The green synthesis and molecular docking of novel N-substituted rhodanines as effective inhibitors for carbonic anhydrase and acetylcholinesterase enzymes-Reference-Cited by-同舟云学术

The green synthesis and molecular docking of novel N-substituted rhodanines as effective inhibitors for carbonic anhydrase and acetylcholinesterase enzymes

Published:2019-09 Issue: Volume:90 Page:103096
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

Bayindir Sinan,Caglayan Cuneyt,Karaman Muhammet,Gülcin İlhami

Funder

Department of Chemistry and Bingöl University

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

Reference105 articles.

1. Targeting tyrosine kinase: development of acridone–pyrrole–oxindole hybrids against human breast cancer;Kaur;Bioorg. Med. Chem. Lett.,2019

2. Enantioselective synthesis of substituted oxindoles and spirooxindoles with applications in drug discovery;Badillo;Curr. Opin. Drug Discov. Dev.,2010

3. Comparative α-glucosidase and α-amylase inhibition studies of rhodanine–pyrazole conjugates and their simple rhodanine analogues;Singh;Med. Chem. Res.,2019

4. Discovery, characterization and comparison of inhibitors of Bacillus anthracis and Staphylococcus aureus replicative DNA helicases;Aiello;Bioorg. Med. Chem.,2009

5. Design, synthesis, and structure-activity relationship of a novel series of 2-aryl 5-(4-oxo-3-phenethyl-2-thioxothiazolidinylidenemethyl) furans as HIV-1 entry inhibitors;Katritzky;J. Med. Chem.,2009

Cited by 75 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Dynamics of small molecule-enzyme interactions: Novel benzenesulfonamides as multi-target agents endowed with inhibitory effects against some metabolic enzymes;Archives of Biochemistry and Biophysics;2024-09

2. Determination of in vitro Antioxidant, Anticholinergic, and Antiepileptic Activities of some Medicinal and Aromatic Plant Extracts;Kahramanmaraş Sütçü İmam Üniversitesi Tarım ve Doğa Dergisi;2024-08-09

3. Chemistry of heterocycles as carbonic anhydrase inhibitors: A pathway to novel research in medicinal chemistry review;Archiv der Pharmazie;2024-04-29

4. Exploring rhodanine linked enamine–carbohydrazide derivatives as mycobacterial carbonic anhydrase inhibitors: Design, synthesis, biological evaluation, and molecular docking studies;Archiv der Pharmazie;2024-03-18

5. New 3-amino-2-thioxothiazolidin-4-one-based inhibitors of acetyl- and butyryl-cholinesterase: synthesis and activity;Future Medicinal Chemistry;2024-01