
CAS 1201902-80-8: MLN9708
Formula:C20H23BCl2N2O9
Synonyms:- 4-Carboxy-2-[(1R)-1-[[2-[(2,5-dichlorobenzoyl)amino]acetyl]amino]-3-methylbutyl]-6-oxo-1,3,2-dioxaborinane-4-acetic acid
- Ixazomib
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Found 7 products.
4-(Carboxymethyl)-2-((R)-1-(2-(2,5-Dichlorobenzamido)Acetamido)-3-Methylbutyl)-6-Oxo-1,3,2-Dioxaborinane-4-Carboxylic Acid
CAS:4-(Carboxymethyl)-2-((R)-1-(2-(2,5-Dichlorobenzamido)Acetamido)-3-Methylbutyl)-6-Oxo-1,3,2-Dioxaborinane-4-Carboxylic AcidPurity:99%Molecular weight:517.12g/mol1,3,2-Dioxaborinane-4-acetic acid, 4-carboxy-2-[(1R)-1-[[2-[(2,5-dichlorobenzoyl)amino]acetyl]amino]-3-methylbutyl]-6-oxo-
CAS:Formula:C20H23BCl2N2O9Purity:98%Color and Shape:SolidMolecular weight:517.1216Ref: IN-DA000QJT
1gTo inquire5mg57.00€10mg65.00€25mg93.00€50mg121.00€100mg153.00€250mg264.00€500mg604.00€MLN-9708
CAS:Controlled ProductApplications MLN-9708 is a novel proteasome inhibitor. References Kupperman, Erik., et al.: Cancer Res., 70, 1970 (2010);Formula:C20H23BCl2N2O9Color and Shape:NeatMolecular weight:517.12Ixazomib Citrate
CAS:Controlled ProductFormula:C20H23BCl2N2O9Color and Shape:NeatMolecular weight:517.12MLN9708 analogues
CAS:MLN2238 inhibits 20S proteasome's β5 site (Ki50=0.93 nM, IC50=3.4 nM), active form of Ixazomib Citrate in solutions/plasma.Formula:C20H23BCl2N2O9Purity:98.24% - ≥95%Color and Shape:SolidMolecular weight:517.12Ref: TM-T2016
5mg50.00€10mg66.00€25mg96.00€50mg131.00€100mg215.00€200mg319.00€500mg535.00€1mL*10mM (DMSO)52.00€Ixazomib Citrate (MLN9708)
CAS:Ixazomib Citrate (MLN9708) is a proteasome inhibitor that belongs to the class of investigational agents. It has minimal toxicity and is being investigated for use in the treatment of multiple myeloma, a type of cancer that starts in the bone marrow. Ixazomib Citrate inhibits the activity of proteasomes, which are cellular structures responsible for degrading proteins. This inhibition leads to an increase in the number of cells with damaged DNA and an increase in apoptosis. Ixazomib Citrate synergizes with other chemotherapeutic agents, such as bortezomib, to promote apoptosis by activating caspases and decreasing cell proliferation. The biochemical properties of this drug include its ability to inhibit protein synthesis by inhibiting eukaryotic ribosomes and its ability to bind to DNA at specific sites.Formula:C20H23BCl2N2O9Purity:Min. 95%Molecular weight:517.12 g/mol