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1.
Stereoselective synthesis of MLN4924, an inhibitor of NEDD8-activating enzyme.
J Org Chem
; 76(9): 3557-61, 2011 May 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-21417215
2.
Design, synthesis, and binding of homologated truncated 4'-thioadenosine derivatives at the human A3 adenosine receptors.
Bioorg Med Chem
; 18(19): 7015-21, 2010 Oct 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-20826090
3.
Synthesis and anti-hepatitis C virus (HCV) activity of 3'-C-substituted-methyl pyrimidine and purine nucleosides.
Bioorg Med Chem
; 18(13): 4812-20, 2010 Jul 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-20627592
4.
Structure-activity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonists.
Bioorg Med Chem
; 17(10): 3733-8, 2009 May 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-19375920
5.
Design and synthesis of N(6)-substituted-4'-thioadenosine-5'-uronamides as potent and selective human A(3) adenosine receptor agonists.
Bioorg Med Chem
; 17(23): 8003-11, 2009 Dec 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-19879151
6.
Design, Synthesis, and Anti-RNA Virus Activity of 6'-Fluorinated-Aristeromycin Analogues.
J Med Chem
; 62(13): 6346-6362, 2019 07 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-31244113
7.
First synthesis of 4'-selenonucleosides showing unusual Southern conformation.
Org Lett
; 10(2): 209-12, 2008 Jan 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-18088134
8.
Structure-activity relationships of 2-chloro-N6-substituted-4'-thioadenosine-5'-N,N-dialkyluronamides as human A3 adenosine receptor antagonists.
Bioorg Med Chem Lett
; 18(5): 1612-6, 2008 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-18255292
9.
Design and synthesis of novel 2',3'-dideoxy-4'-selenonucleosides as potential antiviral agents.
Bioorg Med Chem
; 16(23): 9891-7, 2008 Dec 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-18977147
10.
Synthesis of 3'-acetamidoadenosine derivatives as potential A3 adenosine receptor agonists.
Nucleosides Nucleotides Nucleic Acids
; 27(4): 408-20, 2008 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-18404574
11.
Discovery of a new nucleoside template for human A3 adenosine receptor ligands: D-4'-thioadenosine derivatives without 4'-hydroxymethyl group as highly potent and selective antagonists.
J Med Chem
; 50(14): 3159-62, 2007 Jul 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-17555308
12.
Synthesis and anti-HCV activity Of 2''-beta-hydroxymethylated nucleosides.
Nucleosides Nucleotides Nucleic Acids
; 26(6-7): 725-8, 2007.
Artículo
en Inglés
| MEDLINE | ID: mdl-18066889
13.
Stereoselective synthesis of 1'-functionalized-4'-thionucleosides.
Nucleosides Nucleotides Nucleic Acids
; 26(8-9): 1011-4, 2007.
Artículo
en Inglés
| MEDLINE | ID: mdl-18058527
14.
Asymmetric synthesis of cyclopropyl-fused 2'-C-methylcarbanucleosides as potential anti-HCV agents.
Nucleosides Nucleotides Nucleic Acids
; 26(8-9): 1021-4, 2007.
Artículo
en Inglés
| MEDLINE | ID: mdl-18058529
15.
Synthesis of N6-substituted 3'-ureidoadenosine derivatives as highly potent agonists at the mutant A3 adenosine receptor.
Nucleosides Nucleotides Nucleic Acids
; 26(6-7): 717-9, 2007.
Artículo
en Inglés
| MEDLINE | ID: mdl-18066887
16.
Asymmetric synthesis of novel apio carbocyclic nucleoside analogues as potential antiviral and antitumor agent.
Nucleosides Nucleotides Nucleic Acids
; 26(6-7): 721-4, 2007.
Artículo
en Inglés
| MEDLINE | ID: mdl-18066888
17.
Stereoselective synthesis of homo-apioneplanocin A as potential inhibitor of S-adenosylhomocysteine hydrolase.
Nucleosides Nucleotides Nucleic Acids
; 26(6-7): 729-32, 2007.
Artículo
en Inglés
| MEDLINE | ID: mdl-18066890
18.
Design, synthesis, and anti-tumor activity of 4'-thionucleosides as potent and selective agonists at the human A3 adenosine receptor.
Nucleosides Nucleotides Nucleic Acids
; 26(10-12): 1565-8, 2007.
Artículo
en Inglés
| MEDLINE | ID: mdl-18066827
19.
The antitumor effect of LJ-529, a novel agonist to A3 adenosine receptor, in both estrogen receptor-positive and estrogen receptor-negative human breast cancers.
Mol Cancer Ther
; 5(3): 685-92, 2006 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-16546983
20.
Structure-activity relationships of 2-chloro-N6-substituted-4'-thioadenosine-5'-uronamides as highly potent and selective agonists at the human A3 adenosine receptor.
J Med Chem
; 49(1): 273-81, 2006 Jan 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-16392812