9-Aminoacridine: Difference between revisions
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Latest revision as of 18:51, 16 March 2025
9-Aminoacridine is an amino derivative of acridine, an organic compound that is often used in the field of biochemistry and molecular biology. It is a heterocyclic compound, meaning it contains atoms of at least two different elements as members of its rings.
Chemical Structure and Properties[edit]
9-Aminoacridine has a planar, tricyclic structure that is composed of three rings. The central ring is a benzene ring, which is fused to two other rings at its 1,2 and 3,4 positions. The compound is highly fluorescent, which makes it useful in certain biological applications. It is also a strong intercalating agent, meaning it can insert itself between the base pairs of DNA and disrupt its normal function.
Uses[edit]
One of the main uses of 9-aminoacridine is as a fluorescent stain in microscopy. It is particularly useful in fluorescence microscopy, where it can be used to visualize certain structures or molecules within a sample.
In addition, 9-aminoacridine has been studied for its potential use in cancer therapy. As an intercalating agent, it can disrupt the function of DNA in cancer cells and potentially lead to their death. However, more research is needed to fully understand its potential in this area.
Safety and Toxicity[edit]
Like many other acridine derivatives, 9-aminoacridine is potentially toxic and should be handled with care. It can cause skin and eye irritation, and prolonged exposure can lead to more serious health effects.
See Also[edit]
References[edit]
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9-aminoacridine
