Azathioprine Sodium

Modify Date: 2024-01-14 20:34:42

Azathioprine Sodium Structure
Azathioprine Sodium structure
Common Name Azathioprine Sodium
CAS Number 55774-33-9 Molecular Weight 299.244
Density N/A Boiling Point N/A
Molecular Formula C9H6N7NaO2S Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Azathioprine Sodium


Azathioprine (BW 57-322) sodium is an orally active immunosuppressive agent. Azathioprine can be converted in vivo to the active metabolite 6-mercaptopurine (6-MP). Azathioprine has myelosuppressive effects and induces apoptosis[1][3].

 Names

Name Azathioprine Sodium
Synonym More Synonyms

 Azathioprine Sodium Biological Activity

Description Azathioprine (BW 57-322) sodium is an orally active immunosuppressive agent. Azathioprine can be converted in vivo to the active metabolite 6-mercaptopurine (6-MP). Azathioprine has myelosuppressive effects and induces apoptosis[1][3].
Related Catalog
In Vitro Azathioprine (0-50 μM, 48 hours) sodium can induce severe intracellular GSH depletion with relevant concentrations in both primary rat and human hepatocytes[2]. Cell Viability Assay[2] Cell Line: Rat hepatocytes, Human hepatocytes Concentration: 0-50 μM Incubation Time: 24-48 hours Result: Showed the decrease in cell viability and intracellular GSH levels in rat hepatocytes as low concentration of 0.5 μM but no significant decrease in cell viability at concentrations below 50 μM as well as GSH depletion was obviously noted at a concentration as low as 1 μM in human hepatocytes.
In Vivo Azathioprine (oral gavage, 25–400 mg/kg, everyday, 10days) sodium can affect bone marrow cells, red blood cells, and peripheral blood cytokines and other related parameters in a dose-dependent manner, and can induce apoptosis in female CD-1 mice and ICR mice [3]. Animal Model: Outbred female CD-1 mice, Female ICR mice[3] Dosage: 25-400 mg/kg Administration: Oral gavage; everyday; 10days Result: Induced a decrease in erythrocyte-related parameters as well as leukocyte-related parameters in a dose-dependent manner. Induced 52.4%, 35.4%, 17.9%, 16.1% and 15.2% reduction in bone marrow cells at concentrations of 40, 60, 80, 100 and 120 mg/kg, respectively while fms-like tyrosine kinase-3(FLT-3) ligand (FL)-related cytokines were increased. Increased induction of apoptosis.
References

[1]. SoniaChavez-Alvarez, et al. Azathioprine: its uses in dermatology. An Bras Dermatol. 2020 Nov-Dec;95(6):731-736.

[2]. Yue-Ting Wu, et al. Azathioprine hepatotoxicity and the protective effect of liquorice and glycyrrhizic acid. Phytother Res. 2006 Aug;20(8):640-5. doi: 10.1002/ptr.1920.

[3]. Gemma Molyneux, et al. The haemotoxicity of azathioprine in repeat dose studies in the female CD-1 mouse. Int J Exp Pathol. 2008 Apr;89(2):138-58.

 Chemical & Physical Properties

Molecular Formula C9H6N7NaO2S
Molecular Weight 299.244
Exact Mass 299.020142

 Synonyms

Sodium 6-[(1-methyl-4-nitro-1H-imidazol-5-yl)sulfanyl]purin-9-ide
9H-Purine, 6-[(1-methyl-4-nitro-1H-imidazol-5-yl)thio]-, sodium salt (1:1)
Azathioprine Sodium
7H-purine, 6-[(1-methyl-4-nitro-1H-imidazol-5-yl)thio]-, sodium salt
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