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Facile Synthesis of 5-Bromo-N-Alkylthiophene-2-Sulfonamides and Its Activities Against Clinically Isolated New Delhi Metallo-β-Lactamase Producing Klebsiella pneumoniae ST147
by
Usman Qamar, Muhammad
, Rasool, Nasir
, Mahmood, Abid
, Umar Din, Sobia
, Noreen, Mnaza
, Bilal, Muhammad
, Ali Shah, Tawaf
, Bourhia, Mohammed
, Bin Jardan, Yousef
, Ouahmane, Lahcen
in
Acids
/ antibacterial
/ Antibiotics
/ Bacteria
/ Bromides
/ Carbapenems
/ Dehydrogenases
/ Drug development
/ Drug resistance
/ Enzymes
/ Hydrophobicity
/ Klebsiella pneumoniae
/ Metallo-β-lactamase
/ Molecular weight
/ NDM-1
/ Nosocomial infections
/ Original Research
/ Pathogens
/ RNA polymerase
/ Sepsis
/ Sulfonamides
/ Virulence factors
/ Vitamin B
2024
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Facile Synthesis of 5-Bromo-N-Alkylthiophene-2-Sulfonamides and Its Activities Against Clinically Isolated New Delhi Metallo-β-Lactamase Producing Klebsiella pneumoniae ST147
by
Usman Qamar, Muhammad
, Rasool, Nasir
, Mahmood, Abid
, Umar Din, Sobia
, Noreen, Mnaza
, Bilal, Muhammad
, Ali Shah, Tawaf
, Bourhia, Mohammed
, Bin Jardan, Yousef
, Ouahmane, Lahcen
in
Acids
/ antibacterial
/ Antibiotics
/ Bacteria
/ Bromides
/ Carbapenems
/ Dehydrogenases
/ Drug development
/ Drug resistance
/ Enzymes
/ Hydrophobicity
/ Klebsiella pneumoniae
/ Metallo-β-lactamase
/ Molecular weight
/ NDM-1
/ Nosocomial infections
/ Original Research
/ Pathogens
/ RNA polymerase
/ Sepsis
/ Sulfonamides
/ Virulence factors
/ Vitamin B
2024
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Facile Synthesis of 5-Bromo-N-Alkylthiophene-2-Sulfonamides and Its Activities Against Clinically Isolated New Delhi Metallo-β-Lactamase Producing Klebsiella pneumoniae ST147
by
Usman Qamar, Muhammad
, Rasool, Nasir
, Mahmood, Abid
, Umar Din, Sobia
, Noreen, Mnaza
, Bilal, Muhammad
, Ali Shah, Tawaf
, Bourhia, Mohammed
, Bin Jardan, Yousef
, Ouahmane, Lahcen
in
Acids
/ antibacterial
/ Antibiotics
/ Bacteria
/ Bromides
/ Carbapenems
/ Dehydrogenases
/ Drug development
/ Drug resistance
/ Enzymes
/ Hydrophobicity
/ Klebsiella pneumoniae
/ Metallo-β-lactamase
/ Molecular weight
/ NDM-1
/ Nosocomial infections
/ Original Research
/ Pathogens
/ RNA polymerase
/ Sepsis
/ Sulfonamides
/ Virulence factors
/ Vitamin B
2024
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Facile Synthesis of 5-Bromo-N-Alkylthiophene-2-Sulfonamides and Its Activities Against Clinically Isolated New Delhi Metallo-β-Lactamase Producing Klebsiella pneumoniae ST147
Journal Article
Facile Synthesis of 5-Bromo-N-Alkylthiophene-2-Sulfonamides and Its Activities Against Clinically Isolated New Delhi Metallo-β-Lactamase Producing Klebsiella pneumoniae ST147
2024
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Overview
New Delhi Metallo-
-lactamase producing
(NDM-1-KP) sequence type (ST) 147 poses a significant threat in clinical settings due to its evolution into two distinct directions: hypervirulence and carbapenem resistance. Hypervirulence results from a range of virulence factors, while carbapenem resistance stems from complex biological mechanisms. The NDM-1-KP ST147 clone has emerged as a recent addition to the family of successful clones within the species.
In this study, we successfully synthesized 5-bromo-
-alkylthiophene-2-sulfonamides (
) by reacting 5-bromothiophene-2-sulfonamide (
) with various alkyl bromides (
) using LiH. We also synthesized a series of compounds (
) from compound (
) using the Suzuki-Miyaura cross-coupling reaction with fair to good yields (56-72%). Further, we screened the synthesized molecules against clinically isolated New Delhi Metallo-
-lactamase producing
ST147. Subsequently, we conducted in-silico tests on compound
against a protein extracted from NDM-KP ST147 with PDB ID: 5N5I.
The compound (
) with favourable drug candidate status, MIC of 0.39 μg/mL, and MBC of 0.78 μg/mL. This low molecular weight compound exhibited the highest potency against the resistant bacterial strains. The in-silico tests revealed that the compound
against a protein extracted from NDM-KP ST147 with PDB ID: 5N5I demonstrated H-bond and hydrophobic interactions.
The 5-bromo-
-alkylthiophene-2-sulfonamides displayed antibacterial efficacy against New Delhi Metallo-
-lactamase producing
ST147. After the in-vivo trial, this substance might offer an alternative therapeutic option.
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