Syntheses of Sulfo-Glycodendrimers Using Click Chemistry and Their Biological Evaluation

被引:14
|
作者
Miura, Yoshiko [1 ,2 ]
Onogi, Shunsuke [2 ]
Fukuda, Tomohiro [2 ,3 ]
机构
[1] Kyushu Univ, Grad Sch Engn, Dept Chem Engn, Nishi Ku, Fukuoka 8190395, Japan
[2] Japan Adv Inst Sci & Technol, Sch Mat Sci, Nomi, Ishikawa 9231292, Japan
[3] Toyama Natl Coll Technol, Dept Appl Chem & Chem Engn, Toyama 9398630, Japan
来源
MOLECULES | 2012年 / 17卷 / 10期
关键词
glycopolymer; dendrimer; click chemistry; amyloidosis; WHEAT-GERM-AGGLUTININ; AMYLOID AGGREGATION; STRUCTURAL BASIS; MULTIVALENT; PROTEIN; BINDING;
D O I
10.3390/molecules171011877
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of novel glycol-clusters containing sulfonated N-acetyl-D-glucosamine (GlcNAc) have been synthesized using click chemistry. Three dendrimers with aromatic dendrons were synthesized using chlorination, azidation and click chemistries. The resulting dendrimers were modified with azide-terminated sulfonated GlcNAc using click chemistry. The sulfonated dendrimers showed affinity for proteins, including the lectin wheat germ agglutinin and amyloid beta peptide (1-42). The dendrimers of G1 and G2 in particular showed the largest affinity for the proteins. The addition of the sulfonated GlcNAc dendrimers of G1 and G2 exhibited an inhibition effect on the aggregation of the amyloid beta peptide, reduced the beta-sheet conformation, and led to a reduction in the level of nanofiber formation.
引用
收藏
页码:11877 / 11896
页数:20
相关论文
共 50 条
  • [1] SYNTHESES AND BIOLOGICAL PROPERTIES OF GLYCODENDRIMERS
    ZANINI, D
    PARK, WKC
    MEUNIER, SJ
    WU, Q
    ARAVIND, S
    KRATZER, B
    ROY, R
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1995, 210 : 43 - PMSE
  • [2] Syntheses and biological properties of glycodendrimers
    Polym Mater Sci Eng Proc ACS Div Polym Mater Sci Eng, (82):
  • [3] Diazo Transfer and Click Chemistry in the Solid Phase Syntheses of Lysine-Based Glycodendrimers as Antagonists against Escherichia coli FimH
    Papadopoulos, Alex
    Shiao, Tze Chieh
    Roy, Rene
    MOLECULAR PHARMACEUTICS, 2012, 9 (03) : 394 - 403
  • [4] Concise and Reliable Syntheses of Glycodendrimers via Self-Activating Click Chemistry: A Robust Strategy for Mimicking Multivalent Glycan-Pathogen Interactions
    Farabi, Kindi
    Manabe, Yoshiyuki
    Ichikawa, Hiroaki
    Miyake, Shuto
    Tsutsui, Masato
    Kabayama, Kazuya
    Yamaji, Toshiyuki
    Tanaka, Katsunori
    Hung, Shang-Cheng
    Fukase, Koichi
    JOURNAL OF ORGANIC CHEMISTRY, 2020, 85 (24): : 16014 - 16023
  • [5] SYNTHESIS AND BIOLOGICAL EVALUATION OF TRIAZOLYL MONASTROL ANALOGUES USING Cu-CATALYZED CLICK CHEMISTRY
    Hassan, Hani Mutlak A.
    Denetiu, Iuliana
    Sakkaf, Kaltoom
    Khan, Khalid A.
    Pushparaj, Peter N.
    Gauthaman, Kalamegam
    HETEROCYCLES, 2017, 94 (10) : 1856 - 1869
  • [6] Rapid Detection of Copper in Biological Systems Using Click Chemistry
    Zheng, Wenshu
    Li, Huiling
    Chen, Wenwen
    Zhang, Jiangjiang
    Wang, Nuoxin
    Guo, Xuefeng
    Jiang, Xingyu
    SMALL, 2018, 14 (14)
  • [7] The synthesis and biological evaluation of chondroitin sulfate E glycodendrimers
    Yang, Shuang
    Zhang, Haijing
    Liu, Qifeng
    Sun, Shanshan
    Lei, Pingsheng
    Zhao, Zhehui
    Wu, Lianqiu
    Wang, Yinghong
    FUTURE MEDICINAL CHEMISTRY, 2019, 11 (12) : 1403 - 1415
  • [8] Sulfo-click chemistry with 18F-labeled thio acids
    Urkow, Jenna
    Bergman, Cody
    Wuest, Frank
    CHEMICAL COMMUNICATIONS, 2019, 55 (09) : 1310 - 1313
  • [9] Click Chemistry - Inspired Synthesis of Porphyrin Hybrid Glycodendrimers as Fluorescent Sensor for Cu(II) Ions
    Agrahari, Anand K.
    Kumar, Sunil
    Pandey, Mrituanjay D.
    Rajkhowa, Sanchayita
    Jaiswal, Manoj K.
    Tiwari, Vinod K.
    CHEMISTRYSELECT, 2022, 7 (28):
  • [10] Biological Evaluation of New Largazole Analogues: Alteration of Macrocyclic Scaffold with Click Chemistry
    Li, Xianlin
    Tu, Zhenchao
    Li, Hua
    Liu, Chunping
    Li, Zheng
    Sun, Qiao
    Yao, Yiwu
    Liu, Jinsong
    Jiang, Sheng
    ACS MEDICINAL CHEMISTRY LETTERS, 2013, 4 (01): : 132 - 136