Ambeed.cn

首页 / / / 拓扑异构酶 / Mitoxantrone dihydrochloride

盐酸米托蒽醌 /Mitoxantrone dihydrochloride 99%+

货号:A166750 同义名: 米托蒽醌二盐酸盐 / Mitozantrone dihydrochloride;NSC 301739 dihydrochloride Ambeed 开学季,买赠积分,赢豪礼

Mitoxantrone 2HCl is an inhibitor of type II topoisomerase with antineoplastic activity.

Mitoxantrone dihydrochloride 化学结构 CAS号:70476-82-3
Mitoxantrone dihydrochloride 化学结构
CAS号:70476-82-3
Mitoxantrone dihydrochloride 3D分子结构
CAS号:70476-82-3
Mitoxantrone dihydrochloride 化学结构 CAS号:70476-82-3
Mitoxantrone dihydrochloride 3D分子结构 CAS号:70476-82-3
规格 价格 会员价 库存 数量
{[ item.pr_size ]}

{[ getRatePrice(item.pr_rmb, 1,1) ]}

{[ getRatePrice(item.pr_rmb_sale, 1,1) ]}

{[ getRatePrice(item.pr_rmb, 1,1) ]}

{[ getRatePrice(item.pr_rmb,item.pr_rate,1) ]}
{[ getRatePrice(item.pr_rmb, 1,1) ]} {[ getRatePrice(item.pr_rmb_sale, 1,1) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate) ]} 现货 咨询 - +
购物车0 收藏 询单

Mitoxantrone dihydrochloride 纯度/质量文件 产品仅供科研

货号:A166750 标准纯度: 99%+
批次查询: 批次纯度:

全球学术期刊中引用的产品

Cell,2024. Ambeed. [ A125712 ]
Cancer Discov., 2024. Ambeed. [ A285925 ]
JMC, 2024. Ambeed. [ A288696 ]
JMC, 2024. Ambeed. [ A524399 , A633512 , A144280 , A174613 ]
EJNMMI Radiopharm. Chem., 2024, 9, 61. Ambeed. [ A1257961 , A622068 ]
更多 >
产品名称 Topo I Topo II Topo IV Topoisomerase 其他靶点 纯度
Ellagic acid 99%+
β-Lapachone 99%+
(s)-10-hydroxycamptothecin 99%+
Camptothecin ++

Topo I, IC50: 0.68 μM

98%
Betulinic acid ++

Eukaryotic topoisomerase I, IC50: 5 μM

99%+
Topotecan ++++

Topo I (DU-145 Luc cells), IC50: 2 nM

Topo I (MCF-7 Luc cells), IC50: 13 nM

99%+
Irinotecan HCl Trihydrate 98%
SN-38 98%
Levofloxacin hydrate 99%+
Dexrazoxane 99%+
Ofloxacin 98+%
Enoxacin 99%+
Flumequine +

Topo II, IC50: 15 μM

99%+
Levofloxacin 99%+
Etoposide 98%
Pefloxacin mesylate dihydrate 99+%
Marbofloxacin 99%+
Voreloxin HCl 98%
Mitoxantrone dihydrochloride PKC 99%+
Nalidixic acid 99%+
Doxorubicin 98%
Novobiocin sodium 98%+
Amonafide 99%+
Pirarubicin 98%+
Idarubicin HCl +++

Topo II (MCF-7 cells), IC50: 3.3 ng/mL

99%+
Genistein EGFR 98%
Teniposide 98%
Moxifloxacin 98%
Ciprofloxacin 99%+
Clinafloxacin 97%
Gatifloxacin 99%+
Daunorubicin HCl +++

DNA synthesis, Ki: 20 nM

98%
Epirubicin HCl 99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Mitoxantrone dihydrochloride 生物活性

