Bortezomib
Chemical Name: B-[(1R)-3-Methyl-1-[[(2S)-1-oxo-3-phenyl-2-[(2-pyrazinylcarbonyl)amino]propyl]amino]butyl]boronic acid
Purity: ≥98%
Biological Activity
Bortezomib is a high affinity proteasome inhibitor (Ki = 0.6 nM). Inhibits growth of multiple myeloma (MM) cell lines (IC50 values in <50 nM range); induces apoptosis in MM cell lines and MM patient derived cells, including p53 mutant cell lines. Decreases adherence of MM cells lines to bone marrow stromal cells (BMSCs). Acts synergistically with dexamethasone (Cat. No. 1126). Also cytotoxic in MCF-7 breast cancer cell line (IC50 = 50 nM).Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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The proteasome inhibitor PS-341 in cancer therapy.
Teicher et al.
Clin.Cancer Res., 1999;5:2638 -
The proteasome inhibitor PS-341 inhibits growth, induces apoptosis, and overcomes drug resistance in human multiple myeloma cells.
Hideshima et al.
Cancer Res., 2001;61:3071
Product Datasheets
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Citations for Bortezomib
The citations listed below are publications that use Tocris products. Selected citations for Bortezomib include:
2 Citations: Showing 1 - 2
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ATP Consumption Is Coupled with Endocytosis in Exudated Neutrophils.
Authors: Tomo Et al.
Int J Mol Sci 2023;24
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CHIP/STUB1 Ubiquitin Ligase Functions as a Negative Regulator of ErbB2 by Promoting Its Early Post-Biosynthesis Degradation.
Authors: Vimla Et al.
Cancers (Basel) 2021;13
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