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YMU1 是人胸苷酸激酶 (hTMPK) 的选择性抑制剂,其 IC50 为 610 nM。YMU1 可抑制肿瘤增殖。

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YMU1 Chemical Structure

YMU1 Chemical Structure

CAS No. : 902589-96-2

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Customer Review

查看 STAT 亚型特异性产品:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

YMU1 is a selective inhibitor of human thymidylate kinase (hTMPK) with an IC50 of 610 nM. YMU1 inhibits tumor proliferation[1][2].

IC50 & Target

STAT3

 

体外研究
(In Vitro)

YMU1 (0.1-10 μM,10 min) 对 TK1 无抑制作用[1]
YMU1 对基因组没有毒性,并且与 TMPK 沉默相似,损害 DSB 修复[1]
YMU1 (1-10 μM,14 天) 在细胞 H184B5F5M10,MCF10A,MCF-7,HCT-116 中对细胞生长影响很小[1]
YMU1 在体外没有抑制 dUTPase[1]
YMU1 在体外使恶性肿瘤细胞对多柔比星增敏[1]
YMU1 (3-10 μM,72 h) 抑制 A549 细胞增殖,迁移,侵袭[2]
YMU1 (3-10 μM,72 h) 控制 LUAD 细胞中 STAT3 信号通路的激活[2]

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

Cell Proliferation Assay[1]

Cell Line: H184B5F5M10, MCF10A, MCF-7, HCT-116
Concentration: 1, 10 μM
Incubation Time: 14 days; twice a week
Result: Had little effect on cell growth.

Cell Viability Assay[2]

Cell Line: A549
Concentration: 3, 10 μM
Incubation Time: 72 h
Result: Decreased cell viability.

Cell Migration Assay [2]

Cell Line: A549
Concentration: 3, 10 μM
Incubation Time: 72 h
Result: Inhibited cell migration.

Cell Invasion Assay[2]

Cell Line: A549
Concentration: 3, 10 μM
Incubation Time: 72 h
Result: Inhibited cell invasion.

Western Blot Analysis[2]

Cell Line: A549; LUAD
Concentration: 3, 10 μM
Incubation Time: 72 h
Result: Increased E-Cadherin approximately 3-fold, reduced N-Cadherin, fibronectin, and vimentin by more than 50%, and significantly reduced pSTAT3 levels, while total STAT3 levels had no significant change.
体内研究
(In Vivo)

YMU1 (5 mg/kg,腹腔注射,每周三次,25 天) 和多柔比星联合给药小鼠,抑制肿瘤生长[1]
YMU1 (3-10 mg/kg,腹腔注射,两天一次,30 天) 在小鼠中抑制 A549 移植肿瘤的生长[2]

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

Animal Model: HCT-116 p53-/- cell transplantation model in nude mice[1]
Dosage: 5 mg/kg; 3 times a week; 25 days
Administration: Intraperitoneal injection (i.p.)
Result: Showed that tumors grew significantly slower in mice treated with doxorubicin.
Animal Model: A549 nude mouse transplantation model[2]
Dosage: 3,10 mg/kg; once every two days; 30 days
Administration: Intraperitoneal injection (i.p.)
Result: Reduced tumor volume and weight in a dose-dependent manner.
分子量

378.45

Formula

C17H22N4O4S

CAS 号
性状

固体

颜色

Off-white to light yellow

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 : 5.56 mg/mL (14.69 mM; 超声助溶 (<70°C); 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 2.6424 mL 13.2118 mL 26.4236 mL
5 mM 0.5285 mL 2.6424 mL 5.2847 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

纯度: 99.00%

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 2.6424 mL 13.2118 mL 26.4236 mL 66.0589 mL
5 mM 0.5285 mL 2.6424 mL 5.2847 mL 13.2118 mL
10 mM 0.2642 mL 1.3212 mL 2.6424 mL 6.6059 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:
YMU1
目录号:
HY-129125
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