What is the 5-AMINOURIDINE, HYDROCHLORIDE SALT?

5-AMINOURIDINE, HYDROCHLORIDE SALT is , while it's Molecular Formula is C9H13 N3 O6. Used in Pharmaceutical Research: 5-Aminouridine, hydrochloride salt is used as a research tool for studying the molecular mechanisms of viral infections and the development of potential antiviral treatments. Its ability to inhibit viral replication aids in understanding the processes involved in viral life cycles and the identification of new therapeutic targets. Used in Antiviral Drug Development: In the pharmaceutical industry, 5-Aminouridine, hydrochloride salt is used as a lead compound in the development of new antiviral drugs. Its activity against various RNA viruses makes it a valuable asset in the search for effective treatments against viral diseases. Used in Virology Laboratories: 5-Aminouridine, hydrochloride salt is used as an experimental reagent in virology laboratories to study the replication of RNA viruses. It helps researchers to gain insights into the mechanisms of viral replication and to test the efficacy of potential antiviral agents. Used in Molecular Biology: In molecular biology, 5-Aminouridine, hydrochloride salt is used as a nucleoside analog to investigate RNA metabolism and the function of RNA in various biological processes. Its incorporation into RNA molecules allows researchers to study the stability, structure, and function of RNA in cells. Used in Diagnostics: 5-Aminouridine, hydrochloride salt may also be used in the development of diagnostic tools for viral infections. Its ability to interact with viral RNA could be harnessed to create assays that detect the presence of specific viruses or monitor the progression of viral diseases.

What is the CAS number for 5-AMINOURIDINE, HYDROCHLORIDE SALT?

The CAS number of 5-AMINOURIDINE, HYDROCHLORIDE SALT is 2149-76-0.

What is 5-AMINOURIDINE, HYDROCHLORIDE SALT (2149-76-0) used for?

5-Aminouridine, hydrochloride salt, is a nucleoside analog and antiviral agent derived from uridine. It is a chemical compound that is soluble in water and is widely used in research and laboratory settings to investigate viral replication and RNA metabolism. Its antiviral properties have been demonstrated against a range of RNA viruses, positioning it as a promising candidate for drug development and antiviral therapies.InChI:InChI=1/C9H13N3O6/c10-3-1-12(9(17)11-7(3)16)8-6(15)5(14)4(2-13)18-8/h1,4-6,8,13-15H,2,10H2,(H,11,16,17)

What is the 5-AMINOURIDINE, HYDROCHLORIDE SALT?

5-AMINOURIDINE, HYDROCHLORIDE SALT is , while it's Molecular Formula is C9H13 N3 O6. Used in Pharmaceutical Research: 5-Aminouridine, hydrochloride salt is used as a research tool for studying the molecular mechanisms of viral infections and the development of potential antiviral treatments. Its ability to inhibit viral replication aids in understanding the processes involved in viral life cycles and the identification of new therapeutic targets. Used in Antiviral Drug Development: In the pharmaceutical industry, 5-Aminouridine, hydrochloride salt is used as a lead compound in the development of new antiviral drugs. Its activity against various RNA viruses makes it a valuable asset in the search for effective treatments against viral diseases. Used in Virology Laboratories: 5-Aminouridine, hydrochloride salt is used as an experimental reagent in virology laboratories to study the replication of RNA viruses. It helps researchers to gain insights into the mechanisms of viral replication and to test the efficacy of potential antiviral agents. Used in Molecular Biology: In molecular biology, 5-Aminouridine, hydrochloride salt is used as a nucleoside analog to investigate RNA metabolism and the function of RNA in various biological processes. Its incorporation into RNA molecules allows researchers to study the stability, structure, and function of RNA in cells. Used in Diagnostics: 5-Aminouridine, hydrochloride salt may also be used in the development of diagnostic tools for viral infections. Its ability to interact with viral RNA could be harnessed to create assays that detect the presence of specific viruses or monitor the progression of viral diseases.

What is the CAS number for 5-AMINOURIDINE, HYDROCHLORIDE SALT?

The CAS number of 5-AMINOURIDINE, HYDROCHLORIDE SALT is 2149-76-0.

What is 5-AMINOURIDINE, HYDROCHLORIDE SALT (2149-76-0) used for?

5-Aminouridine, hydrochloride salt, is a nucleoside analog and antiviral agent derived from uridine. It is a chemical compound that is soluble in water and is widely used in research and laboratory settings to investigate viral replication and RNA metabolism. Its antiviral properties have been demonstrated against a range of RNA viruses, positioning it as a promising candidate for drug development and antiviral therapies.InChI:InChI=1/C9H13N3O6/c10-3-1-12(9(17)11-7(3)16)8-6(15)5(14)4(2-13)18-8/h1,4-6,8,13-15H,2,10H2,(H,11,16,17)

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2149-76-0

Product Name：5-Aminouridine
Molecular Formula：C9H13 N3 O6
Specifications：99%
Molecular Weight：259.21602

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Product Details;

CasNo： 2149-76-0

Molecular Formula： C9H13 N3 O6

Reliable Quality 5-Aminouridine 2149-76-0 Hot Sale with Chinese Manufacturer

Molecular Formula:C9H13 N3 O6
Molecular Weight:259.21602
Melting Point:214-216 °C
Boiling Point:°Cat760mmHg
PKA:9.31±0.10(Predicted)
Flash Point:°C
PSA：150.80000
Density:1.712g/cm³
LogP:-2.68850

5-AMINOURIDINE, HYDROCHLORIDE SALT(Cas 2149-76-0) Usage

General Description

5-Aminouridine, hydrochloride salt is a chemical compound that functions as an antiviral agent and nucleoside analog. It is derived from uridine and is commonly used in research and laboratory settings to study viral replication and RNA metabolism. As a hydrochloride salt, it is easily soluble in water and can be readily dissolved for use in experimental procedures. It has been shown to have activity against various RNA viruses, making it a potential candidate for further drug development and antiviral therapies. Additionally, its ability to inhibit viral replication makes it a valuable tool for studying the molecular mechanisms of viral infections and the development of potential antiviral treatments.

InChI:InChI=1/C9H13N3O6/c10-3-1-12(9(17)11-7(3)16)8-6(15)5(14)4(2-13)18-8/h1,4-6,8,13-15H,2,10H2,(H,11,16,17)

2149-76-0 Relevant articles

H-phosphonate synthesis of oligoribonucleotides containing modified bases. I. Photoactivatable derivatives of oligoribonucleotides with perfluoroarylazide groups in heterocyclic bases

Repkova,Ivanova,Komarova,Meshchaninova,Kuznetsova,Venyaminova

, p. 612 - 622 (2007/10/03)

H-phosphonate synthesis was proposed for...

2149-76-0 Process route

: 957-75-5
5-bromouridine

: 2149-76-0
5-Amino-uridin

Conditions

Conditions	Yield
With ammonia; In N,N-dimethyl-formamide; at 20 ℃; for 48h;	83%
With ammonia;

: 2149-76-0
5-Amino-uridin

Conditions

Conditions	Yield
5-Nitro-uridin, Pd/Kohle, A., Hydrieren;
5-Bromuridin, fl. NH3;

2149-76-0 Upstream products

957-75-5
5-bromouridine

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