1. TGF-beta/Smad
  2. TGF-β Receptor
  3. SD-208

SD-208 (GMP) 是 GMP 级别的 SD-208 (HY-13227)。GMP 级别的小分子可用做细胞疗法中的辅助试剂。SD-208 是一种选择性的 TGF-βRI (ALK5) 抑制剂,IC50 值为 48 nM,对其选择性是对 TGF-βRII 的 100 多倍。

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SD-208

SD-208 Chemical Structure

CAS No. : 627536-09-8

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

SD-208 (GMP) is SD-208 (HY-13227) produced by using GMP guidelines. GMP small molecules works appropriately as an auxiliary reagent for cell therapy manufacture. SD-208 is a selective TGF-βRI (ALK5) inhibitor with IC50 of 48 nM, and > 100-fold selectivity over TGF-βRII.

体外研究
(In Vitro)

SD-208 (GMP) 可抑制细胞生长和组成性以及 TGF-β 诱发的迁移和侵袭,并增强小鼠 SMA-560 和人类 LN-308 胶质瘤细胞的免疫原性[1]
SD-208 (GMP) 可阻断 TGF-β 诱导的受体相关 Smads、Smad2 和 Smad3 磷酸化,并在体外刺激上皮-间质转分化、迁移和侵袭到 Matrigel 中[2]
SD-208 (GMP) 还可在体外消除 TGF-β 对新生内膜平滑肌样细胞 (SMLC) 增殖和迁移的促进作用[3]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

SD-208 (GMP) (1 mg/mL,口服) 显著延长了 SMA-560 胶质瘤小鼠的中位生存期[1]
在同基因 129S1 小鼠中,SD-208 (GMP) (60 mg/kg/d,口服) 可抑制原发性 R3T 肿瘤生长,并减少肺转移瘤的数量和大小[2]
在小鼠主动脉同种异体移植模型中,SD-208 (GMP) 有效减少移植动脉硬化 (TA) 内膜增生的形成[3]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

352.75

Formula

C17H10ClFN6

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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  • 稀释计算器

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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
SD-208
目录号:
HY-13227G
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