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Doxorubicin hydrochloride试剂

参考价900.00-1600.00
具体成交价以合同协议为准
  • 公司名称杭州昊鑫生物科技股份有限公司
  • 品       牌MCE
  • 型       号HY-15142
  • 所  在  地杭州市
  • 厂商性质代理商
  • 更新时间2023/5/22 15:23:43
  • 访问次数169
产品标签:

盐酸adriamycin

规格
10 mM * 1 mL in DMSO990.00元10000 支可售
50 mg900.00元10000 支可售
100 mg1600.00元10000 支可售
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杭州昊鑫生物科技股份有限公司成立于2009年初,是一家面向生命科学领域,从事科研机构、高校、院所及生产企业所需科研试剂、耗材,仪器销售和服务面向全国。

产品和服务涵盖生命科学研究技术的诸多方面,提供覆盖分子生物学、细胞生物学、植物学、生物化学、蛋白组学、免疫学等领域的实验产品以及生物技术服务等。目前一级代理品牌有:MCE(Medchemexpress)、Biochannel、AATbio、invivogen、Abnova、Atlas、Origene、Biovision、云克隆(Cloud-clone)、艾德莱(Aidlab)、Cayman、Jackson、Epigentek、Prospec、Sciencell、icellbioscience(赛百慷)、hkABCbio、chondrex、Mybiosource、Abbexa、Innovrsrch、HPI、Hitobiotec、Greerlabs,Ostex,4ADI,LDN等。

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胎牛血清、MCE抑制剂激动剂、RNA提取试剂盒、ELISA试剂盒、重组蛋白
产地 进口 级别 其他
Doxorubicin hydrochloride试剂 是一种具有细胞毒性的蒽环类抗生素,是一种抗癌HL试剂。Doxorubicin hydrochloride 是一种有效的人类 DNA topoisomerase I 和 topoisomerase II 抑制剂,IC50 分别为 0.8 μM 和 2.67 μM。Doxorubicin hydrochlo
Doxorubicin hydrochloride试剂 产品信息

注:本产品仅用于科研,不可用于临床


生物活性

Doxorubicin (Hydroxydaunorubicin) hydrochloride, a cytotoxic anthracycline antibiotic, is an anti-cancer chemotherapy agent. Doxorubicin hydrochloride is a potent human DNA topoisomerase I and topoisomerase II inhibitor with IC50s of 0.8 μM and 2.67 μM, respectively. Doxorubicin hydrochloride reduces basal phosphorylation of AMPK and its downstream target acetyl-CoA carboxylase. Doxorubicin hydrochloride induces apoptosis and autophagy[1][2][3].

IC50 & Target[1][2][3]








Topoisomerase I

0.8 μM (IC50)

Topoisomerase II

2.67 μM (IC50)

Daunorubicins/Doxorubicins

HIV-1

体外研究
(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[4].
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[5].
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[4].

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

Cell Viability Assay[4]

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 hours
Result:IC50 was 1 μM for both MCF-10F and MDA-MB-231 cell lines.
IC50 was 4 μM for MCF-7 cell line.
体内研究
(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[6].

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

Animal Model:Female MF1 nu/nu mice bearing MDA-G8 breast tumor xenograft (6-week-old)[6]
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.
Clinical Trial
NCT NumberSponsorConditionStart DatePhase
NCT04535713Sarcoma Oncology Research Center, LLC
Sarcoma
September 30, 2020Phase 2
NCT01078441National Cancer Institute (NCI)
Refractory Multiple Myeloma
September 2010Phase 2
NCT01796197Dana-Farber Cancer Institute
Breast Cancer
August 2013Phase 2
分子量

579.98

性状

Solid

Formula

C27H30ClNO11

CAS 号

25316-40-9

中文名称


结构分类
  • Quinones

  • Anthraquinones

来源

Streptomyces peucetius var. Caesius

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture and light

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

溶解性数据
In Vitro:

DMSO : 35.71 mg/mL (61.57 mM; ultrasonic and warming and heat to 60°C)

H2O : 20 mg/mL (34.48 mM; Need ultrasonic)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM1.7242 mL8.6210 mL17.2420 mL
5 mM0.3448 mL1.7242 mL3.4484 mL
10 mM0.1724 mL0.8621 mL1.7242 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.


    请依序添加每种溶剂: 5% DMSO    40% PEG300    5% Tween-80    50% saline

    Solubility: ≥ 2.75 mg/mL (4.74 mM); Clear solution


  • 2.


    请依序添加每种溶剂: 10% DMSO    40% PEG300    5% Tween-80    45% saline

    Solubility: ≥ 2.08 mg/mL (3.59 mM); Clear solution


  • 3.


    请依序添加每种溶剂: 10% DMSO    90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.08 mg/mL (3.59 mM); Clear solution



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