Atazanavir Sulfate CAS 229975-97-7 Purity ≥99.0% API Factory Anti-HIV HIV-1 Protease Inhibitor

Short Description:

Chemical Name: Atazanavir Sulfate  

CAS: 229975-97-7

Appearance: White or Off-White Powder

Purity: ≥99.0%

HIV-1 Protease Inhibitor

API High Quality, Commercial Production

Inquiry: alvin@ruifuchem.com


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Description:

Supply with High Purity and Stable Quality
Chemical Name: Atazanavir Sulfate  
CAS: 229975-97-7 
HIV-1 Protease Inhibitor
API High Quality, Commercial Production

Chemical Properties:

Chemical Name Atazanavir Sulfate 
Synonyms BMS-232632 Sulfate
CAS Number 229975-97-7
CAT Number RF-API71
Stock Status In Stock, Production Scale Up to Hundreds of Kilograms
Molecular Formula C38H52N6O7.H2SO4
Molecular Weight 802.93
Melting Point 195.0~198.0℃
Solubility  Insoluble in Water, Soluble in DMSO 
Long-Term Storage Store Long-term at -20℃
Brand Ruifu Chemical

Specifications:

Item Specifications
Appearance White or Off-White Powder
Sulfate 12.0~12.5%
Loss on Drying ≤0.50%
Residue on Ignition ≤0.10%
Heavy Metals ≤20ppm
Single Impurity ≤0.30%
Total Impurities ≤1.0%
Purity/Analysis Method ≥99.0% (HPLC)
pH 5.0~8.0
Test Standard Enterprise Standard
Usage HIV-1 Protease Inhibitor Anti-HIV 

Package & Storage:

Package: Bottle, Aluminium foil bag, Cardboard Drum, 25kg/Drum, or according to customer's requirement.

Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture and pest infestation.

Advantages:

1

FAQ:

Application:

Atazanavir Sulfate (BMS-232632 Sulfate) (CAS: 229975-97-7) is a sulfate salt form of atazanavir that is a highly selective HIV-1 protease inhibitor, is the first protease inhibitor approved for once-daily administration. Atazanavir Sulfate is a substrate and inhibitor of CYP3A4, and an inhibitor and inducer of P-glycoprotein (P-gp). Atazanavir Sulfate is also a SARS-CoV 3CLpro inhibitor with an IC50 of 3.49 μM. Atazanavir Sulfate is an azapeptide and HIV-protease inhibitor that is used in the treatment of HIV infections and AIDS in combination with other Anti-HIV Agents, has been developed and launched by Bristol-Myers Squibb (BMS), under worldwide license from Novartis, for the treatment of HIV infection. Atazanavir was launched in the US as Reyataz™ in July 2003. Antiviral. Atazanavir has shown to be generally more potent than the five currently approved HIV-1 protease inhibitors. Atazanavir selectively inhibits the virus-specific processing of viral Gag and Gag-Pol polyproteins in HIV-1 infected cells by binding to the active site of HIV-1 protease, thus preventing the formation of mature virions. Atazanavir is not active against HIV-2.

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