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CAS RN: 147-94-4 | Product Number: C2035
Cytarabine
 
									 
							Purity: >98.0%(T)(HPLC)
Synonyms:
						
						- 4-Amino-1-β-D-arabinofuranosyl-2(1H)-pyrimidinone
- Arabinocytidine
- Cytosine β-D-Arabinofuranoside
- Ara-C
Product Documents:
                    
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|---|---|---|---|---|---|
| 1G | 
                                                $31.00 | ≥40 | 27 | Contact Us | |
| 5G | 
                                                $104.00 | 9 | 15 | Contact Us | 
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Supplemental Product Information:
This product is a sample for RUO (research use only). Do not use this product for any purpose other than testing and research.
| Product Number | C2035 | 
| Purity / Analysis Method   | >98.0%(T)(HPLC) | 
| Molecular Formula / Molecular Weight | C__9H__1__3N__3O__5 = 243.22 | 
| Physical State (20 deg.C) | Solid | 
| Storage Temperature   | Room Temperature (Recommended in a cool and dark place, <15°C) | 
| Packaging and Container   | 1G-Glass Bottle with Plastic Insert (View image) | 
| CAS RN | 147-94-4 | 
| Related CAS RN   | 69-74-9 | 
| Reaxys Registry Number | 89175 | 
| PubChem Substance ID | 87558791 | 
| Merck Index (14) | 2784 | 
Specifications
		  | Appearance | White to Almost white powder to crystal | 
| Purity(HPLC) | min. 98.0 area% | 
| Purity(Nonaqueous Titration) | min. 98.0 % | 
| Specific rotation [a]20/D | +155.0 to +162.0 deg(C=1, H2O) | 
| NMR | confirm to structure | 
		Properties (reference)
	| Melting Point | 214 °C | 
| Specific Rotation | 158° (C=1,H2O) | 
| Maximum Absorption Wavelength | 272 nm (H__2O) | 
| Solubility in water | Soluble | 
 
						 GHS
						  
								 Related Laws: 
							   | RTECS# | HA5425000 | 
 
						Transport Information:
							| H.S.code* | 2934.99-000 | 
			Application
		
			Cytarabine (ara-C): D-Arabinosyl Nucleoside exhibiting Anti-Leukemia and Anti-DNA Virus Activities
		
		Certain D-arabinosyl nucleosides, notably cytarabine (ara-C) and vidarabine (ara-A) [V0098] are used as an anti-leukemia agent and an anti-DNA virus agent. Ara-C and ara-A are cell cycle phase-specific antineoplastic agents, affecting cells only during the S-phase of cell division. Intracellularly, ara-C and ara-A are converted into the 5-triphosphates (ara-CTP and ara-ATP), which are the active metabolites. The mechanism of actions are not completely understood, but it appear that ara-CTP and ara-ATP act through the inhibition of tumor cell or virus-induced DNA polymerases, competing with dCTP and dATP, respectively. Incorporation of them into DNA and RNA also contribute to their cytotoxicity. (The product is for research purpose only.)
References
- The mechanisms of lethal action of arabinosyl cytosine (araC) and arabinosyl adenine (araA) (a review)
- Ara-C: cellular and molecular pharmacology (a review)
- Acute Myeloid Leukemia (a review)
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