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Submit ReviewSM-21 maleate is a potent and selective σ2 antagonist with central effects following systemic administration. Causes increased release of acetylcholine at central muscarinic synapses. Potent analgesic (efficacy comparable to morphine) and nootropic agent.
分子量 | 453.92 |
公式 | C18H24ClNO3.C4H4O4 |
储存 | Store at RT |
纯度 | ≥99% (HPLC) |
CAS Number | 155059-42-0 |
PubChem ID | 11691005 |
InChI Key | BHXGTFUQDGMXHA-BTJKTKAUSA-N |
Smiles | OC(=O)\C=C/C(O)=O.CCC(OC1=CC=C(Cl)C=C1)C(=O)OC1CC2CCC(C1)N2C |
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 | |||
water | 11.35 | 25 |
以下数据基于产品分子量 453.92。 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 |
---|---|---|---|
0.25 mM | 8.81 mL | 44.06 mL | 88.12 mL |
1.25 mM | 1.76 mL | 8.81 mL | 17.62 mL |
2.5 mM | 0.88 mL | 4.41 mL | 8.81 mL |
12.5 mM | 0.18 mL | 0.88 mL | 1.76 mL |
参考文献是支持产品生物活性的出版物。
Ghelardini et al (1997) Antinociceptive profile of 3-α-tropanyl-(2-Cl)-acid phenoxybutyrate (SM-21): a novel analgesic with a presynaptic cholinergic mechanism of action. J.Pharmacol.Exp.Ther. 282 430 PMID: 9223584
Ghelardini et al (2000) Pharmacological identification of SM-21, the novel σ2 antagonist. Pharmacol.Biochem.Behav. 67 659 PMID: 11164098
Matsumoto and Mack (2001) (±)-SM 21 attenuates the convulsive and locomotor stimulatory effects of cocaine in mice. Eur.J.Pharmacol. 417 R1 PMID: 11301071
If you know of a relevant reference for SM-21 maleate, please let us know.
关键词: SM-21 maleate, SM-21 maleate supplier, Selective, σ2, sigma2, receptors, antagonists, Presynaptic, cholinergic, modulators, Muscarinic, Acetylcholine, release, Nicotinic, nAChR, Other, Sigma2, Receptors, Non-selective, Muscarinics, 0751, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 SM-21 maleate 的部分引用包括:
Dolma et al (2016) Inhibition of Dopamine Receptor D4 Impedes Autophagic Flux, Proliferation, and Survival of Glioblastoma Stem Cells. Cancer Cell 29 859 PMID: 27300435
Matsumoto et al (2007) Effects of UMB24 and (+/-)-SM 21, putative σ2-preferring antagonists, on behavioral toxic and stimulant effects of cocaine in mice. PLoS One 86 86 PMID: 17241657
Ishima and Hashimoto (2012) Potentiation of nerve growth factor-induced neurite outgrowth in PC12 cells by ifenprodil: the role of σ-1 and IP3 receptors. J Diabetes Res 7 e37989 PMID: 22655093
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