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O-Methyl-N-acetyl-2-deoxy-a-D-galactosamine is a modified carbohydrate molecule derived from the naturally occurring sugar, 2-deoxy-a-D-galactose. It features a methyl group attached to the oxygen atom and an acetyl group attached to the nitrogen atom, which distinguishes it from its parent compound. This modification may confer unique properties and potential applications in various fields.

6082-22-0

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6082-22-0 Usage

Uses

Used in Medical Research:
O-Methyl-N-acetyl-2-deoxy-a-D-galactosamine is used as a molecular probe for the detection of epiglycanin-related glycoproteins in body fluids of cancer patients. This application is significant because the presence of these glycoproteins can be indicative of certain types of cancer, and their detection can aid in diagnosis and monitoring of the disease.
Used in Diagnostics:
In the diagnostics industry, O-Methyl-N-acetyl-2-deoxy-a-D-galactosamine can be utilized as a component in the development of antibody-based assays. These assays can help in the identification and quantification of specific glycoproteins, which may be crucial for understanding the progression of cancer and the effectiveness of treatments.
Used in Drug Development:
O-Methyl-N-acetyl-2-deoxy-a-D-galactosamine may also have potential applications in drug development, particularly in the design of targeted therapies for cancer. The unique structural features of this molecule could be exploited to enhance the specificity and efficacy of drugs that interact with glycoproteins implicated in cancer progression.
Used in Biochemical Analysis:
In the field of biochemistry, O-Methyl-N-acetyl-2-deoxy-a-D-galactosamine can be employed as a reference compound or standard for the analysis of glycoproteins and their interactions with other biomolecules. This can be valuable for understanding the complex roles that glycoproteins play in various biological processes, including those related to cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 6082-22-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,8 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6082-22:
(6*6)+(5*0)+(4*8)+(3*2)+(2*2)+(1*2)=80
80 % 10 = 0
So 6082-22-0 is a valid CAS Registry Number.

6082-22-0 Well-known Company Product Price

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  • Aldrich

  • (766690)  Methyl 2-acetamido-2-deoxy-α-D-galactopyranoside  

  • 6082-22-0

  • 766690-250MG

  • 2,302.56CNY

  • Detail
  • Aldrich

  • (766690)  Methyl 2-acetamido-2-deoxy-α-D-galactopyranoside  

  • 6082-22-0

  • 766690-1G

  • 5,914.35CNY

  • Detail

6082-22-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl N-acetyl-α-D-galactosaminide

1.2 Other means of identification

Product number -
Other names methyl N-acetyl-alpha-D-galactosaminide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6082-22-0 SDS

6082-22-0Relevant articles and documents

Design, physico-chemical characterization andin vitrobiological activity of organogold(iii) glycoconjugates

Pettenuzzo, Andrea,Vezzù, Keti,Di Paolo, Maria Luisa,Fotopoulou, Eirini,Marchiò, Luciano,Via, Lisa Dalla,Ronconi, Luca

supporting information, p. 8963 - 8979 (2021/07/02)

To develop new metal-based glycoconjugates as potential anticancer agents, four organometallic gold(iii)-dithiocarbamato glycoconjugates of the type [AuIII(2-Bnpy)(SSC-Inp-GlcN)](PF6) (2-Bnpy: 2-benzylpyridine; Inp: isonipecotic moie

Synthetic development of sugar amino acid oligomers towards novel podophyllotoxin analogues

Bouchard, Megan,Tremblay, Thomas,Paré-Lacroix, Marie-Pier,Gagné-Boulet, Mathieu,Fortin, Sébastien,Giguère, Denis

, (2021/11/30)

In this work, we have developed an approach for the synthesis of sugar amino acid oligomers based on the glucosamine scaffold. We found that the solid-phase approach was unsuccessful for the preparation of sugar amino acid oligomers and the limitation of

Ultrasonication-Assisted Synthesis of a d-Glucosamine-Based β-CD Inclusion Complex and Its Application as an Aqueous Heterogeneous Organocatalytic System

Rani, Dhiraj,Sethi, Aaftaab,Kaur, Khushwinder,Agarwal, Jyoti

, p. 9548 - 9557 (2020/09/09)

For the first time, an inclusion complex has been crafted between a carbohydrate-based molecule and a β-cyclodextrin (CD) hydrophobic cavity for asymmetric catalytic applications. This novel d-glucosamine-based inclusion compound has been synthesized in h

Ring-Opening Reactions of the N-4-Nosyl Hough-Richardson Aziridine with Nitrogen Nucleophiles

Ru?il, Tomá?,Trávní?ek, Zdeněk,Canka?, Petr

, p. 723 - 730 (2017/04/26)

Dinosylated α-d-glucopyranoside was directly transformed into α-d-altropyranosides via in situ formed N-4-nosyl Hough-Richardson aziridine with nitrogen nucleophiles under mild conditions in fair to excellent yields. The scope of the aziridine ring-opening reaction was substantially broadened contrary to the conventional methods introducing solely the azide anion at high temperatures. If necessary, the N-4-nosyl Hough-Richardson aziridine can be isolated by filtration in a very good yield and high purity.

