(2R,3S,4S,5R)-2-(6-Amino-9H-purin-9-yl)-4-fluoro-5-(hydroxymethyl)tetrahydrofuran-3-ol

≥95%

Reagent Code: #43857
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CAS Number 75059-22-2

science Other reagents with same CAS 75059-22-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.23 g/mol
Formula C₁₀H₁₂FN₅O₃
badge Registry Numbers
MDL Number MFCD20134043
thermostat Physical Properties
Boiling Point 628.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a modified nucleoside, often incorporated into the development of antiviral and anticancer drugs. Its fluorinated structure enhances its ability to inhibit viral replication by interfering with the synthesis of viral DNA or RNA. This makes it a valuable component in the design of treatments for viral infections, particularly those caused by DNA viruses. Additionally, its potential to disrupt cellular processes in rapidly dividing cells has led to its exploration in cancer therapy, where it may act as a chemotherapeutic agent. Researchers also study its role in understanding enzyme mechanisms and nucleotide metabolism, contributing to advancements in biochemistry and molecular biology.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿31,563.00
inventory 10mg
10-20 days ฿12,618.00

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(2R,3S,4S,5R)-2-(6-Amino-9H-purin-9-yl)-4-fluoro-5-(hydroxymethyl)tetrahydrofuran-3-ol
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a modified nucleoside, often incorporated into the development of antiviral and anticancer drugs. Its fluorinated structure enhances its ability to inhibit viral replication by interfering with the synthesis of viral DNA or RNA. This makes it a valuable component in the design of treatments for viral infections, particularly those caused by DNA viruses. Additionally, its potential to disrupt cel
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a modified nucleoside, often incorporated into the development of antiviral and anticancer drugs. Its fluorinated structure enhances its ability to inhibit viral replication by interfering with the synthesis of viral DNA or RNA. This makes it a valuable component in the design of treatments for viral infections, particularly those caused by DNA viruses. Additionally, its potential to disrupt cellular processes in rapidly dividing cells has led to its exploration in cancer therapy, where it may act as a chemotherapeutic agent. Researchers also study its role in understanding enzyme mechanisms and nucleotide metabolism, contributing to advancements in biochemistry and molecular biology.
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