52222-74-9

52222-74-9 - Names and Identifiers

Name	Kaempferol-4'-glucoside Kaempferol-4'-O-β-D-glucopyranoside
Synonyms	-O-β-D-glucopyranoside KAEMPFEROL-4'-GLUCOSIDE KaeMpferol-4'-glucoside Kaempferol 4'-O-glucoside Kaempferol 4'-beta-glucoside KaeMpferol-4'-O-β-D-glucopyranoside KAEMPFEROL-4'-O-Β-D-GLUCOPYRANOSIDE KaeMpferol-4'-O-beta-D-glucopyranoside Kaempferol-4'-glucoside Kaempferol-4'-O-β-D-glucopyranoside
CAS	52222-74-9

52222-74-9 - Physico-chemical Properties

Molecular Formula	C21H20O11
Molar Mass	448.38
Density	1.736
Melting Point	223-225℃
Boling Point	784.5±60.0 °C(Predicted)
Solubility	Slightly soluble in water, soluble in hot ethanol, ether and alkali.
Appearance	Powder
pKa	6.32±0.40(Predicted)
Storage Condition	2-8℃
MDL	MFCD27951973

52222-74-9 - Reference

Reference

1. [IF=6.576] Junkun Pan et al."Inhibition of Dipeptidyl Peptidase-4 by Flavonoids: Structure–Activity Relationship, Kinetics and Interaction Mechanism."Frontiers in Nutrition. 2022; 9: 892426

52222-74-9 - Introduction

Kaempferol-4 '-glucosides; Kaempferol-4'-o-β-D-glucopyranosides (Kaempferol-4; Kaempferol-4 '-o-β-D-glucopyranosides) is a plant compound that belongs to the class of flavonoids. It consists of kaempferol and glucose molecules linked by O-glycosidic bonds.

Nature:
-Appearance: White or light yellow crystalline powder.
-Solubility: Soluble in hot water, ethanol and dimethyl sulfoxide, slightly soluble in ether and chloroform.

Use:
-pharmacological effects: Kaempferol-4 '-glucoside; Kaempferol-4'-o-β-D-glucopyranoside has antioxidant, anti-inflammatory, antibacterial, anti-tumor and anti-cancer and other pharmacological effects. It has a certain preventive and therapeutic effect on cardiovascular diseases, inflammatory diseases and tumors.
-Herbal Application: Kaempferol-4 '-glucoside; Kaempferol-4'-o-β-D-glucopyranoside is found in a variety of plants, such as aloe, tea, onion, etc. These plants are widely used in traditional Chinese medicine preparations for the treatment of cardiovascular diseases, inflammation and tumors.

Method:
- Kaempferol-4 '-glucoside; Kaempferol-4'-o-β-D-glucopyranoside can be obtained by plant extraction, synthesis and enzymatic synthesis. The most common method is to extract kaempferol from plants, and then react with glucose molecules to form the Kaempferol-4 '-glucosides; Kaempferol-4'-o-β-D-glucopyranosides.

Safety Information:
Kaempferol-4 '-glucoside; Kaempferol-4'-o-β-D-glucopyranoside There are no clear reports of toxicity and pathogenicity. As a natural product, it is considered safe in general use. However, adverse reactions may be triggered if used in excess or if you are allergic to the substance. When using or applying, it is recommended to follow the relevant dosage guidelines and follow correct handling and safety precautions. If you feel uncomfortable during use, please consult a doctor in time.

Last Update：2024-04-09 20:45:29

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