2555-24-0 Usage
Description
4-HYDROXY-7-METHOXY-3-PHENYLCOUMARIN 9& is a chemical compound that belongs to the coumarin family. It is a derivative of coumarin and is characterized by the presence of a hydroxyl group at the 4th position, a methoxy group at the 7th position, and a phenyl group at the 3rd position of the coumarin ring. 4-HYDROXY-7-METHOXY-3-PHENYLCOUMARIN 9& has exhibited various pharmacological activities, including antioxidant, anti-inflammatory, and antimicrobial properties. It has also been studied for its potential therapeutic applications in the treatment of cancer and neurodegenerative diseases. Additionally, 4-HYDROXY-7-METHOXY-3-PHENYLCOUMARIN 9 has been found to have potential as an ingredient in cosmetics and skincare products due to its antioxidant and anti-aging properties.
Uses
Used in Pharmaceutical Industry:
4-HYDROXY-7-METHOXY-3-PHENYLCOUMARIN 9& is used as a therapeutic agent for its potential applications in the treatment of cancer and neurodegenerative diseases. Its pharmacological activities, such as antioxidant, anti-inflammatory, and antimicrobial properties, contribute to its potential as a promising candidate for these applications.
Used in Cosmetics and Skincare Industry:
4-HYDROXY-7-METHOXY-3-PHENYLCOUMARIN 9& is used as an ingredient in cosmetics and skincare products for its antioxidant and anti-aging properties. Its ability to protect the skin from oxidative stress and promote a youthful appearance makes it a valuable component in these products.
Check Digit Verification of cas no
The CAS Registry Mumber 2555-24-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,5 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2555-24:
(6*2)+(5*5)+(4*5)+(3*5)+(2*2)+(1*4)=80
80 % 10 = 0
So 2555-24-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H12O4/c1-19-11-7-8-12-13(9-11)20-16(18)14(15(12)17)10-5-3-2-4-6-10/h2-9,17H,1H3
2555-24-0Relevant articles and documents
3-phenylcoumarins as inhibitors of HIV-1 replication
Olmedo, Dionisio,Sancho, Rocio,Bedoya, Luis M.,Lopez-Perez, Jose L.,Del Olmo, Esther,Munoz, Eduardo,Alcami, Jose,Gupta, Mahabir P.,Feliciano, Arturo San
, p. 9245 - 9257 (2013/01/14)
We have synthesized fourteen 3-phenylcoumarin derivatives and evaluated their anti-HIV activity. Antiviral activity was assessed on MT-2 cells infected with viral clones carrying the luciferase gene as reporter. Inhibition of HIV transcription and Tat function were tested on cells stably transfected with the HIV-LTR and Tat protein. Six compounds displayed NF-κB inhibition, four resulted Tat antagonists and three of them showed both activities. Three compounds inhibited HIV replication with IC50 values 25 μM. The antiviral effect of the 4-hydroxycoumarin derivative 19 correlates with its specific inhibition of Tat functions, while compound 8, 3-(2-chlorophenyl) coumarin, seems to act through a mechanism unrelated to the molecular targets considered in this research.
Phase transfer catalyst mediated one-pot synthesis of 4-hydroxy-3- phenylcoumarin
Sripathi, Shubashini K.,Sivakamasundari
, p. 789 - 790 (2007/10/03)
The synthesis of two new 3-aryl-4-hydroxycoumarins under phase transfer catalyst conditions is described.
The chemistry of pentavalent organobismuth reagents. Part XII. Synthesis of isoflavanones and 3-aryl-4-hydroxycoumarins
Barton,Donnelly,Finet,Stenson
, p. 6387 - 6396 (2007/10/02)
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