Detalles de la búsqueda
1.
The discovery of IDX21437: Design, synthesis and antiviral evaluation of 2'-α-chloro-2'-ß-C-methyl branched uridine pronucleotides as potent liver-targeted HCV polymerase inhibitors.
Bioorg Med Chem Lett
; 27(18): 4323-4330, 2017 09 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-28835346
2.
Synthesis and SAR studies of analogues of 4-(3,3-dimethyl-butyrylamino)-3,5-difluoro-N-thiazol-2-yl-benzamide (Lu AA41063) as adenosine A2A receptor ligands with improved aqueous solubility.
Bioorg Med Chem Lett
; 25(6): 1212-6, 2015 Mar 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-25701253
3.
Synthesis and antiviral evaluation of a novel series of homoserine-based inhibitors of the hepatitis C virus NS3/4A serine protease.
Bioorg Med Chem Lett
; 25(18): 3984-91, 2015 Sep 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-26231161
4.
Discovery and structural diversity of the hepatitis C virus NS3/4A serine protease inhibitor series leading to clinical candidate IDX320.
Bioorg Med Chem Lett
; 25(22): 5427-36, 2015 Nov 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-26410074
5.
Structure-based design of a novel series of azetidine inhibitors of the hepatitis C virus NS3/4A serine protease.
Bioorg Med Chem Lett
; 24(18): 4444-4449, 2014 Sep 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-25155387
6.
The synthesis and SAR of 2-arylsulfanyl-phenyl piperazinyl acetic acids as glyT-1 inhibitors.
Bioorg Med Chem Lett
; 14(15): 4027-30, 2004 Aug 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-15225720
Resultados
1 -
6
de 6
1
Próxima >
>>