Jennifer L. Woodring, Ph.D.
Affiliations: | 2015 | Chemistry and Chemical Biology | Northeastern University, Boston, MA, United States |
Area:
Medicinal chemistry, neglected tropical diseasesGoogle:
"Jennifer Woodring"Mean distance: 9.62 | S | N | B | C | P |
Parents
Sign in to add mentor| Michael P. Pollastri | grad student | 2015 | Northeastern University | |
| (Enhancing Physicochemical Properties through Synthesis and Formulation of Piclamilast- and Lapatinib-Derived Analogs.) | ||||
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Publications
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| Woodring J, Lu SH, Krasnova L, et al. (2019) Disrupting the Conserved Salt Bridge in the Trimerization of Influenza A Nucleoprotein. Journal of Medicinal Chemistry |
| Woodring JL, Behera R, Sharma A, et al. (2018) Series of Alkynyl-Substituted Thienopyrimidines as Inhibitors of Protozoan Parasite Proliferation. Acs Medicinal Chemistry Letters. 9: 996-1001 |
| Woodring JL, Bachovchin KA, Brady KG, et al. (2018) Corrigendum to "Optimization of physicochemical properties for 4-Anilinoquinazoline inhibitors of trypanosome proliferation" [Eur. J. Med. Chem. 141 (2017) 446-459]. European Journal of Medicinal Chemistry. 152: 515 |
| Woodring JL, Bachovchin KA, Brady KG, et al. (2017) Optimization of physicochemical properties for 4-anilinoquinazoline inhibitors of trypanosome proliferation. European Journal of Medicinal Chemistry. 141: 446-459 |
| Devine W, Woodring JL, Swaminathan U, et al. (2015) Protozoan Parasite Growth Inhibitors Discovered by Cross-Screening Yield Potent Scaffolds for Lead Discovery. Journal of Medicinal Chemistry. 58: 5522-37 |
| Woodring JL, Patel G, Erath J, et al. (2015) EVALUATION OF AROMATIC 6-SUBSTITUTED THIENOPYRIMIDINES AS SCAFFOLDS AGAINST PARASITES THAT CAUSE TRYPANOSOMIASIS, LEISHMANIASIS, AND MALARIA. Medchemcomm. 6: 339-346 |
| Woodring JL, Pollastri MP. (2014) Inhibitors of Protozoan Phosphodiesterases as Potential Therapeutic Approaches for Tropical Diseases Phosphodiesterases and Their Inhibitors. 61: 191-210 |
| Woodring JL, Bland ND, Ochiana SO, et al. (2013) Synthesis and assessment of catechol diether compounds as inhibitors of trypanosomal phosphodiesterase B1 (TbrPDEB1). Bioorganic & Medicinal Chemistry Letters. 23: 5971-4 |