N-(N-(((2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)carbamoyl)carbamimidoyl)formamide

95%

Reagent Code: #215043
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CAS Number 65126-88-7

science Other reagents with same CAS 65126-88-7

blur_circular Chemical Specifications

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Weight 262.22 g/mol
Formula C₈H₁₄N₄O₆
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in biochemical research as an intermediate in nucleotide metabolism studies, particularly in the synthesis of modified nucleosides and antiviral agents. It serves as a building block in the development of pharmaceuticals targeting RNA viruses due to its structural similarity to natural nucleotide components. Also employed in enzymatic assays to investigate the activity of amidotransferases and other enzymes involved in purine and pyrimidine pathways. Its functional groups allow for conjugation in prodrug designs, enhancing cellular uptake and targeted delivery.

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inventory 25mg
10-20 days ฿648,000.00

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N-(N-(((2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)carbamoyl)carbamimidoyl)formamide
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Used in biochemical research as an intermediate in nucleotide metabolism studies, particularly in the synthesis of modified nucleosides and antiviral agents. It serves as a building block in the development of pharmaceuticals targeting RNA viruses due to its structural similarity to natural nucleotide components. Also employed in enzymatic assays to investigate the activity of amidotransferases and other enzymes involved in purine and pyrimidine pathways. Its functional groups allow for conjugation in pr

Used in biochemical research as an intermediate in nucleotide metabolism studies, particularly in the synthesis of modified nucleosides and antiviral agents. It serves as a building block in the development of pharmaceuticals targeting RNA viruses due to its structural similarity to natural nucleotide components. Also employed in enzymatic assays to investigate the activity of amidotransferases and other enzymes involved in purine and pyrimidine pathways. Its functional groups allow for conjugation in prodrug designs, enhancing cellular uptake and targeted delivery.

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