Detalhe da pesquisa
1.
Structure-Enabled Discovery of a Stapled Peptide Inhibitor to Target the Oncogenic Transcriptional Repressor TLE1.
Chemistry
; 23(40): 9577-9584, 2017 Jul 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-28326635
2.
Discovering cell-active BCL6 inhibitors: effectively combining biochemical HTS with multiple biophysical techniques, X-ray crystallography and cell-based assays.
Sci Rep
; 12(1): 18633, 2022 11 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36329085
3.
Stereoselective preparation of ß,γ-methano-GABA derivatives.
Org Biomol Chem
; 9(21): 7517-24, 2011 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21938296
4.
Two methods for catalytic generation of reactive enolates promoted by a chiral poly gd complex: application to catalytic enantioselective protonation reactions.
J Am Chem Soc
; 131(11): 3858-9, 2009 Mar 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-19249830
5.
A C-linked glycomimetic in the gas phase and in solution: synthesis and conformation of the disaccharide Manalpha(1,6)-C-ManalphaOPh.
Chemistry
; 15(16): 4057-69, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19283818
6.
4-Methoxy-phenyl 2,3,4,6-tetra-O-acetyl-1-thio-α-d-mannopyran-oside.
Acta Crystallogr Sect E Struct Rep Online
; 64(Pt 8): o1401, 2008 Jul 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-21203121
7.
At point of use sono-electrochemical generation of hydrogen peroxide for chemical synthesis: the green oxidation of benzonitrile to benzamide.
Ultrason Sonochem
; 14(2): 113-6, 2007 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-16870485
8.
2,3,4,6-Tetra-O-benzoyl-4-nitro-phenyl-1-thio-α-d-mannopyran-oside-dichloro-methane-diethyl ether mixed solvate (1/0.53/0.38).
Acta Crystallogr Sect E Struct Rep Online
; 64(Pt 1): o236, 2007 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-21200803
9.
Voltammetric and electrochemical ESR studies of oxidation reactions mediated by tris(4-bromophenyl)amine in acetonitrile.
J Phys Chem B
; 110(6): 2681-91, 2006 Feb 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-16471872
10.
Structure of the Epigenetic Oncogene MMSET and Inhibition by N-Alkyl Sinefungin Derivatives.
ACS Chem Biol
; 11(11): 3093-3105, 2016 11 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-27571355
11.
Structure enabled design of BAZ2-ICR, a chemical probe targeting the bromodomains of BAZ2A and BAZ2B.
J Med Chem
; 58(5): 2553-9, 2015 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-25719566