3-Methoxyazetidin-2-one Functionalized CuO–CB Microfibrils: A Drug Formulation with Controlled Release and Enhanced Synergistic Antibacterial Activities-Reference-Cited by-同舟云学术

3-Methoxyazetidin-2-one Functionalized CuO–CB Microfibrils: A Drug Formulation with Controlled Release and Enhanced Synergistic Antibacterial Activities

Published:2023-04-19 Issue:5 Volume:6 Page:1849-1862
ISSN:2576-6422
Container-title:ACS Applied Bio Materials
language:en
Short-container-title:ACS Appl. Bio Mater.

Author:

Vijeata Anjali¹,Chaudhary Ganga Ram¹,Bhalla Aman¹^ORCID,Chaudhary Savita¹^ORCID

Affiliation:

1. Department of Chemistry and Centre of Advanced Studies in Chemistry, Panjab University, Chandigarh 160014, India

Funder

Council of Scientific and Industrial Research, India

University Grants Commission

Science and Engineering Research Board

Haryana State Council for Science and Technology

Department of Science and Technology, Ministry of Science and Technology, India

Publisher

American Chemical Society (ACS)

Subject

Biochemistry (medical),Biomedical Engineering,General Chemistry,Biomaterials

Link

https://pubs.acs.org/doi/pdf/10.1021/acsabm.3c00064

Reference58 articles.

1. Design and Application of Conjugated Polymer Nanomaterials for Detection and Inactivation of Pathogenic Microbes

2. RNA-seq analysis of virR and revR mutants of Clostridium perfringens

3. Challenges in drug delivery to tumors of the central nervous system: An overview of pharmacological and surgical considerations

4. Advancing antimicrobial strategies for managing oral biofilm infections

5. Treatment of urinary tract infections in the era of antimicrobial resistance and new antimicrobial agents

Cited by 3 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. Optimization and Effect of Substituents on the Transformation of 3-(Substituted acetoxy)azetidin-2-ones to Chiral 3-Hydroxyazetidin-2-ones, Molecular Docking and Enantiomeric Excess Determination;Letters in Organic Chemistry;2024-06

2. Asymmetric synthesis, characterization of chiral trans and cis -3-chloro/oxo/thio-4-styryl- β -lactams using ( R )-(+)-1-phenylethylamine and their efficient column chromatographic separation;Synthetic Communications;2024-02-27

3. Aroyl-isothiocyanates/isoselenocyanates as precursors to obtain novel cis-3-aroyl-thiourea/urea-β-lactams: design, synthesis, docking and biological evaluation;New Journal of Chemistry;2024