2-Deoxy-d-riboside

95%

Reagent Code: #167191
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CAS Number 22900-10-3

science Other reagents with same CAS 22900-10-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 134.13 g/mol
Formula C₅H₁₀O₄
badge Registry Numbers
MDL Number MFCD00075730
thermostat Physical Properties
Boiling Point 332.1±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.516±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used in biochemical research and pharmaceutical development, particularly in the synthesis of nucleoside analogs for antiviral and anticancer drugs. Serves as a key intermediate in the preparation of modified nucleosides that mimic natural substrates in DNA replication, helping to inhibit viral polymerases or disrupt tumor cell proliferation. Also employed in enzymatic and metabolic studies to understand nucleotide metabolism and enzyme mechanisms. Its structural role in forming stable glycosidic bonds makes it valuable in designing therapeutic oligonucleotides and prodrugs.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,640.00
inventory 5g
10-20 days ฿11,900.00
inventory 25g
10-20 days ฿35,210.00
inventory 100g
10-20 days ฿92,400.00
inventory 250mg
10-20 days ฿1,780.00

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2-Deoxy-d-riboside
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Used in biochemical research and pharmaceutical development, particularly in the synthesis of nucleoside analogs for antiviral and anticancer drugs. Serves as a key intermediate in the preparation of modified nucleosides that mimic natural substrates in DNA replication, helping to inhibit viral polymerases or disrupt tumor cell proliferation. Also employed in enzymatic and metabolic studies to understand nucleotide metabolism and enzyme mechanisms. Its structural role in forming stable glycosidic bonds m

Used in biochemical research and pharmaceutical development, particularly in the synthesis of nucleoside analogs for antiviral and anticancer drugs. Serves as a key intermediate in the preparation of modified nucleosides that mimic natural substrates in DNA replication, helping to inhibit viral polymerases or disrupt tumor cell proliferation. Also employed in enzymatic and metabolic studies to understand nucleotide metabolism and enzyme mechanisms. Its structural role in forming stable glycosidic bonds makes it valuable in designing therapeutic oligonucleotides and prodrugs.

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