Nitro-substituted tetrahydroindolizines and homologs: Design, kinetics, and mechanism of α-glucosidase inhibition-Reference-Cited by-同舟云学术

Nitro-substituted tetrahydroindolizines and homologs: Design, kinetics, and mechanism of α-glucosidase inhibition

Published:2017-09 Issue:17 Volume:27 Page:3980-3986
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Tavani Cinzia,Bianchi Lara,De Palma Annalisa,Passeri Giovanna Ilaria,Punzi Giuseppe,Pierri Ciro Leonardo,Lovece Angelo,Cavalluzzi Maria Maddalena,Franchini Carlo,Lentini Giovanni^ORCID,Petrillo Giovanni^ORCID

Funder

Ministero dell'Istruzione, dell'Università e della Ricerca

MIUR

NANO Molecular tEchnologies for Drug delivery e NANOMED

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference45 articles.

1. α-Glucosidases and α-1,4-glucan lyases: structures, functions, and physiological actions

2. Untapped diamonds for untamed diabetes: The α-glucosidase inhibitors

3. Acid a-Glucosidase Deficiency (Glycogenosis Type II, Pompe Disease)

4. Glycosidase Activity;Corfield,2000

5. Inhibitors of Endoplasmic Reticulum α-Glucosidases Potently Suppress Hepatitis C Virus Virion Assembly and Release

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