N-[(1R,2R)-2-(1-pyrrolidinyl)cyclohexyl]-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-Thiourea

98%

Reagent Code: #70682
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CAS Number 942939-99-3

science Other reagents with same CAS 942939-99-3

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scatter_plot Molecular Information
Weight 557.66 g/mol
Formula C₂₅H₃₉N₃O₉S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of glycosidase inhibitors, which are crucial for studying carbohydrate metabolism and designing therapeutic agents for diseases like diabetes and viral infections. The thiourea moiety in the structure enhances its binding affinity to enzymes, making it valuable for enzyme inhibition studies. Additionally, its acetylated sugar component allows for selective deprotection and further functionalization, enabling the synthesis of complex glycoconjugates. These glycoconjugates are explored for their potential in drug delivery systems and as bioactive molecules in cancer research.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿19,620.00
inventory 10mg
10-20 days ฿4,914.00

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N-[(1R,2R)-2-(1-pyrrolidinyl)cyclohexyl]-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-Thiourea
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This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of glycosidase inhibitors, which are crucial for studying carbohydrate metabolism and designing therapeutic agents for diseases like diabetes and viral infections. The thiourea moiety in the structure enhances its binding affinity to enzymes, making it valuable for enzyme inhibition studies. Additionally, its acetylated sugar component allows for selective depr

This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of glycosidase inhibitors, which are crucial for studying carbohydrate metabolism and designing therapeutic agents for diseases like diabetes and viral infections. The thiourea moiety in the structure enhances its binding affinity to enzymes, making it valuable for enzyme inhibition studies. Additionally, its acetylated sugar component allows for selective deprotection and further functionalization, enabling the synthesis of complex glycoconjugates. These glycoconjugates are explored for their potential in drug delivery systems and as bioactive molecules in cancer research.

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