Detalhe da pesquisa
1.
Assessing the dual activity of a chalcone-phthalocyanine conjugate: design, synthesis, and antivascular and photodynamic properties.
Mol Pharm
; 10(10): 3706-16, 2013 Oct 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23937202
2.
Design, synthesis and biological evaluation of conformationnally-restricted analogues of E7010 as inhibitors of tubulin assembly (ITA) and vascular disrupting agents (VDA).
Eur J Med Chem
; 244: 114809, 2022 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36208509
3.
Correction to "assessing the dual activity of a chalcone-phthalocyanine conjugate: design, synthesis, and antivascular and photodynamic properties".
Mol Pharm
; 12(2): 663, 2015 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25590168
4.
Optimization of the synthesis of a key intermediate for the preparation of glucocorticoids.
Steroids
; 137: 14-21, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30017852
5.
Development of the First Two-Pore Domain Potassium Channel TWIK-Related K+ Channel 1-Selective Agonist Possessing in Vivo Antinociceptive Activity.
J Med Chem
; 60(3): 1076-1088, 2017 02 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28051863
6.
Perspectives on the Two-Pore Domain Potassium Channel TREK-1 (TWIK-Related K(+) Channel 1). A Novel Therapeutic Target?
J Med Chem
; 59(11): 5149-57, 2016 06 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26588045
7.
Synthesis of S-linked thiooligosaccharide analogues of Nod factors: synthesis of new protected thiodisaccharide and thiotrisaccharide intermediates.
Carbohydr Res
; 338(13): 1369-79, 2003 Jun 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-12801710
8.
Synthesis and structure-activity relationship study of substituted caffeate esters as antinociceptive agents modulating the TREK-1 channel.
Eur J Med Chem
; 75: 391-402, 2014 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-24561669