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Propargyl-PEG5-tetra-Ac-beta-D-glucose is a versatile crosslinker designed for use in Click Chemistry, featuring a propargyl group and a beta-D-glucose molecule. This unique structure allows for efficient and stable triazole linkages with azide-bearing compounds or biomolecules through copper-catalyzed azide-alkyne Click Chemistry. The presence of D-glucose enhances solubility in aqueous media and improves the selectivity of the PEGylation reaction, making it a valuable tool in various applications.

1360446-31-6

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1360446-31-6 Usage

Uses

Used in Bioconjugation:
Propargyl-PEG5-tetra-Ac-beta-D-glucose is used as a crosslinker for bioconjugation, allowing the selective and stable attachment of biomolecules through Click Chemistry. The propargyl group's reactivity with azide-bearing compounds enables the formation of covalent bonds, while the D-glucose moiety increases solubility and selectivity of the reaction.
Used in Drug Delivery Systems:
In the pharmaceutical industry, Propargyl-PEG5-tetra-Ac-beta-D-glucose is used as a component in drug delivery systems. Its ability to form stable triazole linkages with azide-bearing drug molecules allows for the development of targeted and controlled-release drug formulations, improving the efficacy and safety of therapeutic treatments.
Used in Materials Science:
In materials science, Propargyl-PEG5-tetra-Ac-beta-D-glucose is used as a building block for the synthesis of functional polymers and hydrogels. The propargyl group's reactivity and the D-glucose's solubility-enhancing properties facilitate the creation of advanced materials with tailored properties for various applications, such as tissue engineering and sensor development.
Used in Diagnostics:
Propargyl-PEG5-tetra-Ac-beta-D-glucose is used as a labeling agent in diagnostic applications. Its ability to form stable covalent bonds with target molecules through Click Chemistry allows for the development of highly specific and sensitive diagnostic tools, such as imaging agents and biosensors.
Used in Chemical Synthesis:
In chemical synthesis, Propargyl-PEG5-tetra-Ac-beta-D-glucose serves as a versatile intermediate for the preparation of various complex molecules. The propargyl group's reactivity and the D-glucose's solubility-enhancing properties make it an attractive candidate for the synthesis of bioactive compounds, pharmaceuticals, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 1360446-31-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,4,4 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1360446-31:
(9*1)+(8*3)+(7*6)+(6*0)+(5*4)+(4*4)+(3*6)+(2*3)+(1*1)=136
136 % 10 = 6
So 1360446-31-6 is a valid CAS Registry Number.

1360446-31-6Relevant academic research and scientific papers

Click Chemistry-Assisted Synthesis of a β- D -Galactose-Targeted SiO2@RC Shell-Core Structure as a Nanoplatform for Metal-Based Complex Delivery

Xu, Xiuling,Hu, Fan,Shuai, Qi

, p. 10694 - 10701 (2018)

A facile reversed-phase microemulsion method was used to synthesize shell-core nanospheres of SiO2@RCs (SiO2-encapsuled rare-earth metal complexes). β-d-Galactose was then grafted onto the surfaces of the nanospheres through the copper(I)-catalyzed azide-alkyne cycloaddition click reaction for targeted delivery. The chemical characteristics and surface profiles of the nanocarriers were investigated by Fourier transform infrared spectroscopy, dynamic light scattering, transmission electron microscopy, and scanning electron microscopy. A high-efficiency microwave synthesis method was applied to prepare five complex cores by the reaction of different rare-earth metal salts with two isomeric ligands, o-CPA (2-chlorophenoxyacetic acid) and m-CPA (3-chlorophenoxyacetic acid). The crystal structures of the five synthesized RC cores were confirmed through X-ray diffraction, which revealed the formulas of five RCs, [Dy(o-CPA)3(H2O)]·H2O RC1, [Ho(o-CPA)3(H2O)]·H2O RC2, 2[Er(m-CPA)3(H2O)]·3H2O RC3, 2[Gd(m-CPA)3(H2O)]·3H2O RC4, and [Ce2(m-CPA)6(H2O)3]·2H2O RC5. An in vitro cell study revealed that all RCs exhibited certain anticancer activities. RC2, in particular, showed the strongest cytotoxicity against HepG2 cells. The enhanced cell permeability and drug retention considerably improved the cytotoxicity of all SiO2@RC2-gal relative to that of RC2. The selective uptake of the β-d-galactose-conjugated nanospheres by HepG2 cells through mechanisms mediated by cell surface receptors resulted in fewer side effects on extrahepatic tissues. Our contribution provides a novel design concept of a target SiO2@RCs-gal nanocarrier for delivering affordable antitumor complexes in cancer therapy.

