Donald Eugene Bergstrom
Affiliations: | Medicinal Chemistry and Molecular Pharmacology | Purdue University, West Lafayette, IN, United States |
Area:
BiochemistryWebsite:
https://www.mcmp.purdue.edu/faculty/dbergstrGoogle:
"Donald Eugene Bergstrom"Bio:
http://www.oac.cdlib.org/findaid/ark:/13030/kt0000162r/dsc/
Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Henry Rapoport | grad student | 1970 | UC Berkeley | |
| (Porphyrin synthesis.) | ||||
| Nelson J. Leonard | post-doc | 1970-1972 | UIUC | |
Children
Sign in to add trainee| Natasha Paul | grad student | 2000 | Purdue |
| Maneesh R. Pingle | grad student | 2000 | Purdue |
| Olga V. Adelfinskaya | grad student | 2004 | Purdue |
| Pei-Sze Ng | grad student | 2004 | Purdue |
| Vishal C. Nashine | grad student | 2006 | Purdue |
| Bridget D. Hines | grad student | 2009 | Purdue |
| Timothy W. Husk | grad student | 2010 | Purdue |
| Brian M. Laing | grad student | 2010 | Purdue |
| Shiyue Fang | post-doc | 2001-2004 | Purdue |
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Publications
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| Giardina SF, Werner DS, Pingle M, et al. (2020) Novel, Self-Assembling Dimeric Inhibitors of Human β Tryptase. Journal of Medicinal Chemistry |
| Giardina SF, Werner DS, Pingle M, et al. (2018) A Novel, Nonpeptidic, Orally Active Bivalent Inhibitor of Human β-Tryptase. Pharmacology. 102: 233-243 |
| Giardina SF, Werner DS, Pingle M, et al. (2018) Target-Directed Self-Assembly of Homodimeric Drugs Against β-Tryptase. Acs Medicinal Chemistry Letters. 9: 827-831 |
| Wanner J, Romashko D, Werner DS, et al. (2015) Reversible linkage of two distinct small molecule inhibitors of Myc generates a dimeric inhibitor with improved potency that is active in myc over-expressing cancer cell lines. Plos One. 10: e0121793 |
| Wanner J, Romashko D, Werner DS, et al. (2015) Abstract B43: Reversible linkage of two distinct small molecule inhibitors of MYC generates a more potent and selective dimeric inhibitor that is active in cancer cell lines over-expressing MYC Molecular Cancer Research. 13 |
| Zohrabi-Kalantari V, Jarrahian A, Bissantz C, et al. (2013) 4-Aminocyclopentane-1,3-diols as platforms for diversity: synthesis of anandamide analogs. Medicinal Chemistry (ShāRiqah (United Arab Emirates)). 9: 881-8 |
| Dolash BD, Lahiji RR, Zemlyanov DY, et al. (2013) Sonication mediated covalent cross-linking of DNA to single-walled carbon nanotubes Chemical Physics. 413: 11-19 |
| Guan Y, Bissantz C, Bergstrom DE, et al. (2012) 1,2,4-trisubstituted cyclopentanes as platforms for diversity. Archiv Der Pharmazie. 345: 677-86 |
| Laing BM, Bergstrom DE. (2012) Evaluation of end-capped DNA modules for pRNA capture and functionalization. Bioconjugate Chemistry. 23: 683-7 |
| Laing BM, Guo P, Bergstrom DE. (2011) Optimized method for the synthesis and purification of adenosine--folic acid conjugates for use as transcription initiators in the preparation of modified RNA. Methods (San Diego, Calif.). 54: 260-6 |