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Gary Eugene Keck, Ph.D.

Affiliations: 
1980-2015 Chemistry University of Utah, Salt Lake City, UT 
Area:
Synthetic Organic Chemistry
Website:
http://www.chem.utah.edu/directory/faculty/keck.html
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"Gary E. Keck"
Mean distance: 7.12
 
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Publications

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Zhao X, Kedei N, Michalowski AM, et al. (2018) Deletion of the C-26 Methyl Substituent from the Bryostatin Analogue Merle 23 has Negligible Impact on Its Biological Profile or Potency. Chembiochem : a European Journal of Chemical Biology
Cummins TJ, Kedei N, Czikora A, et al. (2018) Synthesis and Biological Evaluation of Fluorescent Bryostatin Analogues. Chembiochem : a European Journal of Chemical Biology
Petersen ME, Kedei N, Lewin NE, et al. (2016) Replacement of the Bryostatin A- and B-Pyran Rings With Phenyl Rings Leads to Loss of High Affinity Binding With PKC. Tetrahedron Letters. 57: 4749-4753
Baumann DO, McGowan KM, Kedei N, et al. (2016) Synthesis and Biological Evaluation of Several Bryostatin Analogues Bearing a Diacylglycerol Lactone C-ring. The Journal of Organic Chemistry
Kelsey JS, Cataisson C, Chen J, et al. (2016) Biological activity of the bryostatin analog Merle 23 on mouse epidermal cells and mouse skin. Molecular Carcinogenesis
Kedei N, Kraft MB, Keck GE, et al. (2015) Neristatin 1 provides critical insight into bryostatin 1 structure-function relationships. Journal of Natural Products. 78: 896-900
Kraft MB, Poudel YB, Kedei N, et al. (2014) Synthesis of a des-B-ring bryostatin analogue leads to an unexpected ring expansion of the bryolactone core. Journal of the American Chemical Society. 136: 13202-8
Kedei N, Chen JQ, Herrmann MA, et al. (2014) Molecular systems pharmacology: isoelectric focusing signature of protein kinase Cδ provides an integrated measure of its modulation in response to ligands. Journal of Medicinal Chemistry. 57: 5356-69
Kelsey J, Kedei N, Cataisson C, et al. (2014) Abstract 1642: Bryostatin 1 and the simplified analog Merle 23 have similar and opposing properties on mouse epidermal cells and mouse skin Cancer Research. 74: 1642-1642
Kedei N, Lewin NE, Géczy T, et al. (2013) Biological profile of the less lipophilic and synthetically more accessible bryostatin 7 closely resembles that of bryostatin 1. Acs Chemical Biology. 8: 767-77
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