What are glycosides give examples?

Examples of this large group of glycosides include: Hesperidin (aglycone: hesperetin, glycone: rutinose) Naringin (aglycone: naringenin, glycone: rutinose) Rutin (aglycone: quercetin, glycone: rutinose) Quercitrin (aglycone: quercetin, glycone: rhamnose)

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What is flavone C glycosides?

Flavonoid C-glycosides showed significant antioxidant activity, anticancer and antitumor activity, hepatoprotective activity, anti-inflammatory activity, anti-diabetes activity, antiviral activity, antibacterial and antifungal activity, and other biological effects. People also ask what tests identify c glycosides? (i)3,5-dinitro benzoic acid test : Alcoholic solution of drug sample + few drops of NaOH + 2 % solution of 3,5- dinitro benzoic acid →appearance of pink colour → indicates the presence of cardiac glycosides.

Then, how glycosides are formed?

Glycosides are formed when the anomeric (hemiac-etal or hemiketal) hydroxyl group of a monosaccharide undergoes condensation with the hydroxyl group of a second molecule, with the elimination of water. Which among the following is an example of C-glycosides? Examples of C-glycosides isolated from different plant genus and characterized spectroscopically are: Carminic acid, Aloin, Scoparin, Saponarin, and more recently Cucumerins (flavonoid phytoalexins) and C-glucosylxanthones and complex benzoquinone Altromycin B among others (Figure 5.1).

And another question, where are glycosides found?

Many glycosides occur in plants, often as flower and fruit pigments; for example, anthocyanins. Various medicines, condiments, and dyes from plants occur as glycosides; of great value are the heart-stimulating glycosides of Digitalis and Strophanthus, members of a group known as cardiac glycosides. Regarding this, what do you mean by glycosides? Glycosides can be defined as the compounds in which one or more sugars are combined with nonsugar molecules through glycosidic linkage.