(S)-2-Amino-3-(5-(tert-butyl)-3-(phosphonomethoxy)isoxazol-4-yl)propanoic acid

95%

Reagent Code: #235753
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CAS Number 252930-37-3

science Other reagents with same CAS 252930-37-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 322.25 g/mol
Formula C₁₁H₁₉N₂O₇P
badge Registry Numbers
MDL Number MFCD32200403
thermostat Physical Properties
Boiling Point 569.2±60.0 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of antiviral agents, particularly in prodrugs targeting hepatitis B virus (HBV). Its phosphonate group enables mimicry of nucleotide monophosphates, allowing incorporation into viral DNA chains and causing chain termination. The (S)-amino acid moiety supports cellular uptake via amino acid transporters, enhancing delivery to hepatocytes. This compound plays a key role in developing nucleotide analogs with improved metabolic stability and targeted antiviral activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿40,000.00
inventory 50mg
10-20 days ฿56,000.00
inventory 100mg
10-20 days ฿96,000.00
(S)-2-Amino-3-(5-(tert-butyl)-3-(phosphonomethoxy)isoxazol-4-yl)propanoic acid
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Used as an intermediate in the synthesis of antiviral agents, particularly in prodrugs targeting hepatitis B virus (HBV). Its phosphonate group enables mimicry of nucleotide monophosphates, allowing incorporation into viral DNA chains and causing chain termination. The (S)-amino acid moiety supports cellular uptake via amino acid transporters, enhancing delivery to hepatocytes. This compound plays a key role in developing nucleotide analogs with improved metabolic stability and targeted antiviral activit

Used as an intermediate in the synthesis of antiviral agents, particularly in prodrugs targeting hepatitis B virus (HBV). Its phosphonate group enables mimicry of nucleotide monophosphates, allowing incorporation into viral DNA chains and causing chain termination. The (S)-amino acid moiety supports cellular uptake via amino acid transporters, enhancing delivery to hepatocytes. This compound plays a key role in developing nucleotide analogs with improved metabolic stability and targeted antiviral activity.

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