靶点
  • Topo II

描述 Mitoxantrone dihydrochloride is a potent topoisomerase II inhibitor. It is also showed inhibitory effect on protein kinase C (PKC) activity with IC50=8.5μM. Mitoxantrone inhibited PKC in a competitive manner with respect to histone H1 (Ki=6.3μM) and in a non-competitive manner with respect to phophatidylserine and ATP[3]. Mitoxantrone dihydrochloride (0.5 μg/mL, 48 h) induces a decrease in B-CLL cells. Mitoxantrone dihydrochloride induces DNA fragmentation and the proteolytic cleavage of poly(ADP-ribose) polymerase (PARP), demonstrating that the cytotoxic effect of Mitoxantrone dihydrochloride is due to induction of apoptosis[4]. Mitoxantrone dihydrochloride (IP, 0-3.2 mg/kg/day) produces a statistically significant number of 60-day survivors at 1.6 mg/kg in mice with IP implanted L1210 leukemia. Mitoxantrone dihydrochloride (IV, 0-3.2 mg/kg/day) shows effective antitumor activities and produces a 60% ILS (increase in lifespan) at 3.2 mg/kg in SC implanted Lewis lung carcinoma[5].

Mitoxantrone dihydrochloride 细胞研究

细胞系 浓度 检测类型 检测时间 活动说明 数据源
A2780-cell Growth inhibition assay Concentration required to inhibit A2780-cell growth by 50%, IC50=0.55 nM 9703471
A549 cells Function assay Activity against A549 cancer cell line, IC50=3.1 nM 8960558
CCRF-CEM cells Cytotoxicity assay 48 h Cytotoxicity against human CCRF-CEM cells assessed as cell viability after 48 hrs by celltiter-blue assay, IC50=0.036 μM 22582991
CH1 cell Cytotoxicity assay Cytotoxic potency required to inhibit CH1 cell growth by 50%, IC50=2.65 nM 9371240

Mitoxantrone dihydrochloride 临床研究

NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT00004001 Prostate Cancer Phase 3 Completed - United States, Arizona ... 展开 >> CCOP - Scottsdale Oncology Program Scottsdale, Arizona, United States, 85259-5404 United States, Florida Mayo Clinic Jacksonville, Florida, United States, 32224 United States, Illinois CCOP - Illinois Oncology Research Association Peoria, Illinois, United States, 61602 CCOP - Carle Cancer Center Urbana, Illinois, United States, 61801 United States, Iowa CCOP - Cedar Rapids Oncology Project Cedar Rapids, Iowa, United States, 52403-1206 CCOP - Iowa Oncology Research Association Des Moines, Iowa, United States, 50309-1016 Siouxland Hematology-Oncology Sioux City, Iowa, United States, 51101-1733 United States, Minnesota Mayo Clinic Cancer Center Rochester, Minnesota, United States, 55905 CentraCare Health Plaza Saint Cloud, Minnesota, United States, 56303 United States, Nebraska CCOP - Missouri Valley Cancer Consortium Omaha, Nebraska, United States, 68106 United States, North Dakota Medcenter One Health System Bismarck, North Dakota, United States, 58501 CCOP - Merit Care Hospital Fargo, North Dakota, United States, 58122 Altru Health System Grand Forks, North Dakota, United States, 58201 United States, Pennsylvania CCOP - Geisinger Clinic and Medical Center Danville, Pennsylvania, United States, 17822-2001 United States, South Dakota Rapid City Regional Hospital Rapid City, South Dakota, United States, 57709 CCOP - Sioux Community Cancer Consortium Sioux Falls, South Dakota, United States, 57104 收起 <<
NCT00002498 Breast Cancer Phase 2 Unknown - Netherlands ... 展开 >> Leiden University Medical Center Leiden, Netherlands, 2300 ZA St. Radboud University Hospital Nijmegen, Netherlands, 6500 HB 收起 <<
NCT00219908 Relapsing-Remitting Multiple S... 展开 >>clerosis 收起 << Phase 2 Terminated - France ... 展开 >> Hôpital Cote de Nacre Caen, France, 14033 Hôpital Gabriel Montpied Clermont-Ferrand, France, 63003 CHU Henri Mondor Creteil, France, 94000 Hôpital Général Dijon, France, 21033 CHU Limoges Limoges, France, 87042 Institut Catholique de Lille Lomme, France, 59462 Pierre Weitheimer Hospital Lyon, France, 69394 Chu Timone Marseille, France, 13385 Centre Guy de Chauliac Montpellier, France, 34295 CHU Hôpital Central Nancy, France, 54035 CHU Nice, France, 06000 CHU Pitié-Salpétrière Paris, France, 75013 Hôpital Saint-Anne Paris, France, 75014 Centre Fondation Rotschild Paris, France, 75019 Tenon Hospital Paris, France, 759170 CHU Strasbourg Strasbourg, France, 67000 CHU Purpan Toulouse, France, 31059 Italy Psichiatriche dell'Università di Bari, Policlinico Bari, Italy, 70122 Dipartimento di Scienze Neurologiche e Psichiatriche Firenze, Italy, 50134 Hospedal Civile Gallarate, Italy, 21013 Neuroriabilitazione dell'Università Genova, Italy, 16132 Fondazionz SAN Raffaele del monte tabor Milano, Italy, 20132 Clinica Neurologica Università di Torino Torino, Italy, 10126 收起 <<

