Results 11 to 20 of about 8,103 (214)

Benzenesulfonamide Analogs: Synthesis, Anti-GBM Activity and Pharmacoprofiling

open access: yesInternational Journal of Molecular Sciences, 2023
The tropomyosin receptor kinase A (TrkA) family of receptor tyrosine kinases (RTKs) emerge as a potential target for glioblastoma (GBM) treatment. Benzenesulfonamide analogs were identified as kinase inhibitors possessing promising anticancer properties.
Konda Mani Saravanan   +2 more
exaly   +6 more sources

The crystal structures and Hirshfeld surface analysis of the 2-iodophenyl- and 4,5-difluoro-2-iodophenyl derivatives of benzenesulfonamide [PDF]

open access: yesActa Crystallographica Section E: Crystallographic Communications
Two new benzenesulfonyl derivatives, N-(2-iodophenyl)benzenesulfonamide, C12H10INO2, (I), and N-(4,5-difluoro-2-iodophenyl)benzenesulfonamide, C12H8F2INO2S, (II) were synthesized and structurally characterized.
Sundarasamy Madhan   +3 more
doaj   +3 more sources

Synthesis and Structure of N-(1-(Bromomethyl)-7,7-dimethylbicyclo[2.2.1]heptan-2-yl)benzenesulfonamide

open access: yesMolbank, 2023
A new bicyclic sulfonamide derivative, N-(1-(bromomethyl)-7,7-dimethylbicyclo[2.2.1]heptan-2-yl)benzenesulfonamide, was synthesized in the reaction of benzenesulfonamide and camphene in the presence of N-bromosuccinimide in acetonitrile.
Ivan A. Garagan   +3 more
doaj   +2 more sources

Discovery of Pyrazoline Benzenesulfonamide Derivatives as Anticancer Agents: A Review. [PDF]

open access: yesDrug Des Devel Ther
Pyrazoline benzenesulfonamide derivatives represent a distinctive class of heterocyclic compounds that synergistically combine the pharmacological versatility of the pyrazoline scaffold with the enzyme-inhibitory prowess of benzenesulfonamide moieties. These hybrids have emerged as promising candidates in anticancer drug discovery.
Hasyim DM   +5 more
europepmc   +4 more sources

N-(4-Methoxyphenyl)benzenesulfonamide [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2011
في مركب العنوان، C(13)H(13)NO(3)S، تكون حلقة البنزين لشطر البنزين- سلفوناميد مضطربة بنسبة إشغال 0.56 (3):0.44 (3)، ويتم لف مكونات الاضطراب بزاوية 21 (1) درجة مع بعضها البعض. مجموعة الميثوكسي بنزين مستوية تقريبًا (انحراف الجذر التربيعي = 0.0144 Å) ويتم إزاحة ذرة أميد N من هذا المستوى بمقدار 0.090 (6) Å.
Slamet Ibrahim   +4 more
openaire   +3 more sources

Synthesis and Monoamine Oxidase Inhibition Properties of 4-(2-Methyloxazol-4-yl)benzenesulfonamide

open access: yesMolbank
4-(2-Methyloxazol-4-yl)benzenesulfonamide was synthesized by the reaction of 4-(2-bromoacetyl)benzenesulfonamide with an excess of acetamide. The compound was evaluated as a potential inhibitor of human monoamine oxidase (MAO) A and B and was found to ...
Anton A. Shetnev   +4 more
doaj   +2 more sources

Carbonic anhydrase inhibition with a series of novel benzenesulfonamide-triazole conjugates

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry, 2018
We report the synthesis and characterisation of a novel series of triazole benzenesulfonamide derivatives, which incorporate the general pharmacophore associated with carbonic anhydrase (CA, EC 4.2.1.1) inhibitors.
Marwa G El-Gazzar   +2 more
exaly   +2 more sources

Synthesis of Novel Benzenesulfonamide-Bearing Functionalized Imidazole Derivatives as Novel Candidates Targeting Multidrug-Resistant Mycobacterium abscessus Complex

open access: yesMicroorganisms, 2023
Infections caused by drug-resistant (DR) Mycobacterium abscessus (M. abscessus) complex (MAC) are an important public health concern, particularly when affecting individuals with various immunodeficiencies or chronic pulmonary diseases.
Benas Balandis   +8 more
doaj   +2 more sources

Small-molecule screen in C. elegans identifies benzenesulfonamides as inhibitors of microsporidia spores [PDF]

open access: yesnpj Antimicrobials and Resistance
Microsporidia, a large group of fungal-related intracellular parasites, infect several economically significant animals, leading to substantial economic losses.
Qingyuan Huang   +6 more
doaj   +2 more sources

The Identification and synthesis of metabolites of 4-(5-methyl-1,3,4-oxadiazole-2-yl)-benzenesulfonamide

open access: yesResearch Results in Pharmacology
Introduction: 4-(5-methyl-1,3,4-oxadiazole-2-yl)-benzenesulfonamide is a new selective type II carbonic anhydrase inhibitor with local action through instillation into the eyes. For a complete pharmacokinetic study of this drug, it is necessary to detect
Alexander L. Khokhlov   +8 more
doaj   +2 more sources

Home - About - Disclaimer - Privacy