1. Signaling Pathways
  2. Neuronal Signaling
  3. Glucosylceramide Synthase (GCS)

Glucosylceramide Synthase (GCS) (葡萄糖神经酰胺合成酶)

Glucosylceramide synthase (GCS), converting ceramide to glucosylceramide, catalyzes the first reaction of ceramide glycosylation in sphingolipid metabolism. This glycosylation by GCS is a critical step regulating the modulation of cellular activities by controlling ceramide and glycosphingolipids (GSLs). An increase of ceramide in response to stresses, such as chemotherapy, drives cells to proliferation arrest and apoptosis or autophagy; however, ceramide glycosylation promptly eliminates ceramide and consequently, these induced processes, thus protecting cancer cells. Furthermore, persistently enhanced ceramide glycosylation can increase GSLs, participating in selecting cancer cells to drug resistance. GCS is overexpressed in diverse drug-resistant cancer cells and in tumors of breast, colon, and leukemia that display poor response to chemotherapy. As ceramide glycosylation by GCS is a rate-limiting step in GSL synthesis, inhibition of GCS sensitizes cancer cells to anticancer drugs and eradicates cancer stem cells.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-155715
    G43 Inhibitor
    G43 是一种有效的选择性 glucosyltransferase 抑制剂,对 GtfB 和 GtfC 的Kd 值分别为3.7 μM和46.9 nM。G43 在体内外具有抗变形链球菌 (S. mutans) 的作用,可用于龋齿研究。
    G43
  • HY-114615
    AMP-Deoxynojirimycin Inhibitor
    AMP-Deoxynojirimycin (AMP-DNM) 是一种有效的神经酰胺葡萄糖基转移酶 (ceramide glucosyltransferase) 和 GCase 2 抑制剂。AMP-Deoxynojirimycin 也是一种 GlcCer 生物合成抑制剂。
    AMP-Deoxynojirimycin
  • HY-155716
    G43-C3-TEG Inhibitor
    G43-C3-TEG 是一种 糖基转移酶 抑制剂。G43-C3-TEG 通过减少 EPS (细胞外多糖) 的产生来减少生物膜的形成。
    G43-C3-TEG
  • HY-E70139
    UDP-GalNAc:β-1,3-N-acetylgalactosaminyltransferase 2
    UDP-GalNAc:β-1,3-N-acetylgalactosaminyltransferase 2 ( EC:2.4.1.313; B3GALNT2; β-1,3-N-acetylgalactosaminyltransferase II) 是一种糖基转移酶。
    UDP-GalNAc:β-1,3-N-acetylgalactosaminyltransferase 2
  • HY-116535C
    D-threo-PPMP
    D-threo-PPMP 是一种有效的葡萄糖神经酰胺 (GlcCer) 合酶的抑制剂。D-threo-PPMP 可以阻断核分裂,减少囊肿的产生。
    D-threo-PPMP
  • HY-17020S
    Miglustat-d9
    Miglustat-d9 是 Miglustat 的氘代物。Miglustat (N-Butyldeoxynojirimycin) 是葡萄糖神经酰胺合成酶抑制剂,可作用于I型戈谢病。
    Miglustat-d<sub>9</sub>
  • HY-12744A
    Genz-123346
    Genz-123346 是一种口服有效的葡萄糖神经酰胺合酶 (glucosylceramide synthase) 抑制剂。Genz-123346 阻断神经酰胺向葡萄糖神经酰胺 (GL1) 的转化,并抑制 GM1,IC50 值为 14 nM。
    Genz-123346
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