Synthesis and cholinesterase inhibiting potential of A-ring azepano- and 3-amino-3,4-seco-triterpenoids-Reference-Cited by-同舟云学术

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Synthesis and cholinesterase inhibiting potential of A-ring azepano- and 3-amino-3,4-seco-triterpenoids

Published:2020-08 Issue: Volume:101 Page:104001
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

Kazakova Oxana,Smirnova Irina,Lopatina Tatyana,Giniyatullina Gul'nara,Petrova Anastasiya,Khusnutdinova Elmira,Csuk René,Serbian Immo,Loesche Anne

Funder

Russian Foundation for Basic Research

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

Reference35 articles.

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2. Cholinesterase inhibitors for the treatment of Alzheimer's disease: getting on and staying on;Grossberg;Curr. Ther. Res. Clin. Exp.,2003

3. D.J. Newman, G.M. Cragg, Natural products as sources of new drugs from 1981 to 2014, J. Nat. Prod. 79 (2016) 629-661. https://doi.org/10.1021/acs.jnatprod.5b01055.

4. Synthesis, biology and clinical significance of pentacyclic triterpenes: a multi-target approach to prevention and treatment of metabolic and vascular diseases;Sheng;Nat. Prod. Rep.,2011

5. Synthetic oleanane triterpenoids: multifunctional drugs with a broad range of applications for prevention and treatment of chronic disease;Liby;Pharmacol. Rev.,2012

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1. Diethoxyphosphoryloxy‐oleanolic acid is a nanomolar‐inhibitor of butyrylcholinesterase;Chemical Biology & Drug Design;2024-03

2. Evaluation of A-ring hydroxymethylene-amino- triterpenoids as inhibitors of SARS-CoV-2 spike pseudovirus and influenza H1N1;The Journal of Antibiotics;2023-11-24

3. Inhibitory properties of quinopimaric acid derivatives towards cholinesterases;Natural Product Research;2023-10-09

4. α-Glucosidase Inhibitors Based on Oleanolic Acid for the Treatment of Immunometabolic Disorders;Applied Sciences;2023-08-15

5. Acetylcholinesterase Inhibitory Activity of Modified Lupane, Oleanane, and Ursane A‐seco‐Triterpenoids;Chemistry & Biodiversity;2023-03-31

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