Misplaced Pages

Mannosamine

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Mannosamine
Names
IUPAC name 2-Amino-2-deoxy-D-mannopyranose
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
MeSH mannosamine
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C6H13NO5/c7-3-5(10)4(9)2(1-8)12-6(3)11/h2-6,8-11H,1,7H2/t2-,3+,4-,5-,6?/m1/s1Key: MSWZFWKMSRAUBD-CBPJZXOFSA-N
  • InChI=1/C6H13NO5/c7-3-5(10)4(9)2(1-8)12-6(3)11/h2-6,8-11H,1,7H2/t2-,3+,4-,5-,6?/m1/s1Key: MSWZFWKMSRAUBD-CBPJZXOFBL
SMILES
  • C(1(((C(O1)O)N)O)O)O
Properties
Chemical formula C6H13NO5
Molar mass 179.171 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

D-Mannosamine (2-amino-2-deoxymannose) is a hexosamine derivative of mannose.

See also

References

  1. Lisanti MP, Field MC, Caras IW, Menon AK, Rodriguez-Boulan E (August 1991). "Mannosamine, a novel inhibitor of glycosylphosphatidylinositol incorporation into proteins". The EMBO Journal. 10 (8): 1969–1977. doi:10.1002/j.1460-2075.1991.tb07726.x. PMC 452876. PMID 1829673.
  2. Patwari P, Kurz B, Sandy JD, Grodzinsky AJ (February 2000). "Mannosamine inhibits aggrecanase-mediated changes in the physical properties and biochemical composition of articular cartilage". Archives of Biochemistry and Biophysics. 374 (1): 79–85. doi:10.1006/abbi.1999.1538. PMID 10640399.
Stub icon

This article about an organic compound is a stub. You can help Misplaced Pages by expanding it.

Categories: