• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

Doxorubicin hydrochloride

CAS No. 25316-40-9

Doxorubicin hydrochloride ( DOX )

产品货号. M13752 CAS No. 25316-40-9

Doxorubicin (Adriamycin) 是一种抗生素,可抑制 DNA 拓扑异构酶 II 并诱导 DNA 损伤和细胞凋亡。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥147 有现货
10MG ¥259 有现货
25MG ¥423 有现货
50MG ¥693 有现货
100MG ¥1188 有现货
200MG ¥1935 有现货
500MG ¥2862 有现货
1G ¥3789 有现货
1 mL x 10 mM in DMSO ¥312 有现货

生物学信息

  • 产品名称
    Doxorubicin hydrochloride
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    Doxorubicin (Adriamycin) 是一种抗生素,可抑制 DNA 拓扑异构酶 II 并诱导 DNA 损伤和细胞凋亡。
  • 产品描述
    Doxorubicin (Adriamycin) is an antibiotic agent that inhibits DNA topoisomerase II and induces DNA damage and apoptosis. (In Vitro):Doxorubicin hydrochloride (1-8 μM; 24 and 48 hours) decreases the viability of MCF-10F, MCF-7 and MDA-MB-231 cells in a time- and dose-dependent manner.Doxorubicin hydrochloride (1 μM; 3 and 24 hours) results in Hct-116 human colon carcinoma cells reduction in G0/G1 phase and accumulation in G2 phase.Doxorubicin hydrochloride (1 μM for MCF-10F and MDA-MB-231 cells, 4 μM for MCF-7 cells; 48 hours) induces apoptosis by upregulating Bax, caspase-8 and caspase-3 and downregulation of Bcl-2 protein expression.(In Vivo):Treatment with Doxorubicin (2 mg/kg) or Zoledronic acid (100 μg/kg) alone does not statistically significantly decrease final tumor volume compared with saline. Mice treated with Doxorubicin plus Zoledronic acid have statistically significantly smaller final tumor volumes than those treated with Doxorubicin alone.
  • 体外实验
    Cell Viability Assay Cell Line:Breast cancer cell lines MCF-10F, MCF-7 and MDA-MB-231 Concentration:0, 1, 2, 4 and 8 μM Incubation Time:24 and 48 hoursResult:IC50 was 1 μM for both MCF-10F and MDA-MB-231 cell lines.IC50 was 4 μM for MCF-7 cell line.Cell Cycle Analysis Cell Line:Hct-116 human colon carcinoma cells Concentration:1 μM Incubation Time:3 hours and 24 hours Result:Both, bolus (3 h) and continuous (24 h) incubation led to a significant reduction of cells in G0/G1 and accumulation in G2 phase. Western Blot Analysis Cell Line:Breast cancer cell lines MCF-10F, MCF-7 and MDA-MB-231 Concentration:1 μM for MCF-10F and MDA-MB-231 cells, 4 μM for MCF-7 cells Incubation Time:48 hours Result:Bax protein expression was upregulated in MCF-10F and MDA-MB-231 cell lines but MCF-7 cells did not show any significant increase. Caspase-8 gene expression was upregulated in MCF-10F, but it was downregulated in MCF-7 and MDA-MB-231 cells.
  • 体内实验
    Animal Model:Female MF1 nu/nu mice bearing MDA-G8 breast tumor xenograft (6-week-old)Dosage:Doxorubicin (2 mg/kg); Zoledronic acid (100 μg/kg)Administration:Intravenous injection; once a week; 6 weeks Result:Moderate inhibition of subcutaneous tumor growth in mice that were treated with 2 mg/kg Doxorubicin alone or with 100 μg/kg Zoledronic acid alone compared to the saline control.Mice treated with Zoledronic acid and Doxorubicin together had statistically significant smaller mean tumor volumes on day 42 than those treated with Doxorubicin alone.Animal Model:Male Sprague-Dawley rats Dosage:1%, 2%, 4%, 5%, 6%, 10%, 20% Administration:Intrastriatal injection; Single dose Result:In doses of 4, 5, 6, 10 or 20% caused obvious loss of ipsilateral SNc and VTA neuronsz and doses of 1 or 2% failed to produce obvious neuron loss.
  • 同义词
    DOX
  • 通路
    Cell Cycle/DNA Damage
  • 靶点
    Topoisomerase
  • 受体
    Topo II
  • 研究领域
    Cancer
  • 适应症
    ——

化学信息

  • CAS Number
    25316-40-9
  • 分子量
    579.99
  • 分子式
    C27H29NO11·HCl
  • 纯度
    >98% (HPLC)
  • 溶解度
    Water: 20 mg/mL (34.48 mM); DMSO: 100 mg/mL warmed (172.41 mM)
  • SMILES
    C[C@H]1[C@H]([C@H](C[C@@H](O1)O[C@H]2C[C@@](CC3=C(C4=C(C(=C23)O)C(=O)C5=C(C4=O)C=CC=C5OC)O)(C(=O)CO)O)N)O.Cl
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Sun W, et al. Y Res, 2009, 69(10), 4294-4300.
产品手册
关联产品
  • Genz-644282

    Genz-644282,一种用于癌症治疗的新型非喜树碱拓扑异构酶 I 抑制剂。

  • Topovale

    Topovale 是拓扑异构酶 I 的有效抑制剂。Topovale 抑制缺氧介导的缺氧诱导因子 1α 的积累。

  • Nalidixic acid

    Nalidixic Acid 是一种合成的 1,8-萘啶抗菌剂,杀菌谱有限。