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Clasto-lactacystin(Omuralide)_Molecular_structure_CAS_154226-60-5)
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Clasto-lactacystin(Omuralide)

Catalog No. C562500 Name Toronto Research Chemicals
CAS Number 154226-60-5 Website http://www.trc-canada.com
M. F. C10H15NO4 Telephone +1 (416) 665-9696
M. W. 213.2304 Fax +1 (416) 665-4439
Purity Email info@trc-canada.com
Storage -20°C Freezer Chembase ID: 132558

SYNONYMS

IUPAC name
(1R,4R,5S)-1-[(1S)-1-hydroxy-2-methylpropyl]-4-methyl-6-oxa-2-azabicyclo[3.2.0]heptane-3,7-dione
IUPAC Traditional name
(1R,4R,5S)-1-[(1S)-1-hydroxy-2-methylpropyl]-4-methyl-6-oxa-2-azabicyclo[3.2.0]heptane-3,7-dione
Synonyms
Clasto-lactacystin β-Lactone
(1R,4R,5S)-1-[(1S)-1-Hydroxy-2-methylpropyl]-4-methyl-6-oxa-2-azabicyclo[3.2.0]heptane-3,7-dione
Omuralide

DATABASE IDS

CAS Number 154226-60-5

PROPERTIES

Certificate of Analysis Download
Apperance White Solid
Melting Point 186-187°C
Solubility DMF
Solubility Ethanol
Solubility Hot Ethyl Acetate
Solubility Methanol
Solubility Pyridine
MSDS Link Download
Storage Condition -20°C Freezer

DETAILS

Description (English)
A cell permeable, irreversible proteasome inhibitor. It is 20-fold more potent than Lactacystin. Lactacytstin spontaneously converts to clasto-lactacystin in biological systems. Clasto-lactacystin is the only cell permeable form of lactacystin. Induce

REFERENCES

  • Craiu, A., et al.: J. Biol. Chem., 272, 13437 (1997)
  • Dick, G.L.R., et al.: J. Biol. Chem., 272, 182 (1997)
  • Fenteany, G. and Schreiber, S.: J. Biol. Chem., 273, 8545 (1997)
  • Corey, E.J., et al.: J.A.C.S., 120, 2330 (1998)