Literature DB >> 2497772

Australine, a pyrrolizidine alkaloid that inhibits amyloglucosidase and glycoprotein processing.

J E Tropea1, R J Molyneux, G P Kaushal, Y T Pan, M Mitchell, A D Elbein.   

Abstract

Australine [(1R,2R,3R,7S,7aR)-3-(hydroxymethyl)-1,2,7-trihydroxypyrrolizid ine] is a polyhydroxylated pyrrolizidine alkaloid that was isolated from the seeds of the Australian tree Castanospermum australe and characterized by NMR and X-ray diffraction analysis [Molyneux et al. (1988) J. Nat. Prod. (in press)]. Since swainsonine and catanospermine are polyhydroxylated indolizidine alkaloids that inhibit specific glycosidases, we tested australine against a variety of exoglycosidases to determine whether it would inhibit any of these enzymes. This alkaloid proved to be a good inhibitor of the alpha-glucosidase amyloglucosidase (50% inhibition at 5.8 microM), but it did not inhibit beta-glucosidase, alpha- or beta-mannosidase, or alpha- or beta-galactosidase. The inhibition of amyloglucosidase was of a competitive nature. Australine also inhibited the glycoprotein processing enzyme glucosidase I, but had only slight activity toward glucosidase II. When incubated with cultured cells, this alkaloid inhibited glycoprotein processing at the glucosidase I step and caused the accumulation of glycoproteins with Glc3Man7-9(GlcNAc)2-oligosaccharides.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2497772     DOI: 10.1021/bi00431a010

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  7 in total

1.  The structural basis of the inhibition of human alpha-mannosidases by azafuranose analogues of mannose.

Authors:  B Winchester; S al Daher; N C Carpenter; I Cenci di Bello; S S Choi; A J Fairbanks; G W Fleet
Journal:  Biochem J       Date:  1993-03-15       Impact factor: 3.857

2.  Total Synthesis of Hyacinthacine A2: Stereocontrolled 5-aza-cyclooctene Photoisomerization and Transannular Hydroamination with Planar-to-Point Chirality Transfer.

Authors:  Maksim Royzen; Michael T Taylor; Andrew Deangelis; Joseph M Fox
Journal:  Chem Sci       Date:  2011-11       Impact factor: 9.825

3.  Characterizing the selectivity of ER α-glucosidase inhibitors.

Authors:  Sarah O'Keefe; Quentin P Roebuck; Izumi Nakagome; Shuichi Hirono; Atsushi Kato; Robert Nash; Stephen High
Journal:  Glycobiology       Date:  2019-07-01       Impact factor: 4.313

Review 4.  Recent advances on the synthesis of natural pyrrolizidine alkaloids: alexine, and its stereoisomers.

Authors:  Ghodsi Mohammadi Ziarani; Negar Jamasbi; Fatemeh Mohajer
Journal:  Nat Prod Bioprospect       Date:  2022-02-07

Review 5.  Exploring the Potential of Chemical Inhibitors for Targeting Post-translational Glycosylation of Coronavirus (SARS-CoV-2).

Authors:  Nancy Tripathi; Bharat Goel; Nivedita Bhardwaj; Ram A Vishwakarma; Shreyans K Jain
Journal:  ACS Omega       Date:  2022-07-28

6.  An Intramolecular Hydroaminomethylation-Based Approach to Pyrrolizidine Alkaloids under Microwave-Assisted Heating.

Authors:  Elena Petricci; Simone Zurzolo; Camilla Matassini; Samuele Maramai; Francesca Cardona; Andrea Goti; Maurizio Taddei
Journal:  Molecules       Date:  2022-07-25       Impact factor: 4.927

Review 7.  Pyrrolizidine Alkaloids: Biosynthesis, Biological Activities and Occurrence in Crop Plants.

Authors:  Sebastian Schramm; Nikolai Köhler; Wilfried Rozhon
Journal:  Molecules       Date:  2019-01-30       Impact factor: 4.411

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.