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1.
New phthalimide-based derivatives as EGFR-TK inhibitors: Synthesis, biological evaluation, and molecular modeling study.
Bioorg Chem
; 127: 105966, 2022 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-35728294
2.
Synthesis, antitumour and antioxidant activities of novel α,ß-unsaturated ketones and related heterocyclic analogues: EGFR inhibition and molecular modelling study.
J Enzyme Inhib Med Chem
; 33(1): 507-518, 2018 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-29455554
3.
Synthesis and biological evaluation of 2-styrylquinolines as antitumour agents and EGFR kinase inhibitors: molecular docking study.
J Enzyme Inhib Med Chem
; 33(1): 199-209, 2018 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-29251017
4.
Synthesis, anti-inflammatory, analgesic, COX-1/2 inhibition activities and molecular docking study of pyrazoline derivatives.
Bioorg Med Chem
; 24(9): 2032-42, 2016 May 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-27025563
5.
Synthesis, antitumor activity and molecular docking study of some novel 3-benzyl-4(3H)quinazolinone analogues.
J Enzyme Inhib Med Chem
; 31(1): 78-89, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-25815668
6.
Antitumor evaluation and molecular docking study of substituted 2-benzylidenebutane-1,3-dione, 2-hydrazonobutane-1,3-dione and trifluoromethyl-1H-pyrazole analogues.
J Enzyme Inhib Med Chem
; 30(4): 679-87, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-25472776
7.
Cyanopyridinone- and Cyanopyridine-Based Cancer Cell Pim-1 Inhibitors: Design, Synthesis, Radiolabeling, Biodistribution, and Molecular Modeling Simulation.
ACS Omega
; 8(22): 19351-19366, 2023 Jun 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-37305261
8.
New Pyrazole-Clubbed Pyrimidine or Pyrazoline Hybrids as Anti-Methicillin-Resistant Staphylococcus aureus Agents: Design, Synthesis, In Vitro and In Vivo Evaluation, and Molecular Modeling Simulation.
ACS Omega
; 8(46): 44250-44264, 2023 Nov 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-38027391
9.
Synthesis, biological evaluation and molecular modeling study of pyrazole and pyrazoline derivatives as selective COX-2 inhibitors and anti-inflammatory agents. Part 2.
Bioorg Med Chem
; 20(10): 3306-16, 2012 May 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-22516672
10.
Synthesis and Molecular Docking Study of New Thiazole Derivatives as Potential Tubulin Polymerization Inhibitors.
ACS Omega
; 7(37): 33599-33613, 2022 Sep 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-36157722
11.
Design, synthesis, and biological evaluation of substituted hydrazone and pyrazole derivatives as selective COX-2 inhibitors: Molecular docking study.
Bioorg Med Chem
; 19(11): 3416-24, 2011 Jun 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-21570309
12.
Structural alterations based on naproxen scaffold: Synthesis, evaluation of antitumor activity and COX-2 inhibition, and molecular docking.
Eur J Med Chem
; 158: 134-143, 2018 Oct 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-30216848
13.
Synthesis, anti-inflammatory, analgesic and COX-1/2 inhibition activities of anilides based on 5,5-diphenylimidazolidine-2,4-dione scaffold: Molecular docking studies.
Eur J Med Chem
; 115: 121-31, 2016 Jun 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-26999325
14.
Structure-based design of phthalimide derivatives as potential cyclooxygenase-2 (COX-2) inhibitors: anti-inflammatory and analgesic activities.
Eur J Med Chem
; 92: 115-23, 2015 Mar 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-25549551
15.
Synthesis and biological evaluation of new curcumin analogues as antioxidant and antitumor agents: molecular modeling study.
Eur J Med Chem
; 101: 584-94, 2015 Aug 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-26197162
16.
Synthesis and anti-inflammatory activity of novel (substituted)benzylidene acetone oxime ether derivatives: molecular modeling study.
Eur J Med Chem
; 45(4): 1403-14, 2010 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-20079558
17.
Design, synthesis and biological evaluation of novel quinazoline derivatives as potential antitumor agents: molecular docking study.
Eur J Med Chem
; 45(9): 4188-98, 2010 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-20599299
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