Bendamustine-d4 (hydrochloride)
(Synonyms: 盐酸苯达莫司汀 d4 (盐酸盐)) 目录号 : GC46914
A neuropeptide with diverse biological activities
Cas No.:2802569-31-7
Sample solution is provided at 25 µL, 10mM.
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Bendamustine-d4 is intended for use as an internal standard for the quantification of bendamustine by GC- or LC-MS. Bendamustine is a purine analog and DNA alkylating agent.1 It inhibits growth of SKW-3, Reh, CML-T1, BV-173, and HL-60 leukemia cell lines (IC50s = 27.0, 28.6, 15.6, 20.8, and 57.7 μM, respectively) but not MCF-7 and MDA-MB-231 breast cancer cell lines (IC50s = >200 μM for both).2 It is cytotoxic to patient-derived lymphocytic leukemia (B-CLL) cells (LD50s = 6.8-8.3 mg/ml).3 Bendamustine (50 mg/kg) inhibits tumor growth by 9 and 96% alone and in combination with ofatumumab, respectively, in a JVM-3 CLL mouse xenograft model.4 It activates the DNA-damage stress response, the base excision DNA repair pathway, and apoptosis, as well as inhibits mitotic checkpoints and induces mitotic catastrophe.1 Formulations containing bendamustine have been used to treat CLL and non-Hodgkin lymphoma.
1.Leoni, L.M., Bailey, B., Reifert, J., et al.Bendamustine (Treanda) displays a distinct pattern of cytotoxicity and unique mechanistic features compared with other alkylating agentsClin. Cancer Res.14(1)309-317(2008) 2.Konstantinov, S.M., Kostovski, A., Topashka-Ancheva, M., et al.Cytotoxic efficacy of bendamustine in human leukemia and breast cancer cell linesJ. Cancer Res. Clin. Oncol.128(5)271-278(2002) 3.SchwÄnen, C., Hecker, T., HÜbinger, G., et al.In vitro evaluation of bendamustine induced apoptosis in B-chronic lymphocytic leukemiaLeukemia16(10)2096-2105(2002) 4.Haskova, Z., Whitacre, M.N., Dede, K.A., et al.Combination therapy with ofatumumab and bendamustine in xenograft model of chronic lymphocytic leukaemiaBr. J. Haematol.156(3)402-404(2012)
| Cas No. | 2802569-31-7 | SDF | |
| 别名 | 盐酸苯达莫司汀 d4 (盐酸盐) | ||
| Canonical SMILES | ClCCN(C1=CC=C(N(C)C(CCCC(O)=O)=N2)C2=C1)C([2H])([2H])C([2H])([2H])Cl.Cl | ||
| 分子式 | C16H17Cl2D4N3O2.HCl | 分子量 | 398.8 |
| 溶解度 | DMSO: Soluble,Methanol: Soluble | 储存条件 | Store at -20°C |
| General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液；一旦配成溶液，请分装保存，避免反复冻融造成的产品失效。 储备液的保存方式和期限：-80°C 储存时，请在 6 个月内使用，-20°C 储存时，请在 1 个月内使用。 为了提高溶解度，请将管子加热至37℃，然后在超声波浴中震荡一段时间。 |
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| Shipping Condition | 评估样品解决方案：配备蓝冰进行发货。所有其他可用尺寸：配备RT，或根据请求配备蓝冰。 | ||
| 制备储备液 | |||
 |
1 mg | 5 mg | 10 mg |
| 1 mM | 2.5075 mL | 12.5376 mL | 25.0752 mL |
| 5 mM | 0.5015 mL | 2.5075 mL | 5.015 mL |
| 10 mM | 0.2508 mL | 1.2538 mL | 2.5075 mL |
| 第一步：请输入基本实验信息（考虑到实验过程中的损耗，建议多配一只动物的药量） | ||||||||||
| 给药剂量 | mg/kg |  |
动物平均体重 | g | |
每只动物给药体积 | ul | |
动物数量 | 只 |
| 第二步：请输入动物体内配方组成（配方适用于不溶于水的药物；不同批次药物配方比例不同，请联系GLPBIO为您提供正确的澄清溶液配方） | ||||||||||
| % DMSO % % Tween 80 % saline | ||||||||||
| 计算重置 | ||||||||||
计算结果:
工作液浓度： mg/ml；
DMSO母液配制方法： mg 药物溶于 μL DMSO溶液（母液浓度 mg/mL，
体内配方配制方法：取 μL DMSO母液，加入 μL PEG300，混匀澄清后加入μL Tween 80，混匀澄清后加入 μL saline，混匀澄清。
1. 首先保证母液是澄清的；
2.
一定要按照顺序依次将溶剂加入，进行下一步操作之前必须保证上一步操作得到的是澄清的溶液，可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
Quality Control & SDS
- View current batch:
- Purity: >99.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet