62584-08-1 Usage
Chemical class
Alkaloid compound
Natural occurrence
Derived from the bark of tropical tree species found in Asia and South America
Anticancer activity
Investigated for its potential to combat cancer cells
Antifungal activity
Exhibits properties that may help fight fungal infections
Antibacterial activity
Demonstrates potential to inhibit bacterial growth
Anti-inflammatory activity
May help reduce inflammation in the body
Antioxidant
Canthin-6-one has shown potential as an antioxidant, which can help protect cells from damage caused by free radicals
Neuroprotective agent
It has also shown promise as a neuroprotective agent, which may help protect and preserve brain function
Preclinical studies
Promising results have been observed in preclinical studies, indicating potential for further research and development
Traditional medicine
Has been used in traditional medicine for its various therapeutic properties
Modern medicine
Its potential applications in modern medicine are still being explored, with a focus on developing new pharmaceutical drugs
This list provides a comprehensive overview of the main properties and specific content of 12-hydroxyindolo[2,1-b]quinazolin-6(12H)-one (canthin-6-one) based on the information provided.
Check Digit Verification of cas no
The CAS Registry Mumber 62584-08-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,8 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62584-08:
(7*6)+(6*2)+(5*5)+(4*8)+(3*4)+(2*0)+(1*8)=131
131 % 10 = 1
So 62584-08-1 is a valid CAS Registry Number.
62584-08-1Relevant academic research and scientific papers
Isatin chloride: A phantom. Reactions of 2-(2,2-dichloro-2,3-dihydro-3-oxoindol-1-yl)-3H-indol-3-one
Cornforth, John,Hitchcock, Peter B.,Rozos, Panteleimon
, p. 2787 - 2792 (2007/10/03)
It is shown that 2-chloro-3H-indol-3-one 1 and analogues have never actually been isolated and that their reactions, reported over 115 years in 40 papers and 4 patents, are those of more or less impure 2-(2,2-dichloro-2,3-dihydro-3-oxoindol-1-yl)-3H-indol-3-one 14. Several reactions of the parent compound and its 5,5′-dimethyl and 5,5′-dibromo derivatives are reported, especially a reaction with dry methanol leading to the known indoloquinazoline 25 ('methylisatoid') and to the known alkaloid tryptanthrin 21 via a photolabile orthoester.
