664366-06-7 Usage
Uses
Used in Pharmaceutical Development:
(3-tert-Butyl-5,9-dimethyl-7-oxo-7H-furo[3,2-g]-chromen-6-yl)acetic acid is used as a lead compound in drug development for its potential to be synthesized into new molecules with improved biological activities. Its complex structure and furochromene ring system provide a foundation for creating innovative pharmaceuticals.
Used in Anti-inflammatory Applications:
In the field of medicine, (3-tert-Butyl-5,9-dimethyl-7-oxo-7H-furo[3,2-g]-chromen-6-yl)acetic acid is used as an anti-inflammatory agent due to its potential to modulate inflammatory responses, which could be beneficial in treating various inflammatory conditions.
Used in Antioxidant Formulations:
(3-tert-Butyl-5,9-dimethyl-7-oxo-7H-furo[3,2-g]-chromen-6-yl)acetic acid is utilized as an antioxidant, where its potential to combat oxidative stress and protect cells from damage makes it a candidate for formulations aimed at promoting health and preventing disease.
Used in Anti-tumor Research:
In oncology, (3-tert-Butyl-5,9-dimethyl-7-oxo-7H-furo[3,2-g]-chromen-6-yl)acetic acid is used as an anti-tumor agent. Its potential to exhibit anti-tumor properties in preclinical research positions it as a promising candidate for further investigation into cancer treatment.
Used in Prodrug Design:
(3-tert-Butyl-5,9-dimethyl-7-oxo-7H-furo[3,2-g]-chromen-6-yl)acetic acid is used as a prodrug, leveraging its acetic acid moiety to improve the compound's solubility and bioavailability, which is essential for effective drug delivery and therapeutic efficacy.
Check Digit Verification of cas no
The CAS Registry Mumber 664366-06-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,4,3,6 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 664366-06:
(8*6)+(7*6)+(6*4)+(5*3)+(4*6)+(3*6)+(2*0)+(1*6)=177
177 % 10 = 7
So 664366-06-7 is a valid CAS Registry Number.
664366-06-7Relevant articles and documents
Development of a novel furocoumarin derivative inhibiting NF-κB dependent biological functions: Design, synthesis and biological effects
Borgatti, Monica,Chilin, Adriana,Piccagli, Laura,Lampronti, Ilaria,Bianchi, Nicoletta,Mancini, Irene,Marzaro, Giovanni,Francesco Dall'Acqua,Guiotto, Adriano,Gambari, Roberto
, p. 4870 - 4877 (2011/11/29)
Nuclear Factor kappaB (NF-κB) plays a very important role in the control of gene expression and is deeply involved in several human pathologies. Accordingly, molecules targeting NF-κB dependent biological functions are considered of great interest. Virtua
Modified coumarins. 10. Synthesis of substituted 2-(7-oxofuro[3,2-g] chromen-6-yl) acetic acids
Nagorichna,Dubovik,Garazd,Khilya
, p. 253 - 261 (2007/10/03)
Substituted 2-(7-oxofuro[3,2-g]chromen-6-yl) acetic acids, modified psoralen analogs, were synthesized by linear fusion of a furan ring to the coumarin system.