Mitoxantrone dihydrochloride 参考文献

[1]Seitz M. Molecular and cellular effects of methotrexate. Curr Opin Rheumatol. 1999 May;11(3):226-32.

[2]Hirata S, Matsubara T, et al. Inhibition of in vitro vascular endothelial cell proliferation and in vivo neovascularization by low-dose methotrexate. Arthritis Rheum. 1989 Sep;32(9):1065-73.

[3]Takeuchi N, Nakamura T, Takeuchi F, Hashimoto E, Yamamura H. Inhibitory effect of mitoxantrone on activity of protein kinase C and growth of HL60 cells. J Biochem. 1992;112(6):762-767.

[4]Bellosillo B, Colomer D, Pons G, Gil J. Mitoxantrone, a topoisomerase II inhibitor, induces apoptosis of B-chronic lymphocytic leukaemia cells. Br J Haematol. 1998;100(1):142-146. 

[5]Fujimoto S, Ogawa M. Antitumor activity of mitoxantrone against murine experimental tumors: comparative analysis against various antitumor antibiotics. Cancer Chemother Pharmacol. 1982;8(2):157-162.

Mitoxantrone dihydrochloride 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.93mL

0.39mL

0.19mL

9.66mL

1.93mL

0.97mL

19.33mL

3.87mL

1.93mL

Mitoxantrone dihydrochloride 技术信息

CAS号70476-82-3
分子式C22H30Cl2N4O6
分子量 517.4
别名 米托蒽醌二盐酸盐 ;Mitozantrone dihydrochloride;NSC 301739 dihydrochloride;NSC 301739;NCI 301739;Mitoxantrone (hydrochloride);Mitozantrone 2HCl;NSC-301739 2HCl;Mitoxantrone 2HCl
运输蓝冰
存储条件

粉末 Keep in dark place,Inert atmosphere,Room temperature

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 30 mg/mL(57.98 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 100 mg/mL(193.27 mM),配合低频超声助溶

动物实验配方

PO 0.5% CMC-Na 30 mg/mL suspension

Ambeed 相关网站 Ambeed.cn Ambeed.com
Ambeed
关于我们
联系我们
资讯中心
网站地图
产品手册
  • 批次文件查询
  • 客户支持
    专业术语
    缩略词释义
    质量手册
    产品咨询
    计算器
    活动政策
    订购方法
    活动声明
    联系我们
    400-920-2911 sales@ambeed.cn tech@ambeed.cn
    Ambeed 只为有资质的科研机构、医药企业基于科学研究或药证申报的用途提供医药研发服务,不为任何个人或者非科研性质用途提供服务。