Methyl-α-D-galactose
Names
IUPAC name
Methyl α-D-galactopyranoside
Systematic IUPAC name
(2R,3R,4S,5R,6S)-2-(Hydroxymethyl)-6-methoxyoxane-3,4,5-triol
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.020.229
UNII
  • InChI=1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4+,5+,6-,7+/m1/s1
    Key: HOVAGTYPODGVJG-PZRMXXKTSA-N
  • InChI=1/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4+,5+,6-,7+/m1/s1
    Key: HOVAGTYPODGVJG-PZRMXXKTBV
  • CO[C@@H]1[C@@H]([C@H]([C@H]([C@H](O1)CO)O)O)O
Properties
C7H14O6
Molar mass 194.183 g·mol−1
Melting point 114-115 °C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Methyl-α-D-galactose is a constituent of Eleutherococcus senticosus.[1][2][3]

References

  1. ↑ No authors Listed (2021-05-17). Eleuthero. NBK501806 (1st ed.). Drugs and Lactation Database. p. 1. PMID 30000865.
  2. ↑ Bai Y, Tohda C, Zhu S, Hattori M, Komatsu K (July 2011). "Active components from Siberian ginseng (Eleutherococcus senticosus) for protection of amyloid β(25-35)-induced neuritic atrophy in cultured rat cortical neurons". Journal of Natural Medicines. 65 (3–4): 417–423. doi:10.1007/s11418-011-0509-y. PMID 21301979. S2CID 9716082.
  3. ↑ "Methyl-alpha-d-galactose". pubchem.ncbi.nlm.nih.gov. National Library of Medicine. Archived from the original on 2022-08-20. Retrieved 2022-08-20.


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