479-98-1 Usage
Description
Aucubin is an iridoid compound characterized by its bitter taste and high solubility in water, ethanol, and methanol. It is insoluble in chloroform, ether, petroleum ether, and other solvents. Aucubin is widely found in various plant species in nature and has garnered interest for its potential applications in different industries.
Uses
Used in Pharmaceutical Industry:
Aucubin is used as a pharmaceutical compound for its potential therapeutic properties. Its bitter taste and solubility characteristics make it a candidate for the development of new drugs and treatments, particularly in the areas of natural medicine and herbal remedies.
Used in Cosmetics Industry:
Due to its solubility in water and alcohol-based solvents, Aucubin can be used as an active ingredient in the cosmetics industry. It may be incorporated into skincare products, hair care formulations, or other beauty products for its potential benefits to skin and hair health.
Used in Agricultural Industry:
Aucubin's presence in various plant species suggests that it may have applications in the agricultural industry. It could be used as a natural pesticide or as a component in the development of more sustainable and environmentally friendly agricultural practices.
Used in Food and Beverage Industry:
Given its bitter taste, Aucubin may find use in the food and beverage industry as a natural flavoring agent or as a component in the development of new and unique flavors for various products.
Mechanism of action
Aucubin can be used to clear dampness and heat, facilitate urination, relieving pain, reduce blood pressure and protecting liver. It can promote the regeneration of stem cells, significantly inhibit the replication of hepatitis B virus DNA.
Check Digit Verification of cas no
The CAS Registry Mumber 479-98-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 479-98:
(5*4)+(4*7)+(3*9)+(2*9)+(1*8)=101
101 % 10 = 1
So 479-98-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H22O9/c16-4-6-3-8(18)7-1-2-22-14(10(6)7)24-15-13(21)12(20)11(19)9(5-17)23-15/h1-3,7-21H,4-5H2/t7?,8?,9-,10?,11-,12+,13-,14?,15+/m1/s1
479-98-1Relevant articles and documents
Stereoselective hydrogenation and ozonolysis of iridoids. Conversion into carbocyclic nucleoside analogues
Franzyk, Henrik,Stermitz, Frank R.
, p. 1646 - 1654 (2007/10/03)
Stereoselective hydrogenation of the iridoids geniposide (9) and aucubin (19) was achieved by using the 1-methyl-1- methoxyethyl ether as a protecting group for the allylic alcohol, as it enhanced the stereoselectivity and prevented undesired hydrogenolysis. Ozonolysis of the hydrogenation product from 9, adoxoside (11), with reductive workup, afforded either a chiral lactone (25) or a chiral polyol (26), depending on the reduction conditions. Polyol 26 was subjected to protecting-group manipulation and subsequent oxidation and reductions to yield cyclopentane building blocks (29-34), which, by Mitsunobu couplings with purines, afforded carbocyclic nucleoside analogues (7, 8, and 35).
Iridoids and other glucosides from Penstemon acuminatus
Vesper,Seifert
, p. 1087 - 1089 (2007/10/02)
-
Chemistry and Stereochemistry of Iridoids, XIV. - Aucubin and Scandoside from Catalpol
Weinges, Klaus,Ziegler, Hans Juergen
, p. 715 - 717 (2007/10/02)
Aucubin (9), scandoside (10), and its methyl ester were obtained, in good yields, from catalpol (1).The absolute configurations of 9-11 were established by correlation to catalpol, whose X-ray structure has previously been determined.