1. PI3K/Akt/mTOR
  2. PI3K PI4K
  3. (S)-GSK-F1

(S)-GSK-F1 (Compound 28) 是 III 型磷脂酰肌醇 4-激酶 α (PI4KIIIα) 的抑制剂。(S)-GSK-F1 抑制 PI4Kα、PI4Kβ、PI4Kγ、PI3Kα、PI3Kβ 和 PI3KδpIC50 分别为 8.3、6.0、5.6、5.6、5.1 和 5.6。(S)-GSK-F1 通过抑制 HCV 复制表现出抗丙型肝炎病毒 (HCV) 活性。(S)-GSK-F1 在大鼠模型中表现出中等药代动力学特性。

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(S)-GSK-F1 Chemical Structure

(S)-GSK-F1 Chemical Structure

CAS No. : 1384097-27-1

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Other Forms of (S)-GSK-F1:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

(S)-GSK-F1 (Compound 28) is an inhibitor for type III phosphatidylinositol 4-kinase α (PI4KIIIα). (S)-GSK-F1 inhibits PI4Kα, PI4Kβ, PI4Kγ, PI3Kα, PI3Kβ and PI3Kδ with pIC50 of 8.3, 6.0, 5.6, 5.6, 5.1 and 5.6, respectively. (S)-GSK-F1 exhibits anti-hepatitis C virus (HCV) activity through inhibition of HCV replication. (S)-GSK-F1 exhibits moderate pharmacokinetic characters in rat model[1].

IC50 & Target

PI4KIIIα

8.3 (pIC50)

PI4KIIIβ

6.0 (pIC50)

PI3Kα

5.6 (pIC50)

PI3Kδ

5.6 (pIC50)

PI3Kβ

5.1 (pIC50)

分子量

603.52

Formula

C27H18F5N5O4S

CAS 号
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

(S)-GSK-F1 相关分类

  • 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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(S)-GSK-F1
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HY-100603A
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