(2S,3S,4S,5R,6S)-6-[5-(2,5-dimethylphenoxy)-2,2-bis(trideuteriomethyl)pentanoyl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid

98 atom % D

Reagent Code: #221179
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CAS Number 1703747-47-0

science Other reagents with same CAS 1703747-47-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 432.49 g/mol
Formula C₂₁H₂₄D₆O₉
thermostat Physical Properties
Melting Point 74-79 °C
inventory_2 Storage & Handling
Storage -20°C, Sealed, Inert Gas

description Product Description

Used in pharmaceutical research as a deuterated analog in metabolic stability studies, particularly for probing the pharmacokinetics and degradation pathways of similar ester-containing compounds. The trideuteriomethyl groups enhance resistance to oxidative metabolism, making it valuable in designing more durable drug candidates. Its structural complexity supports investigations into glycoside ester transformations and enzyme-substrate interactions in carbohydrate-based biochemistry.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿38,300.00

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(2S,3S,4S,5R,6S)-6-[5-(2,5-dimethylphenoxy)-2,2-bis(trideuteriomethyl)pentanoyl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid
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Used in pharmaceutical research as a deuterated analog in metabolic stability studies, particularly for probing the pharmacokinetics and degradation pathways of similar ester-containing compounds. The trideuteriomethyl groups enhance resistance to oxidative metabolism, making it valuable in designing more durable drug candidates. Its structural complexity supports investigations into glycoside ester transformations and enzyme-substrate interactions in carbohydrate-based biochemistry.

Used in pharmaceutical research as a deuterated analog in metabolic stability studies, particularly for probing the pharmacokinetics and degradation pathways of similar ester-containing compounds. The trideuteriomethyl groups enhance resistance to oxidative metabolism, making it valuable in designing more durable drug candidates. Its structural complexity supports investigations into glycoside ester transformations and enzyme-substrate interactions in carbohydrate-based biochemistry.

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