Arylsulfonamides and selectivity of matrix metalloproteinase-2: An overview

N Adhikari, A Mukherjee, A Saha, T Jha - European Journal of Medicinal …, 2017 - Elsevier
Uncontrolled regulation of specific metalloenzymes plays important roles in several
diseases like tumor metastasis and inflammation. Therefore, selective metalloenzyme …

Bacterial Zinc Metalloenzyme Inhibitors: Recent Advances and Future Perspectives

R Di Leo, D Cuffaro, A Rossello, E Nuti - Molecules, 2023 - mdpi.com
Human deaths caused by Gram-negative bacteria keep rising due to the multidrug
resistance (MDR) phenomenon. Therefore, it is a priority to develop novel antibiotics with …

Binding Mode Characterization and Early in Vivo Evaluation of Fragment-Like Thiols as Inhibitors of the Virulence Factor LasB from Pseudomonas aeruginosa

AM Kany, A Sikandar, J Haupenthal… - ACS Infectious …, 2018 - ACS Publications
The increasing emergence of antibiotic resistance necessitates the development of anti-
infectives with novel modes of action. Targeting bacterial virulence is considered a …

Tackling Pseudomonas aeruginosa Virulence by a Hydroxamic Acid-Based LasB Inhibitor

AM Kany, A Sikandar, S Yahiaoui… - ACS Chemical …, 2018 - ACS Publications
In search of novel antibiotics to combat the challenging spread of resistant pathogens,
bacterial proteases represent promising targets for pathoblocker development. A common …

Synthesis and biological activity of iron (II), iron (III), nickel (II), copper (II) and zinc (II) complexes of aliphatic hydroxamic acids

IS Sow, M Gelbcke, F Meyer, M Vandeput… - Journal of …, 2023 - Taylor & Francis
Aliphatic hydroxamic acids (HA) with varying numbers of carbon atoms, C2, C6, C8, C10,
C12 and C17, and corresponding Fe (II), Fe (III), Ni (II), Cu (II) and Zn (II) complexes have …

Inhibition of bacterial and human zinc-metalloproteases by bisphosphonate-and catechol-containing compounds

F Rahman, TM Nguyen, OA Adekoya… - Journal of Enzyme …, 2021 - Taylor & Francis
Compounds containg catechol or bisphosphonate were tested as inhibitors of the zinc
metalloproteases, thermolysin (TLN), pseudolysin (PLN) and aureolysin (ALN) which are …

QSAR modelling on a series of arylsulfonamide-based hydroxamates as potent MMP-2 inhibitors

S Sanyal, SA Amin, N Adhikari, T Jha - SAR and QSAR in …, 2019 - Taylor & Francis
ABSTRACT Matrix metalloproteinase-2 (MMP-2) is a lucrative therapeutic target as far as
anticancer drug discovery is concerned. Overexpression of MMP-2 is found to facilitate …

[HTML][HTML] The selectivity of galardin and an azasugar-based hydroxamate compound for human matrix metalloproteases and bacterial metalloproteases

I Sylte, R Dawadi, N Malla, S von Hofsten, TM Nguyen… - PLoS …, 2018 - journals.plos.org
Inhibitors targeting bacterial enzymes should not interfere with enzymes of the host, and
knowledge about structural determinants for selectivity is important for designing inhibitors …

Structural exploration of arylsulfonamide-based ADAM17 inhibitors through validated comparative multi-QSAR modelling studies

SK Baidya, SA Amin, S Banerjee, N Adhikari… - Journal of Molecular …, 2019 - Elsevier
Zinc-dependent ADAM17 takes part in a number of life-threatening conditions such as
inflammatory diseases, cancer, Alzheimer's disease and rheumatoid arthritis. Therefore …

Zinc binding and chelating compounds as inhibitors of bacterial metalloproteases and human matrix metalloproteases

FA Rahman - 2023 - munin.uit.no
Bacterial multi-drug resistance is a major health problem worldwide. Inhibition of bacterial
virulence is suggested to be a promising strategy in the development of new antibacterial …