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Siramesine HCl

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Chemical Structure| 224177-60-0 同义名 : Lu 28-179 hydrochloride;Lu 28-179 HCl;Siramesine hydrochloride
CAS号 : 224177-60-0
货号 : A459463
分子式 : C30H32ClFN2O
纯度 : 98%
分子量 : 491.039
MDL号 : MFCD28144522
存储条件:

粉末 Sealed in dry,Room Temperature

液体 -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 40 mg/mL(81.46 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方:
生物活性
描述 Sigma receptors are ubiquitously expressed in mammals with high levels found in the central nervous system (CNS) and in cancer. There are two subtypes of sigma receptors, sigma-1 and sigma-2. Although sigma-1 receptors promote cell growth and thus inhibit cell death, activation of sigma-2 receptors was reported to trigger cell death[3]. Siramesine hydrochloride is a selective sigma receptors agonist with IC50s of 17 and 0.12 nM for sigma-1 and sigma-2 receptors, respectively[4]. In all cell lines tested, the siramesine concentration found to induce significant cell death within 8 h was in the range of 20 -30 μM, whereas 90% of cells were dead after treatment with 40–50 μM siramesine. Six hours post treatment with 25 or 40 μM siramesine, HaCaT cells exhibited characteristic apoptotic morphology with chromatin condensation and apoptotic body formation. In HaCaT cells, significant accumulation of the proforms of cysteine cathepsin L and cathepsins B and C was observed upon treatment with siramesine concentrations ≤15 μM[3].
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

2.04mL

0.41mL

0.20mL

10.18mL

2.04mL

1.02mL

20.36mL

4.07mL

2.04mL

参考文献

[1]Cesen MH, Repnik U, et al. Siramesine triggers cell death through destabilisation of mitochondria, but not lysosomes. Cell Death Dis. 2013 Oct 3;4:e818.

[2]Spirkoski J, Melo FR, Grujic M, et al. Mast cell apoptosis induced by siramesine, a sigma-2 receptor agonist. Biochem Pharmacol. 2012 Dec 15;84(12):1671-80.

[3]Česen MH, Repnik U, Turk V, Turk B. Siramesine triggers cell death through destabilisation of mitochondria, but not lysosomes. Cell Death Dis. 2013;4(10):e818

[4]Perregaard J, Moltzen EK, Meier E, Sánchez C. Sigma ligands with subnanomolar affinity and preference for the sigma 2 binding site. 1. 3-(omega-aminoalkyl)-1H-indoles. J Med Chem. 1995;38(11):1998‐2008