5-Carboxy-2'-deoxyuridine

98%

Reagent Code: #97235
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Alias Trifluridine impurity A
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CAS Number 14599-46-3

science Other reagents with same CAS 14599-46-3

blur_circular Chemical Specifications

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Weight 272.21 g/mol
Formula C₁₀H₁₂N₂O₇
badge Registry Numbers
MDL Number MFCD22495153
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used primarily in biochemical research, this compound serves as a modified nucleoside for studying DNA repair mechanisms and nucleotide metabolism. It is often incorporated into DNA strands to investigate the effects of modified bases on DNA replication and repair processes. Additionally, it is utilized in the development of antiviral and anticancer drugs, where its incorporation into nucleic acids can inhibit the replication of viral or cancerous cells. The carboxyl group allows for further chemical modifications, making it valuable in the synthesis of nucleotide analogs for therapeutic and diagnostic applications.

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inventory 1mg
10-20 days ฿32,238.00

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5-Carboxy-2'-deoxyuridine
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Used primarily in biochemical research, this compound serves as a modified nucleoside for studying DNA repair mechanisms and nucleotide metabolism. It is often incorporated into DNA strands to investigate the effects of modified bases on DNA replication and repair processes. Additionally, it is utilized in the development of antiviral and anticancer drugs, where its incorporation into nucleic acids can inhibit the replication of viral or cancerous cells. The carboxyl group allows for further chemical mod

Used primarily in biochemical research, this compound serves as a modified nucleoside for studying DNA repair mechanisms and nucleotide metabolism. It is often incorporated into DNA strands to investigate the effects of modified bases on DNA replication and repair processes. Additionally, it is utilized in the development of antiviral and anticancer drugs, where its incorporation into nucleic acids can inhibit the replication of viral or cancerous cells. The carboxyl group allows for further chemical modifications, making it valuable in the synthesis of nucleotide analogs for therapeutic and diagnostic applications.

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