Detalhe da pesquisa
1.
Antibiotic class with potent in vivo activity targeting lipopolysaccharide synthesis in Gram-negative bacteria.
Proc Natl Acad Sci U S A
; 121(15): e2317274121, 2024 Apr 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38579010
2.
Structure-activity relationship studies on the inhibition of the bacterial translation of novel Odilorhabdins analogues.
Bioorg Med Chem
; 28(11): 115469, 2020 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32279921
3.
Synthesis and evaluation of (E)-2-(5-phenylpent-2-en-4-ynamido)cyclohex-1-ene-1-carboxylate derivatives as HCA2 receptor agonists.
Bioorg Med Chem
; 25(16): 4314-4329, 2017 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28668361
4.
Synthesis and evaluation of (E)-2-(acrylamido)cyclohex-1-enecarboxylic acid derivatives as HCA1, HCA2, and HCA3 receptor agonists.
Bioorg Med Chem
; 22(14): 3654-69, 2014 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24864041
5.
Sulfur containing acyclovir derivatives: synthesis, cytotoxic activity, and cell phenotype studies.
Nucleosides Nucleotides Nucleic Acids
; 26(10-12): 1269-71, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-18066766
6.
Efficient synthesis of 8-thiosubstituted guanine derivatives as potential tools for biochemical and biological studies.
Nucleosides Nucleotides Nucleic Acids
; 22(5-8): 755-8, 2003.
Artigo
em Inglês
| MEDLINE | ID: mdl-14565271
7.
Synthesis and antitumor effect in vitro and in vivo of substituted 1,3-dihydroindole-2-ones.
J Med Chem
; 53(19): 7140-5, 2010 Oct 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-20845961