Scott T. Harrison, Ph.D. - Publications

Scripps Research Institute, La Jolla, La Jolla, CA, United States 
chemistry, biology, and medicine of natural and designed molecules

11 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Zhao Z, Harrison ST, Schubert JW, Sanders JM, Polsky-Fisher S, Zhang NR, McLoughlin D, Gibson CR, Robinson RG, Sachs NA, Kandebo M, Yao L, Smith SM, Hutson PH, Wolkenberg SE, et al. Synthesis and optimization of N-heterocyclic pyridinones as catechol-O-methyltransferase (COMT) inhibitors. Bioorganic & Medicinal Chemistry Letters. PMID 27133481 DOI: 10.1016/j.bmcl.2016.03.095  0.96
2015 Harrison ST, Poslusney MS, Mulhearn JJ, Zhao Z, Kett NR, Schubert JW, Melamed JY, Allison TJ, Patel SB, Sanders JM, Sharma S, Smith RF, Hall DL, Robinson RG, Sachs NA, et al. Synthesis and Evaluation of Heterocyclic Catechol Mimics as Inhibitors of Catechol-O-methyltransferase (COMT). Acs Medicinal Chemistry Letters. 6: 318-23. PMID 25815153 DOI: 10.1021/ml500502d  0.96
2012 Robinson RG, Smith SM, Wolkenberg SE, Kandebo M, Yao L, Gibson CR, Harrison ST, Polsky-Fisher S, Barrow JC, Manley PJ, Mulhearn JJ, Nanda KK, Schubert JW, Trotter BW, Zhao Z, et al. Characterization of non-nitrocatechol pan and isoform specific catechol-O-methyltransferase inhibitors and substrates. Acs Chemical Neuroscience. 3: 129-40. PMID 22860182 DOI: 10.1021/cn200109w  0.96
2011 Harrison ST, Mulhearn J, Wolkenberg SE, Miller PJ, O'Malley SS, Zeng Z, Williams DL, Hostetler ED, Sanabria-Bohórquez S, Gammage L, Fan H, Sur C, Culberson JC, Hargreaves RJ, Cook JJ, et al. Synthesis and Evaluation of 5-Fluoro-2-aryloxazolo[5,4-b]pyridines as β-Amyloid PET Ligands and Identification of MK-3328. Acs Medicinal Chemistry Letters. 2: 498-502. PMID 24900338 DOI: 10.1021/ml200018n  0.96
2011 Hostetler ED, Sanabria-Bohórquez S, Fan H, Zeng Z, Gammage L, Miller P, O'Malley S, Connolly B, Mulhearn J, Harrison ST, Wolkenberg SE, Barrow JC, Williams DL, Hargreaves RJ, Sur C, et al. [18F]Fluoroazabenzoxazoles as potential amyloid plaque PET tracers: synthesis and in vivo evaluation in rhesus monkey. Nuclear Medicine and Biology. 38: 1193-203. PMID 21741254 DOI: 10.1016/j.nucmedbio.2011.04.004  0.96
2011 Wolkenberg SE, Zhao Z, Mulhearn JJ, Harrison ST, Sanders JM, Cato MJ, Jovanovska A, Panigel J, Cook SP, Henze DA, Kane SA, Hartman GD, Barrow JC. High concentration electrophysiology-based fragment screen: discovery of novel acid-sensing ion channel 3 (ASIC3) inhibitors. Bioorganic & Medicinal Chemistry Letters. 21: 2646-9. PMID 21257308 DOI: 10.1016/j.bmcl.2010.12.115  0.96
2009 Nicolaou KC, Harrison ST, Chen JS. Discoveries from the Abyss: The Abyssomicins and Their Total Synthesis. Synthesis. 2009: 33-42. PMID 20047014 DOI: 10.1055/s-0028-1083259  0.96
2007 Nicolaou KC, Harrison ST. Total synthesis of abyssomicin C, atrop-abyssomicin C, and abyssomicin D: implications for natural origins of atrop-abyssomicin C. Journal of the American Chemical Society. 129: 429-40. PMID 17212423 DOI: 10.1021/ja067083p  0.96
2006 Nicolaou KC, Harrison ST. Total synthesis of abyssomicin C and atrop-abyssomicin C. Angewandte Chemie (International Ed. in English). 45: 3256-60. PMID 16634106 DOI: 10.1002/anie.200601116  0.96
2006 Nicolaou KC, Denton RM, Lenzen A, Edmonds DJ, Li A, Milburn RR, Harrison ST. Stereocontrolled synthesis of model core systems of lomaiviticins A and B. Angewandte Chemie (International Ed. in English). 45: 2076-81. PMID 16496276 DOI: 10.1002/anie.200504466  0.96
2002 Nicolaou KC, Gray DL, Montagnon T, Harrison ST. Oxidation of silyl enol ethers by using IBX and IBX.N-oxide complexes: a mild and selective reaction for the synthesis of enones. Angewandte Chemie (International Ed. in English). 41: 996-1000. PMID 12491292 DOI: 10.1002/1521-3773(20020315)41:6<996::AID-ANIE996>3.0.CO;2-I  0.96
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