CYM 5541

Pricing Availability   Qty
说明: Selective S1P3 receptor allosteric agonist
化学名: N,N-Dicyclohexyl-5-cyclopropyl-3-isoxazolecarboxamide
纯度: ≥97% (HPLC)
说明书
引用文献 (6)
评论

生物活性 for CYM 5541

CYM 5541 is a selective sphingosine-1-phosphate receptor 3 (S1P3) allosteric agonist (EC50 = 72-132 nM). Occupies a different space within the ligand binding pocket of S1P3 than S1P. Displays no activity at S1P1, S1P2, S1P4 and S1P5 receptors at concentrations up to 10 μM. Shows no significant activities in a profiling panel of 55 GPCRs, ion channels and transporters.

化合物库 for CYM 5541

CYM 5541 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 5541

分子量 316.44
公式 C19H28N2O2
储存 Store at +4°C
纯度 ≥97% (HPLC)
CAS Number 945128-26-7
PubChem ID 17253208
InChI Key NDKGACIWVAOUQH-UHFFFAOYSA-N
Smiles O=C(N(C3CCCCC3)C2CCCCC2)C1=NOC(C4CC4)=C1

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 5541

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 31.64 100
ethanol 15.82 50

制备储备液 for CYM 5541

以下数据基于产品分子量 316.44。 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 3.16 mL 15.8 mL 31.6 mL
5 mM 0.63 mL 3.16 mL 6.32 mL
10 mM 0.32 mL 1.58 mL 3.16 mL
50 mM 0.06 mL 0.32 mL 0.63 mL

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参考文献 for CYM 5541

参考文献是支持产品生物活性的出版物。

Jo et al (2012) Novel selective allosteric and bitopic ligands for the S1P3 receptor. ACS Chem.Biol. 7 1975 PMID: 22971058


If you know of a relevant reference for CYM 5541, please let us know.

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关键词: CYM 5541, CYM 5541 supplier, CYM5541, Selective, S1P3, receptors, allosteric, agonists, SIP, Sphingosine-1-phosphate, Sphingosine, Receptors, 4897, Tocris Bioscience

6 篇 CYM 5541 的引用文献

引用文献是使用了 Tocris 产品的出版物。 CYM 5541 的部分引用包括:

Antonio et al (2020) Developmental potential of aneuploid human embryos cultured beyond implantation. Nat Commun 11 3987 PMID: 32778678

Tzu-Ming et al (2020) Utilizing Designed Receptors Exclusively Activated by Designer Drug Chemogenetic Tools to Identify Beneficial G Protein-Coupled Receptor Signaling for Fibrosis. J Pharmacol Exp Ther 375 357-366 PMID: 32848074

Matsushima-Nishiwaki et al (2018) Sphingosine 1-phosphate (S1P) reduces hepatocyte growth factor-induced migration of hepatocellular carcinoma cells via S1P receptor 2. PLoS One 13 e0209050 PMID: 30543684

Hoffmann et al (2015) Fingolimod induces neuroprotective factors in human astrocytes. J Neuroinflammation 12 184 PMID: 26419927


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