211815-97-3 Usage
Uses
Used in Pharmaceutical Industry:
Nudicaucin A is used as a potential therapeutic agent for its ability to modulate cell differentiation, proliferation, and apoptosis. Its biological activities make it a candidate for the development of new drugs targeting various diseases.
Used in Research Applications:
Nudicaucin A is used as a research tool in the study of cell biology, particularly in understanding the mechanisms of cell differentiation, proliferation, and apoptosis. Its role as a secondary metabolite also makes it valuable in investigating the functions and interactions of plant-derived compounds within biological systems.
Used in Drug Discovery:
Nudicaucin A is used as a lead compound in drug discovery, with its unique structural properties and biological activities providing a foundation for the development of new therapeutic agents. Its potential medicinal uses are still being explored, and further research is needed to fully elucidate its applications in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 211815-97-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,8,1 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 211815-97:
(8*2)+(7*1)+(6*1)+(5*8)+(4*1)+(3*5)+(2*9)+(1*7)=113
113 % 10 = 3
So 211815-97-3 is a valid CAS Registry Number.
211815-97-3Relevant academic research and scientific papers
Jitsuno, Maki,Mimaki, Yoshihiro
, p. 2157 - 2167 (2010)
Chemical study of the aerial parts of Larrea tridentata (Zygophyllaceae) resulted in the isolation of 25 triterpene glycosides, 13 of which were previously unknown. Their structures were determined on the basis of comprehensive spectroscopic analyses, including 2D NMR spectroscopy, and hydrolytic cleavage followed by chromatographic and spectroscopic analyses. This is the first systematic phytochemical study of L. tridentata with attention paid to its triterpene glycoside constituents. The isolated compounds were evaluated for their cytotoxic activity against HL-60 human promyelocytic leukemia cells.
