Enocitabine (Synonyms: 依诺他滨)
目录号: PL02607 纯度: ≥98%
CAS No. :55726-47-1
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中文名称
Enocitabine
中文别名
依诺他滨;山嵛阿糖嘧啶;N-[1-[3,4-二羟基-5-(羟甲基)氧杂环戊-2-基]-2-氧代嘧啶-4-基]山嵛酸酰胺;6-[[5-氟-2-[(3,4,5-三甲氧基苯基)氨基]-4-嘧啶基]氨基]-2,2-二甲基-4-[(磷酰氧)甲基]-2H-吡啶并[3,2-B]-1,4-恶嗪-3(4H)-酮二钠盐六水合物;Enocitabine 抑制剂;山嵛阿糖啶
英文名称
Enocitabine
英文别名
Enocitabine;N-[1-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-oxopyrimidin-4-yl]docosanamide;N-(1-BETA-D-ARABINOFURANOSYL-1,2-DIHYDRO-2-OXO-4-PYRIMIDINYL)DOCOSANAMIDE;BEHENOYLCYTOSINE ARABINOSIDE;BH-AC;ENOCITABINE ANTINEOPLASTIC DRUGS;n(sup4)-behenoylcytosinearabinoside;N4-Behenoylcytosine arabinoside;SUNRABIN
Cas No.
55726-47-1
分子式
C31H55N3O6
分子量
565.78
包装储存
Powder -20°C 3 years;In solvent -80°C 6 months
产品详情
Enocitabine 是一种核苷类似物,是一种有效的 DNA 复制抑制剂和 DNA链终止剂。Enocitabine 抑制人巨细胞病毒的复制,具有抗白血病和抗病毒活性。
生物活性
Enocitabine is a nucleoside analog, and is a potent DNA replication inhibitor, and a DNA chain terminator. Enocitabine inhibits the replication of human cytomegalovirus. Enocitabine has antileukemic and antiviral activities.
性状
Solid
IC50 & Target[1][2]
DNA replication; CMV
体外研究(In Vitro)
Enocitabine is resistant to deamination because Enocitabine bears a highly lipophilic group at the 4-amino position of the cytosine moiety of cytarabine.
The combined effects of Pirarubicin and Enocitabine on HeLa S3 human uterine cervix carcinoma and K562 human myelocytic leukemia cells are determined by enhancement of their cytotoxic activities. Enocitabine or etoposide shows synergistic effects on HeLa S3 and K562 cells.
In the presence of Enocitabine, triphosphate forms of the nucleoside analogs are detected in the human cytomegalovirus (HCMV)-infected cells, and synthesis of HCMV DNA is strongly suppressed. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;In solvent -80°C 6 months
参考文献
[1]. Hamada A, et al. Clinical pharmacokinetics of cytarabine formulations.Clin Pharmacokinet. 2002;41(10):705-18.
[2]. Nagasawa M, et al.In vitro combined effects of pirarubicin (THP) and various antitumor drugs on human tumor cell lines. Gan To Kagaku Ryoho. 1990 Apr;17(4 Pt 1):633-8.
[3]. Nakamura K, et al. Antiv
溶解度数据
In Vitro: DMSO : 2 mg/mL (3.53 mM; ultrasonic and warming and heat to 60°C)H2O : < 0.1 mg/mL (ultrasonic;warming;heat to 60°C) (insoluble)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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