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Home > Biochemical Engineering > Nucleoside Drugs (Find 69 items)

Nucleoside Drugs

2,6-Dichloropurine

(5451-40-1)
2,6-Dichloropurine is used in the synthesis of 2,6-diamino-substituted purine derivatives as potential cardiomyogenesis inducing agents.

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2,6-Diaminopurine

(1904-98-9)
Used as an intermediate in organic synthesis

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2'-DEOXYGUANOSINE

(312693-72-4)

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2,2′-Anhydrouridine

(3736-77-4)
Research tool for antiviral and anticancer studies.1

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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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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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