19879-30-2

Usage

Uses

Used in Pharmaceutical Industry:
BAVACHININ A is used as a therapeutic agent for the treatment of diabetes. It improves insulin-dependent glucose uptake by activating AMPK signaling, which aids in better management of blood sugar levels.
Additionally, BAVACHININ A is used as a PPARγ agonist, which plays a crucial role in the treatment of diabetes by regulating glucose metabolism and insulin sensitivity.

InChI:InChI=1/C21H22O4/c1-13(2)4-5-15-10-17-18(23)11-20(14-6-8-16(22)9-7-14)25-21(17)12-19(15)24-3/h4,6-10,12,20,22H,5,11H2,1-3H3

Upstream product

• 128961-19-3 7-methoxy-2-(4-(methoxymethoxy)phenyl)-6-(3-methylbut-2-en-1-yl)chroman-4-one 
• 123-08-0 4-hydroxy-benzaldehyde 
• 6515-21-5 4-methoxymethoxy-benzaldehyde 
• 552-41-0 1-(2-hydroxy-4-methoxyphenyl)ethanone 
• 128961-25-1 1-(4-methoxy-2-((3-methylbut-2-en-1-yl)oxy)phenyl)ethan-1-one 
• 28448-83-1 2′-hydroxyl-4′-methoxyl-5′-isopentenylacetophenone 
• 129097-15-0 2-(4-hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-en-1-yl)chroman-4-one 
• 128961-13-7 (E)-1-(2-hydroxy-4-methoxy-5-(3-methylbut-2-en-1-yl)phenyl)-3-(4-(methoxymethoxy)phenyl)prop-2-en-1-one 
• 20784-60-5 (E)-1-(2-hydroxy-4-methoxy-5-(3-methylbut-2-en-1-yl)phenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one 

Relevant academic research and scientific papers

2-phenylchroman-4-one derivatives and antiviral composition comprising the same

The present invention relates to a 2-phenylchroman-4-one derivative or a pharmaceutically acceptable salt thereof, a method for manufacturing the same, and a therapeutic agent for MERS containing the same as an active component. A compound containing the

Synthesis method of active component of Chinese herb psoralea corylifolia

The invention relates to a synthesis method of an active component of a Chinese herb psoralea corylifolia. The synthesis method comprises the following steps: (a), mixing paeonol, 1-bromo-3-methyl-2-butene and acetone, adding potassium carbonate, and then

Separation and peroxisome proliferator-activated receptor-γ agonist activity evaluation of synthetic racemic bavachinin enantiomers

Abstract Bavachinin, isolated from Psoralea corylifolia seeds, has been reported to demonstrate peroxisome proliferator-activated receptor-γ (PPAR-γ) agonist activity. However, isolated bavachinin is actually a mixture of S and R configurations, with an e

Isolation of chalkones from the seeds of Psoralea corylifolia Linn.

Isolation and characterization of a new chalkone namely 4,2′-dihydroxy-2″-(1?-methyl ethyl)-2′-3″- dihydro-(4″,5″,3′,4′) furano chalkone 1 along with a known chalkone 4,2′-dihydroxy-4′-methoxy-5′-(3?, 3?-dimethyl allyl)-chalkone 2 have been carried out from the seeds of the desert variety of Psoralea corylifolia Linn on the basis of spectral data analysis i.e. IR, 1H NMR, mass and chemical reactions.

An Improved Procedure for Cyclisation of Chalcones to Flavanones Using Celite Supported Potassium Fluoride in Methanol: Total Synthesis of Bavachinin

Chalcones may be cyclised to the corresponding flavanones by stirring with KF - celite suspended in methanol at reflux.This method gives consistently higher conversion than other reported procedures and its utility is illustrated by the synthesis of the l