DuP-697

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DuP-697_structure.png



DuP-697 is a nonsteroidal anti-inflammatory drug (NSAID) that selectively inhibits the enzyme cyclooxygenase-2 (COX-2). It is part of a class of drugs known as COX-2 inhibitors, which are used to reduce pain and inflammation with a lower risk of gastrointestinal side effects compared to traditional NSAIDs that inhibit both COX-1 and COX-2 enzymes.

Mechanism of Action[edit | edit source]

DuP-697 works by selectively inhibiting the COX-2 enzyme, which is responsible for the synthesis of prostaglandins that mediate inflammation and pain. Unlike COX-1, which is involved in the protection of the gastric mucosa and platelet aggregation, COX-2 is primarily expressed at sites of inflammation. By targeting COX-2, DuP-697 reduces inflammation and pain while minimizing gastrointestinal toxicity.

Pharmacokinetics[edit | edit source]

The pharmacokinetic profile of DuP-697 includes its absorption, distribution, metabolism, and excretion. DuP-697 is absorbed orally and has a bioavailability that allows it to effectively reach therapeutic concentrations in the bloodstream. It is metabolized in the liver and excreted primarily through the kidneys.

Clinical Applications[edit | edit source]

DuP-697 has been studied for its potential use in treating conditions such as rheumatoid arthritis, osteoarthritis, and other inflammatory disorders. Its selective inhibition of COX-2 makes it a candidate for patients who require long-term NSAID therapy but are at risk for gastrointestinal complications.

Side Effects[edit | edit source]

While DuP-697 is designed to minimize gastrointestinal side effects, it may still cause adverse effects such as renal impairment, cardiovascular events, and hypersensitivity reactions. Patients should be monitored for these potential side effects, especially if they have pre-existing conditions that may be exacerbated by NSAID use.

Research and Development[edit | edit source]

DuP-697 was developed as part of a broader effort to create safer NSAIDs by targeting COX-2 specifically. Research continues into the development of COX-2 inhibitors with improved safety profiles and efficacy.

Also see[edit | edit source]

Template:Nonsteroidal anti-inflammatory drugs Template:Cyclooxygenase inhibitors

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Contributors: Prab R. Tumpati, MD