Detalhe da pesquisa
1.
Recent advances of vacuolar protein-sorting 34 inhibitors targeting autophagy.
Bioorg Chem
; 143: 107039, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38134519
2.
Design, synthesis, and biological evaluation of novel protopanoxadiol derivatives based PROTACs technology for the treatment of lung cancer.
Bioorg Chem
; 131: 106327, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36549254
3.
Design, synthesis and evaluation of dihydro-1H-indene derivatives as novel tubulin polymerisation inhibitors with anti-angiogenic and antitumor potency.
J Enzyme Inhib Med Chem
; 38(1): 2247579, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37587873
4.
The Functional Roles of ISG15/ISGylation in Cancer.
Molecules
; 28(3)2023 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-36771004
5.
Discovery of Norbornene as a Novel Hydrophobic Tag Applied in Protein Degradation.
Angew Chem Int Ed Engl
; 62(13): e202217246, 2023 03 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36670545
6.
Spirolactone-type and enmein-type derivatives as potential anti-cancer agents derived from oridonin.
Bioorg Med Chem
; 72: 116977, 2022 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36037626
7.
Identification of a Hydrogen-Sulfide-Releasing Isochroman-4-One Hybrid as a Cardioprotective Candidate for the Treatment of Cardiac Hypertrophy.
Molecules
; 27(13)2022 Jun 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35807360
8.
First total synthesis of hoshinoamide A.
Beilstein J Org Chem
; 17: 2924-2931, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34956412
9.
Hotel employees' fun climate at work: Effects on work-family conflict and employee deep acting through a collectivistic perspective.
Int J Hosp Manag
; 91: 102666, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32934433
10.
Design, synthesis and biological evaluation of isochroman-4-one hybrids bearing piperazine moiety as antihypertensive agent candidates.
Bioorg Med Chem
; 27(13): 2764-2770, 2019 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31078380
11.
Discovery of novel quinazolines as potential anti-tubulin agents occupying three zones of colchicine domain.
Bioorg Chem
; 83: 380-390, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30408650
12.
Synthesis, molecular properties prediction and biological evaluation of indole-vinyl sulfone derivatives as novel tubulin polymerization inhibitors targeting the colchicine binding site.
Bioorg Chem
; 85: 49-59, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30599412
13.
Hydrogen sulfide releasing enmein-type diterpenoid derivatives as apoptosis inducers through mitochondria-related pathways.
Bioorg Chem
; 82: 192-203, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30326401
14.
Metal-Free Synthesis of N-(Pyridine-2-yl)amides from Ketones via Selective Oxidative Cleavage of C(O)-C(Alkyl) Bond in Water.
J Org Chem
; 83(23): 14307-14313, 2018 12 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30450904
15.
Cobalt-catalyzed carbon-sulfur/selenium bond formation: synthesis of benzo[b]thio/selenophene-fused imidazo[1,2-a]pyridines.
Org Biomol Chem
; 16(20): 3721-3725, 2018 05 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-29737996
16.
Concise Total Synthesis of (±)-Deguelin and (±)-Tephrosin Using a Vinyl Iodide as a Key Building Block.
J Nat Prod
; 81(4): 1055-1059, 2018 04 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-29442505
17.
Bioactive Natural Spirolactone-Type 6,7-seco-ent-Kaurane Diterpenoids and Synthetic Derivatives.
Molecules
; 23(11)2018 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30413071
18.
Discovery of acylguanidine oseltamivir carboxylate derivatives as potent neuraminidase inhibitors.
Bioorg Med Chem
; 25(10): 2772-2781, 2017 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28385598
19.
6,7-Seco-ent-Kauranoids Derived from Oridonin as Potential Anticancer Agents.
J Nat Prod
; 80(9): 2391-2398, 2017 09 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-28901767
20.
Novel nitric oxide-releasing spirolactone-type diterpenoid derivatives with in vitro synergistic anticancer activity as apoptosis inducer.
Bioorg Med Chem Lett
; 26(17): 4191-6, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27491707