Selective anomeric acetylation of unprotected sugars in water

Lim, David,Fairbanks, Antony J.

, p. 1896 - 1900 (2017/03/09)

High yielding selective acetylation of only the anomeric hydroxyl of unprotected sugars is possible in aqueous solution using 2-chloro-1,3-dimethylimidazolinium chloride (DMC), thioacetic acid, and a suitable base. The reaction, which may be performed on a multi-gram scale, is stereoselective for sugars that possess a hydroxyl group at position-2, exclusively yielding the 1,2-trans products. The use of an iterative reagent addition procedure allows the use of sodium carbonate as the base, avoiding the formation of triethylammonium salts, which may hamper product purification. The glycosyl acetate products may be used as donor substrates for glycosidase-catalysed synthesis. The crude aqueous acetylation reaction mixture may also be used for this purpose.

Sugar derived alkamine catalytic imine reduction method

-

Paragraph 0035; 0036; 0037, (2016/10/07)

The invention discloses a method used for catalytic reduction of imine with saccharide-derivatized amino alcohol. According to the method, imine is taken as a substrate. The method comprises following steps: 1) imine and saccharide-derivatized amino alcohol are dissolved in an organic solvent I, wherein molar ratio of imine to saccharide-derivatized amino alcohol ranges from 100:1-20; 2) trichlorosilane with 1.5 to 5 times equivalent weights is added into a solution obtained via step 1) dropwise, an obtained mixture is stirred and reacted for 12 to 36h at a temperature of -20 to 40 DEG C, and a saturated sodium bicarbonate solution is used for quenching; 3) a material obtained via step 2) is extracted with an organic solvent II, and is subjected to column chromatography isolation so as to obtain amine compounds.

Synthetic heparin pentasaccharides

-

Page/Page column 36; 37, (2016/02/12)

Preparation and use of synthetic monosaccharides, disaccharides, trisaccharides, tetrasaccharides and pentasaccharides useful for the preparation of synthetic heparinoids.

N-acetylgalactosamine green synthetic method

-

Paragraph 0037; 0038, (2016/11/28)

The present invention discloses a N-acetylgalactosamine green synthetic method. According to the method, N-acetylglucosamine as a raw material is successively condensed with an alcohol and pivaloyl chloride, and then N-acetylgalactosamine can be obtained

A de Novo-Designed Monomeric, Compact Three-Helix-Bundle Protein on a Carbohydrate Template

Malik, Leila,Nygaard, Jesper,Cristensen, Niels J.,Madsen, Charlotte S.,R?sner, Heike I.,Kragelund, Birthe B.,Hoiberg-Nielsen, Rasmus,Streicher, Werner W.,Arleth, Lise,Thulstrup, Peter W.,Jensen, Knud J.

, p. 1905 - 1918 (2015/09/02)

De novo design and chemical synthesis of proteins and of other artificial structures that mimic them is a central strategy for understanding protein folding and for accessing proteins with new functions. We have previously described carbohydrates that act as templates for the assembly of artificial proteins, so-called carboproteins. The hypothesis is that the template preorganizes the secondary structure elements and directs the formation of a tertiary structure, thus achieving structural economy in the combination of peptide, linker, and template. We speculate that the structural information from the template could facilitate protein folding. Here we report the design and synthesis of three-helix-bundle carboproteins on deoxyhexopyranosides. The carboproteins were analyzed by CD, analytical ultracentrifugation (AUC), small-angle X-ray scattering (SAXS), and NMR spectroscopy, and this revealed the formation of the first compact and folded monomeric carboprotein, distinctly different from a molten globule. En route to this carboprotein we observed a clear effect originating from the template on protein folding.

A mechanistic study on the α-N-acetylgalactosaminidase from E. meningosepticum: A family 109 glycoside hydrolase

Chakladar, Saswati,Shamsi Kazem Abadi, Saeideh,Bennet, Andrew J.

, p. 1188 - 1192 (2014/08/05)

A recombinant glycoside hydrolase family 109 α-N- acetylgalactosaminidase from the pathogenic bacteria E. meningosepticum catalyses the hydrolysis of aryl 2-acetamido-2-deoxy-α-d- galactopyranosides. The sensitivities to leaving group abilities (βlg values) on V and V/K are -0.08 ± 0.06 and -0.31 ± 0.12, respectively. These results are consistent with an E2 elimination following hydride transfer from C3. This journal is the Partner Organisations 2014.

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