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1.
Development of new thiazolidine-2,4-dione hybrids as aldose reductase inhibitors endowed with antihyperglycaemic activity: design, synthesis, biological investigations, and in silico insights.
J Enzyme Inhib Med Chem
; 38(1): 2231170, 2023 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-37470409
2.
2-Arylquinolines as novel anticancer agents with dual EGFR/FAK kinase inhibitory activity: synthesis, biological evaluation, and molecular modelling insights.
J Enzyme Inhib Med Chem
; 37(1): 349-372, 2022 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-34923887
3.
Design and synthesis of benzothiazole-based SLC-0111 analogues as new inhibitors for the cancer-associated carbonic anhydrase isoforms IX and XII.
J Enzyme Inhib Med Chem
; 37(1): 2635-2643, 2022 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-36146927
4.
Discovery of 2,4-thiazolidinedione-tethered coumarins as novel selective inhibitors for carbonic anhydrase IX and XII isoforms.
J Enzyme Inhib Med Chem
; 37(1): 531-541, 2022 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-34991416
5.
Discovery of indolinone-bearing benzenesulfonamides as new dual carbonic anhydrase and VEGFR-2 inhibitors possessing anticancer and pro-apoptotic properties.
Eur J Med Chem
; 259: 115707, 2023 Nov 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-37556946
6.
1,5-Diaryl-1,2,4-triazole Ureas as New SLC-0111 Analogues Endowed with Dual Carbonic Anhydrase and VEGFR-2 Inhibitory Activities.
J Med Chem
; 66(15): 10558-10578, 2023 08 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-37501287
7.
Design and synthesis of 6-arylpyridine-tethered sulfonamides as novel selective inhibitors of carbonic anhydrase IX with promising antitumor features toward the human colorectal cancer.
Eur J Med Chem
; 258: 115538, 2023 Oct 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-37321108
8.
Development of 4-((3-oxo-3-phenylpropyl)amino)benzenesulfonamide derivatives utilizing tail/dual-tail approaches as novel carbonic anhydrase inhibitors.
Eur J Med Chem
; 238: 114412, 2022 Aug 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-35551035
9.
Discovery of 4-alkoxy-2-aryl-6,7-dimethoxyquinolines as a new class of topoisomerase I inhibitors endowed with potent in vitro anticancer activity.
Eur J Med Chem
; 215: 113261, 2021 Apr 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33631697
10.
Identification of N-phenyl-2-(phenylsulfonyl)acetamides/propanamides as new SLC-0111 analogues: Synthesis and evaluation of the carbonic anhydrase inhibitory activities.
Eur J Med Chem
; 218: 113360, 2021 Jun 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33773285
11.
Design, Synthesis and Cytotoxicity Evaluation of New 3, 5-Disubstituted-2-Thioxoimidazolidinones.
Anticancer Agents Med Chem
; 18(4): 573-582, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29189182
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