A-86929

From WikiMD.com Medical Encyclopedia

Chemical compound



Chemical structure of A-86929

A-86929 is a synthetic compound that acts as a potent and selective dopamine receptor agonist, specifically targeting the D1-like dopamine receptors. It was developed for its potential therapeutic effects in treating Parkinson's disease and other neurological disorders.

Chemical properties[edit | edit source]

A-86929 is classified as a phenylbenzazepine derivative. Its chemical structure is characterized by a benzazepine core with a phenyl group attached, which is crucial for its activity at dopamine receptors. The compound is known for its high affinity and selectivity for the D1 receptor subtype, which distinguishes it from other dopamine agonists that may also target D2-like receptors.

Pharmacology[edit | edit source]

A-86929 functions primarily as a full agonist at D1-like receptors, which include the D1 and D5 subtypes. Activation of these receptors leads to increased production of cyclic adenosine monophosphate (cAMP) via stimulation of adenylate cyclase. This signaling pathway is important for modulating neuronal activity and has implications in motor control and cognitive functions.

The compound's selectivity for D1 receptors makes it a valuable tool in research for understanding the role of these receptors in the central nervous system. Unlike non-selective dopamine agonists, A-86929 does not significantly activate D2-like receptors, which are associated with different physiological and behavioral effects.

Therapeutic potential[edit | edit source]

Chemical structure of Adrogolide, a related compound

A-86929 has been investigated for its potential use in treating Parkinson's disease, a neurodegenerative disorder characterized by the loss of dopamine-producing neurons in the substantia nigra. By selectively stimulating D1 receptors, A-86929 may help alleviate motor symptoms associated with dopamine deficiency.

In addition to Parkinson's disease, A-86929 has been studied for its effects on cognitive function and schizophrenia. The compound's ability to enhance dopaminergic signaling in the prefrontal cortex suggests potential benefits in improving cognitive deficits and negative symptoms in schizophrenia.

Research and development[edit | edit source]

While A-86929 showed promise in preclinical studies, its development for clinical use has been limited. Challenges such as optimizing its pharmacokinetic properties and minimizing side effects have been areas of focus in ongoing research. Derivatives and analogs of A-86929, such as Adrogolide, continue to be explored for their therapeutic potential.

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