70868-78-9

Usage

Uses

Used in Pharmaceutical and Medicinal Applications:
23-Hydroxytormentic acid is used as a therapeutic agent for its potential anti-inflammatory, antioxidant, and anti-diabetic properties. Its ability to inhibit pro-inflammatory enzymes and reduce oxidative stress makes it a promising candidate for treating inflammatory disorders and diabetes.
Used in Anti-Diabetic Treatments:
23-Hydroxytormentic acid is used as an anti-diabetic agent due to its protective effect on pancreatic beta cells. This property suggests its potential as a treatment for diabetes, helping to improve insulin secretion and glucose tolerance.
Used in Anti-Cancer Research:
23-Hydroxytormentic acid is used as an anti-cancer agent, as research has shown its ability to induce apoptosis and inhibit the growth of cancer cells. This makes it a promising compound for further investigation and development in oncology.
Used in Antioxidant Formulations:
23-Hydroxytormentic acid is used as an antioxidant in various formulations, capitalizing on its ability to reduce oxidative stress. This application can be beneficial in preventing or treating conditions associated with oxidative damage, such as neurodegenerative diseases and aging.
Used in Inflammatory Disorder Treatments:
23-Hydroxytormentic acid is used as an anti-inflammatory agent, targeting the activity of pro-inflammatory enzymes. This makes it a potential treatment for various inflammatory disorders, where reducing inflammation can alleviate symptoms and improve patient outcomes.

Upstream product

• 70868-72-3 (1R,2R,4aS,6aS,6bR,8aR,9R,10R,11R,12aR,12bR,14bS)-1,10,11-Trihydroxy-9-hydroxymethyl-1,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-octadecahydro-2H-picene-4a-carboxylic acid methyl ester 
• 82843-98-9 2α,3β,19α,23-tetrahydroxy-urs-12-en-28-oic acid 3-O-β-D-glucopyranosyl-28-O-β-D-glucopyranosyl ester 
• 109750-36-9 2α,3β,19α-trihydroxyurs-12-ene-23-carboxyl-28-O-β-D-glucopyranosyl ester 
• 87340-30-5 4-epi-Niga-ichigoside F₁ 
• 87340-30-5 nigaichigoside F₁ 
• 132282-70-3 2α,3β,19α-trihydroxyurs-12-ene-23,28-dioic acid 
• 52986-11-5 (2R,3R,4S,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bR)-2,3,12-Trihydroxy-4,6a,6b,11,12,14b-hexamethyl-2,3,4,4a,5,6,6a,6b,7,8,9,10,11,12,12a,14,14a,14b-octadecahydro-1H-picene-4,8a-dicarboxylic acid dimethyl ester 
• 87340-30-5 1-O-[(2α,3β,5ξ,9ξ,18ξ,19α)-2,3,19,23-tetrahydroxy-28-oxoolean-12-en-28-yl]-β-D-glucopyranose 

Relevant academic research and scientific papers

Cytotoxic triterpene glycosides from the roots of Sanguisorba officinalis

Phytochemical investigation of the ethanol extract of the roots of Sanguisorba officinalis resulted in the isolation of three new triterpene glycosides, 3β-[(α-L-arabinopyranosyl)oxy]-19α,23-dihydroxyolean-12-en-28-oic acid 28-[6-O-acetyl-β-D-glucopyranosyl] ester (1), 2α,3β,19α,23-tetrahydroxyurs-12-en-28-oic acid 28-[6-O-acetyl-β-D-glucopyranosyl] ester (2), and 3β-[(α-L-arabinopyranosyl)oxy]-19α-hydroxyurs-12,20(30)-dien-28-oic acid 28-[6-O-acetyl-β-D-glucopyranosyl] ester (3). All the triterpene glycosides exhibited the significant cytotoxic potential with low IC50 values (IC50 5.0 μM) against six tumor cell lines (MCF-7, HeLa, HepG2, SGC-7901, NCI-H460, and BGC-823).

Retrovirus protease inhibitors

A compound composition and method of treating a retrovirus infection are disclosed. In particular, isolated triterpenes have been shown to have significant inhibitory activity against HIV-1.

Constituents of cupuliferae, XVII: Triterpene saponins and flavonoids from Quercus laurifolia Michx.

