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CAS RN: 75607-67-9 | Product Number: F0913
Fludarabine Monophosphate
Purity: >98.0%(T)(HPLC)
Synonyms:
- 2-Fluoroadenine 9-β-D-Arabinofuranoside 5'-Monophosphate
- 9-(β-D-Arabinofuranosyl)-2-fluoroadenine 5'-Monophosphate
- 2-F-ara-AMP
Product Documents:
Size | Unit Price | Saitama (Kawaguchi) | Hyogo (Amagasaki) | Stock in other WH | Shipping Information |
---|---|---|---|---|---|
25MG |
¥7,900
|
4 | 2 | Contact Us | |
100MG |
¥22,600
|
4 | It can be shipped from Saitama warehouse on the same day* | 10 |
* Available Stock: Prompt shipment (for products) in Saitama/Hyogo warehouse. Stock In Other WH: Shipment in about 2-3 Business Days from Saitama warehouse. Please contact us
if you need further information.
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*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
* The displayed price is the unit price and does not include consumption tax. The unit prices displayed are the latest and are subject to change without notice.
* To send your quote request for bulk quantities, please click on the "Request Bulk Quote" button. Please note that we cannot offer bulk quantities for some products.
*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
Product Number | F0913 |
Purity / Analysis Method | >98.0%(T)(HPLC) |
Molecular Formula / Molecular Weight | C__1__0H__1__3FN__5O__7P = 365.21 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Hygroscopic |
Packaging and Container | 100MG-Glass Bottle with Plastic Insert (View image), 25MG-Glass Bottle with Plastic Insert (View image) |
CAS RN | 75607-67-9 |
Reaxys Registry Number | 8167686 |
PubChem Substance ID | 253660324 |
Merck Index (14) | 4126 |
MDL Number | MFCD00866418 |
Specifications
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) |
Properties (reference)
Melting Point | 203 °C(dec.) |
Specific Rotation | 12° (C=0.5,H2O) |
Degree of solubility in water | 8.9 g/l 20 °C |
Solubility (insoluble in) | Ethanol, Ether |
GHS
Pictogram | |
Signal Word | Warning |
Hazard Statements | 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. |
Precautionary Statements | 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. |
Related Laws:
RTECS# | UO7440900 |
Transport Information:
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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