72944-06-0 Usage
Description
30-Hydroxylup-20(29)-en-3-one is a lupane triterpenoid chemical compound derived from the lupin plant. It has been studied for its potential pharmaceutical properties, including anti-inflammatory, anti-cancer, and immunomodulatory effects. 30-Hydroxylup-20(29)-en-3-one has shown promise in preclinical studies for its ability to inhibit the growth of cancer cells and modulate the immune response, as well as demonstrating anti-inflammatory activity.
Uses
Used in Pharmaceutical Industry:
30-Hydroxylup-20(29)-en-3-one is used as a potential pharmaceutical agent for its anti-inflammatory properties, making it a candidate for the development of new drugs for treating inflammatory diseases.
Used in Oncology:
30-Hydroxylup-20(29)-en-3-one is used as an anti-cancer agent in preclinical studies, where it has shown the ability to inhibit the growth of cancer cells. Its potential applications in medicine include the development of new cancer therapies.
Used in Immunology:
30-Hydroxylup-20(29)-en-3-one is used for its immunomodulatory effects, which could be beneficial in the development of treatments for immune-related disorders or conditions.
Further research is needed to fully understand the therapeutic potential of 30-Hydroxylup-20(29)-en-3-one and its possible applications in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 72944-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,9,4 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 72944-06:
(7*7)+(6*2)+(5*9)+(4*4)+(3*4)+(2*0)+(1*6)=140
140 % 10 = 0
So 72944-06-0 is a valid CAS Registry Number.
72944-06-0Relevant articles and documents
Studies on ketene dithioacetalization and hypervalent iodine oxidation of lupenone
Roy, Kamal,Raj,Bhaduri
, p. 774 - 777 (2007/10/03)
Ketene dithioacetalization at the activated C-2 centre of triterpenic lupenone 2 has been carried out successfully to yield α-oxoketenedithioacetal derivative 3. Compound 3 on ring closure reactions with guanidine hydrochloride and hydrazine hydrate furnished respectively the pyrimidine and pyrazole annealed heterocycles 4-6 of lupenone. Unlike these reactions hypervalent iodine oxidation of lupenone using Koser reagent [PhI(OH)OTs] gave various oxidised products 8-11 and did not show any regio-specificity.