In addition to fourteen known glycosides from leaves of Quercus laurifolia Michx., a new acylated triterpene soponin has been isolated and identified as 3-O-galloyl-28-β-D-glucopyranosyl diester of the 2α,3β,19α,23-tetrahydroxyurs-12-ene-28-oic acid (1). The structure of the previously described α-D-glucopyranosyl ester of the 2α,3β,19α,23-tetrahydroxyurs-12-ene-28-oic acid was revised to β-D-glucopyranosyl ester of the 2α,3β,19α,23-tetrahydroxyurs-12-ene-28-oic acid (2).

OLEANANE AND URSANE GLUCOSIDES FROM RUBUS SPECIES

A new oleanane-glucoside was isolated from the leaves of three Rubus species collected in Yunnan, southern China, along with several known ursane- and oleanane-type triterpene glucosides.The structures of these compounds were established by spectroscopic and chemical means.Key Word Index: Rubus accuminatus; R. ellipticus; R. multibreatus; Rosaceae; triterpene; oleanane; ursane; glycoside; glucoside.

19α-Hydroxyursane-Type Triterpene Glucosyl Esters from the Roots of Rubus suavissimus S. LEE

No diterpene glycoside was isolated from the roots of Rubus suavissimus S.LEE, in contrast to its leaves, which taste sweet and contain a large amount of the sweet diterpene glucoside named rubusoside.Instead, a new 28-β-glucopyranosyl ester of 2α,3β,19α-trihydroxyurs-12-ene-23,28-dioic acid named suavissimoside F1 was isolated from the roots of this plant, along with niga-ichigoside F1 (28-β- glucopyranosyl ester of 19α-hydroxyasiatic acid) which has already been obtained from leaves of other Rubus spp. Keywords -- Rubus suavissimus root; Rosaceae; 19α-hydroxyursolic acid derivative; triterpene 28-β-glucopyranosyl ester; niga-ichigoside F1; suavissimoside F1

TRITERPENOIDS AND GLYCOSIDES FROM GEUM JAPONICUM

Key Word Index - Geum japonicum; Rosaceae; triterpenoids; glycosides; 2α-hydroxyursolic acid; 2α-hydroxyoleanolic acid; 2α,19α-dihydroxyursolic acid; glucosides of 2-isopropyl-5-methylhydroquinone; niga-ichigoside F1; suavissimoside F1; 1H NMR; 13C NMR.Two new glucosides and two known ester glucosides have been isolated from Geum japonicum.The two new glucosides were isolated by formation of their acetates and were identified as glucosides of 2-isopropyl-5-methylhydroquinone by chemical and spectral studies.The two known ester glucosides were identified as nigaichigoside F1 and suavissimoside F1 by direct comparison with authentic samples. 2α,19α-Dihydroxyursolic acid and the known glycoside, gein, were also isolated from the same plant, in addition to a mixture of 2α-hydroxyursolic acid and 2α-hydroxyoleanolic acid.

β-GLUCOSYL ESTERS OF 19α-HYDROXYURSOLIC ACID DERIVATIVES IN LEAVES OF RUBUS SPECIES

Key Word Index-Rubus microphyllus; R. koehneanus; R. trifidus; R. medius; Rosaceae; triterpene glucosyl esters; 19α-hydroxyursolic acid derivatives. β-Glucosyl esters of A-ring oxygenated 19α-hydroxyursolic acids were isolated from the leaves of Rubus microphyllus, R. koehneanus, R. trifidus and R. medius.Comparisons of the glycoside fractions of the leaves of 39 Rubus species were conducted, indicating the chemotaxonomic significance of this type of glucosyl ester in this genus.

Constituents of Cupuliferae, 6. - A Novel Triterpene Saponin from Quercus ilex L.

From leaves of Quercus ilex L. a new triterpene saponin has been isolated and identified as the α-D-glucopyranosyl ester 3 of the 2α,3β,19α,23-tetrahydroxy-12-ursen-28-oic acid (1).

TRITERPENOID SAPONINS FROM THE STEM BARK OF SYMPLOCOS SPICATA

From the stem bark of Symplocos spicata a mixture of triterpenoid saponins was obtained.It behaved as a pure compound in TLC and HPLC, but heterogeneity was suspected on the basis of chemical and NMR spectral data.It was separated to give two analogous glycosides, which were identified as 3,28-O-bis-β-D-glucopyranosides of 19α-hydroxyarjunolic and 19α-hydroxyasiatic acids.Key Word Index - Symplocos spicata; Symplocaceae; separation of analogous glycosides; structure elucidation; triterpenoid saponins; 3,28-O-bisglucosides of 19α-hydroxyarjunolic and 19α-hydroxyasiatic acids.