CAS No. : 3992-42-5
(Synonyms: 2'-Deoxycytidine monohydrochloride; Deoxycytidine hydrochloride; NSC 83251)
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| Cat. No. : | HY-17564 |
| M.Wt: | 263.68 |
| Formula: | C9H14ClN3O4 |
| Purity: | >98 % |
| Solubility: | H2O : ≥ 41 mg/mL;DMSO : 25 mg/mL (ultrasonic;warming;heat to 80°C) |
2'-Deoxycytidine hydrochloride is an orally effective nucleic acid biosynthesis enzyme inhibitor. 2'-Deoxycytidine hydrochloride competes with nucleic acid biosynthesis enzymes and nucleoside transporters, thereby reducing the toxicity of cytarabine. 2'-Deoxycytidine (hydrochloride) can be used in the research of L1210 lymphoblastic leukemia[1].
In Vivo:2'-Deoxycytidine (hydrochloride) (40-480 mg/kg; p.o.; three/four times daily; 4-18 days) co-administration completely prevents araC-induced lethal toxicity in normal mice, partially or fully protects most hematopoietic cell lineages except bone marrow lymphocytes, and normalizes araC-induced cellular immune suppression without reversing araC's humoral immune suppression[1].
2'-Deoxycytidine (hydrochloride) (360-480 mg/kg; p.o.; three/four times daily; days 5-26) co-administration prevents araC-induced lethal toxicity in leukemia-bearing mice, maintains or enhances araC's antitumor efficacy against L1210 lymphoblastic leukemia, and reduces araC's antitumor effect against non-lymphoid Graffi MG and Rauscher ER leukemias[1].
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