1185737-16-9

Basic information

• Product Name: Steviol-19-O-Glucoside
• Synonyms: Steviol-19-O-Glucoside
• CAS NO: 1185737-16-9
• Molecular Weight: 0
• Mol File: 1185737-16-9.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Steviol-19-O-Glucoside(CAS DataBase Reference)
• NIST Chemistry Reference: Steviol-19-O-Glucoside(1185737-16-9)
• EPA Substance Registry System: Steviol-19-O-Glucoside(1185737-16-9)

Safety Data

• Hazardous Substances Data: 1185737-16-9(Hazardous Substances Data)

Usage

General Description

Steviol-19-O-Glucoside, also known as Rebaudioside D, is a natural sweetener extracted from the leaves of the Stevia rebaudiana plant. It is a glycoside compound that is 250-450 times sweeter than sucrose, making it a popular alternative to sugar in foods and beverages. The compound is stable under a wide range of pH and temperature conditions, making it suitable for use in a variety of products. Additionally, it has been found to have potential health benefits, such as anti-inflammatory and antioxidant properties, and may also help in regulating blood sugar levels. As a result, Steviol-19-O-Glucoside is increasingly being used as a sugar substitute in natural and low-calorie foods and drinks.

Upstream product

• 133-89-1 UDP-glucose 
• 29584-19-8 steviol 
• 57817-89-7 stevioside 
• 51576-10-4 ent-13-acetoxykaur-16-en-19-oic acid 
• 1353022-67-9 C₃₆H₅₀O₁₃ 
• 58543-16-1 rebaudioside A 
• 492-61-5 β-D-glucose 
• 471-80-7 ent-13-hydroxykaur-16-en-19-oic acid 

Relevant articles and documents

Application of 13C NMR spectroscopy to chemistry of natural glycosides: rebaudioside-C, a new sweet diterpene glycoside of Stevia rebaudiana

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Glucosyltransferase Capable of Catalyzing the Last Step in Neoandrographolide Biosynthesis

ApUGT, a diterpene glycosyltransferase from Andrographis paniculata, could transfer a glucose to the C-19 hydroxyl moiety of andrograpanin to form neoandrographolide. This glycosyltransferase has a broad substrate scope, and it can glycosylate 26 natural and unnatural compounds of different structural types. This study provides a basis for exploring the glycosylation mechanism of ent-labdane-type diterpenes and plays an important role in diversifying the structures used in drug discovery.

Synthesis of ent-kaurane diterpene monoglycosides

Synthesis of two ent-kaurane diterpene glycosides, steviol 19-O-β-D-glucopyranosiduronic acid (steviol glucuronide, 5), and 13-hydroxy ent-kaur-16-en-19-oic acid-β-D-glucopyranosyl ester (7) has been achieved from a common starting material, steviol, usin