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S1R agonist 1 hydrochloride

目录号 : GC71102

S1R agonist 1 hydrochloride是选择性S1R激动剂,S1R和S2R的Kis分别为0.93nM和72nM。

S1R agonist 1 hydrochloride Chemical Structure

Cas No.:242487-82-7

规格 价格 库存 购买数量
5 mg
¥540.00
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10 mg
¥900.00
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25 mg
¥1,800.00
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50 mg
¥2,700.00
现货
100 mg
¥4,320.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

S1R agonist 1 (Compound 6b) hydrochloride is a selective S1R agonist with Kis of 0.93 nM and 72 nM for S1R and S2R, respectively. S1R agonist 1 hydrochloride exhibits neuroprotection against ROS and NMDA-induced neurotoxicity.

S1R agonist 1 (Compound 6b; 0.1-5 μM) hydrochloride significantly increases the nerve growth factor (NGF) induced neurite outgrowth at all the tested concentrations in a dose-dependent manner in PC12 cell lines[1].
S1R agonist 1 (24 h) hydrochloride significantly prevents cell damage induced by Rotenone when tested at the concentration of 1 μM in SHSY5Y cells[1].
S1R agonist 1 (0.1-5 μM; 24 h) hydrochloride demonstrates a neuroprotective effect against NMDA stimuli in SHSY5Y cells[1].
S1R agonist 1 (0-10 μM; 24-72 h) hydrochloride shows no cytotoxicity against A549, LoVo and Panc-1 cells[1].

S1R agonist 1 (Compound 6b; 0.1-50 μM; 120 h) hydrochloride induces the death of 4 Zebrafish embryos out of 8 at 10 μM[1].

References:
[1]. Linciano P, et al. Novel S1R agonists counteracting NMDA excitotoxicity and oxidative stress: A step forward in the discovery of neuroprotective agents. Eur J Med Chem. 2023 Mar 5;249:115163.

Chemical Properties

Cas No. 242487-82-7 SDF
分子式 C20H26ClNO 分子量 331.88
溶解度 DMSO : 100 mg/mL (301.31 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO) 储存条件 -20°C, sealed storage, away from moisture
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1 mg 5 mg 10 mg
1 mM 3.0131 mL 15.0657 mL 30.1314 mL
5 mM 0.6026 mL 3.0131 mL 6.0263 mL
10 mM 0.3013 mL 1.5066 mL 3.0131 mL
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