56259-20-2 Usage
Uses
Used in Pharmaceutical Industry:
7,7-Ethylenedithio-3β-(acetyloxy)-11-oxo-5α-lanostane is used as a precursor in the synthesis of cholesterol, which is essential for various biological processes. Its unique functional groups may also allow it to serve as a building block for the development of novel pharmaceutical agents targeting cholesterol-related diseases.
Used in Chemical Research:
In the field of chemical research, 7,7-Ethylenedithio-3β-(acetyloxy)-11-oxo-5α-lanostane is utilized as a model compound to study the reactivity and binding interactions of its ethylenedithio and acetyloxy groups with biological molecules. This research can provide insights into the design of new chemical entities with potential therapeutic applications.
Used in Drug Development:
7,7-Ethylenedithio-3β-(acetyloxy)-11-oxo-5α-lanostane is employed as a lead compound in drug discovery and development. Its unique structure and functional groups may offer opportunities for the design of innovative therapeutic agents with improved efficacy and selectivity for various diseases, including cholesterol-related disorders.
Used in Biochemical Studies:
In biochemical studies, 7,7-Ethylenedithio-3β-(acetyloxy)-11-oxo-5α-lanostane is used to investigate its potential biological activity and interactions with cellular targets. Understanding its mode of action can contribute to the development of new drugs with novel mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 56259-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,5 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56259-20:
(7*5)+(6*6)+(5*2)+(4*5)+(3*9)+(2*2)+(1*0)=132
132 % 10 = 2
So 56259-20-2 is a valid CAS Registry Number.
56259-20-2Relevant academic research and scientific papers
Synthesis of a 24-Epimeric Mixture of 4α,14α,24-Trimethyl-9(11)-cholesten-3-one
Yamashita, Masahiko,Naora (nee Namikawa), Misuzu,Murae, Tatsushi,Tsuyuki, Takahiko,Takahashi, Takeyoshi
, p. 1383 - 1390 (2007/10/02)
A 24-epimeric mixture of a 4α,14α,24-trimethyl-9(11)-cholesten-3-one was synthesized from lanosterol through 4α,14α,24-trimethyl-8-cholesten-β-ol and 4α,14α,24-trimethyl-7,11-dioxocholestan-3β-yl acetate as key intermediates.
