Results 1 to 10 of about 8,103 (214)

Intracellular Binding of Novel Fluorinated Compounds to Carbonic Anhydrase Isoforms Explored by In-Cell <sup>19</sup>F NMR. [PDF]

open access: yesJ Med Chem
Costantino A   +8 more
europepmc   +1 more source

An ureido-substituted benzenesulfonamide carbonic anhydrase inhibitor exerts a potent antitumor effect in vitro and in vivo. [PDF]

open access: yesExp Hematol Oncol
Gazzaroli G   +12 more
europepmc   +1 more source

Design, synthesis, biological evaluation and in silico studies of 2-anilino- 4-(benzimidazol- 1-yl)pyrimidine scaffold as antitumor agents. [PDF]

open access: yesSaudi Pharm J
Al-Rasheed LS   +6 more
europepmc   +1 more source

Novel Derivatives of 3-Amino-4-hydroxy-benzenesulfonamide: Synthesis, Binding to Carbonic Anhydrases, and Activity in Cancer Cell 2D and 3D Cultures. [PDF]

open access: yesInt J Mol Sci
Vainauskas V   +12 more
europepmc   +1 more source
Some of the next articles are maybe not open access.

Pharmacophoric 2-hydroxyalkyl benzenesulfonamide: A single-step synthesis from benzenesulfonamide via hemiaminal

European Journal of Medicinal Chemistry, 2007
ortho-Acylation attempt of benzenesulfonamide afforded the corresponding hemiaminal as major product. The in situ reduction of the reaction mixture, reported herein, directly provided 2-hydroxyalkyl benzenesulfonamide, an important pharmacophoric element for designing drug-like scaffolds. Its application is demonstrated through designing a novel series
P Praveen Kumar, J Moses Babu, K Vyas
exaly   +4 more sources

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