Original Factory Uracil 1-β-D-Arabinofuranoside - 2′-Deoxycytidine CAS 951-77-9 Purity ≥99.0% (HPLC) High Purity – Ruifu
Original Factory Uracil 1-β-D-Arabinofuranoside - 2′-Deoxycytidine CAS 951-77-9 Purity ≥99.0% (HPLC) High Purity – Ruifu Detail:
Manufacturer Supply Deoxynucleosides Intermediates with High Purity and Stable Quality
2′-Deoxyguanosine monohydrate CAS: 961-07-9 | 2′-Deoxyadenosine CAS: 958-09-8 |
2′-Deoxyuridine CAS: 951-78-0 | 2′-Deoxycytidine CAS: 951-77-9 |
5-Iodo-2′-Deoxyuridine CAS: 54-42-2 |
Chemical Name | 2′-Deoxycytidine |
CAS Number | 951-77-9 |
CAT Number | RF-PI206 |
Stock Status | In Stock, Production Scale Up to Hundreds of Kilograms |
Molecular Formula | C9H13N3O4 |
Molecular Weight | 227.22 |
Brand | Ruifu Chemical |
Item | Specifications |
Appearance | White or Almost White Crystalline Powder |
Heavy Metals | ≤20ppm |
Loss on Drying | ≤0.50% |
Residue on Ignition | ≤0.20% |
Purity / Analysis Method | ≥99.0% (HPLC) |
Test Standard | Enterprise Standard |
Package: Bottle, Aluminum foil bag, Cardboard drum, 25kg/Drum, or according to customer’s requirement.
Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture and pest infestation.
2-Deoxycytidine is a cytidine analog. 2′-Deoxycytidine is a deoxyribonucleoside as Eg5 kinesin modulator with apoptosis-inducing and antiproliferative activity.
2-Deoxycytidine prevents DNA methylation by incorporating itself into newly synthesizing DNA strand. 2-Deoxycytidine also binds to DNA methyltransferase irreversibly and hinders its activity. Thus, 2-deoxycytidine was approved as the most efective demethylating agent for the treatment of cancer .
2-Deoxycytidine at clinically achievable and nontoxic concentrations (≥ 100 μmol/L) protected normal bone marrow progenitor cells against the inhibitory effects of co-administered, high concentrations of 3’-azido-3’-deoxythymidine (AZT) (≥ 10 μmol/L). In normal bone marrow mononuclear cells (BMMC), 2-deoxycytidine also significantly corrected AZT-mediated depletion of intracellular thymidine triphosphate and 2-deoxycytidine triphosphate levels. Furthermore, 2-deoxycytidine reduced the intracellular accumulation of AZT triphosphate and its DNA incorporation in BMMC.
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