Results 11 to 20 of about 8,103 (214)
Benzenesulfonamide Analogs: Synthesis, Anti-GBM Activity and Pharmacoprofiling
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]
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
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]
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]
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
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
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
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]
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
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

