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5'-O-Acetyl-2',3'-dideoxy-2',3'-didehydro-5-fluoro-uridine is a complex chemical compound that contains elements such as carbon, hydrogen, oxygen, nitrogen, and fluorine. It is a modified form of uridine, a nucleoside found in RNA and involved in the synthesis of nucleic acids. The chemical modifications in 5'-O-Acetyl-2',3'-dideoxy-2',3'-didehydro-5-fluoro-uridine make it a potential antiviral drug, as it has been found to inhibit the replication of the human immunodeficiency virus (HIV). Its unique structure and properties make it a promising candidate for future drug development and research in the field of virology and antiviral therapies.

160203-74-7

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160203-74-7 Usage

Uses

Used in Antiviral Applications:
5'-O-Acetyl-2',3'-dideoxy-2',3'-didehydro-5-fluoro-uridine is used as an antiviral agent for inhibiting the replication of the human immunodeficiency virus (HIV). Its chemical modifications allow it to interfere with the viral replication process, making it a potential candidate for the development of new antiviral therapies.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5'-O-Acetyl-2',3'-dideoxy-2',3'-didehydro-5-fluoro-uridine is used as a key compound for the development of new antiviral drugs. Its unique structure and antiviral properties make it a valuable asset in the search for effective treatments against HIV and other viral infections.
Used in Virology Research:
5'-O-Acetyl-2',3'-dideoxy-2',3'-didehydro-5-fluoro-uridine is used as a research tool in virology to study the mechanisms of viral replication and the development of antiviral resistance. Its unique properties allow researchers to gain insights into the molecular interactions between the compound and viral enzymes, contributing to the understanding of viral pathogenesis and the design of novel antiviral strategies.
Used in Drug Delivery Systems:
To enhance the efficacy and bioavailability of 5'-O-Acetyl-2',3'-dideoxy-2',3'-didehydro-5-fluoro-uridine, various drug delivery systems have been developed. These systems, such as nanoparticles and liposomes, aim to improve the compound's stability, solubility, and targeted delivery to infected cells, thereby increasing its therapeutic potential and reducing side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 160203-74-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,2,0 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 160203-74:
(8*1)+(7*6)+(6*0)+(5*2)+(4*0)+(3*3)+(2*7)+(1*4)=87
87 % 10 = 7
So 160203-74-7 is a valid CAS Registry Number.

160203-74-7Upstream product

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