Detalhe da pesquisa
1.
Synthesis of pyrazole acrylic acid based oxadiazole and amide derivatives as antimalarial and anticancer agents.
Bioorg Chem
; 77: 106-124, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29353728
2.
Preparation, characterization and cytotoxic evaluation of bovine serum albumin nanoparticles encapsulating 5-methylmellein: A secondary metabolite isolated from Xylaria psidii.
Bioorg Med Chem Lett
; 27(23): 5126-5130, 2017 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29100800
3.
Fusion of Structure and Ligand Based Methods for Identification of Novel CDK2 Inhibitors.
J Chem Inf Model
; 57(8): 1957-1969, 2017 08 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-28723151
4.
Targeted SLNs for management of HIV-1 associated dementia.
Drug Dev Ind Pharm
; 41(8): 1321-7, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25113430
5.
Dual targeted polymeric nanoparticles based on tumor endothelium and tumor cells for enhanced antitumor drug delivery.
Mol Pharm
; 11(3): 697-715, 2014 Mar 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24512060
6.
Cell cycle inhibitory activity of Piper longum against A549 cell line and its protective effect against metal-induced toxicity in rats.
Indian J Biochem Biophys
; 51(5): 358-64, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25630105
7.
Correction to 1,2,3-Triazole Tethered Hybrid Capsaicinoids as Antiproliferative Agents Active against Lung Cancer Cells (A549).
ACS Omega
; 9(9): 11026, 2024 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38463328
8.
Mechanistic investigation of synergistic interaction of tocopherol succinate with a quinoline-based inhibitor of mammalian target of rapamycin.
J Pharm Pharmacol
; 74(4): 605-617, 2022 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34468737
9.
1,2,3-Triazole Tethered Hybrid Capsaicinoids as Antiproliferative Agents Active against Lung Cancer Cells (A549).
ACS Omega
; 7(36): 32078-32100, 2022 Sep 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36119972
10.
2-Anilinonicotinyl linked 2-aminobenzothiazoles and [1,2,4]triazolo[1,5-b] [1,2,4]benzothiadiazine conjugates as potential mitochondrial apoptotic inducers.
Bioorg Med Chem
; 19(23): 7136-50, 2011 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22047801
11.
Synthesis of 4ß-N-polyaromatic substituted podophyllotoxins: DNA topoisomerase inhibition, anticancer and apoptosis-inducing activities.
Bioorg Med Chem
; 18(24): 8493-500, 2010 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21074444
12.
Design, synthesis and comparative analysis of triphenyl-1,2,3-triazoles as anti-proliferative agents.
Eur J Med Chem
; 207: 112813, 2020 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32947093
13.
Evaluation of fluoren-NU as a novel antitumor agent.
Oncol Res
; 17(9): 387-96, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19718945
14.
Design of Novel 3-Pyrimidinylazaindole CDK2/9 Inhibitors with Potent In Vitro and In Vivo Antitumor Efficacy in a Triple-Negative Breast Cancer Model.
J Med Chem
; 60(23): 9470-9489, 2017 12 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-29144137
15.
Tailored polymer-lipid hybrid nanoparticles for the delivery of drug conjugate: dual strategy for brain targeting.
Colloids Surf B Biointerfaces
; 126: 414-25, 2015 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25601092
16.
Design, synthesis and anticancer activity of Michael-type thiol adducts of α-santonin analogue with exocyclic methylene.
Eur J Med Chem
; 101: 769-79, 2015 Aug 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-26222449
17.
ß-Ionone derived apoptosis inducing endoperoxides; Discovery of potent leads for anticancer agents.
Eur J Med Chem
; 87: 228-36, 2014 Nov 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-25259515
18.
Parthenium hysterophorus: a probable source of anticancer, antioxidant and anti-HIV agents.
Biomed Res Int
; 2013: 810734, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24350290
19.
Synthesis and anticancer activity of novel spiro-isoxazoline and spiro-isoxazolidine derivatives of α-santonin.
Eur J Med Chem
; 63: 279-89, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23501113
20.
Bakuchiol derivatives as novel and potent cytotoxic agents: a report.
Eur J Med Chem
; 49: 55-67, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22245048