70858-45-6

Paucimannose Chemical Structure
70858-45-6

Chemical Structure

Paucimannose

  • CAS No.: 70858-45-6
  • Formula:C34H58N2O26
  • Molecular Weight:910.82

IUPAC Name: 5-bromo-4-methylthiophene-2-carboxamide

InChIKey: DJUIFTOHRFYXSA-YONMKSMASA-N

SMILES: OC[C@@H](O[C@H]([C@@H]([C@H]1O)NC(C)=O)O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)NC(C)=O)[C@H]1O[C@H]2[C@H]([C@H]([C@@H]([C@H](O2)CO[C@H]3O[C@@H]([C@H]([C@@H]([C@@H]3O)O)O)CO)O)O[C@H]4O[C@@H]([C@H]([C@@H]([C@@H]4O)O)O)CO)O

Biological Activity: Paucimannose is a mannosidic N-glycan epitope. It acts as a carcinoembryonic antigen, and a marker for cancer, stem cell properties and inflammation. Paucimannose mainly exists in plants and invertebrates. It consists of oligomannose-type N-glycans that preferentially bind to mannose-binding lectin. Paucimannose localizes on the surface of resting cells and translocates upon cell activation. It can be used in studies related to Pseudomonas aeruginosa infection, cancer and pancreatitis[1][2][3].

Cat. No. Product Name Purity Description Pricing
HY-N10631
Paucimannose Paucimannose is a mannosidic N-glycan epitope. It acts as a carcinoembryonic antigen, and a marker for cancer, stem cell properties and inflammation. Paucimannose mainly exists in plants and invertebrates. It consists of oligomannose-type N-glycans that preferentially bind to mannose-binding lectin. Paucimannose localizes on the surface of resting cells and translocates upon cell activation. It can be used in studies related to Pseudomonas aeruginosa infection, cancer and pancreatitis.
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