甲磺酸苯扎托品产品图

甲磺酸苯扎托品

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  • ¥390 - 490
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  • 北京
  • IB1540
  • 2026年08月13日
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    • 详细信息
    • 技术资料
    • 保存条件:

      Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year

    • 保质期:

      Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year

    • 英文名:

      Benztropine Mesylate

    • 库存:

      999

    • 供应商:

      北京索莱宝科技有限公司

    • CAS号:

      132-17-2

    • 规格:

      500mg/1g

    规格:500mg产品价格:¥390.00
    规格:1g产品价格:¥490.00
    CAS132-17-2
    中文名称甲磺酸苯扎托品
    英文名称Benztropine Mesylate
    别名苯甲托品甲烷磺酸盐
    分子式C21H25NO·CH4SO3
    分子量403.54
    规格1g ; 500mg
    溶解性Soluble in Water/DMSO ≥5mg/mL
    纯度≥98%
    外观(性状)White to light yellow Solid
    储存条件Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
    运输条件冷藏运输
    ECEINECS 205-048-8
    MDLMFCD00074784
    SMILESCN1[C@@H]2CC[C@H]1CC(C2)OC(C3=CC=CC=C3)C4=CC=CC=C4.CS(=O)(=O)O
    InChIKeyCPFJLLXFNPCTDW-IIPFOPBBSA-N
    InChIInChI=1S/C21H25NO.CH4O3S/c1-22-18-12-13-19(22)15-20(14-18)23-21(16-8-4-2-5-9-16)17-10-6-3-7-11-17;1-5(2,3)4/h2-11,18-21H,12-15H2,1H3;1H3,(H,2,3,4)/t18-,19+,20?;
    PubChem CID3246155
    靶点mAChR
    通路Neuronal Signaling;GPCR & G Protein
    背景说明是抗毒蕈碱的化合物,可用于帕金森病的相关研究。
    生物活性Benztropine mesylate inhibits functions of CSCs via the acetylcholine receptors, dopamine transporters/receptors, and/or histamine receptors. [1]
    In VitroBenztropine mesylate(0.1-10 μM; 72 hours)treatment inhibits the cell growth of MDA-MB-231 cells with an IC50 of ~5 μM. In MDA-MB-231 cells and 4T1-luc2 cells,Benztropine mesylate reduces the size as well as the number of mammospheres significantly in a dose-dependent manne[1].Benztropine mesylate inhibits functions of cancer stem cells(CSCs)via the acetylcholine receptors,dopamine transporters/receptors,and/or histamine receptors[1].Benztropine mesylate induces the differentiation of oligodendrocytes through M1 and M3 muscarinic receptors and enhanced re-myelination[1].
    In VivoBenztropine mesylate(1.5 mg/kg; daily; for 3 weeks; Balb/c mice)treatment significantly reduces both tumor size and tumor weight in a 4T1 mouse model[1].
    动物实验Mice were housed in microisolator cages and in pathogen free conditions. Surgical procedures were performed under anesthesia and all efforts were made to minimize suffering of the animals. 4T1-luc2 spheres were maintained in ultra-low attachment plates with SCM and pretreated for 6 days with benztropine mesylate (5 μM) or DMSO (0.1%) in vitro. Single cells were injected in 50 μl 1:1 matrigel:DMEM/F12 solution into the fourth mammary fat pad of 8-week old female Balb/c mice (Janvier) at varying cell numbers ranging from 10 to 1,000 cells/mouse [1].
    数据来源文献[1]. Jihong Cui, et al. New use of an old drug: inhibition of breast cancer stem cells by benztropine mesylate. Oncotarget. 2017 Jan 3;8(1):1007-1022.
    单位瓶
    表格1|*|1mg|5mg|10mg|$$|1mM|2.4781mL|12.3903mL|24.7807mL|$$|5mM|0.4956mL|2.4781mL|4.9561mL|$$|10mM|0.2478mL|1.239mL|2.4781mL|

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