Detalhe da pesquisa
1.
EBV+ tumors exploit tumor cell-intrinsic and -extrinsic mechanisms to produce regulatory T cell-recruiting chemokines CCL17 and CCL22.
PLoS Pathog
; 18(1): e1010200, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35025968
2.
Structure, Chemical Synthesis, and Biosynthesis of Prodiginine Natural Products.
Chem Rev
; 116(14): 7818-53, 2016 07 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-27314508
3.
Catalytic Enantioselective Dihalogenation and the Selective Synthesis of (-)-Deschloromytilipin A and (-)-Danicalipin A.
J Am Chem Soc
; 138(15): 5150-8, 2016 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-27018981
4.
Catalytic chemo-, regio-, and enantioselective bromochlorination of allylic alcohols.
J Am Chem Soc
; 137(11): 3795-8, 2015 Mar 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-25738419
5.
Catalytic enantioselective dibromination of allylic alcohols.
J Am Chem Soc
; 135(35): 12960-3, 2013 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-23952929
6.
Elimination of butylcycloheptylprodigiosin as a known natural product inspired by an evolutionary hypothesis for cyclic prodigiosin biosynthesis.
J Nat Prod
; 76(10): 1937-45, 2013 Oct 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-24053736
7.
Rotamers or diastereomers? An overlooked NMR solution.
J Org Chem
; 77(11): 5198-202, 2012 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22594462
8.
Structure-Based Design of Potent, Selective, and Orally Bioavailable VPS34 Kinase Inhibitors.
J Med Chem
; 65(17): 11500-11512, 2022 09 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34779204
9.
Potent GCN2 Inhibitor Capable of Reversing MDSC-Driven T Cell Suppression Demonstrates In Vivo Efficacy as a Single Agent and in Combination with Anti-Angiogenesis Therapy.
J Med Chem
; 65(19): 12895-12924, 2022 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36127295
10.
Enantioselective total synthesis and confirmation of the absolute and relative stereochemistry of streptorubin B.
J Am Chem Soc
; 133(6): 1799-804, 2011 Feb 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-21166419
11.
Novel Piperidinyl-Azetidines as Potent and Selective CCR4 Antagonists Elicit Antitumor Response as a Single Agent and in Combination with Checkpoint Inhibitors.
J Med Chem
; 63(15): 8584-8607, 2020 08 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-32667798
12.
Discovery of Potent, Selective, and Orally Bioavailable Inhibitors of USP7 with In Vivo Antitumor Activity.
J Med Chem
; 63(10): 5398-5420, 2020 05 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32302140
13.
Novel, Selective Inhibitors of USP7 Uncover Multiple Mechanisms of Antitumor Activity In Vitro and In Vivo.
Mol Cancer Ther
; 19(10): 1970-1980, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32788207
14.
Discovery of a Potent and Selective CCR4 Antagonist That Inhibits Treg Trafficking into the Tumor Microenvironment.
J Med Chem
; 62(13): 6190-6213, 2019 07 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31259550
15.
Continuous multiple liquid-liquid separation: diazotization of amino acids in flow.
Org Lett
; 14(16): 4246-9, 2012 Aug 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-22866828
16.
A synthesis of the carbocyclic core of maoecrystal V.
Org Lett
; 12(13): 3010-3, 2010 Jul 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-20521835