Omuralide结构式
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常用名 | Omuralide | 英文名 | Omuralide |
|---|---|---|---|---|
| CAS号 | 154226-60-5 | 分子量 | 213.230 | |
| 密度 | 1.3±0.1 g/cm3 | 沸点 | 462.9±45.0 °C at 760 mmHg | |
| 分子式 | C10H15NO4 | 熔点 | N/A | |
| MSDS | 美版 | 闪点 | 233.7±28.7 °C | |
| 符号 |
GHS06 |
信号词 | Danger |
Omuralide用途A potent 20S proteasome inhibitor with IC50 of 49 nM (inhibition of proteasomal chymotrypsin-like proteolytic activity).. |
| 英文名 | CLASTO-LACTACYSTIN β-LACTONE |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.3±0.1 g/cm3 |
|---|---|
| 沸点 | 462.9±45.0 °C at 760 mmHg |
| 分子式 | C10H15NO4 |
| 分子量 | 213.230 |
| 闪点 | 233.7±28.7 °C |
| 精确质量 | 213.100113 |
| PSA | 75.63000 |
| LogP | -1.40 |
| InChIKey | FWPWHHUJACGNMZ-BSZUBZAZSA-N |
| SMILES | CC(C)C(O)C12NC(=O)C(C)C1OC2=O |
| 蒸汽压 | 0.0±2.6 mmHg at 25°C |
| 折射率 | 1.534 |
| 符号 |
GHS06 |
|---|---|
| 信号词 | Danger |
| 危害声明 | H301-H315-H319-H335 |
| 警示性声明 | P261-P301 + P310-P305 + P351 + P338 |
| 危险品运输编码 | UN 2811 6.1 / PGIII |
| Omuralide上游产品 4 | |
|---|---|
| Omuralide下游产品 0 | |
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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... |
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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... |
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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... |
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实验名称:Inhibition of clasto-lactacystin binding to beta2 subunit of 20S proteasome in human ...
来源:ChEMBL
靶标:Proteasome subunit beta type-2
External Id:CHEMBL1007984
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实验名称:Inhibition of clasto-lactacystin binding to beta5 subunit of 20S proteasome in human ...
来源:ChEMBL
靶标:Proteasome subunit beta type-5
External Id:CHEMBL1007983
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| (3S,4S,7R,8S)-8-Hydroxy-3-isopropyl-7-methyl-2-oxa-5-azaspiro[3.4]octane-1,6-dione |
| Tri-p-tolylstibine |
| Tri-p-tolylantimony |
| Clasto-Lactacystin Beta-lactone |
| 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 |