Tandospirone
Tandospirone, sold under the brand name Sediel, is an anxiolytic and antidepressant medication used in Japan and China, where it is marketed by Dainippon Sumitomo Pharma. It is a member of the azapirone class of drugs and is closely related to other azapirones like buspirone and gepirone.
Tandospirone was introduced for medical use in Japan in 1996 and in China in 2004.
Medical uses
Anxiety and depression
Tandospirone is most commonly used as a treatment for anxiety and depressive disorders, such as generalised [anxiety disorder] and dysthymia respectively. For both indications it usually takes a couple of weeks for therapeutic effects to begin to be seen, although at higher doses more rapid anxiolytic responses have been seen. It has also been used successfully as a treatment for bruxism.Augmentation for depression
Tandospirone can be used as an effective augmentation, especially when coupled with fluoxetine or clomipramine.Other uses
Tandospirone might been tried successfully as an adjunctive treatment for cognitive symptoms in schizophrenic individuals.Side effects
Common adverse effects include:- Dizziness
- Drowsiness
- Insomnia
- Headache
- Gastrointestinal disorders
- Dry mouth
- Negative influence on explicit memory function
- Nausea
It is not believed to be addictive but is known to produce mild withdrawal effects after abrupt discontinuation.
Pharmacology
Pharmacodynamics
Tandospirone acts as a potent and selective 5-HT1A receptor partial agonist, with a Ki affinity value of 27 ± 5 nM and approximately 55 to 85% intrinsic activity. It has relatively weak affinity for the 5-HT2A, 5-HT2C, α1-adrenergic, α2-adrenergic, D1, and D2 receptors, and is essentially inactive at the 5-HT1B, 5-HT1D, β-adrenergic, and muscarinic acetylcholine receptors, serotonin transporter, and benzodiazepine allosteric site of the GABAA receptor. There is evidence of tandospirone having low but significant antagonistic activity at the α2-adrenergic receptor through its active metabolite 1-(2-pyrimidinyl)piperazine. Tandospirone has been found to produce antiaggressive effects in rodents.Chemistry
Synthesis
- The Noreximide precursor also has dual uses to make Taglutimide & Tripamide & Lurasidone.
The catalytic hydrogenation of cis-5-Norbornene-exo-2,3-dicarboxylic anhydride gives Norbornane-2exo,3exo-dicarboxylic Acid-anhydride . Reaction with aqueous ammonia leads to Exo-2,3-norbornanedicarboximide . Alkylation with 1,4-dibromobutane gives . Alkylation of the remaining halogen with 2-Pyrimidine completed the synthesis of Tandospirone.