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Arbidol Hydrochloride  CAS 131707-25-0
Arbidol Hydrochloride  CAS 131707-25-0

Arbidol Hydrochloride CAS 131707-25-0

Arbidol Hydrochloride

CAS No.: 131707-25-0

Purity:99.5%

Molecular weight:  531.06 g/mol

Molecular formula: C₂₂H₃₀Br₂N₂O₃S·HCl

Appearance:White to white crystalline powder

Package:  1g10g100g1000g

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Arbidol Hydrochloride  CAS 131707-25-0

Arbidol Hydrochloride CAS 131707-25-0

  • Category:Active  Pharmaceutical  ingredient API

  • MF:C22H26BrClN2O3S

  • CAS:131707-25-0

  • Purity:99.5%

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Product Details
Category:
Active  Pharmaceutical  Ingredient API
MF:
C22H26BrClN2O3S
CAS:
131707-25-0
Purity:
99.5%
Package:
25kg/drum  Or 1kg Ziplock Bag
Color:
White
Form:
Solid
Synonym:
Monohydrochloride
Highlight: 131707-25-0 Active Pharmaceutical Ingredient99.5% Active Pharmaceutical IngredientArbidol Hydrochloride
Payment & Shipping Terms
Minimum Order Quantity
No limit  It ups customers' demand
Price
USD Different quantity  different price
Packaging Details
Fiber drum   50cm✖60cm ×50cm  or  ziplock bag
Delivery Time
4-8 days
Payment Terms
L/C, T/T, Western Union
Supply Ability
200kg/per month
Product Description

CAS 131707-25-0Arbidol hydrochloride API Fine Chemicals

Description:

Arbidol is a kind of double-effect anti-influenza various drug developed by the research center of the chemical drug (former Soviet) and can simultaneously fight against the influenza caused by both influenza virus A and B while may also have antiviral activity against other kinds of certain respiratory viral infections. It has been first approved for entering into market in 1993 in Russia for the control of influenza s well as other acute respiratory viral infections.

Pharmaceutical effects:

Arbidol hydrochloride having carboxylic acid ester structure and may be a carrier pro-drug. Structure of this drug is mostly lipophilic. As the hydrolysis substrate, it is subject to simple in vivo hydrolysis and the carrier is removed. It then forms active compound and accumulates in the cells, ultimately playing its pharmacological role. The mechanism of action of Arbidol hydrochloride is through activating Arbidol hydrochloride 2,5-oligoadenylate synthetase and specifically preventing the contact, adhesion and fusion between influenza virus envelope with the host cell membrane, thereby blocking the replication of influenza virus, and can penetrate the nucleus to directly inhibit the viral RNA and DNA synthesis; on the other hand, it has immunomodulatory, interferon-induction and antioxidant properties. It is able to stimulate the host cells to produce interferon and stimulate humoral response and phagocytosis of macrophages, causing cellular and humoral immunity, suggesting that its anti-viral effect is closely related to improving the immune function. Anti-infection mechanisms: acidic condition (pH 5.0) is the necessary condition for influenza virus-mediated fusion with a slight increase in pH being capable of preventing the fusion process. Water soluble arbidol is a weak alkaline drug and is capable of increasing the pH of cytoplasm of the host cells so that the virus can not complete the process of membrane fusion for release of the viral genome which effectively suppresses the acute and chronic infection caused by HCV belonging to the Orthomyxoviridae.

Chemical Formula:

20230524170505_75533.png

Basic Parameters:

MW531.06
SynonymETHYL ESTER
StabilityHygroscopic
SolubilityDMSO: soluble20mg/mL protein, clear
Melting point133-137℃

Uses:

Arbidol hydrochloride (ARB) is a small monocular compound. It is used to prevent severe pneumonia and virus-associated cytokine dysregulation induced by influenza viruses (IFV). ARB also possesses some immunomodulatory properties, including the effects of interferon induction and macrophage activation.
Arbidol is a broad-spectrum antiviral that has demonstrated activity against a number of enveloped and non-enveloped viruses, and is used clinically to treat influenza. Arbidol inhibits viral entry into host cell and stimulates immune response. Arbidol inhibits fusion between the viral capsid and the cell membrane of the target cell, thus preventing viral entry.

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