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171032-74-9

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171032-74-9 Usage

Description

1,3,4,6-TETRA-O-ACETYL-2-AZIDO-2-DEOXY-D-GLUCOPYRANOSE, also known as 2-Azido-2-deoxy-D-glucopyranose 1,3,4,6-tetraacetate, is a synthetic azidosugar derivative with a unique chemical structure. It is characterized by the presence of an azido group at the C2 position and four acetyl groups at the C1, C3, C4, and C6 positions. 1,3,4,6-TETRA-O-ACETYL-2-AZIDO-2-DEOXY-D-GLUCOPYRANOSE is of interest in the field of glycobiology and medicinal chemistry due to its potential applications in studying carbohydrate interactions and developing new therapeutic agents.
Used in Research Applications:
1,3,4,6-TETRA-O-ACETYL-2-AZIDO-2-DEOXY-D-GLUCOPYRANOSE is used as a research tool for investigating the cellular metabolism of synthetic azidosugars. It aids in understanding the interactions between these compounds and cellular machinery, which can provide insights into their potential use in therapeutic applications.
Used in Pharmaceutical Industry:
1,3,4,6-TETRA-O-ACETYL-2-AZIDO-2-DEOXY-D-GLUCOPYRANOSE is used as a starting material or intermediate in the synthesis of various glycoconjugates and glycodrugs. Its unique structure allows for the development of novel compounds with potential therapeutic properties, such as anti-inflammatory, antiviral, or anticancer activities.
Used in Chemical Biology:
1,3,4,6-TETRA-O-ACETYL-2-AZIDO-2-DEOXY-D-GLUCOPYRANOSE is used as a probe in chemical biology to study the function and mechanism of action of carbohydrate-binding proteins, such as lectins. This can help in elucidating the role of carbohydrates in cellular processes and the development of new drugs targeting these interactions.

Check Digit Verification of cas no

The CAS Registry Mumber 171032-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,0,3 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 171032-74:
(8*1)+(7*7)+(6*1)+(5*0)+(4*3)+(3*2)+(2*7)+(1*4)=99
99 % 10 = 9
So 171032-74-9 is a valid CAS Registry Number.

171032-74-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-azido-2-deoxy-3,4,6-tri-O-acetyl-α,β-D-glucopyranosyl acetate

1.2 Other means of identification

Product number -
Other names 2-Azido-2-deoxy-D-glucopyranose 1,3,4,6-Tetraacetate

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:171032-74-9 SDS

171032-74-9Relevant articles and documents

The Small Molecule 2-Azido-2-deoxy-glucose Is a Metabolic Chemical Reporter of O-GlcNAc Modifications in Mammalian Cells, Revealing an Unexpected Promiscuity of O-GlcNAc Transferase

Zaro, Balyn W.,Batt, Anna R.,Chuh, Kelly N.,Navarro, Marisol X.,Pratt, Matthew R.

, p. 787 - 794 (2017)

Glycans can be directly labeled using unnatural monosaccharide analogs, termed metabolic chemical reporters (MCRs). These compounds enable the secondary visualization and identification of glycoproteins by taking advantage of bioorthogonal reactions. Most widely used MCRs have azides or alkynes at the 2-N-acetyl position but are not selective for one class of glycoprotein over others. To address this limitation, we are exploring additional MCRs that have bioorthogonal functionality at other positions. Here, we report the characterization of 2-azido-2-deoxy-glucose (2AzGlc). We find that 2AzGlc selectively labels intracellular O-GlcNAc modifications, which further supports a somewhat unexpected, structural flexibility in this pathway. In contrast to the endogenous modification N-acetyl-glucosamine (GlcNAc), we find that 2AzGlc is not dynamically removed from protein substrates and that treatment with higher concentrations of per-acetylated 2AzGlc is toxic to cells. Finally, we demonstrate that this toxicity is an inherent property of the small-molecule, as removal of the 6-acetyl-group renders the corresponding reporter nontoxic but still results in protein labeling.

