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| | [2H8]-Bendamustine Hydrochloride Basic information |
| Product Name: | [2H8]-Bendamustine Hydrochloride | | Synonyms: | [2H8]-Bendamustine Hydrochloride;[2H8]-Bendamustine hydrochloride salt;Bendamustine-d8 HCl;Bendamustine hydrochloride salt;Bendamustine-[D8] Hydrochloride (Standard) | | CAS: | 1185068-23-8 | | MF: | C16H22Cl3N3O2 | | MW: | 394.72 | | EINECS: | | | Product Categories: | | | Mol File: | 1185068-23-8.mol | ![[2H8]-Bendamustine Hydrochloride Structure](CAS/20211123/GIF/1185068-23-8.gif) |
| | [2H8]-Bendamustine Hydrochloride Chemical Properties |
| | [2H8]-Bendamustine Hydrochloride Usage And Synthesis |
| Uses | Bendamustine-d8 (hydrochloride) is deuterium labeled Bendamustine (hydrochloride). Bendamustine hydrochloride (SDX-105), a purine analogue, is a DNA cross-linking agent. Bendamustine hydrochloride activats DNA-damage stress response and apoptosis. Bendamustine hydrochloride has potent alkylating, anticancer and antimetabolite properties[1]. | | References | [1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. DOI:10.1177/1060028018797110 [2] 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. DOI:10.1158/1078-0432.CCR-07-1061 [3] Cives M, et al. Bendamustine overcomes resistance to melphalan in myeloma cell lines by inducing cell death through mitotic catastrophe. Cell Signal. 2013 May;25(5):1108-17. DOI:10.1016/j.cellsig.2013.01.020 [4] Ackler S, et al. Navitoclax (ABT-263) and bendamustine ± rituximab induce enhanced killing of non-Hodgkin's lymphoma tumours in vivo. Br J Pharmacol. 2012 Oct;167(4):881-91. DOI:10.1111/j.1476-5381.2012.02048.x |
| | [2H8]-Bendamustine Hydrochloride Preparation Products And Raw materials |
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