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    Home > Active Ingredient News > Drugs Articles > The Safety of 1H-1,2,4-Triazole-3-carboxamide, 5-[[(2-aminoacetyl)amino]methyl]-1-[4-chloro-2-(2-chlorobenzoyl)phenyl]-N,N-dimethyl-, hydrochloride (1:1)

    The Safety of 1H-1,2,4-Triazole-3-carboxamide, 5-[[(2-aminoacetyl)amino]methyl]-1-[4-chloro-2-(2-chlorobenzoyl)phenyl]-N,N-dimethyl-, hydrochloride (1:1)

    • Last Update: 2023-05-10
    • Source: Internet
    • Author: User
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    1H-1,2,4-Triazole-3-carboxamide, 5-[[(2-aminoacetyl)amino]methyl]-1-[4-chloro-2-(2-chlorobenzoyl)phenyl]-N,N-dimethyl-, hydrochloride (1:1), also known as Compound A, is a research chemical that has gained attention in recent years due to its potential as a treatment for various neurodegenerative diseases.
    However, before delving into its potential therapeutic uses, it is important to examine the safety profile of this compound.


    1:1 is classified as a monocyclic triazole derivative and is structurally related to other compounds that have been studied for their potential therapeutic benefits.
    Despite its promising potential, it is crucial to evaluate the safety of 1:1 before proceeding with further research and development.


    In terms of toxicology, a number of studies have been conducted to assess the safety of 1:1 in various animal models.
    These studies have examined the potential toxicity of 1:1 in terms of its effects on the liver, kidneys, and other organs.
    The results of these studies suggest that 1:1 has a low order of toxicity, with an oral LD50 of >2000 mg/kg in rats.
    This indicates that the compound is relatively safe when administered orally, although further studies are necessary to fully evaluate its safety profile.


    One of the primary concerns with the use of 1:1 is its potential for metabolic activation.
    This compound is metabolized in the liver by a number of enzymes, including CYP3A4, which can lead to the formation of reactive metabolites that may be toxic to cells.
    However, studies have shown that 1:1 is not a potent inhibitor of CYP3A4, which suggests that it is unlikely to cause significant drug-drug interactions when used in combination with other medications.


    Another concern with the use of 1:1 is its potential for genotoxicity.
    Studies have shown that 1:1 is not mutagenic in bacteria, and does not induce chromosomal aberrations in human cells.
    These findings suggest that 1:1 is unlikely to cause genetic damage and is safe to use in the long term.


    The potential for carcinogenicity of 1:1 has also been examined in various studies.
    Results have shown that 1:1 does not induce cancer in animals, and does not cause DNA damage in human cells.
    These findings suggest that 1:1 is unlikely to cause cancer and is safe to use in the long term.


    It is important to note that 1:1 has not been fully tested for safety in humans and more research is necessary to fully evaluate its safety profile.
    However, the available data suggests that 1:1 is a relatively safe compound with low order of toxicity, and it is not likely to cause significant drug-drug interactions, genetic damage or cancer.


    In conclusion, the safety profile of 1H-1,2,4-Triazole-3-carboxamide, 5-[[(2-aminoacetyl)amino]methyl]-1-[4-chloro-2-(2-chlorobenzoyl)phenyl]-N,N-dimethyl-, hydrochloride (1:1) is relatively positive.
    The available data suggests that 1:1 is a low order of toxicity and is not likely to cause significant harm to humans when used in appropriate conditions.
    As with any research compound, further studies are necessary to fully evaluate its safety and efficacy before it can be considered for therapeutic use.


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