Home Amines 14116-68-8
14116-68-8,MFCD00079413
Catalog No.:AA001FXC

14116-68-8 | D-Glucose, O-β-D-galactopyranosyl-(1→3)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)-O-β-D-galactopyranosyl-(1→4)-

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1mg
98%
1 week  
$156.00   $109.00
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5mg
98%
1 week  
$390.00   $273.00
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10mg
98%
1 week  
$616.00   $432.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA001FXC
Chemical Name:
D-Glucose, O-β-D-galactopyranosyl-(1→3)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)-O-β-D-galactopyranosyl-(1→4)-
CAS Number:
14116-68-8
Molecular Formula:
C26H45NO21
Molecular Weight:
707.6296
MDL Number:
MFCD00079413
SMILES:
OC[C@H]1O[C@@H](O[C@@H]2[C@@H](CO)OC([C@@H]([C@H]2O)O)O)[C@@H]([C@H]([C@H]1O)O[C@@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1NC(=O)C)O[C@@H]1O[C@H](CO)[C@@H]([C@@H]([C@H]1O)O)O)O)O
Properties
Computed Properties
 
Complexity:
1030  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
19  
Heavy Atom Count:
48  
Hydrogen Bond Acceptor Count:
21  
Hydrogen Bond Donor Count:
14  
Rotatable Bond Count:
11  
Undefined Atom Stereocenter Count:
1  
XLogP3:
-7.9  

Downstream Synthesis Route
17625-83-1    14116-68-8   
<i>N</i>-4-(4-{4-3-acetylamino-5-hydroxy-6-hydroxymethyl-4-(3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy-3,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy}-2,3,5,6-tetrahydroxy-hexylamino)-phenyl-benzamide 

[1]Blixt;Norberg[JournalofCarbohydrateChemistry,1997,vol.16,#2,p.143-154]

14116-68-8   
4-O-3-O-(2-acetamido-2-deoxy-3-O-(β-D-galactopyranosyl)-β-D-glucopyranosyl)-β-D-galactopyranosyl-N-(N-tert-butyloxycarbonylglycyl)-β-D-glucopyranosylamine 

[1]Likhosherstov;Novikova;Kolotyrkina;Piskarev[RussianChemicalBulletin,2019,vol.68,#2,p.411-415][Izv.Akad.Nauk,Ser.Khim.,2019,#2,p.411-415,5]

14116-68-8   
4-O-3-O-(2-acetamido-2-deoxy-3-O-(β-D-galactopyranosyl)-β-D-glucopyranosyl)-β-D-galactopyranosyl-N-glycyl-β-D-glucopyranosylamine 

[1]Likhosherstov;Novikova;Kolotyrkina;Piskarev[RussianChemicalBulletin,2019,vol.68,#2,p.411-415][Izv.Akad.Nauk,Ser.Khim.,2019,#2,p.411-415,5]

14116-68-8   
N-((2S,3R,4R,5S,6R)-2-(((2S,3R,4S,5S,6R)-2-(((2R,3S,4R,5R)-6-amino-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)-oxy)-3,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-4-yl)-oxy)-5-hydroxy-6-(hydroxymethyl)-4-(((2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro2H-pyran-3-yl)acetamide 

[1]Likhosherstov;Novikova;Kolotyrkina;Piskarev[RussianChemicalBulletin,2019,vol.68,#2,p.411-415][Izv.Akad.Nauk,Ser.Khim.,2019,#2,p.411-415,5]

Literature

Title: Release and utilization of N-acetyl-D-glucosamine from human milk oligosaccharides by Bifidobacterium longum subsp. infantis.

Journal: Anaerobe 20120801

Title: Urinary excretion of in vivo ¹³C-labelled milk oligosaccharides in breastfed infants.

Journal: The British journal of nutrition 20120401

Title: Bifidobacterium longum subsp. infantis uses two different β-galactosidases for selectively degrading type-1 and type-2 human milk oligosaccharides.

Journal: Glycobiology 20120301

Title: Human lipooligosaccharide IGG that prevents endemic meningococcal disease recognizes an internal lacto-N-neotetraose structure.

Journal: The Journal of biological chemistry 20111223

Title: Characterization and synthetic application of a novel beta1,3-galactosyltransferase from Escherichia coli O55:H7.

Journal: Bioorganic & medicinal chemistry 20090715

Title: The fine structure of Neisseria meningitidis lipooligosaccharide from the M986 strain and three of its variants.

Journal: The Journal of biological chemistry 20090213

Title: Chemo-enzymatic supported synthesis of the 3-sulfated Lewis a pentasaccharide on a multimeric polyethylene glycol.

Journal: Carbohydrate research 20080407

Title: Factor H binding and function in sialylated pathogenic neisseriae is influenced by gonococcal, but not meningococcal, porin.

Journal: Journal of immunology (Baltimore, Md. : 1950) 20070401

Title: Syntheses of a series of lacto-N-neotetraose clusters using a carbosilane dendrimer scaffold.

Journal: Carbohydrate research 20060320

Title: Identification and structural characterization of a sialylated lacto-N-neotetraose structure in the lipopolysaccharide of Haemophilus influenzae.

Journal: European journal of biochemistry 20020801

Title: In vivo fucosylation of lacto-N-neotetraose and lacto-N-neohexaose by heterologous expression of Helicobacter pylori alpha-1,3 fucosyltransferase in engineered Escherichia coli.

Journal: Glycoconjugate journal 20010601

Title: Molecular mimicry of host structures by lipooligosaccharides of Neisseria meningitidis: characterization of sialylated and nonsialylated lacto-N-neotetraose (Galbeta1-4GlcNAcbeta1-3Galbeta1-4Glc) structures in lipooligosaccharides using monoclonal antibodies and specific lectins.

Journal: Advances in experimental medicine and biology 20010101

Title: Recognition of type 1 chain oligosaccharides and lacto-series glycolipids by an antibody to human secretory component.

Journal: Archives of biochemistry and biophysics 19951001

Title: Monoclonal antibodies against Haemophilus lipopolysaccharides: clone DP8 specific for Haemophilus ducreyi and clone DH24 binding to lacto-N-neotetraose.

Journal: Infection and immunity 19950701

Title: Further studies of the specificities of monoclonal anti-i and anti-I antibodies using chemically synthesized, linear oligosaccharides of the poly-N-acetyllactosamine series.

Journal: Molecular immunology 19841101

Title: Two mouse hybridoma antibodies against human milk-fat globules recognise the I(Ma) antigenic determinant beta-D-Galp-(1 leads to 4)-beta-D-GlcpNAc-(1 leads to 6).

Journal: Carbohydrate research 19830816

Title: Further evidence that carbohydrates are the immunodeterminant structures of blood group M and N specificities.

Journal: Immunological communications 19810101

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SDS
Tags:14116-68-8 Molecular Formula|14116-68-8 MDL|14116-68-8 SMILES|14116-68-8 D-Glucose, O-β-D-galactopyranosyl-(1→3)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)-O-β-D-galactopyranosyl-(1→4)-