2465-11-4 Usage
Description
(22E)-5α-Ergosta-7,22-dien-3β-ol, also known as Stellasterol, is a 3β-sterol with an ergostane skeleton featuring double bonds at the 7and 22-positions. It is one of the six sterols isolated from the fruiting bodies of Boletus pulverulentus Opat. (Boletaceae).
Uses
Used in Pharmaceutical Industry:
(22E)-5α-Ergosta-7,22-dien-3β-ol is used as a pharmaceutical compound for its potential therapeutic applications. As a sterol, it may have various biological activities that can be harnessed for the development of new drugs or supplements.
Used in Nutritional Supplements:
(22E)-5α-Ergosta-7,22-dien-3β-ol is used as an ingredient in nutritional supplements due to its sterol content, which may contribute to maintaining healthy cholesterol levels and overall health.
Used in Research and Development:
(22E)-5α-Ergosta-7,22-dien-3β-ol is used as a research compound for studying the structure, function, and potential applications of sterols in various biological systems. This can lead to a better understanding of their role in human health and the development of new therapeutic strategies.
Used in Cosmetics Industry:
(22E)-5α-Ergosta-7,22-dien-3β-ol may be used as an ingredient in the cosmetics industry for its potential benefits to skin health, such as promoting skin hydration and elasticity.
Check Digit Verification of cas no
The CAS Registry Mumber 2465-11-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,6 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2465-11:
(6*2)+(5*4)+(4*6)+(3*5)+(2*1)+(1*1)=74
74 % 10 = 4
So 2465-11-4 is a valid CAS Registry Number.
InChI:InChI=1/C28H46O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h7-8,10,18-22,24-26,29H,9,11-17H2,1-6H3/b8-7+/t19-,20+,21-,22-,24+,25-,26-,27-,28+/m0/s1
2465-11-4Relevant articles and documents
A LANOSTANOID OF FORMOSAN GANODERMA LUCIDUM
Lin, Chun-Nan,Tome, Whey-Pin,Won, Shen-Jeu
, p. 673 - 675 (2007/10/02)
A new steryl ester, ergosta-7,22-dien-3β-yl palmitate, a novel lanostanoid, named ganoderic aldehyde A (3β-hydroxy-26-oxo-5α-lanosta-8,24-dien-11-one, ergosta-7,22-dien-3β-ol, ergosta-7,22-dien-3-one, and ergosterol peroxide, were isolated from the fruit bodies of Formosan Ganoderma lucidum and characterized by chemical degradation, synthesis, and spectral data.
Selective Reduction of the 7(8)-Double Bond in Ergosterol
Barton, Derek H. R.,Lusinchi, Xavier,Magdzinski, Leon,Ramirez, Jesus Sandoval
, p. 1236 - 1238 (2007/10/02)
Reduction of ergosterol alkoxide derivatives with lithium metal gives better yields of the 7(8)-reduced product brassicasterol than previous procedures; the mixed products of the reduction are easily converted into ergosta-2,22-dien-6-one, a convenient in
A Simple Method for the Reduction of the 7,8-Double Bond of Steroidal 5,7-Dienes
Anastasia, Mario,Ciuffreda, Pierangela,Fiecchi, Alberto
, p. 1169 - 1170 (2007/10/02)
1,4-Cycloadducts of various steroidal 5,7-dienes and 4-phenyl-1,2,4-triazoline-3,5-dione gave a separable mixture (3 : 2) of the corresponding Δ5- and Δ7-sterols in good yield when treated with lithium dissolved in refluxing ethylamine.
