Forma Therapeutics, Inc. 2016 - Feb 2019
Principal Scientist
Forma Therapeutics, Inc. 2012 - 2016
Senior Scientist
Biogen 2008 - 2012
Senior Scientist
Gsk 2002 - 2008
Principal Scientist
Camp4 Therapeutics 2002 - 2008
Director, Chemistry
Education:
Massachusetts Institute of Technology 1996 - 2002
Doctorates, Doctor of Philosophy, Chemistry
Duke University 1992 - 1996
Bachelors, Bachelor of Science, Chemistry
Skills:
Drug Discovery Computational Chemistry Drug Design Antibodies Biotechnology Monoclonal Antibodies Virtual Screening Biochemistry Cheminformatics Molecular Dynamics Bioinformatics Molecular Modeling Computational Biology Protein Engineering Biophysics Protein Structure Lifesciences Structural Bioinformatics Nuclear Receptors Biophysical Chemistry Pharmaceutical Research Ligand Binding System Administration Scientific Computing Quantum Chemistry Homology Modeling Biological Physics
John Loren Collins - Durham NC, US Eugene Lee Stewart - Durham NC, US William Zuercher - Durham NC, US Esther Chao - Durham NC, US Robert Wiethe - Durham NC, US Justin Caravella - Durham NC, US
This invention relates to compounds that are modulators of the liver X receptors (LXRs), and also to the methods for the making and use of such compounds.
David Norman Deaton - Durham NC, US Justin Caravella - Durham NC, US Robert Blount McFadyen - Durham NC, US Frank Navas, III - Durham NC, US Paul Kenneth Spearing - Durham NC, US
The present invention provides novel substituted isoxazole compounds, pharmaceutical compositions, therapeutic uses and processes for preparing the same.
Ann M. Ranger - Northborough MA, US Ellen Garber - Cambridge MA, US Justin A. Caravella - Cambridge MA, US Alexey A. Lugovskoy - Woburn MA, US Joseph Arndt - Peabody MA, US Frederick R. Taylor - Milton MA, US Giovanna Antognetti - Foxboro MA, US Eric Day - Cambridge MA, US
The instant invention is based, at least in part on the identification of a new class of antibodies that result, e.g., in improved LT blocking capabilities. Methods of making the subject binding molecules and methods of using the binding molecules of the invention to antagonize LTβR signaling are also provided.
Brian Robert Miller - San Diego CA, US Scott Glaser - San Diego CA, US Justin Caravella - Cambridge MA, US Susan Foley - Milford MA, US Tigran Dikran Alvazian - San Diego CA, US
The invention is based, at least in part, on the finding that linker peptides which lack the amino acid sequence GSG reduce or eliminate the addition of posttranslational modifications to the polypeptides which comprise them. More specifically, the novel linker peptides disclosed herein reduce the ability of enzymes to link carbohydrate adducts to polypeptides comprising these linker peptides, e.g., reduce the ability of xylosyltransferase to link xylose to polypeptides. These novel linker peptides, molecules comprising same, and methods of their use are described.
BIOGEN IDEC MA INC. - , US Ellen GARBER - Cambridge MA, US Justin A. CARAVELLA - Cambridge MA, US Alexey A. LUGOVSKOY - Woburn MA, US Joseph ARNDT - Peabody MA, US Frederick R. TAYLOR - Milton MA, US Giovanna ANTOGNETTI - Foxboro MA, US Eric DAY - Cambridge MA, US
The instant invention is based, at least in part on the identification of a new class of antibodies that result, e.g., in improved LT blocking capabilities. Methods of making the subject binding molecules and methods of using the binding molecules of the invention to antagonize LTβR signaling are also provided.
Justin Caravella - Durham NC, US David Norman Deaton - Durham NC, US Robert Blount McFadyen - Durham NC, US Frank Navas, III - Durham NC, US Paul Kenneth Spearing - Durham NC, US
Assignee:
GlaxoSmithKline LLC - Philadelphia PA
International Classification:
C07D 401/00
US Classification:
546167
Abstract:
The present invention provides novel substituted isoxazole compounds, pharmaceutical compositions, therapeutic uses and processes for preparing the same.
Purinones As Ubiquitin-Specific Protease 1 Inhibitors
- Watertown MA, US Stephanos Ioannidis - Natick MA, US Bruce Follows - Littleton MA, US Gary Gustafson - Ridgefield CT, US Minghua Wang - Acton MA, US Justin Andrew Caravella - Cambridge MA, US Zhongguo Wang - Lexington MA, US Edward L. Fritzen - Niantic CT, US Jian Lin - Acton MA, US
International Classification:
C07D 473/00 A61K 31/522
Abstract:
The application relates to inhibitors of USP1 useful in the treatment of cancers, and other USP1 associated diseases and disorders, having the Formula:where R, R, R, R, R, R, X, X, X, X, and n are described herein.
Pyridin-2(1H)-One Quinolinone Derivatives As Mutant-Isocitrate Dehydrogenase Inhibitors
- Watertown MA, US Anna Ericsson - Shrewsbury MA, US Ann-Marie Campbell - Monroe CT, US Gary Gustafson - Ridgefield CT, US Zhongguo Wang - Lexington MA, US R. Bruce Diebold - Waltham MA, US Susan Ashwell - Carlisle MA, US Justin Andrew Caravella - Cambridge MA, US Wei Lu - Newton MA, US
Assignee:
FORMA Therapeutics, Inc. - Watertown MA
International Classification:
C07D 401/12 C07D 401/14 C07D 471/04 A61P 35/00
Abstract:
The invention relates to inhibitors of mutant isocitrate dehydrogenase (mt-IDH) proteins with neomorphic activity useful in the treatment of cell-proliferation disorders and cancers, having the Formula:where A, U, W, W, W, R-R, and Rare described herein.
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