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 mentorHenry Rapoport | grad student | 1970 | UC Berkeley | |
(Porphyrin synthesis.) | ||||
Nelson J. Leonard | post-doc | 1970-1972 | UIUC |
Children
Sign in to add traineeNatasha 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 |
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. |
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 |