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| Product | Description | |
|---|---|---|
| 2'-Chloro-2'-deoxycytidine | 2'-Chloro-2'-deoxycytidine is a nucleoside analogue, orchestrating its antineoplastic prowess via impeding DNA synthesis and evoking apoptosis exclusively within malignant cells. Synonyms: 2'-Deoxy-2'-chloro-cytidine; 4-Amino-1-((2R,3R,4R,5R)-3-chloro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one. Grades: ≥95%. CAS No. 10212-19-8. Molecular formula: C9H12ClN3O4. Mole weight: 261.66. |  |
| 2'-Chloro-2'-deoxycytidine | 2'-Chloro-2'-deoxycytidine is a nucleoside derivative. Group: Biochemicals. Grades: Highly Purified. CAS No. 10212-19-8. Pack Sizes: 5mg, 10mg. Molecular Formula: C9H12ClN3O4, Molecular Weight: 261.66. US Biological Life Sciences. |  Worldwide |
| 5-Chloro-2'-deoxycytidine | 5-Chloro-2'-deoxycytidine. Group: Biochemicals. Grades: Highly Purified. CAS No. 32387-56-7. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C9H12CIN3O4. US Biological Life Sciences. | Worldwide |
| 5-Chloro-5'-deoxy-2',3'-O-isopropylidenecytidine | 5-Chloro-5'-deoxy-2',3'-O-isopropylidenecytidine, a remarkable antiviral agent, showcases immense potential in the realm of viral infection therapy. Specifically, it displays its efficacy against RNA viruses like hepatitis C and respiratory syncytial virus (RSV). Facilitating the obstruction of viral RNA replication, its mechanism prevents viral escalation and obstructs the progression of associated diseases. Synonyms: 2',3'-O-Isopropylidene-5-chlorocytidine; 5-Chloro-5'-deoxy-2',3'-O-isopropylidene-D-cytidine; 5-Chloro-2',3'-O-isopropylidene-5'-deoxycytidine. Molecular formula: C12H16ClN3O4. Mole weight: 301.73. | |
| Cytochlor | Cytochlor is a radio-sensitizing pyrimidine nucleoside with potential antineoplastic activity. Cytochlor is metabolized first to a phosphate derivative, CldCMP, by the enzyme deoxycytidine kinase and then to the active uracyl derivative, CldUMP, by the enzyme dCMP deaminase; deoxycytidine kinase and dCMP deaminase have been found in abnormally high concentrations in most cancers. CldUMP, the active metabolite, incorporates into DNA and, upon exposure to radiation, induces the formation of uracil radicals and double-strand DNA breaks. Synonyms: 5-Chloro-2'-deoxycytidine; 5-Chlorodeoxycytidine; 2'-Deoxy-5-chlorocytidine; NSC-371331; NSC 371331. Grades: ≥ 97%. CAS No. 32387-56-7. Molecular formula: C9H12ClN3O5. Mole weight: 261.66. | |
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