Sulfonamide drugs: Structure, antibacterial property, toxicity, and biophysical interactions
A Ovung, J Bhattacharyya - Biophysical reviews, 2021 - Springer
Sulfonamide (or sulphonamide) functional group chemistry (SN) forms the basis of several
groups of drug. In vivo sulfonamides exhibit a range of pharmacological activities, such as …
groups of drug. In vivo sulfonamides exhibit a range of pharmacological activities, such as …
Ciprofloxacin derivatives and their antibacterial activities
GF Zhang, X Liu, S Zhang, B Pan, ML Liu - European journal of medicinal …, 2018 - Elsevier
Bacterial infections represent a significant health threat globally, and are responsible for the
majority of hospital-acquired infections, leading to extensive mortality and burden on global …
majority of hospital-acquired infections, leading to extensive mortality and burden on global …
[HTML][HTML] Folic acid antagonists: antimicrobial and immunomodulating mechanisms and applications
Bacterial, protozoan and other microbial infections share an accelerated metabolic rate. In
order to ensure a proper functioning of cell replication and proteins and nucleic acids …
order to ensure a proper functioning of cell replication and proteins and nucleic acids …
[HTML][HTML] Synthesis, DFT studies, molecular docking and biological activity evaluation of thiazole-sulfonamide derivatives as potent Alzheimer's inhibitors
Alzheimer's disease is a major public brain condition that has resulted in many deaths, as
revealed by the World Health Organization (WHO). Conventional Alzheimer's treatments …
revealed by the World Health Organization (WHO). Conventional Alzheimer's treatments …
Ciprofloxacin removal from non-clinical environment: A critical review of current methods and future trend prospects
Antibiotics in the environment represent a significant threat to global public health.
Ciprofloxacin (CIP) is one of the second generation groups of synthetic fluoroquinolones …
Ciprofloxacin (CIP) is one of the second generation groups of synthetic fluoroquinolones …
Development of sulfonamide-based Schiff bases targeting urease inhibition: Synthesis, characterization, inhibitory activity assessment, molecular docking and ADME …
A series of Sulfonamide-based Schiff bases (E)-4-(benzylideneamino)-N-(6-
methoxypyridazin-3-yl) benzenesulfonamide (3a-r) targeting Urease Inhibition was …
methoxypyridazin-3-yl) benzenesulfonamide (3a-r) targeting Urease Inhibition was …
Facile synthesis of ZnO-clay minerals composites using an ultrasonic approach for photocatalytic performance
WA Freitas, BECF Soares, MS Rodrigues… - … of Photochemistry and …, 2022 - Elsevier
Photocatalysts based on ZnO-clay minerals were prepared using palygorskite (Pal) and/or
halloysite (Hal) as supports. The photocatalysts were obtained by the method of ultrasonic …
halloysite (Hal) as supports. The photocatalysts were obtained by the method of ultrasonic …
[HTML][HTML] sulfonamides
CT Supuran - Molecules, 2017 - mdpi.com
The sulfonamides and their structurally related derivatives, such as the sulfamates and
sulfamides, possess the general formula A-SO2NHR, in which the functional group is either …
sulfamides, possess the general formula A-SO2NHR, in which the functional group is either …
Recent efforts in the discovery of urease inhibitor identifications
WQ Song, ML Liu, SY Li, ZP Xiao - Current Topics in Medicinal …, 2022 - ingentaconnect.com
Urease is an attractive drug target for designing anti-infective agents against pathogens
such as Helicobacter pylori, Proteus mirabilis, and Ureaplasma urealyticum. In the past …
such as Helicobacter pylori, Proteus mirabilis, and Ureaplasma urealyticum. In the past …
Current pharmaceutical aspects of synthetic quinoline derivatives
Quinoline derivatives are considered broad-spectrum pharmacological compounds that
exhibit a wide range of biological activities. Integration of quinoline moiety can improve its …
exhibit a wide range of biological activities. Integration of quinoline moiety can improve its …