Dexelvucitabine (Synonyms: Reverset; d-d4FC)
目录号: PL10980 纯度: ≥99%
CAS No. :134379-77-4
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中文名称
Dexelvucitabine
中文别名
5-氟-1-(2',3'-二脱氧-2',3'-二脱氢β-D-呋喃阿糖基)-胞嘧啶(Dexelvucitabine)
英文名称
Dexelvucitabine
英文别名
Cytidine,2',3'-didehydro-2',3'-dideoxy-5-fluoro-;Dexelvucitabine;INCB 8721;2',3'-didehydro-2,3-dideoxy-5-fluorocytidine;D-D4FC;DFC;DPC 817;DPC-817;INCB-8721;RA 131423;Reverset;YZ-817
Cas No.
134379-77-4
分子式
C9H10N3O3F
分子量
227.19
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
Dexelbucitabine (Reverset; d-d4FC) 是一种胞苷 (HY-B0158) 类似物,一种具有口服活性的核苷逆转录酶 (nucleoside reverse transcriptase) 抑制剂。Dexelbucitabine 是一种有效的抗 HIV-1 病毒剂,这些病毒聚合酶中含有胸苷类似物和/或 M184V 突变。Dexelvucitabine 是一种 2'-脱氧胞苷抗逆转录病毒剂。
生物活性
Dexelvucitabine (Reverset; d-d4FC), a Cytidine (HY-B0158) analog, is an orally active nucleoside reverse transcriptase inhibitor. Dexelvucitabine is a powerful drug against HIV-1-resistant viruses containing a thymidine analog and/or M184V mutation in the viral polymerase. Dexelvucitabine is a 2′-Deoxycytidine antiretroviral agent.
性状
Solid
IC50 & Target[1][2]
HIV-1
体内研究(In Vivo)
Dexelvucitabine (Reverset; d-d4FC; 33.3 mg/kg by i.v. or p.o.) has distribution and elimination half-lives (t 1/2α  and t 1/2β , respectively) of 0.7 and 3.6 h in monkeys, respectively. The C max ranges from 21.1 to 47.5 μM.
Dexelvucitabine has a favorable pharmacokinetic profile with a long half-life (4.71 and 10.75 h after administration by the intravenous [i.v.] and oral [p.o.] routes, respectively) in woodchucks.
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;4°C 2 years
ClinicalTrial
参考文献
[1]. Brenda I Hernandez-Santiago, et al. Antiviral and cellular metabolism interactions between Dexelvucitabine and lamivudine. Antimicrob Agents Chemother. 2007 Jun;51(6):2130-5.
[2]. L Ma, et al. Pharmacokinetics of the antiviral agent beta-D-2,3-didehydro-2,3-dideoxy-5-fluorocytidine in rhesus monkeys. Antimicrob Agents Chemother. 1999 Feb;43(2):381-4.
溶解度数据
In Vitro: DMSO : 50 mg/mL (220.08 mM; Need ultrasonic)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。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2