3798-86-5 Usage
Description
6-[(2-fluorobenzyl)sulfanyl]-5H-purine is a purine derivative featuring a purine ring with a sulfur atom attached to a benzyl group that contains a fluorine atom. 6-[(2-fluorobenzyl)sulfanyl]-5H-purine is part of the purine class, which is commonly found in nucleic acids such as DNA and RNA. The unique structure, including the sulfur atom and the fluorinated benzyl group, endows it with potential biological and pharmaceutical significance. Sulfur-containing compounds have been recognized for their diverse biological activities, such as antioxidant, anti-inflammatory, and anticancer properties. The presence of the fluorine atom in the benzyl group can further influence the chemical and biological properties of the compound, making 6-[(2-fluorobenzyl)sulfanyl]-5H-purine a promising candidate for exploration in medicinal chemistry, pharmacology, and biochemistry.
Uses
Used in Pharmaceutical Industry:
6-[(2-fluorobenzyl)sulfanyl]-5H-purine is used as a potential pharmaceutical agent for its diverse biological activities. The sulfur atom in the compound may contribute to antioxidant, anti-inflammatory, and anticancer properties, making it a candidate for the development of new drugs targeting various diseases and conditions.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 6-[(2-fluorobenzyl)sulfanyl]-5H-purine serves as a subject of study for its potential to be modified and optimized for specific therapeutic applications. 6-[(2-fluorobenzyl)sulfanyl]-5H-purine's structure allows for further chemical modifications that could enhance its biological activity or target specificity.
Used in Biochemical Studies:
6-[(2-fluorobenzyl)sulfanyl]-5H-purine is utilized in biochemical research to understand its interactions with biological systems, including its potential binding to enzymes, receptors, or other biomolecules. This can provide insights into its mechanism of action and its effects on cellular processes.
Used in Drug Design and Development:
The unique structure of 6-[(2-fluorobenzyl)sulfanyl]-5H-purine makes it a valuable compound in drug design and development. Its properties can be harnessed to create new drugs with improved efficacy, selectivity, and reduced side effects.
Used in Chemical Biology:
6-[(2-fluorobenzyl)sulfanyl]-5H-purine is applied in chemical biology to investigate its interactions with biological targets and to elucidate the underlying molecular mechanisms. This can aid in the discovery of new biological pathways and potential therapeutic targets.
Check Digit Verification of cas no
The CAS Registry Mumber 3798-86-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,9 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3798-86:
(6*3)+(5*7)+(4*9)+(3*8)+(2*8)+(1*6)=135
135 % 10 = 5
So 3798-86-5 is a valid CAS Registry Number.
