114297-20-0 Usage
General Description
Soya-cerebroside I is a type of sphingolipid found in soybeans and other plant-based sources. It is primarily composed of a fatty acid, sphingosine, and a carbohydrate group. Soya-cerebroside I has been studied for its potential health benefits, including its anti-inflammatory and antioxidant properties. It has also been shown to have potential neuroprotective effects, making it a promising candidate for the treatment and prevention of neurodegenerative diseases. Additionally, soya-cerebroside I is being investigated for its role in improving skin health and reducing the risk of cardiovascular disease. Overall, the unique composition and potential health benefits of soya-cerebroside I make it an interesting area of study for researchers in the fields of nutrition, medicine, and cosmetic science.
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
Synthesis of Sphingosine Relatives, VII. - Synthesis fo Anti-Ulcerogenic Cerebrosides Isolated from Tetragonia tetragonoides
Mori, Kenji,Kinsho, Takeshi
, p. 807 - 814 (2007/10/02)
The synthesis of (2S,3R,4E,8E,2'R)-1-O-(β-D-glucopyranosyl)-N-(2'-hydroxyhexadecanoyl)-4,8-sphingadienine (1a) and its (8Z) isomer (1b) was accomplished by employing (R)-2-aminohexadecanoic acid, D-glucose, and (S)-serine as chiral sources.
