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Submit ReviewTandospirone hydrochloride is a 5-HT1A receptor partial agonist (Ki = 27 nM) that displays selectivity over 5-HT2, 5-HT1C, α1, α2, D1 and D2 receptors (Ki values ranging from 1300 - 41000 nM). Inactive at 5-HT uptake sites, 5-HT1B, β-adrenergic, muscarinic and benzodiazepine receptors. Displays anxiolytic activity.
分子量 | 419.95 |
公式 | C21H29N5O2.HCl |
储存 | Store at +4°C |
纯度 | ≥98% (HPLC) |
CAS Number | 99095-10-0 |
PubChem ID | 13422623 |
InChI Key | ACVFJYKNBOHIMH-DPFKZJTMSA-N |
Smiles | [H][C@]13[C@](C(N(CCCCN4CCN(C5=NC=CC=N5)CC4)C3=O)=O)([H])[C@@H]2CC[C@H]1C2.Cl |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 41.99 | 100 | |
water | 41.99 | 100 |
以下数据基于产品分子量 419.95。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 2.38 mL | 11.91 mL | 23.81 mL |
5 mM | 0.48 mL | 2.38 mL | 4.76 mL |
10 mM | 0.24 mL | 1.19 mL | 2.38 mL |
50 mM | 0.05 mL | 0.24 mL | 0.48 mL |
参考文献是支持产品生物活性的出版物。
Hamik et al (1990) Analysis of tandospirone (SM-3997) interactions with neurotransmitter receptor binding sites. Biol.Psychiatry 28 99 PMID: 1974152
Pollard et al (1992) Effects of tandospirone in three behavioral tests for anxiolytics. Eur.J.Pharmacol. 221 297 PMID: 1358655
Matsubara et al (2006) Tandospirone, a 5-HT1A agonist, ameliorates movement disorder via non-DArgic systems in rats with unilateral 6-hydroxyDA-generated lesions. Brain Res. 1112 126 PMID: 16884702
If you know of a relevant reference for Tandospirone hydrochloride, please let us know.
关键词: Tandospirone hydrochloride, Tandospirone hydrochloride supplier, Selective, 5-HT1A, partial, agonists, Serotonin, Receptors, SM3997, SM-3997, 2854, Tocris Bioscience
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