Pyrazolone: Difference between revisions
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File:Lactam-Lactim-Tautomerie_Pyrazolone.svg|Lactam-Lactim Tautomerism of Pyrazolone | |||
File:KnorrPrep.png|Knorr Synthesis Preparation | |||
File:Phenazone2DCSD.svg|Phenazone 2D Chemical Structure | |||
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Latest revision as of 01:25, 18 February 2025
Pyrazolone is a class of organic compounds that are derived from pyrazole. Pyrazolones are often used in the synthesis of various pharmaceuticals due to their wide range of biological activities. They are known for their analgesic, anti-inflammatory, antipyretic, and antirheumatic properties.
History[edit]
The first pyrazolone derivative, Antipyrine, was synthesized in 1883 by Ludwig Knorr. Since then, many other pyrazolone derivatives have been developed and used in medicine.
Structure and Properties[edit]
Pyrazolones have a five-membered ring structure with two nitrogen atoms and three carbon atoms. The basic structure of pyrazolone can be modified by adding different substituents to the ring, which can significantly alter its properties and biological activity.
Medical Uses[edit]
Pyrazolones are used in the treatment of various conditions due to their analgesic, anti-inflammatory, antipyretic, and antirheumatic properties. Some of the most commonly used pyrazolone derivatives in medicine include Phenylbutazone, Aminopyrine, and Metamizole.
Phenylbutazone is used in the treatment of rheumatoid arthritis and gout. Aminopyrine is used as an analgesic and antipyretic. Metamizole, also known as dipyrone, is used as a powerful painkiller and fever reducer.
Safety and Side Effects[edit]
While pyrazolones are generally considered safe for use, they can cause side effects in some individuals. These can include gastrointestinal disturbances, allergic reactions, and, in rare cases, blood disorders such as agranulocytosis and aplastic anemia.
See Also[edit]
References[edit]
<references />
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Lactam-Lactim Tautomerism of Pyrazolone
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Knorr Synthesis Preparation
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Phenazone 2D Chemical Structure

