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Usage

Uses

Used in Pharmaceutical Industry:
(20R)-3β,29-Dihydroxyolean-12-en-28-oic acid is used as a pharmaceutical compound for its potential therapeutic properties. (20R)-3β,29-Dihydroxyolean-12-en-28-oic acid's unique structure and biological activities make it a promising candidate for the development of new drugs and treatments.
Used in Cosmetic Industry:
In the cosmetic industry, (20R)-3β,29-Dihydroxyolean-12-en-28-oic acid is used as an active ingredient for its potential skin benefits. Its presence in plant sources suggests that it may have properties that can be harnessed for skincare products, such as anti-aging or moisturizing effects.
Used in Research and Development:
(20R)-3β,29-Dihydroxyolean-12-en-28-oic acid is also used in research and development for its potential applications in various fields. Scientists and researchers may study (20R)-3β,29-Dihydroxyolean-12-en-28-oic acid to better understand its properties and how it can be utilized in the development of new products and treatments.
Used in Traditional Medicine:
Given that (20R)-3β,29-Dihydroxyolean-12-en-28-oic acid is derived from plant sources, it may also have applications in traditional medicine. It could be used as a component in herbal remedies or traditional treatments, where its potential therapeutic properties are valued.

InChI:InChI=1/C30H48O4/c1-25(2)21-9-12-29(6)22(27(21,4)11-10-23(25)32)8-7-19-20-17-26(3,18-31)13-15-30(20,24(33)34)16-14-28(19,29)5/h7,20-23,31-32H,8-18H2,1-6H3,(H,33,34)/t20-,21?,22-,23+,26?,27+,28-,29-,30+/m1/s1

Upstream product

• 120726-94-5 ciwujianoside A₃ 

Relevant academic research and scientific papers

Ebenamariosides A-D: Triterpene glucosides and megastigmanes from the leaves of diospyros maritima

The 1-BuOH-soluble fraction of the methanol (MeOH) extract of Diospyros maritima was separated by chromatographic techniques to give three new oleanane-type and one new ursane-type triterpene glucoside, named ebenamariosides A-D (1-4); two megastigmanes were also isolated. The structures of triterpene glucosides was elucidated with extensive investigation by one and two dimensional NMR spectroscopy and the structures were confirmed by partial enzymatic hydrolyses to give the corresponding mono-glucosides and aglycones. The structures of the megastigmanes, including their absolute stereochemistries, were elucidated by spectroscopic evidence and by the modified Mosher's method. Two megastigmanes were chemically correlated and their absolute structures were unambiguously determined. The cytotoxicity of the triterpene glucosides and their degradation products were assayed. They did not show any significant activity.

Saponins from Leaves of Acanthopanax senticosus HARMS., Ciwujia. II. Structures of Ciwujianosides A1, A2, A3 A4 and D3

Further investigation of the chemical constituents of the leaves of Acanthopanax senticosus HARMS. resulted in the isolation of five new triterpenoid saponins, named ciwujianosides A1 (1), A2 (2), A3 (3), D3 (4) and A4 (5).The structures of these saponins were elucidated as follows: 1, 3-O-β-glucopyranosyl-(1->2)-α-arabinopyranosyloleanolic acid 28-O-α-rhamnopyranosyl-(1->4)-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; 2, 3-O-β-glucopyranosyl-(1->2)-α-arabinopyranosyl-30-norolean-12,20(29)-dien-28-oic acid 28-O-α-rhamnopyranosyl-(1->4)-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; 3, 3-O-α-rhamnopyranosyl-(1->2)-α-arabinopyranosylmesembryanthemoidigenic acid 28-O-α-rhamnopyranosyl-(1->4)-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; 4, 3-O-α-arabinopyranosylmesembryanthemoidigenic acid 28-O-α-rhamnopyranosyl-(1->4)-6-O-acetyl-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; 5, 3-O-β-glucopyranosyl-(1->2)-α-arabinopyranosylmesembryanthemoidigenic acid 28-O-α-rhamnopyranosyl-(1->4)-6-O-acetyl-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester.Keywords: Acanthopanax senticosus; Araliaceae; saponin; Chinese folk medicine; ciwujianoside; oleanolic acid glycoside; noroleanolic acid glycoside; mesembryanthemoidigenic acid glycoside; ciwujia