AS 1949490

Pricing Availability   Qty
说明: SH2 domain-containing inositol 5'-phosphatase 2 (SHIP2) inhibitor
化学名: 3-[(4-Chlorophenyl)methoxy]-N-[(1S)-1-phenylethyl]thiophene-2-carboxamide
纯度: ≥99% (HPLC)
说明书
引用文献 (9)
评论

生物活性 for AS 1949490

AS 1949490 is a selective SHIP2 (SH2 domain-containing inositol 5'-phosphatase 2) inhibitor (IC50 values are 0.34 μM and 0.62 μM for mouse and human respectively); displays approximately 30-fold affinity for SHIP2 over SHIP1. Increases insulin-induced phosphorylation of Akt in L6 myotubules. Stimulates activation of glucose metabolism; regulates gluconeogenesis in vitro and in vivo and exhibits antidiabetic effects. Also promotes increased BDNF mRNA levels in cultured cortical neurons and has memory enhancing and antidepressant effects in vivo.

化合物库 for AS 1949490

AS 1949490 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 AS 1949490

分子量 371.88
公式 C20H18ClNO2S
储存 Store at RT
纯度 ≥99% (HPLC)
CAS Number 1203680-76-5
PubChem ID 44473434
InChI Key RFZPGNRLOKVZJY-AWEZNQCLSA-N
Smiles ClC(C=C2)=CC=C2COC1=C(C(N[C@@H](C)C3=CC=CC=C3)=O)SC=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 AS 1949490

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 37.19 100
ethanol 37.19 100

制备储备液 for AS 1949490

以下数据基于产品分子量 371.88。 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 2.69 mL 13.45 mL 26.89 mL
5 mM 0.54 mL 2.69 mL 5.38 mL
10 mM 0.27 mL 1.34 mL 2.69 mL
50 mM 0.05 mL 0.27 mL 0.54 mL

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参考文献 for AS 1949490

参考文献是支持产品生物活性的出版物。

Suwa et al (2010) Glucose metabolism activation by SHIP2 inhibitors via up-regulation of GLUT1 gene in L6 myotubes. Eur.J.Pharmacol. 642 177 PMID: 20558154

Suwa et al (2009) Discovery and functional characterization of a novel small molecule inhibitor of the intracellular phosphatase, SHIP2. Br.J.Pharmcol. 158 879 PMID: 19694723

Tsuneki et al (2019) AS1949490, an inhibitor of 5'-lipid phosphatase SHIP2, promotes protein kinase C-dependent stabilization of brain-derived neurotrophic factor mRNA in cultured cortical neurons. Eur.J.Pharmacol. 851 69 PMID: 30753865


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关键词: AS 1949490, AS 1949490 supplier, AS1949490, SHIP2, inhibitor, inhibits, SH2, domain, containing, inositol, 5'phosphate, 2, diabetes, antidiabetic, inhibitors, Inositol, Phosphatases, 3718, Tocris Bioscience

9 篇 AS 1949490 的引用文献

引用文献是使用了 Tocris 产品的出版物。 AS 1949490 的部分引用包括:

Sérgio B et al (2017) Fibroblasts derived from patients with opsismodysplasia display SHIP2-specific cell migration and adhesion defects. Hum Mutat 38 1731-1739 PMID: 28869677

Justyna et al (2022) Cell Culture Media, Unlike the Presence of Insulin, Affect α-Synuclein Aggregation in Dopaminergic Neurons. Biomolecules 12 PMID: 35454152

Hak et al (2018) FBP17 and CIP4 recruit SHIP2 and lamellipodin to prime the plasma membrane for fast endophilin-mediated endocytosis. Nat Cell Biol 20 1023 PMID: 30061681

Ghosh et al (2018) Inhibition of SHIP2 activity inhibits cell migration and could prevent metastasis in breast cancer cells. J Cell Sci 131 PMID: 30012834


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