List of corticosteroid cyclic ketals

From WikiMD.com - Food, Medicine & Wellness Encyclopedia

List of corticosteroid cyclic ketals


Overview[edit | edit source]

Corticosteroid cyclic ketals are a class of corticosteroids that have been chemically modified to include a cyclic ketal group. This modification can alter the pharmacokinetic and pharmacodynamic properties of the corticosteroid, potentially enhancing its therapeutic effects or reducing side effects. Cyclic ketals are formed by the reaction of a ketone group with a diol, resulting in a five- or six-membered ring structure.

Structure and Function[edit | edit source]

Corticosteroids are steroid hormones that are produced in the adrenal cortex and are involved in a wide range of physiological processes, including the regulation of inflammation, immune response, and metabolism. The addition of a cyclic ketal group to a corticosteroid molecule can influence its solubility, stability, and receptor binding affinity.

Triamcinolone acetonide structure

One of the most well-known corticosteroid cyclic ketals is triamcinolone acetonide, which is derived from triamcinolone. The acetonide group in triamcinolone acetonide is a cyclic ketal formed from acetone and the 16,17-dihydroxy group of triamcinolone. This modification enhances the lipophilicity of the molecule, allowing for better penetration into tissues and prolonged duration of action.

List of Corticosteroid Cyclic Ketals[edit | edit source]

The following is a list of some corticosteroid cyclic ketals:

  • Triamcinolone acetonide: A potent glucocorticoid used in various inflammatory and allergic conditions. It is commonly used in dermatology and ophthalmology.
  • Fluocinolone acetonide: Another glucocorticoid with a similar acetonide modification, used in dermatological applications.
  • Flunisolide: A corticosteroid used in the treatment of asthma and allergic rhinitis, which also contains a cyclic ketal group.

Applications[edit | edit source]

Corticosteroid cyclic ketals are primarily used for their anti-inflammatory and immunosuppressive properties. They are commonly employed in the treatment of conditions such as asthma, allergic rhinitis, eczema, psoriasis, and other inflammatory disorders. The cyclic ketal modification often allows for topical formulations that are more effective and have fewer systemic side effects.

Triamcinolone structure

Mechanism of Action[edit | edit source]

Corticosteroid cyclic ketals exert their effects by binding to the glucocorticoid receptor, a type of nuclear receptor that regulates the expression of anti-inflammatory proteins and suppresses the expression of pro-inflammatory proteins. The cyclic ketal group can enhance the binding affinity and selectivity of the corticosteroid for its receptor, leading to more potent anti-inflammatory effects.

Related Pages[edit | edit source]

WikiMD
Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Search WikiMD

Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD

WikiMD's Wellness Encyclopedia

Let Food Be Thy Medicine
Medicine Thy Food - Hippocrates

Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.

Contributors: Prab R. Tumpati, MD