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Ex26

CAS No. 1233332-37-0

Ex26 ( —— )

产品货号. M34404 CAS No. 1233332-37-0

Ex26 (S1P1-IN-Ex26) 是一种强效和选择性的 sphingosine 1-phosphate receptor 1 (S1P1) 拮抗剂 (IC50=0.93 nM),对 S1P1 的选择性大于其他 Sphingosine 1-phosphate receptor 约 3,000 倍。Ex26 可用于实验性自身免疫性脑脊髓炎的研究。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥2432 有现货
10MG ¥3724 有现货
25MG ¥5840 有现货
50MG ¥8017 有现货
100MG ¥10440 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Ex26
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    Ex26 (S1P1-IN-Ex26) 是一种强效和选择性的 sphingosine 1-phosphate receptor 1 (S1P1) 拮抗剂 (IC50=0.93 nM),对 S1P1 的选择性大于其他 Sphingosine 1-phosphate receptor 约 3,000 倍。Ex26 可用于实验性自身免疫性脑脊髓炎的研究。
  • 产品描述
    Ex26 (S1P1-IN-Ex26) is a potent and selective sphingosine 1-phosphate receptor 1 (S1P1) antagonist (IC50=0.93 nM). Ex26 shows >3,000-fold selectivity for S1P1 over other Sphingosine 1-phosphate receptors. Ex26 can be used in experimental autoimmune encephalomyelitis reseach.
  • 体外实验
    Ex26 (0-10 μM; 1 h) treatment shows excellent selectivity for S1P1 over other Sphingosine 1-phosphate receptors.Cell Viability Assay Cell Line:U2OS cells, and Chinese hamster ovary cells Concentration:0-10 μM Incubation Time:1 hour Result:Confirmed a potent and selective antagonist of S1P1 (IC50=0.93 nM).
  • 体内实验
    Ex26 (i.p.; 3 mg/kg; once daily; 3 d) treatment disrupts S1P1 signaling inhibiting the lymphocyte and thymocyte egress.Ex26 (i.p.; 30 mg/kg; once daily; 15 d) treatment alleviates experimental autoimmune encephalomyelitis by S1P1 antagonism.Animal Model:Eight-week-old male C57Bl/6J mice Dosage:3 mg/kg Administration:Intraperitoneal injection; 3 mg/kg; once daily; 3 days Result:Induced lymphocyte sequestration at low doses, possessing an ED50 of 0.06 mg/kg after 2 hours treatment. Led to significant retention of T and B cells within the lymph nodes and significant decreases in T and B cells within the spleen.Animal Model:Eight-week-old male C57Bl/6J mice induced with experimental autoimmune encephalomyelitis Dosage:30 mg/kg Administration:Intraperitoneal injection; 30 mg/kg; once daily; 15 days Result:Inhibited both lymphocyte infiltration and destruction of the white matter in the spinal cord of mice euthanized at the end of the experiment.
  • 同义词
    ——
  • 通路
    GPCR/G Protein
  • 靶点
    S1P Receptor
  • 受体
    S1P Receptor
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    1233332-37-0
  • 分子量
    494.99
  • 分子式
    C28H28ClFN2O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    O=C(O)C1(NC(=O)C2=C(C=C(C=C2C)C=3C=C(C=CC3F)NC(C4=CC=C(Cl)C(=C4)C)C)C)CC1
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1. Stuart M Cahalan, et al. Sphingosine 1-phosphate receptor 1 (S1P(1)) upregulation and amelioration of experimental autoimmune encephalomyelitis by an S1P(1) antagonist. Mol Pharmacol. 2013 Feb;83(2):316-21.?
产品手册
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