Results 121 to 130 of about 8,103 (214)

SYNTHESIS, CHARACTERIZATION AND ANTIMICROBIAL STUDY OF SOME BENZENESULFONAMIDE BASED BIPYRAZOLES

open access: yes, 2014
Objectives: To synthesize, characterize and evaluate antimicrobial properties of some benzenesulfonamide based bipyrazole. Methods: The benzenesulfonamide based bipyrazole 1a-d & 2a-f have been synthesized by the reaction between 1-[1-aryl ...
Sharma, Pawan K., Singh, Karan
core  

Reaction of mesoionic compounds deriving from cyclic N-acyl-alpha-aminoacids with N-(phenylmethylene)benzenesulfonamide

open access: yes, 1999
We studied the behaviour of bicyclic mesoionic compounds derived from the cyclodehydration of cyclic N-acyl-α-aminoacids 1-4 with N- (phenylmethylene)benzenesulfonamide 5. The reaction affords spirocyclic β- lactams and/or imidazo-condensed products (the
C. La Rosa   +2 more
core   +1 more source

Designing, synthesis and bioactivities of 4-[3-(4-hydroxyphenyl)-5-aryl-4,5-dihydro-pyrazol-1-yl]benzenesulfonamides

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry, 2017
In this study, 4-[3-(4-hydroxyphenyl)-5-aryl-4,5-dihydro-pyrazol-1-yl]benzenesulfonamide (1–9) types compounds were synthesized and their chemical structures were confirmed by 1H NMR, 13C NMR and HRMS spectra.
Halise Inci Gul   +5 more
doaj   +1 more source

Synthesis of Anti-Microtubule N-(2-Arylindol-7-yl)benzenesulfonamide Derivatives and Their Antitumor Mechanisms

open access: yes, 2010
Breaking the cycle: A series of N-(2-arylindol-7-yl)benzenesulfonamide derivatives were prepared. Among them, compound 2 showed promising antiproliferative activity against hormone-resistant prostate cancer PC-3 cells, induced G2/M-phase arrest, and ...
Chen, Grace Shiahuy   +15 more
core   +1 more source

Benzenesulfonamide

open access: yesActa Crystallographica Section E Structure Reports Online, 2007
B. Thimme Gowda   +4 more
openaire   +1 more source

Docking study of novel designed indazole derivatives against topoisomerase-II DNA gyrase enzyme for antibacterial screening

open access: yesIntelligent Pharmacy
Aim of the study was designed for the design of novel indazole derivatives and evaluation of their docking against topoisomerase-II DNA gyrase enzyme for the antibacterial screening. Different novel substituted indazol-3-yl benzenesulfonamide derivatives
Nabeela Mareyam   +4 more
doaj   +1 more source

Synthesis, antimicrobial and QSAR studies of novel benzenesulfonamide derivatives [PDF]

open access: yes, 2018
852-857Novel benzenesulfonamide derivatives have been synthesized and characterized by various spectroscopical and analytical techniques, such as, FT-IR, UV-Vis, and NMR, and elemental analysis.
Dığrak, Metin   +3 more
core  

(S)-(−)-4-[4-[2-(Isochroman-1-yl)ethyl]piperazin-1-yl]benzenesulfonamide, a Selective Dopamine D4 Antagonist

open access: yes, 2016
(S)-(−)-4-[4-[2-(Isochroman-1-yl)ethyl]piperazin-1-yl]benzenesulfonamide, a Selective Dopamine D4 ...
Robert A. Lahti (3018411)   +12 more
core   +1 more source

An overlap of interacting amino acid in cluster I & II with inositol-(1,3,4,5)-tetrakisphosphate, benzenesulfonamide and sulfonamide derivatives within Akt2 binding cavity.

open access: yes, 2016
An overlap of interacting amino acid in cluster I & II with inositol-(1,3,4,5)-tetrakisphosphate, benzenesulfonamide and sulfonamide derivatives within Akt2 binding cavity.
Noreen Akhtar (3609425)   +1 more
core   +1 more source

The evaluation of pharmacokinetic parameters of 4-(5-methyl-1,3,4-oxadiazole-2-yl)- benzenesulfonamide and its metabolites in rat plasma

open access: yes
4-(5-methyl-1,3,4-oxadiazole-2-yl)-benzenesulfonamide (ODASA) is a new pharmacologically active compound, which is capable of reducing intraocular pressure by inhibiting carbonic anhydrase ...
Korsakov, M. K.   +4 more
core   +1 more source

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