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Home > Biochemical Engineering > Nucleoside Drugs (Find 346 items)

Nucleoside Drugs

5-Fluorouridine

(77180-80-4)
Intermediates, genetic engineering and biochemical reagents used in the production of anti-tumor drugs DFUR and FUDR, etc.

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N4-Benzoylcytosine

(26661-13-2)
Antitumor and antiviral drug intermediates, Sofibuvir intermediates

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2′,3′,5′-Tri-O-acetyluridine

(4105-38-8)
Uridine triacetate (Tri-O-acetyl uridine) is an orally active prodrug of Uridine. Uridine triacetate (Tri-O-acetyl uridine) is lipophilic, is quickly absorbed in the gut, and is rapidly deacetylated in the circulation to yield free uridine. Uridine triacetate (Tri-O-acetyl uridine) is uesd for the prevention and treatment of life-threatening 5-fluorouracil and capecitabine toxicity. Uridine triacetate (Tri-O-acetyl uridine) delivers high concentrations of uridine, which competes with tox

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2-Fluoroadenine

(700-49-2)
A purine nucleoside phosphorylase gene therapy for human malignancy.

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2′-O-Methyluridine

(2140-76-3)
Uridine analog. Used for preparation of antiviral nucleoside derivatives as inhibitors of subgenomic hepatitis C virus RNA replication.

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2-Fluoroadenosine

(146-78-1)
Used as intermediate of drug fludarabine

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Nucleoside drugs are an important class of drugs used clinically to treat viral infectious diseases, tumors, and AIDS. Nearly 50% of the currently used antiviral drugs are nucleoside drugs, and the antitumor drugs Cytarabine, Doxifluridine, etc. also belong to the nucleoside class. Nucleoside and deoxynucleoside series derivatives have a variety of biologically active substances, which can be used directly or indirectly as drugs, and play an extremely important role in the treatment of a variety of major diseases.
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