Literature DB >> 29305216

Selective glycosidase inhibitors: A patent review (2012-present).

Abdul Wadood1, Mehreen Ghufran2, Ajmal Khan3, Syed Sikander Azam4, Musharraf Jelani5, Reaz Uddin6.   

Abstract

In the recent decades, the interest on glycosidases has dramatically increased, mainly because these enzymes play a vital role in many biological processes. Based on the biological potential associated to these enzymes, several glycosidase inhibitors have been developed. In this review, the most important inhibitors targeting these enzymes, including the disaccharides, iminosugars, monocyclic iminosugars, bicyclic iminosugars, thiosugars and carbasugars will be discussed and special attention will be given to the ones that are currently used clinically. This review summarizes and characterizes the current knowledge regarding the classes of glycosidase inhibitors that have therapeutic potential in a wide range of diseases. It highlights the patents, relevant research and patent applications filed in the past years in the field. Since the glycosidase inhibitors are involved in several chronic diseases and possibly pandemic, the pharmaceutical research towards developing new generations of these molecules is very important to public health. Most of the glycosidase inhibitors mimics the structures of monosaccharides or oligosaccharides and are well accepted by the organisms since they benefit from privileged drug-like properties. Disaccharides, iminosugars, carbasugars and thiosugars derivatives are the most popular inhibitors among the glycosidase inhibitors.
Copyright © 2017. Published by Elsevier B.V.

Entities:  

Keywords:  Carbasugars; Disaccharides; Glucosidases; Glycosidases; Iminosugars; Thiosugars

Mesh:

Substances:

Year:  2018        PMID: 29305216     DOI: 10.1016/j.ijbiomac.2017.12.148

Source DB:  PubMed          Journal:  Int J Biol Macromol        ISSN: 0141-8130            Impact factor:   6.953


  8 in total

1.  The endogenous galactofuranosidase GlfH1 hydrolyzes mycobacterial arabinogalactan.

Authors:  Lin Shen; Albertus Viljoen; Sydney Villaume; Maju Joe; Iman Halloum; Loïc Chêne; Alexandre Méry; Emeline Fabre; Kaoru Takegawa; Todd L Lowary; Stéphane P Vincent; Laurent Kremer; Yann Guérardel; Christophe Mariller
Journal:  J Biol Chem       Date:  2020-02-27       Impact factor: 5.157

Review 2.  Transient Sulfenic Acids in the Synthesis of Biologically Relevant Products.

Authors:  Anna Barattucci; Maria Chiara Aversa; Aurora Mancuso; Tania Maria Grazia Salerno; Paola Bonaccorsi
Journal:  Molecules       Date:  2018-04-27       Impact factor: 4.411

3.  Iminosugars: Effects of Stereochemistry, Ring Size, and N-Substituents on Glucosidase Activities.

Authors:  Luís O B Zamoner; Valquiria Aragão-Leoneti; Ivone Carvalho
Journal:  Pharmaceuticals (Basel)       Date:  2019-07-12

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.  Synthesis of N-Substituted Iminosugar C-Glycosides and Evaluation as Promising α-Glucosidase Inhibitors.

Authors:  Haibo Wang; Senling Tang; Guoqing Zhang; Yang Pan; Wei Jiao; Huawu Shao
Journal:  Molecules       Date:  2022-08-27       Impact factor: 4.927

6.  Stereoselective Synthesis of Nojirimycin α-C-Glycosides from a Bicyclic Acyliminium Intermediate: A Convenient Entry to N,C-Biantennary Glycomimetics.

Authors:  Irene Herrera-González; Manuel González-Cuesta; M Isabel García-Moreno; José Manuel García Fernández; Carmen Ortiz Mellet
Journal:  ACS Omega       Date:  2022-06-16

7.  MonteCarbo: A software to generate and dock multifunctionalized ring molecules.

Authors:  Santiago Alonso-Gil
Journal:  J Comput Chem       Date:  2021-05-13       Impact factor: 3.376

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

  8 in total

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