114297-20-0 Usage
Description
Soya-cerebroside I, a sphingolipid derived from soybeans and other plant sources, is composed of a fatty acid, sphingosine, and a carbohydrate group. It has garnered attention for its potential health benefits, such as anti-inflammatory and antioxidant properties, as well as its neuroprotective effects, making it a promising candidate for the treatment and prevention of neurodegenerative diseases. Furthermore, it is being studied for its potential to improve skin health and reduce the risk of cardiovascular disease. The unique composition and potential health benefits of soya-cerebroside I have piqued the interest of researchers in nutrition, medicine, and cosmetic science.
Uses
Used in Pharmaceutical Industry:
Soya-cerebroside I is used as a neuroprotective agent for its potential to treat and prevent neurodegenerative diseases due to its demonstrated neuroprotective effects.
Used in Cosmetic Industry:
Soya-cerebroside I is used as a skin health improver for its potential to enhance skin health and reduce the risk of skin-related issues.
Used in Nutritional Supplements:
Soya-cerebroside I is used as a dietary supplement for its anti-inflammatory and antioxidant properties, which may contribute to overall health and well-being.
Used in Cardiovascular Health Applications:
Soya-cerebroside I is used as a cardiovascular risk reducer for its potential to lower the risk of cardiovascular diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 114297-20-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,2,9 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 114297-20:
(8*1)+(7*1)+(6*4)+(5*2)+(4*9)+(3*7)+(2*2)+(1*0)=110
110 % 10 = 0
So 114297-20-0 is a valid CAS Registry Number.
InChI:InChI=1/C40H75NO9/c1-3-5-7-9-11-13-15-17-19-20-22-24-26-28-33(43)32(31-49-40-38(47)37(46)36(45)35(30-42)50-40)41-39(48)34(44)29-27-25-23-21-18-16-14-12-10-8-6-4-2/h19-20,26,28,32-38,40,42-47H,3-18,21-25,27,29-31H2,1-2H3,(H,41,48)/b20-19+,28-26+/t32?,33-,34-,35-,36-,37+,38-,40+/m1/s1
114297-20-0Relevant articles and documents
Synthesis of sphingadienine-type glucocerebrosides
Murakami, Teiichi,Shimizu, Toshimi,Taguchi, Kazuhiro
, p. 533 - 545 (2007/10/03)
Sphinga-4,8-dienine derivatives were synthesized from a vinyl-epoxide 5 via three routes. First, reaction of 5 with 2-dodecenyl cyanocuprate afforded a 1:1 mixture of (4E,8E)- and (4E,8Z)-sphingadienine derivatives in high yield. Second, the (4E,8E)-isome
Glycosyl Imidates, 35. - Synthesis of a Cerebroside Having a (4E,8E)-Sphingadienine Moiety from Tetragonia tetragonoides with Antiulcerogenic Activity
Baer, Thomas,Schmidt, Richard R.
, p. 669 - 674 (2007/10/02)
The natural cerebroside 1a possessing antiulcerogenig activity and its diastereomer 1b were readily synthesized by the azidosphingosine glycosylation method.The requied (4E,8E)-azidosphingadienine 12 was obtained from (4E)-tetradecenyl bromide (7) and 2,4-O-benzylidene-D-threose (9) by Wittig reaction, subsequent azide introduction and benzylidene group removal.For the glucosylation the corresponding 3-O-benzoyl derivative 15 was prepared; it provided with the trichloroacetimidate 16 as glucosyl donor the desired β-D-glucopyranosyl derivative 17 in high yield.Deprotection and azido group reduction afforded compound 19 with a free amino group.N-Acylation with both enantiomers of 2-hydroxypalmitic acid (using the derivatives 20 a,b) yielded after deacetylation compounds 1a and 1b, respectively.
