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Details

Stereochemistry ABSOLUTE
Molecular Formula C7H14O6
Molecular Weight 194.1825
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Methyl-α-D-galactose

SMILES

CO[C@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O

InChI

InChIKey=HOVAGTYPODGVJG-PZRMXXKTSA-N
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

HIDE SMILES / InChI

Molecular Formula C7H14O6
Molecular Weight 194.1825
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Serological and chemical specificities of twelve monoclonal anti-Lea and anti-Leb antibodies.
1992
A monoclonal IgM kappa from a blood group B individual with specificity for alpha-galactosyl epitopes on partially hydrolyzed blood group B substance.
1993 May 7
Protection of pig kidney (PK15) cells from the cytotoxic effect of anti-pig antibodies by alpha-galactosyl oligosaccharides.
1994 Mar 27
Gal alpha(1,3)Gal is the major xenoepitope expressed on pig endothelial cells recognized by naturally occurring cytotoxic human antibodies.
1994 Oct 27
Purification and characterization of three galactose specific lectins from mulberry seeds (Morus sp.).
2001 Dec
Role of endosymbiotic zooxanthellae and coral mucus in the adhesion of the coral-bleaching pathogen Vibrio shiloi to its host.
2001 May 15
1-O-Acetyl-beta-D-galactopyranose: a novel substrate for the transglycosylation reaction catalyzed by the beta-galactosidase from Penicillium sp.
2002 Apr 2
Synthesis and intramolecular transesterifications of pivaloylated methyl alpha-D-galactopyranosides.
2002 Apr 30
Alpha-galactosyl fluoride in transfer reactions mediated by the green coffee beans alpha-galactosidase in ice.
2002 Feb 11
Binding of hydrophobic D-galactopyranosides to the lactose permease of Escherichia coli.
2002 Oct 29
Efficient transport of saccharides through a liquid membrane mediated by a cyclodextrin dimer.
2003 Oct 17
Evaluation of carbohydrate molecular mechanical force fields by quantum mechanical calculations.
2004 Apr 2
Two orthorhombic crystal structures of a galactose-specific lectin from Artocarpus hirsuta in complex with methyl-alpha-D-galactose.
2004 Aug
Fluorescence quenching and time-resolved fluorescence studies on Trichosanthes dioica seed lectin.
2005 Aug 1
Regioselective synthesis of long-chain ethers and their sulfates derived from methyl beta-D-galactopyranoside and derivatives via dibutylstannylene acetal intermediates.
2005 Oct 17
Identification of a glycosylphosphatidylinositol-anchored plasma membrane protein interacting with the C-terminus of auxin-binding protein 1: a photoaffinity crosslinking study.
2006 Mar
Production, purification, and characterization of a novel galactose oxidase from Fusarium acuminatum.
2007 Jun
Carbohydrate residues downstream of the terminal Galalpha(1,3)Gal epitope modulate the specificity of xenoreactive antibodies.
2007 Nov-Dec
NMR studies on the interaction of sugars with the C-terminal domain of an R-type lectin from the earthworm Lumbricus terrestris.
2009 Apr
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:04:00 GMT 2023
Edited
by admin
on Sat Dec 16 17:04:00 GMT 2023
Record UNII
ESJ6UY55QN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Methyl-α-D-galactose
Common Name English
(2R,3R,4S,5R,6S)-2-(Hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol
Systematic Name English
METHYL .ALPHA.-D-GALACTOPYRANOSIDE
Systematic Name English
GALACTOPYRANOSIDE, METHYL, .ALPHA.-D-
Systematic Name English
NSC-33684
Code English
1-O-METHYL-.ALPHA.-D-GALACTOPYRANOSIDE
Systematic Name English
Code System Code Type Description
NSC
33684
Created by admin on Sat Dec 16 17:04:00 GMT 2023 , Edited by admin on Sat Dec 16 17:04:00 GMT 2023
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PUBCHEM
76935
Created by admin on Sat Dec 16 17:04:00 GMT 2023 , Edited by admin on Sat Dec 16 17:04:00 GMT 2023
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WIKIPEDIA
Methyl-α-D-galactose
Created by admin on Sat Dec 16 17:04:00 GMT 2023 , Edited by admin on Sat Dec 16 17:04:00 GMT 2023
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FDA UNII
ESJ6UY55QN
Created by admin on Sat Dec 16 17:04:00 GMT 2023 , Edited by admin on Sat Dec 16 17:04:00 GMT 2023
PRIMARY
CAS
3396-99-4
Created by admin on Sat Dec 16 17:04:00 GMT 2023 , Edited by admin on Sat Dec 16 17:04:00 GMT 2023
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EPA CompTox
DTXSID30187575
Created by admin on Sat Dec 16 17:04:00 GMT 2023 , Edited by admin on Sat Dec 16 17:04:00 GMT 2023
PRIMARY