A glucose-responsive controlled release system using glucose oxidase-gated mesoporous silica nanocontainers

Chen, Mengjie,Huang, Chusen,He, Chunsheng,Zhu, Weiping,Xu, Yufang,Lu, Yunfeng

, p. 9522 - 9524 (2012)

A glucose-responsive controlled-release system based on the competitive combination between glucose oxidase, glucosamine and glucose has been described, which exhibits perfect controlled release properties and high selectivity for glucose over other monosaccharides. This paved the way for a new generation of stimuli-responsive delivery systems.

Synthesis of 7-O-(2-deoxy-2-sulfamido-α-D-glucopyranosyl)-4-methylcoumarin sodium salt: A fluorogenic substrate for sulfamidase

Dasgupta, Falguni,Masada, R.Irene

, p. 1055 - 1058 (2002)

The title compound, useful for testing the efficacy of heparin sulfamidase, was synthesized in good yield starting from 2-azido-2-deoxy-3,4,6-tri-O-acetyl-D-glucopyranosyl fluoride, reducing the azido group efficiently with SnCl2-PhSH-Et3N reagent and finally crystallizing the N-sulfated product from methanol after deacetylation.

Improvement of the stereoselectivity of the glycosylation reaction with 2-azido-2-deoxy-1-thioglucoside donors

Louren?o,Ventura

, p. 33 - 39 (2016)

2-Azido-2-deoxy-1-thioglucoside donors with an electron withdrawing group at position 6 were employed to study the stereoselectivity of the glycosylation reaction with several acceptors, ranging from unhindered small primary alcohols to other sugars and s

Teniposide derivative, preparation method therefor and application of teniposide derivative

-

Paragraph 0085; 0090-0091, (2020/08/07)

The invention discloses a teniposide derivative, a synthesis method therefor and application of the teniposide derivative. The teniposide derivative represented by a formula (V) shown in the description. The anti-tumor activity of the teniposide derivative is improved remarkably and the toxic or side effects are lowered, is obtained through introducing a heteroaromatic compound with low toxicity such as 5-fluoro-benzothiazol-2-thiol or 5-fluoro-benzoxazol-2-thiol into 2' and 3' positions of a saccharide ring of teniposide by means of an ester bond or amide bond. Shown by in-vitro tumor cell activity inhibiting experiments, the toxic or side effects of the compound represented by the formula (V) disclosed by the invention are remarkably lowered compared with those of the teniposide on the basis that the anti-tumor activity of the compound is equivalent to that of the teniposide.

2 - (1 ', 2', 3 '- Triazole - 4' - methyl pyridine oxyalkylene) - 1, 3, 4, 6 - O - acetyl - D - glucose and its preparation method and application

-

, (2018/04/01)

The invention discloses 2-(1',2',3'-triazolyl-4'-oxymethylenepyridyl)-1,3,4,6-O-acetyl-D-glucose with anti-rectal cancer activity. The 2-(1',2',3'-triazolyl-4'-oxymethylenepyridyl)-1,3,4,6-O-acetyl-D-glucose has a core structure of 1,3,4,6-O-acetyl-D-glucose subjected to 1,2,4-triazole derivative 2-site substitution. The above compound has good rectal cancer cell inhibition activity and can be used as a drug for resisting rectal cancer. A compound synthesis method comprises that 2-amino-D-glucose hydrochloride and an azidation reagent as raw materials undergo a reaction under alkaline conditions to produce a 2-azido-1,3,4,6-O-acetyl-D-glucose intermediate, 3-propargyl bromide and aromatic methanol undergo a reaction under the action of sodium hydride to produce aromatic propargyl ether, and the 2-azido-1,3,4,6-O-acetyl-D-glucose intermediate and the aromatic propargyl ether undergo a click reaction in a solvent in the presence of monovalent copper as a catalyst to produce 2-(1', 2', 3'-triazolyl-4'-oxymethylenepyridyl)-1,3,4,6-O-acetyl-D-glucose.

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