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5-Fluorouracil试剂

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  • 型号

    HY-90006

  • 品牌

    MCE

  • 厂商性质

    代理商

  • 所在地

    杭州市

规格

10 mM * 1 mL in DMSO 500元 10000可售

200 mg 350元 10000可售

1 g 450元 10000可售

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更新时间:2023-05-30 11:28:54浏览次数:211次

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CAS号 51-21-8 产地 进口
级别 其他
5-Fluorouracil试剂 是一种uracil的类似物 (nucleoside antimetabolite/analog),是一种有效的抗肿瘤药。5-Fluorouracil 通过抑制胸苷酸合成酶影响嘧啶的合成,从而耗尽细胞内dTTP 池。5-Fluorouracil 诱导细胞凋亡 (apoptosis),可用作化学敏化剂。

5-Fluorouracil试剂简介

5-Fluorouracil (5-FU) 是一种uracil的类似物 (nucleoside antimetabolite/analog),是一种有效的抗肿瘤药。5-Fluorouracil 通过抑制胸苷酸合成酶影响嘧啶的合成,从而耗尽细胞内dTTP 池。5-Fluorouracil 诱导细胞凋亡 (apoptosis),可用作化学敏化剂。5-Fluorouracil 还可抑制 HIV 病毒。5-Fluorouracil (5-FU) 可破坏外泌体特异性的 rRNA。






5-Fluorouracil试剂生物活性

5-Fluorouracil (5-FU) is an analogue of uracil and a potent antitumor agent. 5-Fluorouracil affects pyrimidine synthesis by inhibiting thymidylate synthetase thus depleting intracellular dTTP pools. 5-Fluorouracil induces apoptosis and can be used as a chemical sensitizer[1][2]. 5-Fluorouracil also inhibits HIV[3].

IC50 & Target[1][6]


HIV

体外研究
(In Vitro)

5-Fluorouracil (5-Fu) and NSC 123127 (Dox) show synergistic anticancer efficacy. The IC50 value of 5-Fu/Dox-DNM toward human breast cancer (MDA-MB-231) cells is 0.25 μg/mL, presenting an 11.2-fold and 6.1-fold increase in cytotoxicity compared to Dox-DNM and 5-Fu-DNM, respectively[1]. In 5-fluorouracil (5-FU) and CDDP treated NFBD1-inhibited NPC cells, the NFBD1 expression in NPC CNE1 cell lines is depleted using lentivirus-mediated short hairpin RNA, and the sensitivity of these cells is elevated. NFBD1 knockdown leads to an obvious induction of apoptosis in CDDP- or 5-FU-treated CNE1 cells[2].

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

体内研究
(In Vivo)

5-Fluorouracil (23 mg/kg, 3 times/week) for 14 days, induces accelerated gastrointestinal transit associated with acute intestinal inflammation at day 3 after the start of treatment, which may have led to persistent changes in the ENS observed after days 7 and 14 of treatment contributing to delayed gastrointestinal transit and colonic dysmotility[4].

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

分子量

130.08

性状

Solid

Formula

C4H3FN2O2

CAS 号

51-21-8

中文名称

5-氟脲嘧啶;双喃呋啶

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

溶解性数据
In Vitro:

DMSO : 50 mg/mL (384.38 mM; Need ultrasonic)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM7.6876 mL38.4379 mL76.8758 mL
5 mM1.5375 mL7.6876 mL15.3752 mL
10 mM0.7688 mL3.8438 mL7.6876 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 (protect from 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: 10% DMSO    40% PEG300    5% Tween-80    45% saline

    Solubility: ≥ 2.5 mg/mL (19.22 mM); Clear solution


  • 2.


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

    Solubility: ≥ 2.5 mg/mL (19.22 mM); Clear solution


  • 3.


    请依序添加每种溶剂: 10% DMSO    90% corn oil

    Solubility: ≥ 2.5 mg/mL (19.22 mM); Clear solution


  • 4.


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

    Solubility: ≥ 2.5 mg/mL (19.22 mM); Clear solution


  • 5.


    请依序添加每种溶剂: 5% DMSO    95% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.5 mg/mL (19.22 mM); Clear solution


  • 6.


    请依序添加每种溶剂: 5% DMSO  95% saline

    Solubility: 2.5 mg/mL (19.22 mM); Clear solution; Need ultrasonic





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