466-09-1

Usage

Uses

Due to the limited information provided about the chemical composition, efficacy, and use of ODORIGENIN B, its applications are not clearly defined. However, based on its classification as a phenylpropanoid and the general properties of such compounds, we can speculate on potential uses in various industries.
Used in Pharmaceutical Industry:
ODORIGENIN B could be used as a potential therapeutic agent for [application reason], given its classification as a phenylpropanoid. Further research is required to understand its potential biological or therapeutic applications.
Used in Cosmetic Industry:
ODORIGENIN B might be used as an active ingredient in skincare products for [application reason], considering its natural origin and bioactivity. Additional studies are needed to confirm its efficacy and safety in cosmetic formulations.
Used in Agricultural Industry:
ODORIGENIN B could potentially be employed as a natural pesticide or plant growth regulator for [application reason], due to its bioactive properties. More research is necessary to determine its effectiveness and impact on crops and the environment.

Upstream product

• 58407-69-5 3β-O-(β-D-diginosyl)-14-hydroxy-5α,14β-card-20(22)-enolide 
• 61217-80-9 3β-O-(β-D-digitalosyl)-14-hydroxy-5α,14β-card-20(22)-enolide 
• 41628-29-9 Uzarin 
• 9007-56-1 odoroside K 
• 143-62-4 digitoxigenin 
• 14364-89-7 Gitoxigenin 3-O-monodigitalosideglucoside, or digitalinum verum 
• 6877-82-3 Desglucouzarin 
• 27127-79-3 17α-digitoxigenin β-Gentiobiosyl-(1*4)-α-L-thevetoside 
• 114590-45-3 17α-digitoxigenin β-Cellobiosyl-(1*4)-α-L-thevetoside 
• 114590-46-4 17α-digitoxigenin β-D-apiosyl-(1*6)-β-D-glucosyl-(1*4)-α-L-thevetoside 
• 41628-29-9 Uzarigenin 3-O-β-D-Glucopyranosyl (1-4)-β-D-Glucopyranoside 
• 1111-39-3 acetyldigitoxin 
• 17575-20-1 Digitoxigenin 3-O-bisdigitoxosideacetyldigilanidobioside, or lanatoside A 
• 71-63-6 digitoxin 

Downstream Products

• 35068-75-8 desglucouzarin tetraacetate 
• 143-62-4 3-epidigitoxigenin 
• 128701-09-7 digitoxigenin myristate 
• 128701-08-6 digitoxigenin palmitate 
• 128701-07-5 digitoxigenin stearate 
• 514-39-6 periplogenin 
• 514-39-6 3-epiperiplogenin 
• 6877-82-3 3-epidigitoxigenin β-D-glucoside 
• 18531-44-7 periplogenin β-D-glucoside 
• 6877-82-3 digitoxigenin β-D-glucoside 
• 20231-81-6 3-epidigitoxigenin β-D-gentiobioside 
• 2287-95-8 3β,14-dihydroxy-5β,14β-card-20(22)-enolide 3-(3-carboxypropanoate) 

Relevant academic research and scientific papers

CARDENOLIDE DIGLYCOSIDES FROM OXYSTELMA ESCULENTUM

Two new cardenolide diglycosides, named oxystelmoside and oxystelmine, were isolated from the dried roots of Oxystelma esculentum.On the basis of chemical and spectroscopic evidence their structures were established as uzarigenin 3-O-β-D-xylopyranosyl(1->4)-O-β-D-digitalopyranoside and periplogenin 3-O-6-deoxy-β-D-glucopyranosyl(1->4)-α-D-digitalopyranoside. Key Word Index - Oxystelma esculentum; Asclepiadaceae; roots; oxystelmoside; oxystelmine; steroid; cardenolide glycoside.

BIOTRANSFORMATION OF DIGITOXIGENIN BY GINSENG HAIRY ROOT CULTURES

Five new compounds (three esters and two glycosides) and seven previously reported compounds were isolated as biotransformation products of digitoxigenin by ginseng hairy root cultures.The new esters and glycosides were elucidated as digitoxigenin stearate, digitoxigenin palmitate, digitoxigenin myristate, 3-epidigitoxigenin β-D-gentiobioside and digitoxigenin β-D-sophoroside using 1H and 13C NMR and FAB mass spectral data.Biotransformations involving esterification (of stearic acid, palmitic acid, myristic acid and lauric acid) and glycosylation (of gentiobiose and sophorose) of digitoxigenin have been demonstrated for the first time in the plant cell and tissue cultures.The hairy roots showed high glycosylation ability to the digitoxigenin molecule.

Degradation of Cardenolide Glycosides

The thermal degradation of cardenolide glycosides consisting of different sugar moieties and aglycones was examined.On simple heating, the sugar - aglycone linkage of cardenolide glycosides having 2,6-dideoxy sugar moieties is readily cleaved, to afford their genuine aglycones.On the contrary, cardenolide glycosides possessing 6-deoxy sugar moieties are resistant to the degradative reaction.Besides the fission of the glycosidic linkages, some interesting reactions also took place.The pyrolyzed products were isolated by chromatography, and the structures were elucidated by spectroscopic evidence.