Human APIs Powder
- Respiratory Drugs Raw Material
- Antiviral Antibacterial
- Antipyretic Analgesics
- Antihistamine Drugs
- Antineoplastic
- Cosmetic Raw Material
Pharmaceutical
OEM & ODM
Veterinary raw materials
Phone: 86-29-89601602
E-mail: sales28@interlgroup.com
Add: Fengcheng 2nd Road, Weiyang District, Xi'an, Shaanxi, China
Daclatasvir CAS 1009119-64-5 Powder Raw Materials
Product Overview:
Daclatasvir Powder (Daklinza) has been granted Priority Review status in combination with Sofosbuvir for the treatment of adult patients with genotype 3 chronic hepatitis C. Daclatasvir CAS 1009119-64-5 is the first drug to demonstrate safe efficacy in the treatment of genotype 3 hepatitis C virus infection without the need for coadministration with interferon or ribavirin. Daclatasvir is the first drug to demonstrate safe and effective treatment of genotype 3 hepatitis C virus infection without co-administration with interferon or ribavirin, and Raw Materials Raw Materials has demonstrated potent antiviral effects across genotypes 1-6 hepatitis C viruses. The current mainstream regimen for daclatasvir is the daclatasvir + sofosbuvir combination. Daclatasvir Powder is characterised by good efficacy, higher SVR, fewer side effects and shorter treatment cycles than other regimens.
Daclatasvir CAS 1009119-64-5 Powder Raw Materials Attributes
CAS: 1009119-64-5
MF: C40H50N8O6
MW: 738.88
EINECS: 1592732-453-0
Specification: 99% min Daclatasvir
Sample: Daclatasvir Powder
Brand: Henrikang
Appearance: White Powder
Storage: Cool Dry Place
Shelf Life: 2 Years
Test Method: HPLC
Daclatasvir CAS 1009119-64-5 Powder Raw Materials Details
Daclatasvir Powder Usage and Synthesis.
Daclatasvir Powder (Daklinza) has been granted Priority Review status in combination with Sofosbuvir for the treatment of adult patients with genotype 3 chronic hepatitis C. Daclatasvir CAS 1009119-64-5 is the first drug to demonstrate safe efficacy in the treatment of genotype 3 hepatitis C virus infection without the need for coadministration with interferon or ribavirin.
Daclatasvir is the first drug to demonstrate safe and effective treatment of genotype 3 hepatitis C virus infection without co-administration with interferon or ribavirin, and Daclatasvir Raw Materials Raw Materials has demonstrated potent antiviral effects across genotypes 1-6 hepatitis C viruses. The current mainstream regimen for daclatasvir is the daclatasvir + sofosbuvir combination.
Daclatasvir Powder is characterised by good efficacy, higher SVR, fewer side effects and shorter treatment cycles than other regimens.
Uses and functions of Daclatasvir Powder.
Dacatavir is a hepatitis C virus (HCV) NS5A inhibitor that is indicated for the treatment of chronic hepatitis C infection with genotype 3 infection. On July 24, 2015, the FDA approved Squibb's chronic hepatitis C drug Daclatasvir-dactamivir for marketing. Squibb's application for FDA approval of dactamivir was also tortuously rejected by the FDA, but was finally approved in mid-2015, and the FDA approved the combination of dactamivir and sofibuvir for the treatment of hepatitis C genotype 3 patients.
Daclatasvir (BMS-790052) is a highly selective HCV NS5A inhibitor with an EC50 of 9-50 pM that acts in cell culture on infectious viruses of multiple HCV replication genotypes and JFH-1 genotype 2a. Phase 3.BMS-790052 is a first-in-class, highly selective NS5A inhibitor of hepatitis C virus (HCV) with an EC50 of picomolarity.
Pharmacological Effects of Daclatasvir Powder.
Daclatasvir Powder is an HCV NS5A protein inhibitor NS5A protein is a multifunctional protein critical for viral replication. It inhibits the replication of HCV RNA and the assembly of viral particles.It should not be used alone, but in combination with sofosbuvir or pegylated interferon and ribavirin.
Production method of Daclatasvir Powder.