5143-05-5

Basic information

• Product Name: Gypsogenic acid
• Synonyms: Gypsogenic acid;PAIBKVQNJKUVCE-JUENUIDLSA-N
• CAS NO: 5143-05-5
• Molecular Formula: C₃₀H₄₆O₅
• Molecular Weight: 486.68324
• Mol File: 5143-05-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: -20°C Freezer
• Solubility: DMSO (Slightly), Methanol (Slightly)
• CAS DataBase Reference: Gypsogenic acid(CAS DataBase Reference)
• NIST Chemistry Reference: Gypsogenic acid(5143-05-5)
• EPA Substance Registry System: Gypsogenic acid(5143-05-5)

Safety Data

• Hazardous Substances Data: 5143-05-5(Hazardous Substances Data)

Usage

Description

Gypsogenic acid, a pentacyclic triterpenoid belonging to the Caryophyllaceae family, is a naturally occurring compound characterized by the presence of carboxy groups at positions 23 and 28 and a hydroxy group at position 3 (the 3beta stereoisomer). It is known for its potential applications in various fields due to its unique chemical structure and properties.

Uses

Used in Dental Applications:
Gypsogenic acid is used as an antiplaque and anticaries agent in the dental industry. Its effectiveness in reducing plaque and preventing dental caries makes it a promising candidate for the development of oral care products and treatments.
Used in Pharmaceutical Applications:
Gypsogenic acid, due to its triterpenoid saponin nature, may also find applications in the pharmaceutical industry. Its potential use in the development of new drugs or as a supplement to existing treatments could be explored, given its unique chemical structure and properties.

Upstream product

• 1207550-46-6 3-O-β-D-glucopyranosyl gypsogenic acid 28-O-α-D-galactopyranosyl-(1->6)-β-D-glucopyranosyl-(1->6)-[β-D-glucopyranosyl-(1->3)]-β-D-glucopyranosyl ester 
• 86438-32-6 copteroside H 
• 86438-31-5 β-D-glucopyranosyl <β-D-glucuronopyranosyl-(1-> 3)>-3β-hydroxyolean-12-en-23-oic-28-oate 
• 84161-94-4 gypsogenic acid 3-O-β-D-glucuronopyranoside 

Relevant articles and documents

Three new triterpenoid saponins from Dianthus superbus

Three new triterpenoid saponins (1-3) were isolated from the dried aerial parts of Dianthus superbus L. (Caryophyllaceae). Their structures were established as 3-O-β-D-glucopyranosyl gypsogenic acid 28-O-[β-D-6-O- ((3S)-3-hydroxyl-3-methylglutaryl)glucopyranosyl(1→6)]-β-D- glucopyranoside (1), 3-O-β-D-glucopyranosyl gypsogenic acid 28-O-[β-D-glucopyranosyl(1→3)][β-D-6-O-((3S)-hydroxyl-3- methylglutaryl)glucopyranosyl(1→6)]-β-D-glucopyranoside (2), 3-O-α-L-arabinopyranosyl-3β,16α-dihydroxyolean-12-en-23, 28-dioic acid 28-O-[β-D-glucopyranosyl-(1→6)]-β-D-glucopyranoside (3), on the basis of various spectroscopic analyses and chemical degradations.

TRITERPENE GLYCOSIDES OF Climacoptera transoxana. IV. STRUCTURES OF COPTEROSIDES G AND H

From the epigeal part of the plant Climacoptera transoxana (Iljin) Botsch. have been isolated new triterpene glycosides - copterosides G and H, which are bisdesmosidic glycosides.On the basis of chemical transformations and spectral characteristics, copteroside G has been assigned the structure of gypsogenic acid 28-O-β-D-glucopyranoside 3-O-β-D-glucuronopyranoside, while copteroside H is gypsogenic acid 28-O-β-D-glucopyranoside 3-O-2)-β-glucuronopyranoside>.