Bendamustine Hydrochloride DNA Synthesis Inhibitors Cas 3543-75-7
Bendamustine Hydrochloride DNA Synthesis Inhibitors Cas 3543-75-7
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Chemical Information
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Product name:Bendamustine hydrochloride |
Purity:98% min |
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CAS NO:3543-75-7 |
Solubility:DMSO100 mg/mL (253.34 mM) |
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Molecular Formula:C16H22Cl3N3O2 |
Package:Package according to customer requirements |
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Molecular Weight:394.724 |
Storage:Store at -20℃ |
Quality control
COA
Remarks
Bendamustine hydrochloride is the hydrochloride salt of bendamustine, a bifunctional mechlorethamine derivative with alkylator and antimetabolite activities. Bendamustine possesses three active moieties: an alkylating group; a benzimidazole ring, which may act as a purine analogue; and a butyric acid side chain. Although its exact mechanism of action is unknown, this agent appears to act primarily as an alkylator. Bendamustine metabolites alkylate and crosslink macromolecules, resulting in DNA, RNA and protein synthesis inhibition, and, subsequently, apoptosis. In October 2008, the FDA granted further approval to market Treanda for the treatment of indolent B-cell non-Hodgkin's lymphoma (NHL) that has progressed during or within six months of treatment with rituximab or a rituximab-containing regimen.
Related Prodcuts:
Moxifloxacin; Moxifloxacin HCL; Fasudil; Fasudil HCL; Pixantrone Maleate; Topotecan Hydrochloride; Irinotecan HCl Trihydrate; Irinotecan; Gemfibrozil; Cicloheximide; Oxaliplatin; Camptothecin; 10-Hydroxycamptothecin
References
[1].Leoni LM, et al. Bendamustine (Treanda) displays a distinct pattern of cytotoxicity and unique mechanistic features compared with other alkylating agents. Clin Cancer Res. 2008 Jan 1;14(1):309-17.
[2].Cives M, et al. Bendamustine overcomes resistance to melphalan i
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