577-26-4 Usage
Uses
Used in Pharmaceutical Applications:
5,6,7,8-tetrahydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one is used as a therapeutic agent for its antioxidant, anti-inflammatory, and anticancer properties, making it a potential treatment for various diseases and conditions.
Used in Cancer Treatment:
In the field of oncology, 5,6,7,8-tetrahydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one is used as an anticancer agent, targeting the inhibition of cancer cell growth and potentially offering a treatment option for a range of malignancies.
Used in Neurological Disorders Treatment:
5,6,7,8-tetrahydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one is used as a neuroprotective agent for its potential role in the treatment of neurological disorders such as Alzheimer's disease, due to its ability to protect against oxidative stress and inflammation.
Used in Cardiovascular Health:
In the cardiovascular industry, 5,6,7,8-tetrahydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one is used to improve cardiovascular health, potentially contributing to the prevention of heart-related diseases through its antioxidant and anti-inflammatory actions.
Used in Longevity Research:
5,6,7,8-tetrahydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one is used in longevity research for its potential to promote a longer and healthier life, possibly through its antioxidant and anti-inflammatory effects that may slow down aging processes.
Check Digit Verification of cas no
The CAS Registry Mumber 577-26-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 577-26:
(5*5)+(4*7)+(3*7)+(2*2)+(1*6)=84
84 % 10 = 4
So 577-26-4 is a valid CAS Registry Number.
577-26-4Relevant academic research and scientific papers
Synthetic Studies of the Flavone Derivatives. VIII. Synthesis of Kanzakiflavones and Their Isomers
Iinuma, Munekazu,Tanaka, Toshiyuki,Matsuura, Shin
, p. 1006 - 1010 (2007/10/02)
Kanzakiflavone-1 and -2, isolates from Iris Unguicularis, and their position isomers were synthesized to confirm the structures of the isolates.The differences among these flavones are discussed on the basis of spectral data.Keywords: kanzakiflavone-1; kanzakiflavone-2; 4',5-dihydroxy-7,8-methylenedioxyflavone; 6,7-methylenedioxy-4',5,8-trimethoxyflavone; 7,8-methylenedioxy-4',5,6-trimethoxyflavone; 3'-acetyl-4',5-dihydroxy-6,7-methylenedioxyflavone
