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  3. Idarubicin

Idarubicin  (Synonyms: 4-Demethoxydaunorubicin)

目录号: HY-17381A
产品使用指南

Idarubicin 是一种口服有效的蒽环类抗白血病剂。Idarubicin 抑制 拓扑异构酶 II,干扰 DNA 复制和 RNA 转录。Idarubicin 可诱导 DNA 损伤。Idarubicin 抑制 DNA 合成和 c-myc 表达。Idarubicin 还抑制细菌和酵母菌的生长。

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Idarubicin Chemical Structure

Idarubicin Chemical Structure

CAS No. : 58957-92-9

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Idarubicin 的其他形式现货产品:

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Other Forms of Idarubicin:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Idarubicin is an orally active and potent anthracycline antileukemic agent. Idarubicin inhibits the topoisomerase II interfering with the replication of DNA and RNA transcription. Idarubicin shows induction of DNA damage. Idarubicin inhibits DNA synthesis and of c-myc expression. Idarubicin inhibits the growth of bacteria and yeasts[1][2][3][4][5].

IC50 & Target

Topoisomerase II

 

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
DA-3 cell line IC50
2.3 μM
Compound: IDR
Cytotoxicity against mouse DA-3 cells after 24 hrs by XTT assay
Cytotoxicity against mouse DA-3 cells after 24 hrs by XTT assay
[PMID: 24900668]
K562 IC50
0.012 μM
Compound: idarubicin
Cytotoxicity against human K562 cells after 5 days by XTT assay
Cytotoxicity against human K562 cells after 5 days by XTT assay
[PMID: 18076140]
K562 GI50
3.3 μM
Compound: idarubicin
Antiproliferative activity against human K562 cells after 72 hrs
Antiproliferative activity against human K562 cells after 72 hrs
[PMID: 25420175]
MCF7 IC50
7.3 μM
Compound: IDR
Cytotoxicity against human MCF7 cells after 24 hrs by XTT assay
Cytotoxicity against human MCF7 cells after 24 hrs by XTT assay
[PMID: 24900668]
SK-OV-3 IC50
4.5 μM
Compound: IDR
Cytotoxicity against human SKOV3 cells after 24 hrs by XTT assay
Cytotoxicity against human SKOV3 cells after 24 hrs by XTT assay
[PMID: 24900668]
体外研究
(In Vitro)

The IC50 of idarubicin is 3.3 ± 0.4 ng/mL on MCF-7 monolayers and 7.9 ± 1.1 ng/mL in multicellular spheroids[1].
Idarubicin shows a greater cytotoxicity than daunorubicin or doxorubicin in various in vitro systems. This has been attributed to a better ability of idarubicin to induce the formation of topoisomerase II -mediated DNA breaks[2].
Idarubicin is about 57.5-fold and 25-fold more active than doxorubicin and epirubicin, respectively[3].
Idarubicin produces a concentration-dependent reduction in MCF-7 cell growth, with an IC50 of approximately 0.01 μM. Idarubicin produces a concentration-dependent inhibition of DNA synthesis and a time- and concentration-dependent suppression of c-myc expression[4].

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

Clinical Trial
分子量

497.49

Formula

C26H27NO9

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
  • 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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