Literature DB >> 30993894

Multivalent Effect in Glycosidase Inhibition: The End of the Beginning.

Philippe Compain1.   

Abstract

Glycosidases are ubiquitous enzymes involved in a diversity of key biological processes such as energy uptake or cell wall degradation. The design of specific glycosidase inhibitors has been therefore the subject of intense research efforts in academia and pharmaceutical industry. However, until recently, the study of the impact of multivalency on glycosidase inhibition was almost completely neglected. The following account will review our ten year journey on the design of multivalent glycomimetics within our research group, from the discovery of the first strong multivalent effect in glycosidase inhibition to the high-resolution crystal structures of Jack bean α-mannosidase in complex with the multimeric inhibitor displaying the largest binding enhancements reported so far.
© 2019 The Chemical Society of Japan & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  biological activities; carbohydrates; click chemistry; cluster compounds; inhibitors

Mesh:

Substances:

Year:  2019        PMID: 30993894     DOI: 10.1002/tcr.201900004

Source DB:  PubMed          Journal:  Chem Rec        ISSN: 1528-0691            Impact factor:   6.771


  12 in total

1.  GH47 and Other Glycoside Hydrolases Catalyze Glycosidic Bond Cleavage with the Assistance of Substrate Super-arming at the Transition State.

Authors:  Jonathan C K Quirke; David Crich
Journal:  ACS Catal       Date:  2021-08-04       Impact factor: 13.700

2.  Glycoside Hydrolases Restrict the Side Chain Conformation of Their Substrates To Gain Additional Transition State Stabilization.

Authors:  Jonathan C K Quirke; David Crich
Journal:  J Am Chem Soc       Date:  2020-09-24       Impact factor: 15.419

Review 3.  Bioisosteres of Carbohydrate Functional Groups in Glycomimetic Design.

Authors:  Rachel Hevey
Journal:  Biomimetics (Basel)       Date:  2019-07-28

4.  Synthesis and Glycosidase Inhibition Properties of Calix[8]arene-Based Iminosugar Click Clusters.

Authors:  Jérémy P Schneider; Stefano Tommasone; Paolo Della Sala; Carmine Gaeta; Carmen Talotta; Céline Tarnus; Placido Neri; Anne Bodlenner; Philippe Compain
Journal:  Pharmaceuticals (Basel)       Date:  2020-11-05

5.  Bambus[4,6]urils as Dual Scaffolds for Multivalent Iminosugar Presentation and Ion Transport: Access to Unprecedented Glycosidase-Directed Anion Caging Agents.

Authors:  Marine Lafosse; Yan Liang; Jérémy P Schneider; Elise Cartier; Anne Bodlenner; Philippe Compain; Marie-Pierre Heck
Journal:  Molecules       Date:  2022-07-26       Impact factor: 4.927

Review 6.  Multivalent Carbonic Anhydrases Inhibitors.

Authors:  Fabrizio Carta; Pascal Dumy; Claudiu T Supuran; Jean-Yves Winum
Journal:  Int J Mol Sci       Date:  2019-10-28       Impact factor: 5.923

Review 7.  Synthesis and Therapeutic Applications of Iminosugars in Cystic Fibrosis.

Authors:  Anna Esposito; Daniele D'Alonzo; Maria De Fenza; Eliana De Gregorio; Anna Tamanini; Giuseppe Lippi; Maria Cristina Dechecchi; Annalisa Guaragna
Journal:  Int J Mol Sci       Date:  2020-05-09       Impact factor: 5.923

8.  N-Alkylated Iminosugar Based Ligands: Synthesis and Inhibition of Human Lysosomal β-Glucocerebrosidase.

Authors:  Andreas Wolfsgruber; Martin Thonhofer; Patrick Weber; Seyed A Nasseri; Roland Fischer; Michael Schalli; Arnold E Stütz; Stephen G Withers; Tanja M Wrodnigg
Journal:  Molecules       Date:  2020-10-11       Impact factor: 4.411

9.  Development of tacrine clusters as positively cooperative systems for the inhibition of acetylcholinesterase.

Authors:  Tereza Cristina Santos Evangelista; Óscar López; Sabrina Baptista Ferreira; José G Fernández-Bolaños; Magne O Sydnes; Emil Lindbäck
Journal:  J Enzyme Inhib Med Chem       Date:  2021-12       Impact factor: 5.051

10.  3,4,5-Trihydroxypiperidine Based Multivalent Glucocerebrosidase (GCase) Enhancers.

Authors:  Costanza Vanni; Francesca Clemente; Paolo Paoli; Amelia Morrone; Camilla Matassini; Andrea Goti; Francesca Cardona
Journal:  Chembiochem       Date:  2022-04-07       Impact factor: 3.461

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