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STEMCELL Technologies (S)-MG132
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Quantity:
1 mg
10 mg
Unit Size:
10mg
1mg
Description
- (S)-MG132 is a reversible, cell-permeable inhibitor of proteasome activity (IC50 = 100 nM; Kisselev & Goldberg) and calpain (IC50 = 1.2 μM; Tsubuki et al.) The ubiquitin-proteasome pathway selectively degrades intracellular proteins, thereby clearing damaged or misfolded proteins, and regulating the availability of key proteins involved in the control of inflammatory processes and cell cycle regulation
- (S)-MG132 suppresses NF-κB activation by preventing IκB degradation (IC50 = 3 μM; Arlt et al.), Palombella et al.), Ortiz-Lazareno et al.)
- Blocks apoptosis triggered by DNA damage in HeLa cells (Zhang et al.)
- Inhibits NF-κB activation, sensitizing a variety of carcinoma cell lines to apoptosis (Arlt et al.)
- Cytotoxic effects on a variety of human cancer cell lines (Banerjee & Liefshitz)
- Inhibits growth of mouse melanoma (B16) and human ocular melanoma (IPC227F) cell lines (Vivier et al.)
Specifications
Specifications
| CAS | 133407-82-6 |
| Synonym | Z-Leu-Leu-Leu-CHO; Calpain inhibitor IV-2 |
| Quantity | 1 mg |
| Molecular Formula | C26H41N3O5 |
| Purity | ≥98% |
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