Anna E. Speers, Ph.D.
Affiliations: | 2005 | Scripps Research Institute, La Jolla, La Jolla, CA, United States |
Area:
Medicinal ChemistryGoogle:
"Anna Speers"Mean distance: 18.87 | S | N | B | C | P |
Parents
Sign in to add mentorMorgan Conn | research assistant | 1999-2000 | Amherst College (Chemistry Tree) | |
Benjamin F. Cravatt | grad student | 2005 | Scripps Institute | |
(Advanced click chemistry strategies for in vivo enzyme activity profiling.) |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Chang JW, Zuhl AM, Speers AE, et al. (2015) Selective inhibitor of platelet-activating factor acetylhydrolases 1b2 and 1b3 that impairs cancer cell survival. Acs Chemical Biology. 10: 925-32 |
Zhao N, Darby CM, Small J, et al. (2015) Target-based screen against a periplasmic serine protease that regulates intrabacterial pH homeostasis in Mycobacterium tuberculosis. Acs Chemical Biology. 10: 364-71 |
Ward J, Spath SN, Pabst B, et al. (2013) Mechanistic characterization of a 2-thioxanthine myeloperoxidase inhibitor and selectivity assessment utilizing click chemistry--activity-based protein profiling. Biochemistry. 52: 9187-201 |
Hsu KL, Tsuboi K, Chang JW, et al. (2013) Discovery and optimization of piperidyl-1,2,3-triazole ureas as potent, selective, and in vivo-active inhibitors of α/β-hydrolase domain containing 6 (ABHD6). Journal of Medicinal Chemistry. 56: 8270-9 |
Hsu KL, Tsuboi K, Whitby LR, et al. (2013) Development and optimization of piperidyl-1,2,3-triazole ureas as selective chemical probes of endocannabinoid biosynthesis. Journal of Medicinal Chemistry. 56: 8257-69 |
Nagano JM, Hsu KL, Whitby LR, et al. (2013) Selective inhibitors and tailored activity probes for lipoprotein-associated phospholipase A(2). Bioorganic & Medicinal Chemistry Letters. 23: 839-43 |
Liu X, Dix M, Speers AE, et al. (2012) Rapid development of a potent photo-triggered inhibitor of the serine hydrolase RBBP9. Chembiochem : a European Journal of Chemical Biology. 13: 2082-93 |
Saario SM, McKinney MK, Speers AE, et al. (2012) Clickable, photoreactive inhibitors to probe the active site microenvironment of fatty acid amide hydrolase(). Chemical Science (Royal Society of Chemistry : 2010). 3: 77-83 |
Adibekian A, Martin BR, Chang JW, et al. (2012) Confirming target engagement for reversible inhibitors in vivo by kinetically tuned activity-based probes. Journal of the American Chemical Society. 134: 10345-8 |
Rowland MM, Bostic HE, Gong D, et al. (2011) Phosphatidylinositol 3,4,5-trisphosphate activity probes for the labeling and proteomic characterization of protein binding partners. Biochemistry. 50: 11143-61 |