1. MAPK/ERK Pathway
  2. p38 MAPK
  3. Talmapimod hydrochloride

Talmapimod hydrochloride  (Synonyms: SCIO-469 hydrochloride)

目录号: HY-10406A
产品使用指南

Talmapimod (SCIO-469) hydrochloride 是 p38α 选择性的,具有口服活性的,ATP 竞争性的抑制剂,IC50 值是 9 nM,约为 p38β 的 10 倍,在 20 个其他激酶 (包括其他 MAPKs) 上显示出至少 2000 倍的选择性。

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Talmapimod hydrochloride Chemical Structure

Talmapimod hydrochloride Chemical Structure

CAS No. : 309915-12-6

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Talmapimod hydrochloride 的其他形式现货产品:

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Other Forms of Talmapimod hydrochloride:

查看 p38 MAPK 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

Talmapimod (SCIO-469) hydrochloride is an orally active, selective, and ATP-competitive p38α inhibitor with an IC50 of 9 nM. Talmapimod hydrochloride shows about 10-fold selectivity over p38β, and at least 2000-fold selectivity over a panel of 20 other kinases, including other MAPKs[1][2][3].

IC50 & Target

p38α

9 nM (IC50)

p38β

90 nM (IC50)

体外研究
(In Vitro)

Talmapimod (SCIO-469) hydrochloride (100-200 nM; 1 hour) inhibits phosphorylation of p38 MAPK in MM cells[1].
Talmapimod hydrochloride inhibits LPS-induced TNF-a production in human whole blood[2].
Talmapimod hydrochloride decreases constitutive p38alpha MAPK phosphorylation of both 5T2MM and 5T33MM cells[3].

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

Western Blot Analysis[1]

Cell Line: MM.1S, U266, RPMI8226, MM.1R, and RPMI-Dox40 cell lines
Concentration: 100, 200 nM
Incubation Time: 1 hour
Result: Strongly inhibits phosphorylation of p38 MAPK.
体内研究
(In Vivo)

Talmapimod hydrochloride (10-90 mg/kg; P.o.; twice daily orally for 14 days) dose-dependently reduced tumor growth and also dose-dependently reduced weight of the palpable tumors at termination[4].

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

Animal Model: Six-week-old male triple immune-deficient BNX mice (RPMI-8226 MM palpable tumors)[4]
Dosage: 10, 30, 90 mg/kg
Administration: P.o.; twice daily orally for 14 days
Result: Dose-dependently reduced tumor growth.
Clinical Trial
分子量

549.46

Formula

C27H31Cl2FN4O3

CAS 号
中文名称

他匹莫德盐酸盐

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

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

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

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

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
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:
Talmapimod hydrochloride
目录号:
HY-10406A
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