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Wender, Paul A., Nakagawa, Yu, Near, Katherine E., Staveness, Daryl (2014) Computer-Guided Design, Synthesis, and Protein Kinase C Affinity of a New Salicylate-Based Class of Bryostatin Analogs. Organic Letters, 16. 5136-5139 doi:10.1021/ol502491f

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Reference TypeJournal (article/letter/editorial)
TitleComputer-Guided Design, Synthesis, and Protein Kinase C Affinity of a New Salicylate-Based Class of Bryostatin Analogs
JournalOrganic Letters
AuthorsWender, Paul A.Author
Nakagawa, YuAuthor
Near, Katherine E.Author
Staveness, DarylAuthor
Year2014 (October 3)Volume16
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ol502491fSearch in ResearchGate
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Mindat Ref. ID10902110Long-form Identifiermindat:1:5:10902110:8
GUID0
Full ReferenceWender, Paul A., Nakagawa, Yu, Near, Katherine E., Staveness, Daryl (2014) Computer-Guided Design, Synthesis, and Protein Kinase C Affinity of a New Salicylate-Based Class of Bryostatin Analogs. Organic Letters, 16. 5136-5139 doi:10.1021/ol502491f
Plain TextWender, Paul A., Nakagawa, Yu, Near, Katherine E., Staveness, Daryl (2014) Computer-Guided Design, Synthesis, and Protein Kinase C Affinity of a New Salicylate-Based Class of Bryostatin Analogs. Organic Letters, 16. 5136-5139 doi:10.1021/ol502491f
In(n.d.) Organic Letters Vol. 16. American Chemical Society (ACS)

See Also

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Wender, Paul A., Staveness, Daryl (2014) Improved Protein Kinase C Affinity through Final Step Diversification of a Simplified Salicylate-Derived Bryostatin Analog Scaffold. Organic Letters, 16. 5140-5143 doi:10.1021/ol502492b
Staveness, Daryl, Abdelnabi, Rana, Near, Katherine E., Nakagawa, Yu, Neyts, Johan, Delang, Leen, Leyssen, Pieter, Wender, Paul A. (2016) Inhibition of Chikungunya Virus-Induced Cell Death by Salicylate-Derived Bryostatin Analogues Provides Additional Evidence for a PKC-Independent Pathway. Journal of Natural Products, 79. 680-684 doi:10.1021/acs.jnatprod.5b01017
Wender, Paul A., Verma, Vishal A. (2008) The Design, Synthesis, and Evaluation of C7 Diversified Bryostatin Analogs Reveals a Hot Spot for PKC Affinity. Organic Letters, 10. 3331-3334 doi:10.1021/ol801235h
Loy, Brian A., Lesser, Adam B., Staveness, Daryl, Billingsley, Kelvin L., Cegelski, Lynette, Wender, Paul A. (2015) Toward a Biorelevant Structure of Protein Kinase C Bound Modulators: Design, Synthesis, and Evaluation of Labeled Bryostatin Analogues for Analysis with Rotational Echo Double Resonance NMR Spectroscopy. Journal Of The American Chemical Society, 137 (10) 3678-3685 doi:10.1021/jacs.5b00886
Staveness, Daryl, Abdelnabi, Rana, Schrier, Adam J., Loy, Brian A., Verma, Vishal A., DeChristopher, Brian A., Near, Katherine E., Neyts, Johan, Delang, Leen, Leyssen, Pieter, Wender, Paul A. (2016) Simplified Bryostatin Analogues Protect Cells from Chikungunya Virus-Induced Cell Death. Journal of Natural Products, 79. 675-679 doi:10.1021/acs.jnatprod.5b01016
Wender, Paul A., Horan, Joshua C., Verma, Vishal A. (2006) Total Synthesis and Initial Biological Evaluation of New B-Ring-Modified Bryostatin Analogs. Organic Letters, 8. 5299-5302 doi:10.1021/ol0620904
Wender, Paul A., Horan, Joshua C. (2006) Synthesis and PKC Binding of a New Class of A-Ring Diversifiable Bryostatin Analogues Utilizing a Double Asymmetric Hydrogenation and Cross-Coupling Strategy. Organic Letters, 8. 4581-4584 doi:10.1021/ol0618149
Wender, Paul A., Verma, Vishal A. (2006) Design, Synthesis, and Biological Evaluation of a Potent, PKC Selective, B-Ring Analog of Bryostatin. Organic Letters, 8. 1893-1896 doi:10.1021/ol060457z
Wender, Paul A., Baryza, Jeremy L. (2005) Identification of a Tunable Site in Bryostatin Analogs:  C20 Bryologs through Late Stage Diversification. Organic Letters, 7. 1177-1180 doi:10.1021/ol0501931
Wender, Paul A., Clarke, Michael O., Horan, Joshua C. (2005) Role of the A-Ring of Bryostatin Analogues in PKC Binding:  Synthesis and Initial Biological Evaluation of New A-Ring-Modified Bryologs. Organic Letters, 7. 1995-1998 doi:10.1021/ol0504650
Wender, Paul A., Koehler, Michael F. T., Sendzik, Martin (2003) A New Synthetic Approach to the C Ring of Known as Well as Novel Bryostatin Analogues. Organic Letters, 5. 4549-4552 doi:10.1021/ol0355332
 
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