(2R,3S,5R)-5-(2-Amino-9H-purin-9-yl)-2-(hydroxymethyl)tetrahydrofuran-3-ol

97%

Reagent Code: #228956
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CAS Number 3616-24-8

science Other reagents with same CAS 3616-24-8

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Weight 251.24 g/mol
Formula C₁₀H₁₃N₅O₃
badge Registry Numbers
MDL Number MFCD01630951
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of antiviral drugs, particularly in the development of nucleoside analogs. These analogs are designed to inhibit viral replication by mimicking natural nucleosides, thereby interfering with viral RNA or DNA synthesis. It plays a key role in the production of medications targeting viruses such as HIV, hepatitis B, and hepatitis C. Its stereochemistry is critical for biological activity, ensuring proper binding to viral polymerases. Commonly utilized in pharmaceutical research and development for creating more effective and selective antiviral agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,440.00
inventory 250mg
10-20 days ฿15,990.00
inventory 1g
10-20 days ฿43,120.00

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(2R,3S,5R)-5-(2-Amino-9H-purin-9-yl)-2-(hydroxymethyl)tetrahydrofuran-3-ol
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Used as an intermediate in the synthesis of antiviral drugs, particularly in the development of nucleoside analogs. These analogs are designed to inhibit viral replication by mimicking natural nucleosides, thereby interfering with viral RNA or DNA synthesis. It plays a key role in the production of medications targeting viruses such as HIV, hepatitis B, and hepatitis C. Its stereochemistry is critical for biological activity, ensuring proper binding to viral polymerases. Commonly utilized in pharmaceutic

Used as an intermediate in the synthesis of antiviral drugs, particularly in the development of nucleoside analogs. These analogs are designed to inhibit viral replication by mimicking natural nucleosides, thereby interfering with viral RNA or DNA synthesis. It plays a key role in the production of medications targeting viruses such as HIV, hepatitis B, and hepatitis C. Its stereochemistry is critical for biological activity, ensuring proper binding to viral polymerases. Commonly utilized in pharmaceutical research and development for creating more effective and selective antiviral agents.

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