Results 11 to 20 of about 110,887 (393)

Special Issue: Sulfonamides [PDF]

open access: yesMolecules, 2017
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 directly bound to an aromatic, heterocyclic, aliphatic, or sugar scaffold ...
Claudiu T. Supuran
doaj   +4 more sources

Amidine Sulfonamides and Benzene Sulfonamides: Synthesis and Their Biological Evaluation [PDF]

open access: yesJournal of Chemistry, 2015
New amidine and benzene sulfonamide derivatives were developed and structures of the new products were confirmed by elemental and spectral analysis (FT-IR, ESI-MS, 1HNMR, and 13CNMR).
Muhammad Abdul Qadir   +4 more
doaj   +3 more sources

Sulfonamide Allergies [PDF]

open access: yesPharmacy, 2019
As one of the earliest developed antimicrobial classes, sulfonamides remain important therapeutic options for the empiric and definitive treatment of various infectious diseases. In the general population, approximately 3–8% of patients are reported to experience a sulfonamide allergy. Sulfonamide allergies can result in various physical manifestations;
Amber Giles   +3 more
openaire   +3 more sources

Deconstructing Protein Binding of Sulfonamides and Sulfonamide Analogues

open access: yesJACS Au, 2023
Sulfonamides are one of the most important pharmacophores in medicinal chemistry and sulfonamide analogs have gained substantial interest in recent years. However, the protein interactions of sulfonamides and especially of their analogs are underexplored.
Patrick L. Purder   +9 more
openaire   +3 more sources

Maternal exposure to sulfonamides and adverse pregnancy outcomes: A systematic review and meta-analysis.

open access: yesPLoS ONE, 2020
BackgroundSulfonamides are widely used to treat infectious diseases during pregnancy. However, the safety of maternal exposure to sulfonamides is controversial.
Peixuan Li   +3 more
doaj   +1 more source

Structure‐guided identification of a selective sulfonamide‐based inhibitor targeting the human carbonic anhydrase VA isoform

open access: yesArchiv der Pharmazie, Volume 356, Issue 1, January 2023., 2023
Combining ligand‐based and structure‐based methodologies, the applied virtual screening approach identified a collection of sulfonamides targeting the human carbonic anhydrase (hCA) VA isoform. 2‐(3,4‐Dihydro‐2H‐quinolin‐1‐yl)‐N‐(4‐sulfamoylphenyl)acetamide was identified as a potent and selective lead compound as a candidate for further exploitation ...
Laura De Luca   +4 more
wiley   +1 more source

Methylfolate Trap Promotes Bacterial Thymineless Death by Sulfa Drugs. [PDF]

open access: yesPLoS Pathogens, 2016
The methylfolate trap, a metabolic blockage associated with anemia, neural tube defects, Alzheimer's dementia, cardiovascular diseases, and cancer, was discovered in the 1960s, linking the metabolism of folate, vitamin B12, methionine and homocysteine ...
Marissa B Guzzo   +14 more
doaj   +1 more source

Synthesis and Antibacterial Activity of N,N-Diethylamide Bearing Benzenesulfonamide Derivatives [PDF]

open access: yes, 2013
Sulfonamides are known to represent a class of medicinally important compounds which are extensively used as antibacterial agents. Hence, a series of new N,N-diethyl amide bearing sulfonamides (2a-k) were synthesized via amidation of easily prepared ...
Ajani, Olayinka O.   +4 more
core   +1 more source

Room Temperature Synthesis and Antibacterial Activity of New Sulfonamides Containing N,N -Diethyl-Substituted AmidoMoieties [PDF]

open access: yes, 2012
Sulfonamide drugs which have brought about an antibiotic revolution in medicine are associated with a wide range of biological activities.
Ajani, Olayinka O.   +4 more
core   +5 more sources

Site-Selective C–H Functionalization–Sulfination Sequence to Access Aryl Sulfonamides

open access: yesOrganic Letters, 2020
Aryl sulfinates are precursors to a diverse number of sulfonyl-derived arenes, which are common motifs in pharmaceuticals and agrochemicals. Here, we report a site-selective two-step C–H sulfination sequence via aryl sulfonium salts to access aryl ...
E. Alvarez   +3 more
semanticscholar   +1 more source

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