2'',4''-Di-O-(Z-p-coumaroyl)afzelin

2'',4''-Di-O-(Z-p-coumaroyl)afzelin - Names and Identifiers

Name	2'',4''-Di-O-(Z-p-coumaroyl)afzelin
Synonyms	-Di-O-(Z-p-couMaroyl)afzelin 2'',4''-Di-O-(Z-p-coumaroyl)afzelin 4H-1-Benzopyran-4-one, 3-[[6-deoxy-2,4-bis-O-[(2Z)-3-(4-hydroxyphenyl)-1-oxo-2-propen-1-yl]-α-L-mannopyranosyl]oxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-
CAS	205534-17-4

2'',4''-Di-O-(Z-p-coumaroyl)afzelin - Physico-chemical Properties

Molecular Formula	C39H32O14
Molar Mass	724.66
Density	1.58±0.1 g/cm3(Predicted)
Boling Point	966.9±65.0 °C(Predicted)
Appearance	Yellow powder
pKa	6.20±0.40(Predicted)
Storage Condition	2-8℃

2'',4''-Di-O-(Z-p-coumaroyl)afzelin - Introduction

2 '',4''-Di-O-(Z-p-coumaroyl)afzelin is a natural plant secondary metabolite, which belongs to flavonoids. Its chemical structure contains two Z-type coumarin derived groups.

2 '',4''-Di-O-(Z-p-coumaroyl)afzelin has antioxidant, anti-inflammatory and anti-tumor activities in plants. It can inhibit tumor growth by interfering with the proliferation and apoptosis pathways of cancer cells. In addition, it also has antibacterial, antiviral and antithrombotic biological activity.

The method for preparing 2 '',4''-Di-O-(Z-p-coumaroyl)afzelin is generally extracted from plants and purified to obtain pure products. Some commonly used plant sources include Inula, Triple, and Caceae, among others.

As for safety information, there are no clinical or toxicological data on 2 '',4''-Di-O-(Z-p-coumaroyl)afzelin. However, as a natural product, use should follow appropriate laboratory safety practices and care should be taken to avoid inhalation, ingestion, or skin contact. At the same time, if necessary, further evaluation and screening are required on a case-by-case basis. Use caution when using or handling this material.

Last Update：2024-04-09 22:09:11