2980-32-7

Usage

Uses

Used in Pharmaceutical Industry:
DESMETHYLBELLIDIFOLIN is used as an α-glucosidase inhibitor for managing and treating diabetes. As an inhibitor, it helps regulate the rate at which carbohydrates are broken down into glucose, thus controlling blood sugar levels and providing a potential therapeutic approach for diabetes management.

InChI:InChI=1/C13H8O6/c14-5-3-8(17)10-9(4-5)19-13-7(16)2-1-6(15)11(13)12(10)18/h1-4,14-17H

Upstream product

• 2798-25-6 bellidifolin 
• 552-00-1 1,3,8-trihydroxy-5-methoxy-9H-xanthen-9-one 
• 521-65-3 methylbellidifolin 
• 103726-10-9 5,8-dihydroxy-1,3-dimethoxy-9H-xanthen-9-one 
• 108-73-6 3,5-dihydroxyphenol 
• 60241-74-9 2,3,6-trimethoxybenzoic acid 
• 5653-53-2 6-hydroxy-2,3-dimethoxy-benzoic acid 
• 13909-60-9 1-(2,3,6-trimethoxy-phenyl)-ethanone 
• 303-07-1 2,6-Dihydroxybenzoic acid 
• 6052-93-3 1,3,8-trihydroxyxanthone 
• 135-77-3 1,2,4-trimethoxy-benzene 
• 25245-34-5 1-bromo-2,5-dimethoxybenzene 
• 22248-13-1 1-(6-hydroxy-2,3-dimethoxyphenyl)ethan-1-one 
• 103726-17-6 C₄₁H₂₄O₁₀ 

Downstream Products

• 49599-09-9 1,8-dihydroxy-3,5,8-trimethoxyxanthone 
• 552-00-1 1,3,8-trihydroxy-5-methoxy-9H-xanthen-9-one 
• 521-65-3 methylbellidifolin 
• 103726-10-9 5,8-dihydroxy-1,3-dimethoxy-9H-xanthen-9-one 
• 103726-23-4 5-benzyloxy-1,3,8-trihydroxy-9H-xanthen-9-one 
• 103726-17-6 C₄₁H₂₄O₁₀ 
• 54954-12-0 bellidin 8-O-β-glucopyranoside 
• 103726-25-6 5-benzyloxy-3,8-dihydroxy-1-methoxy-9H-xanthen-9-one 
• 103726-21-2 1,3,5-tribenzoyloxy-8-hydroxy-9H-xanthen-9-one 
• 2798-25-6 bellidifolin 

Relevant academic research and scientific papers

Method for preparing 1,3,5,8-tetrahydroxy xanthone and 1,3,7,8-tetrahydroxy xanthone

The invention discloses a method for preparing 1,3,5,8-tetrahydroxy xanthone and 1,3,7,8-tetrahydroxy xanthone. The method comprises the following steps: by taking 1,2,4-trimetoxybenzene as an initialraw material, and adding n-butyllithium and a chloro-ca

A bellidifodin preparing method

A bellidifodin preparing method is disclosed. The method includes preparing methanesulfonic acid and phosphorus pentoxide according to a ratio into a composite medium, adding 2,6-dihydroxybenzoic acid and phloroglucinol into the medium, performing a reaction to obtain 1,3,8-trihydroxy xanthenone, performing selective oxidation under alkaline conditions through using potassium persulfate to obtain 1,3,5,8-tetrahydroxy xanthenone, and subjecting the 1,3,5,8-tetrahydroxy xanthenone and iodomethane to methylation to obtain the target compound that is the bellidifodin. According to the method, reaction steps are shortened, reaction operation is simplified, the yield is increased and the method has certain application value.