نتایج جستجو برای: benzenesulfonamides

تعداد نتایج: 93  

2015
Sébastien Fortin Lianhu Wei Lakshmi P. Kotra René C.-Gaudreault

Phenyl 4-(2-oxoimidazolidin-1-yl)benzenesulfonates (PIB-SOs) and phenyl 4-(2-oxoimidazolidin1-yl)benzenesulfonamides (PIB-SAs) are new, potent combretastatin A-4 (CA-4) analogs designed on the basis of their common phenyl 2-imidazolidone moiety. This phenyl 2-imidazolidone group is a bioisosteric equivalent of the trimethoxyphenyl group also found in colchicine, podophyllotoxin and several othe...

Journal: :International Letters of Chemistry, Physics and Astronomy 2013

Journal: :Molecules 2014
Kęstutis Rutkauskas Asta Zubrienė Ingrida Tumosienė Kristina Kantminienė Marytė Kažemėkaitė Alexey Smirnov Justina Kazokaitė Vaida Morkūnaitė Edita Čapkauskaitė Elena Manakova Saulius Gražulis Zigmuntas J Beresnevičius Daumantas Matulis

A series of N-aryl-β-alanine derivatives and diazobenzenesulfonamides containing aliphatic rings were designed, synthesized, and their binding to carbonic anhydrases (CA) I, II, VI, VII, XII, and XIII was studied by the fluorescent thermal shift assay and isothermal titration calorimetry. The results showed that 4-substituted diazobenzenesulfonamides were more potent CA binders than N-aryl-β-al...

Journal: :Journal of enzyme inhibition and medicinal chemistry 2016
Halise Inci Gul Mehtap Tugrak Hiroshi Sakagami Parham Taslimi Ilhami Gulcin Claudiu T Supuran

A series of new 4-(3-(4-substitutedphenyl)-3a,4-dihydro-3H-indeno[1,2-c]pyrazol-2-yl) benzenesulfonamides (7-12) was synthesized starting from 2-(4-substitutedbenzylidene)-2,3-dihydro-1H-inden-1-one (1-6) and 4-hydrazinobenzenesulfonamide. The substituted benzaldehydes from which the key intermediate was prepared by introducing 2- or 4-substituents such as fluorine, hydroxy, methoxy, or the 3,4...

Journal: :Bioorganic & medicinal chemistry letters 2011
Adam J Salmon Michael L Williams Alfonso Maresca Claudiu T Supuran Sally-Ann Poulsen

Carbonic anhydrase IX (CA IX) is a recently validated target for the development of new cancer therapies. In this Letter we describe the synthesis and CA inhibition of a novel series of carbohydrate-based 1,5-disubstituted-1,2,3-triazole benzenesulfonamides. The key step of our synthesis is the regioselective Huisgen's 1,3-dipolar cycloaddition reaction (1,3-DCR) from carbohydrate azide substra...

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