NIR fluorescent DCPO glucose analogues and their application in cancer cell imaging

Chen, Shiguang,Fang, Yanfen,Zhu, Qiwen,Zhang, Wanli,Zhang, Xiongwen,Lu, Wei

, p. 81894 - 81901 (2016)

Given the increased glucose uptake in cancer cells than normal cells, near-infrared (NIR) fluorescent glucose analogues have been previously synthesized and applied in cancer cell imaging. However, most NIR dyes usually have one or more charge in their structures, which may cause low cell membrane permeability and hamper their application in cell imaging. Here we report the synthesis and characterization of a series of DCPO-conjugated glucose analogues (N0-N4), which have no charge in their structures and have different lengths of the spacer arm. Experiments in different cancer cell lines showed the uptake of N0-N4 was dependent on the protein levels of GLUT-1. The distance between the dyes and glucose was adjusted by the length of PEG. Of these five glucose analogues, the length of the linker in N2 which contains a diethylene glycol was the most appropriate spacer arm, a longer or shorter linker exhibited reduced cellular uptake efficiency. Moreover, the uptake of DCPO-conjugated glucose analogues could be inhibited by phloretin, a GLUT-1 inhibitor or competitively inhibited by unlabeled d-glucose. Therefore, our study has reported a novel type of NIR-conjugated glucose analogues, whose cell permeability ensured the potential application for cancer cell bioimaging in the NIR region. We also demonstrated, for the first time, that the length of the linker between the dyes and glucose was also an important factor that will affect the delivery efficiency of the glucose analogues to cells.

Mimicking biological membranes with programmable glycan ligands self-assembled from amphiphilic Janus glycodendrimers

Zhang, Shaodong,Moussodia, Ralph-Olivier,Sun, Hao-Jan,Leowanawat, Pawaret,Muncan, Adam,Nusbaum, Christopher D.,Chelling, Kathleen M.,Heiney, Paul A.,Klein, Michael L.,André, Sabine,Roy, René,Gabius, Hans-J.,Percec, Virgil

, p. 10899 - 10903 (2015/03/30)

An accelerated modular synthesis produced 18 amphiphilic Janus glycodendrimers with three different topologies formed from either two or one carbohydrate head groups or a mixed constellation with a noncarbohydrate hydrophilic arm. By simple injection of their THF solutions into water or buffer, all of the Janus compounds self-assembled into uniform, stable, and soft unilamellar vesicles, denoted glycodendrimersomes. The mixed constellation topology glycodendrimersomes were demonstrated to be most efficient in binding plant, bacterial, and human lectins. This evidence with biomedically relevant receptors offers a promising perspective for the application of such glycodendrimersomes in targeted drug delivery, vaccines, and other areas of nanomedicine.

Second generation specific-enzyme-activated rotaxane propeptides

Fernandes, Antony,Viterisi, Aurelien,Aucagne, Vincent,Leigh, David A.,Papot, Sebastien

supporting information; experimental part, p. 2083 - 2085 (2012/03/26)

A [2]rotaxane, in which the peptidic axle is protected from degradation by the macrocyclic sheath and terminated with a novel glycosidase-cleavable stopper, is rendered water-soluble by derivatisation with tetra(ethylene glycol) (TetEG) or glucosylated te

One-step bioengineering of magnetic nanoparticles via a surface diazo transfer/azide-alkyne click reaction sequence

Polito, Laura,Monti, Diego,Caneva, Enrico,Delnevo, Eleonora,Russo, Giovanni,Prosperi, Davide

, p. 621 - 623 (2008/09/21)

We have developed an efficient conversion of amino iron oxides to carbohydrate and protein derived nanoparticles with highly conserved bioactivity through a combination of diazo transfer and azide-alkyne click technology. The Royal Society of Chemistry.

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