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Usage

Uses

Used in Pharmaceutical Industry:
(25S)-5β-Spirostane-1β,3β,4β,5-tetrol is used as a pharmaceutical agent for its potential anti-inflammatory properties, which can help in reducing inflammation and associated symptoms in various conditions.
(25S)-5β-Spirostane-1β,3β,4β,5-tetrol is used as an antioxidant agent to combat oxidative stress and protect cells from damage, which can contribute to the prevention and treatment of various diseases.
(25S)-5β-Spirostane-1β,3β,4β,5-tetrol is used as an antitumor agent due to its potential to inhibit tumor growth and progression, making it a candidate for cancer research and treatment development.
Used in Nutraceutical Industry:
(25S)-5β-Spirostane-1β,3β,4β,5-tetrol is used as a nutraceutical ingredient for its health-promoting properties, such as supporting anti-inflammatory and antioxidant functions, which can contribute to overall wellness and disease prevention.
Used in Cosmetic Industry:
(25S)-5β-Spirostane-1β,3β,4β,5-tetrol is used as an ingredient in cosmetic products for its potential skin health benefits, such as reducing inflammation and promoting antioxidant protection, which can help maintain skin vitality and appearance.

Upstream product

• 91291-49-5 26-O-β-D-glucopyranosyl 22-methoxy-5β-furostane-1β,3β,4β,5β,26-pentaol 5-O-β-D-glucopyranoside 
• 160789-42-4 (1β,3β,4β,5β,25S)-spirostan-1,3,4,5-tetrol 5-(β-D-glucopyranoside) 

Relevant academic research and scientific papers

Polyhydroxylated steroidal constituents from the fresh rhizomes of Tupistra yunnanensis

Six new polyhydroxylated steroidal saponins, tupistrosides A-F (1-6), together with nine known steroids, were isolated from the fresh rhizomes of Tupistra yunnanensis. Their structures were elucidated to be (25S)-1β,4β,5β-trihydroxy-spirostane-3β-yl O-α-l-arabinopyranoside (1), 1β,24β-dihydroxy-spirost-5,25(27)- dien-3α-yl O-β-d-glucopyranoside (2), (22S,25S)-1α,2β, 3α,5α-tetrahydroxy-furo-spirostane-26-yl O-β-d-glucopyranoside (3), 1β,3α,22 ξ-trihydroxy-furost-5,25(27)-dien-26-yl O-β-d-glucopyranoside (4), 26-O-β-d-glucopyranosyl-1β,22- dihydroxy-furost-5-en-3α-yl O-β-d-glucopyranoside (5) and 22-methoxy-1β,2β,3β,4β,5β,7α-hexahydroxy-furost- 25(27)-en-6-one-26-yl O-β-d-glucopyranoside (6), respectively, by means of spectroscopic analysis and the results of acid hydrolysis.

Studies on the Constituents of Aspidistra elatior BLUME. II. On the Steroidal Glycosides of the Leaves. (1)

Six steroidal glycosides were isolated from the fresh leaves of Aspidistra elatior BLUME (Liliaceae) and the structures of these glycosides, tentatively named glycosides A(I), B(2), C(3), D(4), E(5) and F(6), were established to be neopentologenin 5-O-β-D-glucopyranoside (1), 26-O-β-D-glucopyranosyl 22-methoxy-5β-furostane-1β,3β,4β,5β,26-pentaol 5-O-β-D-glucopyranoside (2), aspidistrin (3), 26-O-β-D-glucopyranosyl 22-methoxy-5-β-furostane-1β,2β,3β,4β,5β,26-hexaol 5-O-β-D-glucopyranoside (4), methyl proto-aspidistrin (5) and magnesium 26-O-β-D-glucopyranosyl 22-methoxy-5β-furostane-1β,3β,4β,5β,26-pentahydroxy-2β-yl-sulfate monohydroxide (6), respectively.The last compound is the first sulfated steroidal glycoside to be isolated from a Liliaceous plant.Keywords - steroidal glycoside; Aspidistra elatior; Liliaceae; leaf; spirostanol glycoside; furostanol glycoside; sulfated steroidal glycoside; diosgenin; neopentologenin; aspidistrin.