18-15(22)6-11/h9,11-13,20H,4-8H2,1-3H3,(H,18,21,22)/t9-,12-,13+,17+/m0/s1
    Key: UFDHNJJHPSGMFX-SQUSCZTCSA-N
  • C[C@H]1C[C@@](C[C@H](C1=O)[C@@H](CC2CC(=O)NC(=O)C2)O)(C)OC(=O)C
Properties
C17H25NO6
Molar mass 339.388 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Acetoxycycloheximide is an organic chemical compound. It can be considered as the acetylated analogue of cycloheximide. It is a potent protein synthesis inhibitor in animal cells[1] and can inhibit the formation of memories.[2][3]

See also

References

  1. ↑ Mahy, Brian W J (2001). A dictionary of virology (3. ed.). San Diego, Calif. [u.a.]: Academic Press. pp. 2. ISBN 0-12-465327-8.
  2. ↑ Flood, James F.; Bennett, Edward L.; Orme, Ann E.; Rosenzweig, Mark R. (February 1975). "Effects of protein synthesis inhibition on memory for active avoidance training" (PDF). Physiology & Behavior. 14 (2): 177–184. doi:10.1016/0031-9384(75)90163-8. PMID 1161822. S2CID 31577844.
  3. ↑ Flexner, L. B.; Flexner, J. B.; Roberts, R. B. (1 August 1966). "Stages of memory in mice treated with acetoxycycloheximide before or immediately after learning". Proceedings of the National Academy of Sciences. 56 (2): 730–735. Bibcode:1966PNAS...56..730F. doi:10.1073/pnas.56.2.730. PMC 224433. PMID 5229991.
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