Detalles de la búsqueda
1.
Design and Synthesis of Pyrazole Carboxamide Derivatives as Selective Cholinesterase and Carbonic Anhydrase Inhibitors: Molecular Docking and Biological Evaluation.
Chem Biodivers
; 21(2): e202301824, 2024 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-38149720
2.
Potent and selective carbonic anhydrase inhibition activities of pyrazolones bearing benzenesulfonamides.
Bioorg Med Chem Lett
; 95: 129479, 2023 10 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-37704010
3.
In vitro multitarget activity of sulfadiazine substituted triazenes as antimicrobial, cytotoxic, and larvicidal agents.
J Biochem Mol Toxicol
; 37(10): e23467, 2023 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-37466109
4.
Evaluation of cytotoxic, antifungal, and larvicidal activities of different bis-sulfonamide Schiff base compounds.
J Biochem Mol Toxicol
; 37(8): e23375, 2023 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-37129082
5.
Novel bis-ureido-substituted sulfaguanidines and sulfisoxazoles as carbonic anhydrase and acetylcholinesterase inhibitors.
Mol Divers
; 27(4): 1735-1749, 2023 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-36136229
6.
Potent carbonic anhydrase I, II, IX and XII inhibition activity of novel primary benzenesulfonamides incorporating bis-ureido moieties.
J Enzyme Inhib Med Chem
; 38(1): 2185762, 2023 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-36880350
7.
Synthesis and Characterization of Novel 1,3-Diaryltriazene-Substituted Sulfaguanidine Derivatives as Selective Carbonic Anhydrase Inhibitors: Biological Evaluation, in Silico ADME/T and Molecular Docking Study.
Chem Biodivers
; 20(8): e202300611, 2023 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-37470688
8.
Biological effects of bis-hydrazone compounds bearing isovanillin moiety on the aldose reductase.
Bioorg Chem
; 117: 105473, 2021 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-34768205
9.
Synthesis, Characterization, and Inhibition Study of Novel Substituted Phenylureido Sulfaguanidine Derivatives as α-Glycosidase and Cholinesterase Inhibitors.
Chem Biodivers
; 18(4): e2000958, 2021 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-33620128
10.
Synthesis, characterization, inhibition effects, and molecular docking studies as acetylcholinesterase, α-glycosidase, and carbonic anhydrase inhibitors of novel benzenesulfonamides incorporating 1,3,5-triazine structural motifs.
Bioorg Chem
; 100: 103897, 2020 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-32413628
11.
Pyridinium derivatives of 3-aminobenzenesulfonamide are nanomolar-potent inhibitors of tumor-expressed carbonic anhydrase isozymes CA IX and CA XII.
Bioorg Chem
; 103: 104204, 2020 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-32891000
12.
Sulphonamides incorporating 1,3,5-triazine structural motifs show antioxidant, acetylcholinesterase, butyrylcholinesterase, and tyrosinase inhibitory profile.
J Enzyme Inhib Med Chem
; 35(1): 424-431, 2020 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-31899985
13.
Synthesis of calix[4]azacrown substituted sulphonamides with antioxidant, acetylcholinesterase, butyrylcholinesterase, tyrosinase and carbonic anhydrase inhibitory action.
J Enzyme Inhib Med Chem
; 35(1): 1215-1223, 2020 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-32401067
14.
Synthesis, characterisation, biological evaluation and in silico studies of sulphonamide Schiff bases.
J Enzyme Inhib Med Chem
; 35(1): 950-962, 2020 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-32249705
15.
Synthesis, characterization, biological evaluation, and in silico studies of novel 1,3-diaryltriazene-substituted sulfathiazole derivatives.
Arch Pharm (Weinheim)
; 353(9): e2000102, 2020 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-32529657
16.
Discovery of new ureido benzenesulfonamides incorporating 1,3,5-triazine moieties as carbonic anhydrase I, II, IX and XII inhibitors.
Bioorg Med Chem
; 27(8): 1588-1594, 2019 04 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-30846402
17.
α-Carbonic anhydrases are strongly activated by spinaceamine derivatives.
Bioorg Med Chem
; 27(5): 800-804, 2019 03 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30683554
18.
Design, synthesis and biological evaluation of novel ureido benzenesulfonamides incorporating 1,3,5-triazine moieties as potent carbonic anhydrase IX inhibitors.
Bioorg Chem
; 82: 117-122, 2019 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-30312866
19.
Activation of α-, ß-, γ- δ-, ζ- and η- class of carbonic anhydrases with amines and amino acids: a review.
J Enzyme Inhib Med Chem
; 34(1): 1652-1659, 2019 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-31530034
20.
Activation of human α-carbonic anhydrase isoforms I, II, IV and VII with bis-histamine schiff bases and bis-spinaceamine substituted derivatives.
J Enzyme Inhib Med Chem
; 34(1): 1193-1198, 2019 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-31237157