57396-78-8

Usage

Uses

Used in Traditional Chinese Medicine:
BAICALEIN 7-O-B-D-GLUCOPYRANOSIDE (BAICALIN) is used as a therapeutic agent for its anti-inflammatory, antioxidant, and antiviral properties, contributing to the treatment of various health concerns.
Used in Immune System Regulation:
BAICALEIN 7-O-B-D-GLUCOPYRANOSIDE (BAICALIN) is used as an immune modulator to study its effects on the immune system, potentially enhancing its function and contributing to the prevention and treatment of diseases.
Used in Disease Treatment:
BAICALEIN 7-O-B-D-GLUCOPYRANOSIDE (BAICALIN) is used as a treatment for various diseases and conditions, such as cancer, cardiovascular diseases, and liver disorders, due to its potential therapeutic effects.
Used in Neuroprotection and Cognitive Function:
BAICALEIN 7-O-B-D-GLUCOPYRANOSIDE (BAICALIN) is used as a neuroprotective agent to investigate its role in cognitive function and the prevention of neurodegenerative diseases.

Upstream product

• 572-09-8 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl bromide 
• 82475-03-4 Baicalin methyl ester 
• 67-56-1 methanol 
• 21967-41-9 baicalin 
• 67047-06-7 7-(benzyloxy)-4-oxo-2-phenyl-4H-1-benzopyran-5,6-diyl diacetate 
• 67047-07-8 5,6-diacetoxy-7-hydroxyflavone 
• 67047-05-6 4-oxo-2-phenyl-4H-1-benzopyran-5,6,7-triyl triacetate 
• 74293-55-3 5,6-Diacetoxy-7-hydroxyflavon-7-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosid) 

Downstream Products

• 29550-13-8 5,6-dihydroxy-7-methoxyflavone 
• 491-67-8 5,6,7-trihydroxy-2-phenyl-4H-1-benzopyran-4-one 

Relevant academic research and scientific papers

A convenient and efficient approach to synthesize negletein from baicalin

A simple two-step/one-pot and highly efficient strategy for the synthesis of negletein from naturally abundant and inexpensive baicalin has been developed. In this one-pot sequence, esterification of baicalin catalyzed by concentrated H2SO

Development of a concise synthetic approach to access oroxin A

A novel environment-friendly method to access bioactive oroxin A through a one-pot/two-step process from naturally abundant and inexpensive baicalin is described. The procedure presented here has several advantages including clean, one-pot, synthetic ease, and large-scale feasibility. This work also provides a model strategy for rapid and diverse access to natural molecules sharing the common skeleton of this family.

Synthese von Baicalin und einiger anderer Baicalein-glycoside

The 6- and 7-O-β-glucopyranosides 14 and 7 and the 6- and 7-O-β-glucopyranosiduronic acids 18 and 9 of baicalein (1) have been synthesized. 9 was identical with baicalin but 14 and tetuin, further 18 and a "baicalin-6-glucuronide" from Oroxylum indicum were different.