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CAS RN: 75607-67-9 | 產品號碼: F0913
Fludarabine Monophosphate
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| 產品號碼 | F0913 |
純度/分析方法 
|
>98.0%(T)(HPLC) |
| 分子式 / 分子量 | C__1__0H__1__3FN__5O__7P = 365.21 |
| 外觀與形狀（20°C） | Solid |
| 儲存條件
|
Room Temperature (Recommended in a cool and dark place, <15°C) |
| 儲存在惰性氣體下 | Store under inert gas |
| 應避免的情況 | Hygroscopic |
| 包裝和容器
|
100MG-Glass Bottle with Plastic Insert （閲覽圖片）, 25MG-Glass Bottle with Plastic Insert （閲覽圖片） |
| CAS RN | 75607-67-9 |
| Reaxys-RN | 8167686 |
| PubChem Substance ID | 253660324 |
| Merck Index(14) | 4126 |
| MDL編號 | MFCD00866418 |
產品規格
| Appearance | White to Almost white powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Purity(Neutralization titration) | min. 98.0 % |
| Specific rotation [a]20/D | +11.0 to +13.0 deg(C=0.5, H2O) |
性質
| 熔點 | 203 °C(dec.) |
| 比旋光 [α]D | 12° (C=0.5,H2O) |
| Degree of solubility in water | 8.9 g/l 20 °C |
| 溶解性（不溶於） | Ethanol, Ether |
GHS
| 圖形表示 |
|
| 信號詞 | Warning |
| 危險性說明 | H302 : Harmful if swallowed. H361 : Suspected of damaging fertility or the unborn child. H362 : May cause harm to breast-fed children. H373 : May cause damage to organs through prolonged or repeated exposure. |
| 防範說明 | P501 : Dispose of contents/ container to an approved waste disposal plant. P263 : Avoid contact during pregnancy/ while nursing. P260 : Do not breathe dust/ fume/ gas/ mist/ vapors/ spray. P270 : Do not eat, drink or smoke when using this product. P202 : Do not handle until all safety precautions have been read and understood. P201 : Obtain special instructions before use. P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection. P308 + P313 : IF exposed or concerned: Get medical advice/ attention. P301 + P312 + P330 : IF SWALLOWED: Call a POISON CENTER/doctor if you feel unwell. Rinse mouth. P405 : Store locked up. |
相關法規
| RTECS # | UO7440900 |
運輸資料
| HS編碼* | 2934.99-000 |
Application
Fludarabine phosphate (2-F-ara-AMP): An Inhibitor of DNA Synthesis
Fludarabine phosphate (2-F-ara-AMP) is an adenine nucleoside analog that is converted first to 9-β-D-arabinofuranosyl-2-fluoradenine (2-F-ara-A) and then into the active metabolite 2-F-ara-A triphosphate (F-ara-ATP). The triphosphate inhibits the synthesis of primer RNA and DNA by DNA polymerase primase complex, and also induces cell death through apoptosis. Fludarabine phosphate shows activity against chronic lymphocytic leukemia (CLL) and indolent lymphoma. (The product is for research purpose only.)
References
- Termination of DNA synthesis by 9-β-D-arabinofuranosyl-2-fluoroadenine. A mechanism for cytotoxicity
- Inhibition of the 3'→5' exonuclease of human DNA polymerase ε by fludarabine-terminated DNA
- The role of fludarabine-induced apoptosis and cell cycle synchronization in enhanced murine tumor radiation response in vivo
- Differential induction of apoptosis by fludarabine monophosphate in leukemic B and normal T cells in chronic lymphocytic leukemia
- In vitro cytotoxic effects of fludarabine (2-F-ara-A) in combination with commonly used antileukemic agents by isobologram analysis
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