17605-67-3 Usage
Description
Fucosterol, also known as a 3beta-sterol, is a compound consisting of stigmastan-3beta-ol with double bonds at positions 5 and 24(28). It is a steroid that plays a significant role in proteomics research, which is the large-scale study of proteins, their structures, and functions.
Uses
Used in Proteomics Research:
Fucosterol is used as a steroid for proteomics research to study the structure, function, and interactions of proteins. Its presence in research helps in understanding the complex biological processes and pathways involving proteins.
Used in Pharmaceutical Industry:
Fucosterol is used as a raw material in the pharmaceutical industry for the development of various drugs and therapeutic agents. Its steroidal nature makes it a valuable component in the synthesis of medications targeting specific health conditions.
Used in Cosmetics Industry:
Fucosterol is also used in the cosmetics industry as an ingredient in various skincare and beauty products. Its properties may contribute to the development of products that promote skin health and address specific skin concerns.
Used in Nutritional Supplements:
Fucosterol can be found in nutritional supplements, particularly those targeting hormonal balance and overall health. Its steroidal nature may provide benefits to individuals seeking to support their endocrine system and general well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 17605-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,0 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17605-67:
(7*1)+(6*7)+(5*6)+(4*0)+(3*5)+(2*6)+(1*7)=113
113 % 10 = 3
So 17605-67-3 is a valid CAS Registry Number.
InChI:InChI=1/C29H48O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h7,10,19-20,23-27,30H,8-9,11-18H2,1-6H3/b21-7+
17605-67-3Relevant articles and documents
Stereochemical fate of C-26 and C-27 during the conversion of isofucosterol to sitosterol and of 24-methylenecholesterol to campesterol and dihydrobrassicasterol in Oryza sativa cell cultures
Nasu, Kozue,Takahashi, Kyoko,Morisaki, Masuo,Fujimoto, Yoshinori
, p. 381 - 385 (2007/10/03)
Administration of pro-R-methyl-13C-labeled isofucosterol to cultured cells of Oryza sativa revealed that the pro-R and pro-S methyls at C-25 become the pro-R and pro-S methyls at C-25 of sitosterol, respectively. Similar administration experime
Partial Synthesis of "Sargasterol" and (20S)-Cholesterol
Sucrow, Wolfgang,Nooy, Michael van
, p. 1897 - 1906 (2007/10/02)
The data of the synthetic (20S)-3β-hydroxy-5-cholestan-24-one (5b) and its acetate 5a differ significantly from those given for the degradation product of "sargasterol".The compounds 5a,b were converted into the E/Z-isomeric (20S)-stigmasta-5,24(28)-dien-3β-ols 8b, 9b, into their acetates 8a, 9a, and into (20S)-cholesterol (10b). (20S)-cholesterol acetate (10a) shows a lower melting point than that which is given in literature.
