1. Signaling Pathways
  2. Metabolic Enzyme/Protease
  3. Sialyltransferase

Sialyltransferase

Sialyltransferase

Sialyltransferases are enzymes that transfer sialic acid to nascent oligosaccharides. Sialyltransferases (SiaTs) exhibit distinct characteristics and preferences, such as for substrates and glycosidic linkages. Sialyltransferases use cytidine monophosphate N-acetylneuraminic acid (CMP-Neu5Ac) as an activated sugar donor. Overexpression of sialyltransferases is associated with tumor hypersialylation and poor outcome[1].

Sialyltransferase Related Products (10):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-110288
    3FAx-Neu5Ac
    99.88%
    3FAx-Neu5Ac (Compound 8), a Sialic acid peracetylated analog, is a sialyltransferase inhibitor. 3FAx-Neu5Ac substantially reduces expression of the sialylated ligand sialyl Lewis X.
    3FAx-Neu5Ac
  • HY-112415
    Lith-O-Asp
    ≥98.0%
    Lith-O-Asp is a sialytransferase (ST) inhibitor, with IC50s of 12-37 μM.
    Lith-O-Asp
  • HY-112535
    α-2,3-sialyltransferase-IN-1
    ≥98.0%
    α-2,3-sialyltransferase-IN-1 (Lith-O-Asp analog) is a noncompetitive α-2,3-sialyltransferase inhibitor with an IC50 of 6 μM.
    α-2,3-sialyltransferase-IN-1
  • HY-E70024
    CMP-sialic acid synthetase (NmCSS)
    CMP-sialic acid synthetase (NmCSS) is an essential enzyme involved in the biosynthesis of carbohydrates and glycoconjugates containing sialic acids. CMP-sialic acid synthetase (NmCSS) activates free Sia, converting it to CMP-Sia, which is the only donor substrate for all sialyltransferases.
    CMP-sialic acid synthetase (NmCSS)
  • HY-E70055
    α-2,6-Sialyltransferase, pasteurella multocida (P-1059)
    alpha-2,6-Sialyltransferase (Pd26ST) (EC 2.4.99.1) is capable of sialylating both terminal and internal galactose and N-acetylgalactosamine, which producing terminal α2,6-sialosides.
    α-2,6-Sialyltransferase, pasteurella multocida (P-1059)
  • HY-E70056
    α2,3-Sialyltransferase, Pasteurella multocida (P-1059)
    α2,3-Sialyltransferase, Pasteurella multocida (P-1059) (PmST1(M144D)), a sialyltransferase, can be isolated from Pasteurella multocida. alpha-2,3-Sialyltransferase (PmST1) can be converted into regioselective α2-6-sialyltransferase by saturation mutagenesis and regioselective screening.
    α2,3-Sialyltransferase, Pasteurella multocida (P-1059)
  • HY-101218
    N-Biotinyl-6-aminohexanoic acid
    99.84%
    N-Biotinyl-6-aminohexanoic acid (N-(+)-Biotinyl-6-aminohexanoic acid) can be used to perform biotinylation.
    N-Biotinyl-6-aminohexanoic acid
  • HY-E70065
    alpha-2,3-Sialyltransferase (PmST2)
    alpha-2,3-Sialyltransferase (PmST2) is a sialyltransferase produced by Pasteurella multocida (Pm) and plays an important role in the pathogenesis of Pm. alpha-2,3-Sialyltransferase (PmST2) can be used to synthesize sialyllactosyl sphingosine (lyso-GM3).
    alpha-2,3-Sialyltransferase (PmST2)
  • HY-E70150
    ST6 Sialyltransferase 1
    ST6 Sialyltransferase 1 (EC:2.4.3.3, ST6GALNAC1, SIAT7A, Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1)? transfers a sialic acid, N-acetylneuraminic acid (NeuAc), in an alpha-2,6 linkage to O-linked GalNAc residues. ST6 Sialyltransferase 1 plays an important role in cancer.
    ST6 Sialyltransferase 1
  • HY-163548
    SPP-002
    Inhibitor ≥98.0%
    SPP-002 is a sulfate analogue that acts as a potential Sialyltransferase (ST) inhibitor. SPP-002 selectively inhibits n-glycosialylation with inhibition at least an order of magnitude greater than that of unmodified parental cholic acid (LCA). SPP-002 reduces tumor cell migration and invasion by inhibiting the integrin /FAK/Paxillin signaling pathway. SPP-002 can be used in the study of tumor metastasis.
    SPP-002