Novel Antibacterial Agents

This book was devoted to the latest advances achieved in the antibacterial field, with a focus on the recent efforts made to develop new antimicrobial agents with novel modes of action, and a perspective on future directions of this line of research. Antimicrobial resistance has become a major threa...

Full description

Saved in:
Bibliographic Details
Other Authors: Meneghetti, Fiorella (Editor), Barlocco, Daniela (Editor)
Format: Book Chapter
Published: Basel MDPI - Multidisciplinary Digital Publishing Institute 2022
Subjects:
AMP
NMR
n/a
Online Access:Get Fullteks
DOAB: description of the publication
Tags: Add Tag
No Tags, Be the first to tag this record!
LEADER 07072naaaa2201861uu 4500
001 doab_20_500_12854_78739
005 20220224
020 |a books978-3-0365-2860-1 
020 |a 9783036528601 
020 |a 9783036528618 
024 7 |a 10.3390/books978-3-0365-2860-1  |c doi 
041 0 |a English 
042 |a dc 
072 7 |a GP  |2 bicssc 
100 1 |a Meneghetti, Fiorella  |4 edt 
700 1 |a Barlocco, Daniela  |4 edt 
700 1 |a Meneghetti, Fiorella  |4 oth 
700 1 |a Barlocco, Daniela  |4 oth 
245 1 0 |a Novel Antibacterial Agents 
260 |a Basel  |b MDPI - Multidisciplinary Digital Publishing Institute  |c 2022 
300 |a 1 electronic resource (409 p.) 
506 0 |a Open Access  |2 star  |f Unrestricted online access 
520 |a This book was devoted to the latest advances achieved in the antibacterial field, with a focus on the recent efforts made to develop new antimicrobial agents with novel modes of action, and a perspective on future directions of this line of research. Antimicrobial resistance has become a major threat to global health, and the twenty-two published articles here reported put in evidence that the discovery and development of new antibiotics are extremely challenging. The antimicrobial research covers a wide area, spanning from the design of new compounds, also supported by molecular modeling techniques, their synthesis and characterization, and biological tests.In this context, the current crisis caused by the COVID-19 pandemic, but also older threats, such as the human immunodeficiency virus or the hepatitis C virus, require greater attention than ever.The research works described in this book provide an extremely useful example of the results achieved in the field of antibacterial drug development. The search for new chemical entities was approached starting from both natural and synthetic compounds and addressing different targets. In addition, recent findings were presented and discussed highlighting the strategies to fight bacterial resistance. Detailed references to the state-of-the-art can be found in this book.We strongly encourage the wide group of readers to explore the book that we are presenting, to get inspired to develop new approaches for the diagnosis and treatment of antibacterial diseases, and to circumvent resistance issues. 
540 |a Creative Commons  |f https://creativecommons.org/licenses/by/4.0/  |2 cc  |4 https://creativecommons.org/licenses/by/4.0/ 
546 |a English 
650 7 |a Research & information: general  |2 bicssc 
653 |a saccharin 
653 |a tetrazole 
653 |a 1,3,4-thiadiazole 
653 |a H7PX glioma cells 
653 |a antimicrobial screening 
653 |a antioxidant capacity 
653 |a oxidative stress 
653 |a natural products 
653 |a medicinal plants 
653 |a anti-infective agents 
653 |a alternative infection models 
653 |a antibacterial 
653 |a anticancer 
653 |a GC-MS 
653 |a LIBS 
653 |a Moringa oleifera 
653 |a seed extract 
653 |a MRSA 
653 |a marine bisindole alkaloids 
653 |a antibiofilm activity 
653 |a adjuvants agents 
653 |a VBNC cells 
653 |a indole 
653 |a thioxothiazolidine 
653 |a antibacterial activity 
653 |a antifungal activity 
653 |a computer-aided prediction 
653 |a docking 
653 |a Mur B 
653 |a CYP 51 
653 |a plant compounds 
653 |a diarrhea 
653 |a selectivity 
653 |a compounds screening 
653 |a quorum sensing inhibition 
653 |a molecular docking 
653 |a AMP 
653 |a antimicrobial activity 
653 |a antiviral activity 
653 |a bacteriocin 
653 |a COVID-19 
653 |a disinfectant 
653 |a Lactobacillus plantarum 
653 |a plantaricin 
653 |a carbon nanotubes 
653 |a quaternary ammonium groups 
653 |a hyperbranched dendritic polymers 
653 |a antibacterial properties 
653 |a anti-cyanobacterial properties 
653 |a 3D-printing 
653 |a dental polymer 
653 |a antibacterial agent 
653 |a coating 
653 |a mesoporous silica nanoparticles 
653 |a polydimethylsiloxane 
653 |a Leishmania tropica and infantum 
653 |a antileishmanial agents 
653 |a lucanthone analogues 
653 |a amitriptyline analogues 
653 |a quinolizidine-derived compounds 
653 |a molecular modelling studies 
653 |a covalent inhibitor 
653 |a MurA 
653 |a cyclobutenaminone 
653 |a irreversible 
653 |a methicillin-resistant Staphylococcus aureus 
653 |a essential oils 
653 |a Origanum majorana 
653 |a Rosmarinus officinalis 
653 |a Thymus zygis 
653 |a biofilm inhibition and eradication 
653 |a urushiol 
653 |a 3-pentylcatechol 
653 |a 3-pentadecylcatechol 
653 |a Helicobacter pylori 
653 |a antimicrobial 
653 |a triple therapy 
653 |a atopic dermatitis 
653 |a skin barrier 
653 |a cutaneous dysbiosis 
653 |a Staphylococcus aureus 
653 |a microbial therapy 
653 |a drug delivery systems 
653 |a tris(1H-indol-3-yl)methylium 
653 |a turbomycin 
653 |a indole derivatives 
653 |a antibacterial action 
653 |a overcoming of drug resistance 
653 |a biological activities 
653 |a essential oil 
653 |a extract 
653 |a Thymus mastichina 
653 |a imidazole and imidazolium salts 
653 |a amino acid 
653 |a antibacterial agents 
653 |a aggregation 
653 |a lipophilicity 
653 |a antimicrobial peptide 
653 |a biomembranes 
653 |a ESKAPE 
653 |a antibiotic resistance 
653 |a NMR 
653 |a molecular dynamics 
653 |a biophysics 
653 |a sequence alignment 
653 |a lytic infection 
653 |a antibiotic-resistance 
653 |a Mycobacterium tuberculosis 
653 |a Acinetobacter baumannii 
653 |a Pseudomonas aeruginosa 
653 |a phage production 
653 |a magistral phage 
653 |a pulmonary delivery 
653 |a oral administration 
653 |a topical delivery 
653 |a Pinus cembra L. 
653 |a Pinus mugo Turra 
653 |a Picea abies L. 
653 |a Abies alba M. 
653 |a chemical investigation 
653 |a HS-GC/MS 
653 |a antioxidant activity 
653 |a tuberculosis 
653 |a mycobactins 
653 |a furan 
653 |a siderophores 
653 |a drug design 
653 |a bioisosterism 
653 |a drug resistance 
653 |a n/a 
856 4 0 |a www.oapen.org  |u https://mdpi.com/books/pdfview/book/4830  |7 0  |z Get Fullteks 
856 4 0 |a www.oapen.org  |u https://directory.doabooks.org/handle/20.500.12854/78739  |7 0  |z DOAB: description of the publication