Synthesis, antimicrobial, SAR, PASS, molecular docking, molecular dynamics and pharmacokinetics studies of 5′-<i>O</i>-uridine derivatives bearing acyl moieties: POM study and identification of the pharmacophore sites-Reference-Cited by-同舟云学术

Synthesis, antimicrobial, SAR, PASS, molecular docking, molecular dynamics and pharmacokinetics studies of 5′-O-uridine derivatives bearing acyl moieties: POM study and identification of the pharmacophore sites

Published:2022-07-07 Issue:10 Volume:41 Page:1036-1083
ISSN:1525-7770
Container-title:Nucleosides, Nucleotides & Nucleic Acids
language:en
Short-container-title:Nucleosides, Nucleotides & Nucleic Acids

Author:

Munia Nasrin S.¹^ORCID,Hosen Mohammed A.¹^ORCID,Azzam Khaldun M. A.²^ORCID,Al-Ghorbani Mohammed³^ORCID,Baashen Mohammed⁴^ORCID,Hossain Mohammed K.⁵^ORCID,Ali Ferdausi⁶^ORCID,Mahmud Shafi⁷^ORCID,Shimu Mst. S. S.⁸^ORCID,Almalki Faisal A.⁹^ORCID,Hadda Taibi B.⁹¹⁰^ORCID,Laaroussi Hamid¹⁰^ORCID,Naimi Souad¹¹,Kawsar Sarkar M. A.¹^ORCID

Affiliation:

1. Department of Chemistry, Faculty of Science, University of Chittagong, Chittagong, Bangladesh

2. Pharmacological and Diagnostic Research Center (PDRC), Department of Pharmaceutical Sciences, Faculty of Pharmacy, Al-Ahliyya Amman University, Amman, Jordan

3. Department of Chemistry, Faculty of Science and Arts, Ulla, Taibah University, Medina, Saudi Arabia

4. Department of Chemistry, Science and Humanities College, Shaqra University, Shaqra, KSA

5. Department of Pharmacy, Faculty of Biological Science, University of Chittagong, Chittagong, Bangladesh

6. Department of Microbiology, Faculty of Biological Science, University of Chittagong, Chittagong, Bangladesh

7. Department of Genome Science, John Curtin School of Medical Research, Australian National University, Canberra, Australia

8. Microbiology Laboratory, Department of Genetic Engineering and Biotechnology, University of Rajshahi, Rajshahi, Bangladesh

9. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Umm Al-Qura University, Makkah, Saudi Arabia

10. Laboratory of Applied Chemistry & Environment, Faculty of Sciences, Mohammed Premier University, Oujda, Morocco

11. Department of Biological Sciences, Sanofi-Aventis, Vitry, France

Funder

Ministry of Education, Government of the People's Republic of Bangladesh

Publisher

Informa UK Limited

Subject

Genetics,Molecular Medicine,Biochemistry,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/15257770.2022.2096898

Reference89 articles.

1. Uridine Function in the Central Nervous System

2. Antidepressant-like effects of uridine and omega-3 fatty acids are potentiated by combined treatment in rats

3. Discovery and Synthesis of a Phosphoramidate Prodrug of a Pyrrolo[2,1-f][triazin-4-amino] Adenine C-Nucleoside (GS-5734) for the Treatment of Ebola and Emerging Viruses

4. Uridine supplementation enhances hepatic mitochondrial function in thymidine-analogue treated HIV-infected patients

5. 5-FdUrd–araC heterodinucleoside re-establishes sensitivity in 5-FdUrd- and AraC-resistant MCF-7 breast cancer cells overexpressing ErbB2

Cited by 19 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. Synthesis, spectral characterization, biological, FMO, MEP, molecular docking, and molecular dynamics simulation studies of cytidine derivatives as antimicrobial and anticancer agents;Chemical Physics Impact;2024-12

2. Computational screening and molecular docking of compounds from Traditional Chinese Medicine (TCM) by targeting DNA topoisomerase I to design potential anticancer drugs;PLOS ONE;2024-09-12

3. Synthesis, Antimicrobial, Molecular Docking Against Bacterial and Fungal Proteins and In Silico Studies of Glucopyranoside Derivatives as Potent Antimicrobial Agents;Chemistry & Biodiversity;2024-08-16

4. Synthesis, Characterization, and Evaluation of Tetrazole Derivatives with Pyrrole‐2,5‐Dione Moieties as Urease Inhibitors: Exploring Structure‐Activity Relationships and Computational Insights;ChemistrySelect;2024-06-18

5. Antimicrobial polymers: elucidating the role of functional groups on antimicrobial activity;Arab Journal of Basic and Applied Sciences;2024-06-18