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S87974

SEW 2871

源叶(MedMol) >98%
  • 英文名:
  • SEW 2871
  • 别名:
  • 5 - [4 - 苯基-5 - (三氟甲基)-2 - 噻吩基] -3 - [3 - (三氟甲基)苯基] -1,2,4 - 恶二唑
  • CAS号:
  • 256414-75-2
  • 分子式:
  • C20H10F6N2OS
  • 分子量:
  • 440.36
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
源叶(MedMol) S87974-5mg >98% ¥400.00元 6 - - - EA 加入购物车
源叶(MedMol) S87974-10mg >98% ¥770.00元 8 - - - EA 加入购物车
源叶(MedMol) S87974-25mg >98% ¥1700.00元 8 - - - EA 加入购物车
源叶(MedMol) S87974-50mg >98% ¥3200.00元 4 - - - EA 加入购物车
源叶(MedMol) S87974-100mg >98% ¥6000.00元 2 - - - EA 加入购物车
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参考文献

质检证书(COA)

摩尔浓度计算器

相关产品

  • 产品描述: SEW2871 is an orally active, potent, highly selective S1P1 (sphingosine-1-phosphate type 1 receptor) agonist, with an EC50 of 13.8 nM. SEW2871 activates ERK, Akt, and Rac signaling pathways and induces S1P1 internalization and recycling. SEW2871 reduces lymphocyte numbers in blood. SEW2871 can be used for the research of diabetes, Alzheimer’s disease, liver fibrosis, and inflammatory responses
  • 靶点: S1PR1:13.8 nM (EC50);S1PReceptor; LPLReceptor
  • 体内研究:
    SEW2871 (20 mg/kg, Gavage, once daily for 2 weeks) ameliorates established experimental colitis in IL-10–/– mice. SEW2871 (0.5 mg/kg, IP, daily for 2 weeks) inhibited β amyloid (Aβ1-42)-induced spatial memory impairment and hippocampal neuronal loss in a rat model of Alzheimer’s disease. SEW2871 (0-0.3 mg/kg, IV) attenuates LPS-induced acute inflammatory lung injury, produces dose-dependent alveolar and vascular barrier protection in C57Bl/6 mice. SEW2871 is effective in protecting kidneys against ischaemia-reperfusion injury by reducing CD4+ T cell infiltration in mice. Animal Model: IL-10–/– (interleukin (IL)-10 gene-deficient) mice, a murine model of Crohn's disease (CD) Dosage: 20 mg/kg Administration: Gavage, once daily for 2 weeks Result: Ameliorated established colitis in IL-10–/– mice, associated with a reduction of serum amyloid A concentration, a decreased colon MPO concentration, a depletion of the peripheral CD4+CD45+ T cells and a reduction of the homing of T cells into colon LP. Suppressed typical cytokines of T helper type 1 (Th1) and Th17 cells and p-STAT-3 expression, and significantly decreased TNF-α, IFN-γ, IL-1β and IL-17A mRNA levels.
  • 参考文献:
    1. Park SJ, et al. Sphingosine 1-Phosphate Receptor Modulators and Drug Discovery. Biomol Ther (Seoul). 2017 Jan 1;25(1):80-90. 2. Jo E, et al. S1P1-selective in vivo-active agonists from high-throughput screening: off-the-shelf chemical probes of receptor interactions, signaling, and fate. Chem Biol. 2005 Jun;12(6):703-15. 3. Dong J, et al. Oral treatment with SEW2871, a sphingosine-1-phosphate type 1 receptor agonist, ameliorates experimental colitis in interleukin-10 gene deficient mice. Clin Exp Immunol. 2014 Jul;177(1):94-101.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.271 ml 11.354 ml 22.709 ml
    5 mM 0.454 ml 2.271 ml 4.542 ml
    10 mM 0.227 ml 1.135 ml 2.271 ml
    50 mM 0.045 ml 0.227 ml 0.454 ml
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