87626-55-9 Usage
Uses
Used in Oncology:
Mitoflaxone is used as an anti-cancer agent for its ability to interfere with the DNA replication process in cancer cells, leading to their death. It is particularly effective against a variety of cancer types, making it a valuable asset in the development of new cancer treatments.
Used in Research and Development:
Mitoflaxone is utilized in ongoing research to explore its potential for use in combination with other drugs or therapies, aiming to enhance the overall effectiveness of cancer treatment regimens and potentially mitigate side effects.
Used in Drug Development:
Mitoflaxone is employed in the development of new pharmaceuticals, as its mechanism of action offers a unique approach to combating cancer. The exploration of its synergistic effects with other agents is a key area of focus in improving cancer treatment outcomes.
Used in Cancer Treatment Optimization:
Mitoflaxone is used to optimize cancer treatment strategies by targeting its application to specific cancer types where it has demonstrated activity. This targeted approach helps in personalizing treatment plans and improving patient outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 87626-55-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,2 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87626-55:
(7*8)+(6*7)+(5*6)+(4*2)+(3*6)+(2*5)+(1*5)=169
169 % 10 = 9
So 87626-55-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H12O4/c18-14-10-15(11-5-2-1-3-6-11)21-17-12(9-16(19)20)7-4-8-13(14)17/h1-8,10H,9H2,(H,19,20)
87626-55-9Relevant academic research and scientific papers
Synthesis of flavone-3-sulfonylureas
Loewe, Werner,Matzanke, Norbert
, p. 943 - 948 (2007/10/03)
The synthesis of new flavone-3-sulfonylurea derivatives is hereby described. The influence of a phenyl group in the 2-position and an acetate group in the 8-position at the chromone nucleus on the activity was studied. Only weak cytostatic activity of the
