1. Signaling Pathways
  2. Immunology/Inflammation
  3. SphK

SphK (鞘氨醇激酶)

Sphingosine kinase

鞘氨醇激酶 (SphK1 和 SphK2) 是一种脂质酶,可催化鞘氨醇磷酸化形成鞘氨醇 1-磷酸 (S1P)。在哺乳动物中发现了两种 SphK 同工酶,即 SphK1 和 SphK2。SphK1 主要存在于红细胞、内皮细胞和肥大细胞的细胞质和质膜中。SphK2 较大,位于内质网、细胞核和线粒体中。

S1P 与五种不同的质膜鞘氨醇 1-磷酸受体 (S1P1-5) 结合,并可调节细胞内靶蛋白。S1P 具有广泛的生物学功能,包括促进细胞增殖和存活、免疫细胞运输、刺激血管生成和调节血管完整性。S1P 的积累与癌症和各种其他疾病的发展/进展有关,包括但不限于哮喘、炎症性肠病、类风湿性关节炎和糖尿病性肾病。因此,S1P 的生物合成途径是药物发现的合理目标。SphK1 和 SphK2 同工酶也是公认的治疗靶点。

Sphingosine kinase (SphK1 and SphK2) is a lipid enzyme that catalyses the phosphorylation of sphingosine to form sphingosine 1-phosphate (S1P). Two isoforms of SphK are found in mammalian organisms, SphK1 and SphK2. SphK1 is found primarily in the cytoplasm and the plasma membrane of erythrocyte, endothelial and mast cells. SphK2 is larger and localized to the endoplasmic reticulum, nucleus, and mitochondria.

S1P binds to five different plasma membrane sphingosine 1-phosphate receptors (S1P1-5) and can regulate intracellular target proteins. S1P has a wide range of biological functions including promotion of cellular proliferation and survival, immune cell trafficking, stimulation of angiogenesis, and regulation of vascular integrity. Accumulation of S1P has been linked to the development/progression of cancer and various other diseases including, but not limited to, asthma, inflammatory bowel disease, rheumatoid arthritis, and diabetic nephropathy. Thus, the biosynthetic route to S1P is a logical target for drug discovery. SphK1 and SphK2 isozymes are also recognized therapeutic targets.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-RS13668
    Sphk2 Mouse Pre-designed siRNA Set A Inhibitor
    Sphk2 Mouse Pre-designed siRNA Set A 包括针对 Sphk2 (Mouse) 基因的不同区域设计三对 siRNA,以及阴性对照、FAM 标记阴性对照和阳性对照。
    Sphk2 Mouse Pre-designed siRNA Set A
  • HY-16015R
    Opaganib (Standard) Inhibitor
    Opaganib (Standard) 是 Opaganib 的分析标准品。本产品用于研究及分析应用。Opaganib (ABC294640) 是一种选择性的竞争性的鞘氨醇激酶 2 (SK2) 抑制剂,Ki 为 9.8 μM。
    Opaganib (Standard)
  • HY-162580
    SphK2-IN-3 Inhibitor
    SphK2-IN-3 (compound 12q) 是一种选择性鞘氨醇激酶 2 抑制剂。SphK2-IN-3 对各种癌细胞具有抗增殖活性,可诱导肝癌细胞 HepG2 的 G2 期停滞和凋亡。
    SphK2-IN-3
  • HY-12900
    RB-005 Inhibitor
    RB-005 是一种对鞘氨醇激酶1 (SK1) 的选择性抑制剂 (IC50=3.6 µM),对另一种同工酶 SK2 的抑制作用较弱。RB-005 的选择性抑制作用有助于区分 SK1 和 SK2 的生物学功能和角色,可用于炎症性疾病和癌症的研究。
    RB-005
  • HY-16015A
    Opaganib hydrochloride Inhibitor
    Opaganib (ABC294640) hydrochloride 是一种选择性的竞争性的鞘氨醇激酶 2 (SK2) 抑制剂,Ki 为 9.8 μM。
    Opaganib hydrochloride
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