1. Epigenetics
  2. Histone Methyltransferase
  3. PRMT5-IN-48

PRMT5-IN-48 (compound D3) 是一种口服有效的 PRMT5 抑制剂 (IC50=20.7 nM),具有抗癌活性。PRMT5-IN-48 可抑制多种癌细胞的生长,诱导细胞凋亡 (apoptosis),并将细胞周期停滞在 G0/G1 期。PRMT5-IN-48 可用于非非霍奇金淋巴瘤 (NHL) 的研究。

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PRMT5-IN-48 Chemical Structure

PRMT5-IN-48 Chemical Structure

CAS No. : 2640287-77-8

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

PRMT5-IN-48 (compound D3) is an orally effective PRMT5 inhibitor (IC50=20.7 nM) with anticancer activity. PRMT5-IN-48 can inhibit the growth of various cancer cells, induce apoptosis (apoptosis), and arrest the cell cycle at the G0/G1 phase. PRMT5-IN-48 can be used for non-Hodgkin lymphoma (NHL) research[1].

IC50 & Target

PRMT5[1]

药代动力学
(Parmacokinetics)
Species Dose Route Indicator value
Rat 10.000mg/kg p.o. T1/2 0.4hr
Rat 2.000mg/kg i.v. T1/2 2.2hr
Rat 10.000mg/kg p.o. Cmax 1366.5ng/mL
Rat 2.000mg/kg i.v. Tmax 0.1hr
Rat 10.000mg/kg p.o. AUC0-t 771ng·h/mL
Rat 2.000mg/kg i.v. Cmax 894ng/mL
Rat 10.000mg/kg p.o. MRT 0.5hr
Rat 2.000mg/kg i.v. AUC0-t 1028.2ng·h/mL
Rat 10.000mg/kg p.o. CL 2.5L/h/kg
Rat 2.000mg/kg i.v. MRT 1.7hr
Rat 10.000mg/kg p.o. Vd 1.4L/kg
Rat 2.000mg/kg i.v. F 26.7%
分子量

515.65

Formula

C30H37N5O3

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
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  • 稀释计算器

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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)
× = ×
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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:
PRMT5-IN-48
目录号:
HY-170792
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