3672-15-9

Mannose 6 phosphate Chemical Structure
3672-15-9

Chemical Structure

Mannose 6 phosphate

  • CAS No.: 3672-15-9
  • Formula:C6H13O9P
  • Molecular Weight:260.14

IUPAC Name: 8-bromo-6-methoxyquinoline-3-carboxylic acid

InChIKey: VFRROHXSMXFLSN-KVTDHHQDSA-N

SMILES: O=C[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)COP(O)(O)=O

Biological Activity: Mannose 6 phosphate is an essential precursor for mannosyl glycoconjugates, including lipid-linked oligosaccharides (LLO; glucose3mannose9GlcNAc2-P-P-dolichol) used for protein N-glycosylation. Mannose 6 phosphate causes specific LLO cleavage. Mannose 6 phosphate causes specific degradation of G3M9Gn2-P-P-Dol. Complexes containing Mannose 6 phosphate can remodel the dermal collagen network, improve skin biomechanical properties, and reverse visible signs of aging. Mannose 6 phosphate can be used in research related to skin aging[1][2].

Cat. No. Product Name Purity Description Pricing
HY-150177
Mannose 6 phosphate Mannose 6 phosphate is an essential precursor for mannosyl glycoconjugates, including lipid-linked oligosaccharides (LLO; glucose3mannose9GlcNAc2-P-P-dolichol) used for protein N-glycosylation. Mannose 6 phosphate causes specific LLO cleavage. Mannose 6 phosphate causes specific degradation of G3M9Gn2-P-P-Dol. Complexes containing Mannose 6 phosphate can remodel the dermal collagen network, improve skin biomechanical properties, and reverse visible signs of aging. Mannose 6 phosphate can be used in research related to skin aging.
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This product is a controlled substance and not for sale in your territory.

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This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References