SB-215505

From WikiMD's WELLNESSPEDIA

SB-215505 is a compound that is used in scientific research. It acts as a potent and selective antagonist for the 5-HT2B receptor, with around 100x selectivity over other related targets.[1]

Pharmacology[edit]

SB-215505 has been used in the study of various diseases and conditions, including schizophrenia, depression, and anxiety disorders. It has been shown to potentiate the effects of other drugs, such as haloperidol, in the brain.[2]

Research[edit]

Research on SB-215505 has focused on its potential therapeutic applications. Studies have suggested that it may have potential in the treatment of conditions such as Parkinson's disease, obsessive-compulsive disorder, and eating disorders.[3]

See also[edit]

References[edit]

  1. "SB-215505, a selective 5-HT2B receptor antagonist, potentiates haloperidol-induced dopamine release in rat striatum and nucleus accumbens".Neuropharmacology.2000;39(5)
    793–802.doi:10.1016/S0028-3908(99)00168-6.PMID:10728886.
  2. "SB-215505, a selective 5-HT2B receptor antagonist, potentiates haloperidol-induced dopamine release in rat striatum and nucleus accumbens".Neuropharmacology.2000;39(5)
    793–802.doi:10.1016/S0028-3908(99)00168-6.PMID:10728886.
  3. "SB-215505, a selective 5-HT2B receptor antagonist, potentiates haloperidol-induced dopamine release in rat striatum and nucleus accumbens".Neuropharmacology.2000;39(5)
    793–802.doi:10.1016/S0028-3908(99)00168-6.PMID:10728886.


Medical Disclaimer: WikiMD is for informational purposes only and is not a substitute for professional medical advice. Content may be inaccurate or outdated and should not be used for diagnosis or treatment. Always consult your healthcare provider for medical decisions. Verify information with trusted sources such as CDC.gov and NIH.gov. By using this site, you agree that WikiMD is not liable for any outcomes related to its content. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.