نتایج جستجو برای: benzenesulfonamides

تعداد نتایج: 93  

Journal: :Molecules 2016
Beata Żołnowska Jarosław Sławiński Aneta Pogorzelska Krzysztof Szafrański Anna Kawiak Grzegorz Stasiłojć Mariusz Belka Szymon Ulenberg Tomasz Bączek Jarosław Chojnacki

A series of novel 5-substituted 2-(arylmethylthio)-4-chloro-N-(5-aryl-1,2,4-triazin-3-yl) benzenesulfonamide derivatives 27-60 have been synthesized by the reaction of aminoguanidines with an appropriate phenylglyoxal hydrate in glacial acetic acid. A majority of the compounds showed cytotoxic activity toward the human cancer cell lines HCT-116, HeLa and MCF-7, with IC50 values below 100 μM. It...

2016
Mostafa M. Ghorab Mansour S. Alsaid Mohamed S. Al-Dosary Yassin M. Nissan Sabry M. Attia

BACKGROUND Many thiourea derivatives have exhibited biological activities including anticancer activity through several mechanisms. On the other hand, benzenesulfonamide derivatives have proven to be good anticancer agents. Hybrids of both moieties could be further developed to explore their biological activity as anticancer. RESULTS Novel series of thioureidobenzenesulfonamides incorporating...

2013
Vijay M. Krishnamurthy Venkata S. Raman Richard A. Mowery Michelle Hentz James D. Baleja Bryan F. Shaw Krishna Kumar

This paper describes a biophysical investigation of residual mobility in complexes of bovine carbonic anhydrase II (BCA) and para-substituted benzenesulfonamide ligands with chains of 1-5 glycine subunits, and explains the previously observed increase in entropy of binding with chain length. The reported results represent the first experimental demonstration that BCA is not the rigid, static gl...

Journal: :Journal of medicinal chemistry 1995
P A Boriack D W Christianson J Kingery-Wood G M Whitesides

A series of competitive inhibitors of carbonic anhydrase II (CAII; EC 4.2.1.1) that consists of oligo(ethylene glycol) units attached to p-benzenesulfonamides with pendant amino acids, H2NSO2C6H4CONHCH2CH2OCH2CH2OCH2CH2NHCOCHRNH3+, have been synthesized and examined using competitive fluorescence assays. Three of the strongest inhibitors, designated EG3NH3+, EG3GlyNH3+, and EG3PheNH3+, have bee...

Journal: :Bioorganic & medicinal chemistry letters 2007
Brendan L Wilkinson Laurent F Bornaghi Todd A Houston Alessio Innocenti Daniela Vullo Claudiu T Supuran Sally-Ann Poulsen

A library of glycoconjugate benzenesulfonamides that contain diverse carbohydrate-triazole tails were investigated for their ability to inhibit the enzymatic activity of the three human transmembrane carbonic anhydrase (CA) isozymes hCA IX, hCA XII and hCA XIV. These isozymes have their CA domains located extracellularly, unlike the physiologically dominant hCA II, and are of immense current in...

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