1-((2R,5S)-2-(Hydroxymethyl)-1,3-oxathiolan-5-yl)pyrimidine-2,4(1H,3H)-dione

98%

Reagent Code: #229018
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CAS Number 145986-07-8

science Other reagents with same CAS 145986-07-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.24 g/mol
Formula C₈H₁₀N₂O₄S
inventory_2 Storage & Handling
Storage -20°C, Sealed

description Product Description

Used in the treatment of viral infections, particularly as an antiretroviral agent against HIV and hepatitis B. It functions as a nucleoside reverse transcriptase inhibitor (NRTI), interfering with the viral replication process by incorporating into viral DNA and causing chain termination. This compound is a key component in certain antiviral therapies, helping to reduce viral load and slow disease progression in patients with HIV/AIDS and chronic hepatitis B. Its structural configuration allows for improved selectivity and reduced toxicity compared to earlier analogs, making it valuable in combination drug regimens.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿39,980.00

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1-((2R,5S)-2-(Hydroxymethyl)-1,3-oxathiolan-5-yl)pyrimidine-2,4(1H,3H)-dione
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Used in the treatment of viral infections, particularly as an antiretroviral agent against HIV and hepatitis B. It functions as a nucleoside reverse transcriptase inhibitor (NRTI), interfering with the viral replication process by incorporating into viral DNA and causing chain termination. This compound is a key component in certain antiviral therapies, helping to reduce viral load and slow disease progression in patients with HIV/AIDS and chronic hepatitis B. Its structural configuration allows for impr

Used in the treatment of viral infections, particularly as an antiretroviral agent against HIV and hepatitis B. It functions as a nucleoside reverse transcriptase inhibitor (NRTI), interfering with the viral replication process by incorporating into viral DNA and causing chain termination. This compound is a key component in certain antiviral therapies, helping to reduce viral load and slow disease progression in patients with HIV/AIDS and chronic hepatitis B. Its structural configuration allows for improved selectivity and reduced toxicity compared to earlier analogs, making it valuable in combination drug regimens.

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