1398-17-0 Usage
Uses
Used in Pharmaceutical Industry:
Villoside is used as a potential therapeutic agent for its anti-tumor properties, as it has demonstrated the ability to inhibit the growth of cancer cells in laboratory studies. Its unique chemical structure and medicinal potential make it an interesting compound for further research and development in the field of cancer therapy.
Used in Natural Product Chemistry:
In the field of natural product chemistry, villoside is used as a subject of study for its potential anti-inflammatory properties. This research could lead to the development of new treatments for various inflammatory conditions, leveraging the compound's natural origins and biological activity.
Used in Cancer Therapy Research:
Villoside is employed as a subject of research in cancer therapy, with a focus on understanding its mechanism of action and potential synergistic effects when combined with conventional chemotherapeutic drugs. This research aims to enhance the chemo-sensitivity and efficacy of existing treatments, particularly in cases of drug resistance.
Used in Drug Delivery Systems:
Similar to gallotannin, villoside's potential applications can be enhanced through the development of novel drug delivery systems. These systems could improve the compound's delivery, bioavailability, and therapeutic outcomes, making it a more effective agent in the treatment of various diseases, including cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 1398-17-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,3,9 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1398-17:
(6*1)+(5*3)+(4*9)+(3*8)+(2*1)+(1*7)=90
90 % 10 = 0
So 1398-17-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H23NO8/c1-2-7-8-3-4-17-14(22)9(8)6-23-15(7)25-16-13(21)12(20)11(19)10(5-18)24-16/h2,6-8,10-13,15-16,18-21H,1,3-5H2,(H,17,22)/t7-,8+,10-,11-,12+,13-,15+,16+/m1/s1
1398-17-0Relevant academic research and scientific papers
SYNTHESIS OF THE MONOTERPENE ALKALOID BAKANKOSIN FROM SECOLOGANIN
Tietze, Lutz F.,Baertels, Christoph
, p. 681 - 686 (2007/10/02)
Reduction of secologanin 1a with sodium borohydride followed by acylation afforded 86percent of sweroside tetraacetate 4 which was transformed to the 8-iodomethylester 5c by treatment with trimethylsilyliodide, hydrolysis and addition of diazomethane in 9
