Ganciclovir
(Synonyms: 更昔洛韦; BW 759; 2'-Nor-2'-deoxyguanosine) 目录号 : GC11331
An antiviral drug that is effective against CMV
Cas No.:82410-32-0
Sample solution is provided at 25 µL, 10mM.
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Quality Control & SDS
- View current batch:
- Purity: >99.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
| Cell experiment [1]: | |
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Cell lines |
BV-2 mouse microglial cells |
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Preparation method |
The solubility of this compound in DMSO is > 10 mM. General tips for obtaining a higher concentration: Please warm the tube at 37 °C for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below - 20 °C for several months. |
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Reacting condition |
0 ~ 1250 μM; 24 hrs |
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Applications |
In BV-2 mouse microglial cells, Ganciclovir inhibited cell proliferation in a dose-dependent manner in the absence of HSVtk, without causing significant cell death at the indicated concentrations. It was implied that Ganciclovir targeted activated microglia at least in part via a mechanism independent of endogenous thymidine kinase (tk). |
| Animal experiment [1]: | |
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Animal models |
C57BL/6 mice |
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Dosage form |
25 or 100 mg/kg; i.p. |
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Applications |
In C57BL/6 mice, Ganciclovir inhibited the proliferation of microglia induced by experimental autoimmune encephalomyelitis (EAE). Ganciclovir attenuated neuroinflammation in a dose-depedent manner without significantly restraining the peripheral immune response. In addition, it was found that Ganciclovir accumulated in the brains of EAE mice but not those of naive mice to exert localized effects. |
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Other notes |
Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal. |
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References: [1]. Ding Z, Mathur V, Ho PP, James ML, Lucin KM, Hoehne A, Alabsi H, Gambhir SS, Steinman L, Luo J, Wyss-Coray T. Antiviral drug ganciclovir is a potent inhibitor of microglial proliferation and neuroinflammation. J Exp Med. 2014 Feb 10; 211(2):189-98. |
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Ganciclovir (DHPG) is a potent antiviral drug used to treatment of cytomegalovirus (CMV) infections [1].
Ganciclovir (DHPG) is a nucleoside analogue and has shown the activity against viral thymidine kinase (tk) in the Herpesviridae family, including human cytomegalovirus and herpes simplex virus types I and II as well as Epstein-Barr virus. In addition, Ganciclovir has been reported to inhibit the proliferation of uninfected cells, most significantly of bone marrow cells, because of the function of inhibiting viral replication. Apart from these, Ganciclovir has been revealed to reduce the activation of microglial in wild-type C57BL/6 mice and inhibit proliferation of microglial in wild-type FvB mice [1].
References:
[1] Ding Z1, Mathur V, Ho PP, James ML, Lucin KM, Hoehne A, Alabsi H, Gambhir SS, Steinman L, Luo J, Wyss-Coray T. Antiviral drug ganciclovir is a potent inhibitor of microglial proliferation and neuroinflammation. J Exp Med. 2014 Feb 10; 211(2):189-98.
| Cas No. | 82410-32-0 | SDF | |
| 别名 | 更昔洛韦; BW 759; 2'-Nor-2'-deoxyguanosine | ||
| 化学名 | 2-amino-9-(1,3-dihydroxypropan-2-yloxymethyl)-3H-purin-6-one | ||
| Canonical SMILES | C1=NC2=C(N1COC(CO)CO)NC(=NC2=O)N | ||
| 分子式 | C9H13N5O4 | 分子量 | 255.23 |
| 溶解度 | >50mg/mL in DMSO (Need ultrasonic) | 储存条件 | Store at 2-8°C |
| General tips | 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 储存时，请在 6 个月内使用，-20°C 储存时，请在 1 个月内使用。 为了提高溶解度，请将管子加热至37℃，然后在超声波浴中震荡一段时间。 |
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| Shipping Condition | 评估样品解决方案：配备蓝冰进行发货。所有其他可用尺寸：配备RT，或根据请求配备蓝冰。 | ||
| 制备储备液 | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 3.918 mL | 19.5902 mL | 39.1803 mL |
| 5 mM | 0.7836 mL | 3.918 mL | 7.8361 mL |
| 10 mM | 0.3918 mL | 1.959 mL | 3.918 mL |
| 第一步：请输入基本实验信息（考虑到实验过程中的损耗，建议多配一只动物的药量） | ||||||||||
| 给药剂量 | mg/kg |  |
动物平均体重 | g | |
每只动物给药体积 | ul | |
动物数量 | 只 |
| 第二步：请输入动物体内配方组成（配方适用于不溶于水的药物；不同批次药物配方比例不同，请联系GLPBIO为您提供正确的澄清溶液配方） | ||||||||||
| % DMSO % % Tween 80 % saline | ||||||||||
| 计算重置 | ||||||||||
计算结果:
工作液浓度： mg/ml；
DMSO母液配制方法： mg 药物溶于 μL DMSO溶液（母液浓度 mg/mL，
体内配方配制方法：取 μL DMSO母液，加入 μL PEG300，混匀澄清后加入μL Tween 80，混匀澄清后加入 μL saline，混匀澄清。
1. 首先保证母液是澄清的；
2.
一定要按照顺序依次将溶剂加入，进行下一步操作之前必须保证上一步操作得到的是澄清的溶液，可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。