1. Neuronal Signaling
  2. Monoamine Oxidase
  3. Tisolagiline monomethylsulfate

Tisolagiline monomethylsulfate  (Synonyms: KDS2010 monomethylsulfate)

目录号: HY-127109A 纯度: 99.83% ee.: 100.00%
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Tisolagiline methylsulfate (KDS2010) 是一种选择性、可逆且具有口服活性的单胺氧化酶 (MAO-B) 抑制剂,IC50 值为 8 nM。Tisolagiline methylsulfate 具有神经保护和抗神经炎活性。

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Tisolagiline monomethylsulfate

Tisolagiline monomethylsulfate Chemical Structure

CAS No. : 1894207-45-4

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Other Forms of Tisolagiline monomethylsulfate:

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Tisolagiline methylsulfate (KDS2010) is the selective, reversible and orally active inhibitor for MAO-B with an IC50 of 8 nM. Tisolagiline methylsulfate exhibits neuroprotective and anti-neuroinflammatory activities[1][2].

IC50 & Target[1]

MAO-B

8 nM (IC50)

体外研究
(In Vitro)

Tisolagiline methylsulfate (1 μM, 4 days) 可降低胶质纤维酸性蛋白 (GFAP) 的表达和糖胺聚糖 (CSPG) 的沉积,从而抑制星形胶质细胞活化和星形胶质细胞瘢痕形成[2]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Immunofluorescence[2]

Cell Line: Human astrocytes
Concentration: 1 μM
Incubation Time: 4 days
Result: Inhibited the expression of GFAP.
体内研究
(In Vivo)

Tisolagiline methylsulfate(10 mg/kg,口服,每日一次,连用 30 天)可改善小鼠模型中 MPTP (HY-15608) 诱发的帕金森病[1]
Tisolagiline methylsulfate (10 mg/kg/天,口服,1-7 天)可抑制星形胶质细胞瘢痕形成,从而增加 Doxorubicin (HY-15142) 向胶质母细胞瘤区域的渗透,增加小鼠模型中胶质母细胞瘤的体积[2]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: MPTP-induced Parkinson’s disease in mouse models[1]
Dosage: 10 mg/kg
Administration: po, once daily for 30 days
Result: Alleviated the motor dysfunction, reversed the reduction in the number of TH-positive neurons, reduced the expression of GFAP and iNOS.
Animal Model: U87 MG xenograft mouse models[2]
Dosage: 10 mg/kg
Administration: po for 1-7 days
Result: Increased the fluorescence signal of DOX in the GBM area, increased the volume of GBM tumors.
分子量

418.43

Formula

C18H21F3N2O4S

CAS 号
性状

固体

颜色

White to off-white

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
溶解性数据
细胞实验: 

DMSO 中的溶解度 : 20 mg/mL (47.80 mM; ultrasonic and adjust pH to 2 with 1 M HCL; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.3899 mL 11.9494 mL 23.8989 mL
5 mM 0.4780 mL 2.3899 mL 4.7798 mL
查看完整储备液配制表

* 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, 6 months; -20°C, 1 month。-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。

  • 摩尔计算器

  • 稀释计算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量
=
浓度
×
体积
×
分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

C1

×
体积 (start)

V1

=
浓度 (final)

C2

×
体积 (final)

V2

动物溶解方案计算器
请输入动物实验的基本信息:

给药剂量

mg/kg

动物的平均体重

g

每只动物的给药体积

μL

动物数量

由于实验过程有损耗,建议您多配一只动物的量
计算结果
工作液所需浓度 : mg/mL
纯度 & 产品资料
参考文献

完整储备液配制表

* 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, 6 months; -20°C, 1 month。-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。

可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.3899 mL 11.9494 mL 23.8989 mL 59.7472 mL
5 mM 0.4780 mL 2.3899 mL 4.7798 mL 11.9494 mL
10 mM 0.2390 mL 1.1949 mL 2.3899 mL 5.9747 mL
15 mM 0.1593 mL 0.7966 mL 1.5933 mL 3.9831 mL
20 mM 0.1195 mL 0.5975 mL 1.1949 mL 2.9874 mL
25 mM 0.0956 mL 0.4780 mL 0.9560 mL 2.3899 mL
30 mM 0.0797 mL 0.3983 mL 0.7966 mL 1.9916 mL
40 mM 0.0597 mL 0.2987 mL 0.5975 mL 1.4937 mL
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
Tisolagiline monomethylsulfate
目录号:
HY-127109A
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