Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Robert Groneberg is active.

Publication


Featured researches published by Robert Groneberg.


Bioorganic & Medicinal Chemistry Letters | 2000

Solid-phase synthesis of an arylsulfone hydroxamate library

Joseph M. Salvino; Rose Mathew; Terence Kiesow; Ramesh Narensingh; Helen J. Mason; Amy Dodd; Robert Groneberg; Christopher J. Burns; Gerald McGeehan; Jane Kline; Edward Orton; Sheng-Yuh Tang; Mathew Morrisette; Richard Labaudininiere

Synthesis of an arylsulfone hydroxamate lead optimization library is presented. Biological activity of representative examples is given to demonstrate the value of this approach for lead optimization.


Angewandte Chemie | 1998

SYNTHESE VON INHIBITOREN FUR ZWEI FAMILIEN BIOLOGISCHER TARGETS IN EINER SEQUENZ : EIN NACHSTER SCHRITT BEIM AUFBAU KOMBINATORISCHER BIBLIOTHEKEN ?

Christopher J. Burns; Robert Groneberg; Joseph M. Salvino; Gerard M. McGeehan; Stephen M. Condon; Robert Morris; Matthew M. Morrissette; Rose Mathew; Shelley Darnbrough; Kent W. Neuenschwander; Anthony C. Scotese; Stevan W. Djuric; John W. Ullrich; Richard Labaudiniere

Uber nureinen Syntheseweg lassen sich Bibliotheken aus niedermolekularen Verbindungen aufbauen, die auf zwei Targetfamilien mit unterschiedlichen Funktionalitaten ausgerichtet sind. Dies wurde anhand der Entdeckung des Strukturtemplats 1 deutlich, das voneinander unabhangige pharmakophore Muster enthalt, uber die Mitglieder aus einer von zwei Targetfamilien, den Matrix-Metalloproteinasen (MMPs) oder den Phosphodiesterasen (PDEs), inhibiert werden konnen. Durch den Einbau von Bausteinen, die gegen mehrere Targets gerichtet sind, in eine Verbindungsbibliothek kann man so moglicherweise das Auffinden pharmazeutischer Leitstrukuren beschleunigen. Z=OR′ (PDE4), H (MMPs).


Archive | 2000

DI-ARYL ACID DERIVATIVES AS PPAR RECEPTOR LIGANDS

Zaid Jayyosi; Gerard M. Mcgeehan; Michael F. Kelley; Richard Labaudiniere; Litao Zhang; Robert Groneberg; Daniel G. Mcgarry; Thomas Caulfield; Anne Minnich; Mark Bobko


Archive | 2003

Substituted oxoazaheterocyclyl compounds

William R. Ewing; Michael R. Becker; Yong Mi Choi-Sledeski; Heinz W. Pauls; Wei He; Stephen M. Condon; Roderick S. Davis; Barbara Hanney; Alfred P. Spada; Christopher J. Burns; John Z. Jiang; Aiwen Li; Michael Myers; Wan F. Lau; Gregory Bernard Poli; Mark Bobko; Robert L. Morris; Joseph M. Karpinski; Timothy F. Gallagher; Kent W. Neuenschwander; Robert Groneberg; Jean-francois Sabuco


Bioorganic & Medicinal Chemistry Letters | 2007

Tetrazole and ester substituted tetrahydoquinoxalines as potent cholesteryl ester transfer protein inhibitors.

C. Todd Eary; Zachary Jones; Robert Groneberg; Laurence E. Burgess; David A. Mareska; Mark Drew; James F. Blake; Ellen R. Laird; Devan Balachari; Michael O’Sullivan; Andrew Allen; Vivienne Marsh


Journal of Medicinal Chemistry | 1999

Dual inhibition of phosphodiesterase 4 and matrix metalloproteinases by an (arylsulfonyl)hydroxamic acid template.

Robert Groneberg; Christopher J. Burns; Matthew M. Morrissette; John W. Ullrich; Robert L. Morris; Shelley Darnbrough; Stevan W. Djuric; Stephen M. Condon; Gerard M. McGeehan; Richard Labaudiniere; Kent W. Neuenschwander; and Anthony C. Scotese; Jane Kline


Archive | 2010

8-substituted benzoazepines as toll-like receptor modulators

George A. Doherty; C. Todd Eary; Robert Groneberg; Zachary Jones


Journal of Medicinal Chemistry | 2014

Discovery of 7-tetrahydropyran-2-yl chromans: β-site amyloid precursor protein cleaving enzyme 1 (BACE1) inhibitors that reduce amyloid β-protein (Aβ) in the central nervous system.

Allen A. Thomas; Kevin W. Hunt; Matthew Volgraf; Ryan J. Watts; Xingrong Liu; Guy Vigers; Darin Smith; Douglas Sammond; Tony P. Tang; Susan P. Rhodes; Andrew T. Metcalf; Karin D. Brown; Jennifer Otten; Michael Burkard; April Cox; Mary K. Geck Do; Darrin Dutcher; Sumeet Rana; Robert Kirk Delisle; Kelly Regal; Albion D. Wright; Robert Groneberg; Kimberly Scearce-Levie; Michael Siu; Hans E. Purkey; Joseph P. Lyssikatos; Indrani W. Gunawardana


Archive | 2011

5, 7-substituted-imidazo [1, 2-c] pyrimidines as inhibitors of jak kinases

Mark Laurence Boys; Laurence E. Burgess; Robert Groneberg; Darren Harvey; Lily Huang; Timothy Kercher; Christopher F. Kraser; Ellen R. Laird; Eugene Tarlton; Qian Zhao


Journal of Medicinal Chemistry | 2007

Potent Nonpeptide Antagonists of the Bradykinin B1 Receptor: Structure−Activity Relationship Studies with Novel Diaminochroman Carboxamides

Kaustav Biswas; Aiwen Li; Jian Jeffrey Chen; Derin C. D'amico; Christopher Fotsch; Nianhe Han; Jason Brooks Human; Qingyian Liu; Mark H. Norman; Bobby Riahi; Chester Chenguang Yuan; Hideo Suzuki; David A. Mareska; James Zhan; David E. Clarke; Andras Toro; Robert Groneberg; Laurence E. Burgess; Dianna Lester-Zeiner; Gloria Biddlecome; Barton H. Manning; Leyla Arik; Hong Dong; Ming Huang; Augustus Kamassah; Richard J. Loeloff; Hong Sun; Feng-Yin Hsieh; Gondi Kumar; Gordon Ng

Collaboration


Dive into the Robert Groneberg's collaboration.

Researchain Logo
Decentralizing Knowledge