Omuralide

Modify Date: 2024-01-02 12:07:31

Omuralide Structure
Omuralide structure
Common Name Omuralide
CAS Number 154226-60-5 Molecular Weight 213.230
Density 1.3±0.1 g/cm3 Boiling Point 462.9±45.0 °C at 760 mmHg
Molecular Formula C10H15NO4 Melting Point N/A
MSDS USA Flash Point 233.7±28.7 °C
Symbol GHS06
GHS06
Signal Word Danger

 Use of Omuralide


A potent 20S proteasome inhibitor with IC50 of 49 nM (inhibition of proteasomal chymotrypsin-like proteolytic activity)..

 Names

Name CLASTO-LACTACYSTIN β-LACTONE
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 462.9±45.0 °C at 760 mmHg
Molecular Formula C10H15NO4
Molecular Weight 213.230
Flash Point 233.7±28.7 °C
Exact Mass 213.100113
PSA 75.63000
LogP -1.40
Vapour Pressure 0.0±2.6 mmHg at 25°C
Index of Refraction 1.534

 Safety Information

Symbol GHS06
GHS06
Signal Word Danger
Hazard Statements H301-H315-H319-H335
Precautionary Statements P261-P301 + P310-P305 + P351 + P338
RIDADR UN 2811 6.1 / PGIII

 Synthetic Route

 Articles31

More Articles
Proteasome inhibitor differentially regulates expression of the major immediate early genes of human cytomegalovirus in human central nervous system-derived cell lines.

Virus Res. 142(1-2) , 68-77, (2009)

Proteasome inhibitor, which inhibits NF-kappaB activation, has been reported to activate c-Jun N-terminal kinase (JNK)-c-Jun pathway. In this study, we investigated the effects of proteasome inhibitor...

Turnover of StAR protein: roles for the proteasome and mitochondrial proteases.

Mol. Cell. Endocrinol. 265-266 , 51-8, (2007)

Steroidogenic acute regulatory protein (StAR) is a mitochondrial protein essential for massive synthesis of steroid hormones in the adrenal and the gonads. Our studies suggest that once synthesized on...

Targeting of a chlamydial protease impedes intracellular bacterial growth.

PLoS Pathog. 7(9) , e1002283, (2011)

Chlamydiae are obligate intracellular bacteria that propagate in a cytosolic vacuole. Recent work has shown that growth of Chlamydia induces the fragmentation of the Golgi apparatus (GA) into ministac...

 Synonyms

(3S,4S,7R,8S)-8-Hydroxy-3-isopropyl-7-methyl-2-oxa-5-azaspiro[3.4]octane-1,6-dione
6-Oxa-2-azabicyclo[3.2.0]heptane-3,7-dione, 1-(1-hydroxy-2-methylpropyl)-4-methyl-
Tri-p-tolylstibine
Tri-p-tolylantimony
Clasto-Lactacystin Beta-lactone
2-Oxa-5-azaspiro[3.4]octane-1,6-dione, 8-hydroxy-7-methyl-3-(1-methylethyl)-, (3S,4S,7R,8S)-
1-(1-Hydroxy-2-methylpropyl)-4-methyl-6-oxa-2-azabicyclo[3.2.0]heptane-3,7-dione
Stibine,tri-p-tolyl
5,6,7,12,6'-pentamethoxy-2-methyl-berbam-1'-ene
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