CMP-Sialic acidCMP-Sialic acid - High-quality laboratory reagent available from Gentaur. Catalog: 804-HY-112942.804-HY-112942804-HY-112942Business & Industrial > Science & LaboratoryCMP-Sialic acid
Gentaur
EUR12027-02-22

CMP-Sialic acid

CAT:
804-HY-112942
Size:
1 Each
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
CMP-Sialic acid - image 1

CMP-Sialic acid

  • Description:

    CMP-Sialic acid (CMP-Neu5Ac) is an allosteric inhibitor of UDP-GlcNAc 2-epimerase. CMP-Sialic acid provides a substrate for Golgi sialyltransferases. CMP-Sialic acid is an important sugar nucleotide for biosynthesis of sialic acid and its conjugates[1].
  • Product Name Alternative:

    CMP-Neu5Ac
  • UNSPSC:

    12352005
  • Hazard Statement:

    H302-H315-H319-H335
  • Target:

    Endogenous Metabolite
  • Type:

    Reference compound
  • Related Pathways:

    Metabolic Enzyme/Protease
  • Applications:

    Metabolism-sugar/lipid metabolism
  • Field of Research:

    Metabolic Disease
  • Assay Protocol:

    https://www.medchemexpress.com/cmp-sialic-acid.html
  • Solubility:

    10 mM in DMSO
  • Smiles:

    O[C@@H]1[C@H](O[C@@H](N2C(N=C(N)C=C2)=O)[C@@H]1O)COP(O[C@@]3(O[C@@]([C@H](NC(C)=O)[C@@H](O)C3)([H])[C@H](O)[C@H](O)CO)C(O)=O)(O)=O
  • Molecular Formula:

    C20H31N4O16P
  • Molecular Weight:

    614.45
  • Precautions:

    P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
  • References & Citations:

    [1]Münster AK, et al. Mammalian cytidine 5'-monophosphate N-acetylneuraminic acid synthetase: a nuclear protein with evolutionarily conserved structural motifs. Proc Natl Acad Sci U S A. 1998 Aug 4;95 (16) :9140-5.|[2]Jing Song, et al. Reassembled Biosynthetic Pathway for a Large-scale Synthesis of CMP-Neu5Ac. Mar Drugs. 2003 Dec; 1 (4) : 34-45.|[3]Mercado CP, et al. A serotonin-induced N-glycan switch regulates platelet aggregation. Sci Rep. 2013 Sep 30;3:2795.
  • Shipping Conditions:

    Room temperature
  • Scientific Category:

    Reference compound1
  • Clinical Information:

    No Development Reported
  • Isoform:

    Human Endogenous Metabolite
  • Citation 01:

    Nature. 2025 Jul;643 (8070) :192-200.|Cell Host Microbe. 2025 Jul 9;33 (7) :1133-1145.e4.
  • CAS Number:

    [3063-71-6]