CYM 5442 hydrochloride

Pricing Availability   Qty
说明: Selective S1P1 receptor agonist
化学名: 2-(4-(5-(3,4-Diethoxyphenyl)-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-inden-1-yl amino) ethanol hydrochloride
纯度: ≥98% (HPLC)
说明书
引用文献 (6)
评论

生物活性 for CYM 5442 hydrochloride

CYM 5442 hydrochloride is a potent and selective S1P1 agonist in vitro (EC50 = 1.35 nM). Activates S1P1-mediated p42/p44 MAPK phosphorylation in CHO-K1 cells transfected with S1P1. Induces acute lymphopenia in mice. Brain penetrant.

化合物库 for CYM 5442 hydrochloride

CYM 5442 hydrochloride is also offered as part of the Tocriscreen 2.0 Max. 了解 Tocris 化合物库的更多信息。

技术数据 for CYM 5442 hydrochloride

分子量 445.94
公式 C23H27N3O4.HCl
储存 Store at -20°C
纯度 ≥98% (HPLC)
CAS Number 1783987-80-3
PubChem ID 90488865
InChI Key KMZLVDAVGXYZDA-UHFFFAOYSA-N
Smiles OCCNC3CCC(C3=CC=C4)=C4C1=NOC(C2=CC(OCC)=C(OCC)C=C2)=N1.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.

溶解性数据 for CYM 5442 hydrochloride

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 44.59 100

制备储备液 for CYM 5442 hydrochloride

以下数据基于产品分子量 445.94。 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.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
1 mM 2.24 mL 11.21 mL 22.42 mL
5 mM 0.45 mL 2.24 mL 4.48 mL
10 mM 0.22 mL 1.12 mL 2.24 mL
50 mM 0.04 mL 0.22 mL 0.45 mL

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产品说明书 for CYM 5442 hydrochloride

分析证书/产品说明书
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参考文献 for CYM 5442 hydrochloride

参考文献是支持产品生物活性的出版物。

Gonzalez-Cabrera et al (2008) Full pharmacological efficacy of a novel S1P1 agonist that does not require S1P-like headgroup interactions Mol.Pharmacol. 74 1308 PMID: 18708635


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关键词: CYM 5442 hydrochloride, CYM 5442 hydrochloride supplier, sphingosine-1-phosphate, S1P1, receptors, agonists, CYM5442, hydrochloride, Sphingosine-1-phosphate, Receptors, 3601, Tocris Bioscience

6 篇 CYM 5442 hydrochloride 的引用文献

引用文献是使用了 Tocris 产品的出版物。 CYM 5442 hydrochloride 的部分引用包括:

Janes et al (2014) The development and maintenance of PacT.-induced neuropathic pain require activation of the sphingosine 1-phosphate receptor subtype 1. J Biol Chem 289 21082 PMID: 24876379

Balaji M et al (2021) Two distinct trophectoderm lineage stem cells from human pluripotent stem cells. J Biol Chem 296 100386 PMID: 33556374

Li et al (2015) Sphingosine 1-phosphate enhances the excitability of rat sensory neurons through activation of sphingosine 1-phosphate receptors 1 and/or 3. J Neuroinflammation 12 70 PMID: 25880547

Hübner et al (2018) Wnt/β-catenin signaling regulates VE-cadherin-mediated anastomosis of brain capillaries by counteracting S1pr1 signaling. Nat Commun 9 4860 PMID: 30451830


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