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1.
HDX reveals unique fragment ligands for the vitamin D receptor.
Bioorg Med Chem Lett
; 24(15): 3459-63, 2014 Aug 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-24974344
2.
Branched-chain α-ketoacids are preferentially reaminated and activate protein synthesis in the heart.
Nat Commun
; 12(1): 1680, 2021 03 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-33723250
3.
Muscle-Liver Trafficking of BCAA-Derived Nitrogen Underlies Obesity-Related Glycine Depletion.
Cell Rep
; 33(6): 108375, 2020 11 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-33176135
4.
An intra/intermolecular suzuki sequence to benzopyridyloxepines containing geometrically pure exocyclic tetrasubstituted alkenes.
Org Lett
; 10(13): 2701-4, 2008 Jul 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-18537249
5.
Cyclocarbopalladation of alkynes: a stereoselective method for preparing dibenzoxapine containing tetrasubstituted exocyclic alkenes.
Org Lett
; 8(8): 1685-8, 2006 Apr 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-16597141
6.
Indole Glucocorticoid Receptor Antagonists Active in a Model of Dyslipidemia Act via a Unique Association with an Agonist Binding Site.
J Med Chem
; 58(16): 6607-18, 2015 Aug 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-26218343
7.
Glucocorticoid receptor modulators informed by crystallography lead to a new rationale for receptor selectivity, function, and implications for structure-based design.
J Med Chem
; 57(3): 849-60, 2014 Feb 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-24446728
8.
Total Synthesis and Proof of Stereochemistry of Natural and Unnatural Pinnaic Acids: A Remarkable Long-Range Stereochemical Effect in the Reduction of 17-Oxo Precursors of the Pinnaic Acids This work was supported by the National Institutes of Health (Grant Numbers: CA28824). Postdoctoral Fellowship support is gratefully acknowledged by M.W.C. (U.S. Army BCRP, DAMD17-98-1-8154). We thank Dr. George Sukenick of the MSKCC NMR Core Facility for NMR and mass spectral analyses. We would like to thank professor Nakanishi for his supportive interest in the project.
Angew Chem Int Ed Engl
; 40(23): 4453-4456, 2001 Dec 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-12404443
9.
Concise Stereoselective Routes to Advanced Intermediates Related to Natural and Unnatural Pinnaic Acid This work was supported by the National Institutes of Health (Grant Numbers: CA28824). Postdoctoral Fellowship support is gratefully acknowledged by M.W.C. (U.S. Army BCRP, DAMD17-98-1-8154), M.F.H. (5T32 CA62948-05), and D.T. (Schering Research Foundation, Berlin). We thank Dr. George Sukenick of the MSKCC NMR Core Facility for NMR and mass spectral analyses.
Angew Chem Int Ed Engl
; 40(23): 4450-4452, 2001 Dec 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-12404442
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