80735-21-3 Usage
Uses
Used in Pharmaceutical Industry:
(1beta,3alpha,5alpha)-spirost-25(27)-en-1,3-diol is used as a pharmaceutical agent for its potential anti-inflammatory properties, which can help in reducing inflammation and alleviating symptoms associated with various inflammatory conditions.
Used in Oncology:
In the field of oncology, (1beta,3alpha,5alpha)-spirost-25(27)-en-1,3-diol is used as an anti-cancer agent, targeting various types of cancer cells and potentially contributing to cancer treatment and therapy.
Used in Diabetes Management:
(1beta,3alpha,5alpha)-spirost-25(27)-en-1,3-diol is utilized as an anti-diabetic compound, which may help in managing blood sugar levels and improving the overall health of individuals with diabetes.
Used in Cardiovascular Health:
(1beta,3alpha,5alpha)-spirost-25(27)-en-1,3-diol is also used in the context of cardiovascular health, as it has been investigated for its potential role in regulating cholesterol levels and reducing the risk of cardiovascular diseases, thus promoting heart health.
Used in Drug Development:
(1beta,3alpha,5alpha)-spirost-25(27)-en-1,3-diol serves as an interesting target for drug development due to its potential biological activities and unique structural features, which can be harnessed to create new therapeutic agents for various health conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 80735-21-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,3 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80735-21:
(7*8)+(6*0)+(5*7)+(4*3)+(3*5)+(2*2)+(1*1)=123
123 % 10 = 3
So 80735-21-3 is a valid CAS Registry Number.
80735-21-3Relevant academic research and scientific papers
Mimaki, Yoshihiro,Kuroda, Minpei,Takaashi, Yoko,Sashida, Yutaka
, p. 79 - 85 (1998)
Three new spirostanol saponins and two new furostanol saponins were isolated from the fresh leaves of Cordyline stricta. Their structures were elucidated on the basis of spectroscopic analysis, including various 2D-NMR techniques, hydrolysis, and by comparison of spectral data of known compounds. Two of the isolated saponins contained a new branched triglycoside moiety assigned as O-α-L-rhamnopyranosyl-(1 → 2)-O-[β-D-xylopyranosyl-(1 → 3)]-β-D-xylopyranose with the formation of an O-glycosidic linkage to C- 1 of the aglycone.
Blunden, G.,Jaffer, J. A.,Jewers, K.,Griffin, W. J.
, p. 2911 - 2915 (1981)
From the leaves of Cordyline stricta Endl. four new steroidal sapogenins crabbogenin , 1β-hydroxycrabbogenin, strictagenin and pompeygenin have been isolated and their structures determined by chemical and spectroscopic methods.
