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Hybrid inhibitors of DNA gyrase A and B : design, synthesis and evaluation
ID
Durcik, Martina
(
Author
),
ID
Skok, Žiga
(
Author
),
ID
Ilaš, Janez
(
Author
),
ID
Zidar, Nace
(
Author
),
ID
Zega, Anamarija
(
Author
),
ID
Szili, Petra
(
Author
),
ID
Draskovits, Gábor
(
Author
),
ID
Revesz, T.
(
Author
),
ID
Kikelj, Danijel
(
Author
),
ID
Nyerges, Ákos
(
Author
),
ID
Pál, Csaba
(
Author
),
ID
Peterlin-Mašič, Lucija
(
Author
),
ID
Tomašič, Tihomir
(
Author
)
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MD5: 55614DE5A88BB31AD352E271FDB12DC6
URL - Source URL, Visit
https://www.mdpi.com/1999-4923/13/1/6
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Abstract
The discovery of multi-targeting ligands of bacterial enzymes is an important strategy to combat rapidly spreading antimicrobial resistance. Bacterial DNA gyrase and topoisomerase IV are validated targets for the development of antibiotics. They can be inhibited at their catalytic sites or at their ATP binding sites. Here we present the design of new hybrids between the catalytic inhibitor ciprofloxacin and ATP-competitive inhibitors that show low nanomolar inhibition of DNA gyrase and antibacterial activity against Gram-negative pathogens. The most potent hybrid 3a has MICs of 0.5 µg/mL against Klebsiella pneumoniae, 4 µg/mL against Enterobacter cloacae, and 2 µg/mL against Escherichia coli. In addition, inhibition of mutant E. coli strains shows that these hybrid inhibitors interact with both subunits of DNA gyrase (GyrA, GyrB), and that binding to both of these sites contributes to their antibacterial activity.
Language:
English
Keywords:
antibacterial
,
ciprofloxacin
,
DNA gyrase
,
dual inhibitor
,
hybrid
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
FFA - Faculty of Pharmacy
Publication status:
Published
Publication version:
Version of Record
Year:
2021
Number of pages:
17 str.
Numbering:
Vol. 13, iss. 1, art. 6
PID:
20.500.12556/RUL-134779
UDC:
615.4:54:615.015.8
ISSN on article:
1999-4923
DOI:
10.3390/pharmaceutics13010006
COBISS.SI-ID:
44007939
Publication date in RUL:
01.02.2022
Views:
981
Downloads:
161
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Record is a part of a journal
Title:
Pharmaceutics
Shortened title:
Pharmaceutics
Publisher:
MDPI
ISSN:
1999-4923
COBISS.SI-ID:
517949977
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:
01.01.2021
Secondary language
Language:
Slovenian
Keywords:
DNK giraze
,
ciprofloksacin
,
zaviralci
,
hibridi
,
bakterijska rezistenca
,
farmacevtska kemija
Projects
Funder:
ARRS - Slovenian Research Agency
Project number:
P1-0208
Name:
Farmacevtska kemija: načrtovanje, sinteza in vrednotenje učinkovin
Funder:
EC - European Commission
Funding programme:
H2020
Project number:
648364
Name:
Bacterial evolution of hypersensitivity and resistance against antimicrobial peptides
Acronym:
Resistance evolution
Funder:
Other - Other funder or multiple funders
Funding programme:
Hungarian Academy of Sciences, Célzott Lendület
Project number:
LP-2017–10/2017
Funder:
Other - Other funder or multiple funders
Funding programme:
Élvonal
Project number:
KKP 126506
Funder:
Other - Other funder or multiple funders
Project number:
GINOP-2.3.2–15–2016–00014
Acronym:
EVOMER
Funder:
Other - Other funder or multiple funders
Project number:
GINOP-2.3.2–15–2016–00020
Acronym:
MolMedEx TUMORDNS
Funder:
Other - Other funder or multiple funders
Project number:
GINOP-2.3.3–15–2016–00001
Funder:
Other - Other funder or multiple funders
Project number:
EFOP 3.6.3-VEKOP-16-2017-00009
Funder:
Other - Other funder or multiple funders
Funding programme:
Ministry for Innovation and Technology, New National Excellence Programme, UNKP-20-3
Funder:
Other - Other funder or multiple funders
Funding programme:
Boehringer Ingelheim Fonds, PhD Fellowship
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