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Organic Letters|September 12, 2003
Concise formal synthesis of (-)-peduncularine via ring-closing metathesisDavid G Washburn, Richard W Heidebrecht, Stephen F MartinJournal of the American Chemical Society|May 16, 2002
Asymmetric total synthesis of spongistatins 1 and 2Michael T Crimmins, Jason D Katz, David G Washburn, et al.Bioorganic & Medicinal Chemistry Letters|January 27, 2009
Synthesis and SAR of potent LXR agonists containing an indole pharmacophoreDavid G Washburn, Tram H Hoang, Nino Campobasso, et al.Bioorganic & Medicinal Chemistry Letters|July 15, 2009
Rational design of orally-active, pyrrolidine-based progesterone receptor partial agonistsScott K Thompson, David G Washburn, James S Frazee, et al.Bioorganic & Medicinal Chemistry Letters|April 21, 2009
Synthesis and SAR of amino acid-derived heterocyclic progesterone receptor full and partial agonistsMarlys Hammond, Jaclyn R Patterson, Sharada Manns, et al.Bioorganic & Medicinal Chemistry Letters|July 21, 2009
Discovery of orally active, pyrrolidinone-based progesterone receptor partial agonistsDavid G Washburn, Tram H Hoang, James S Frazee, et al.Bioorganic & Medicinal Chemistry Letters|June 6, 2009
Design and synthesis of orally bioavailable serum and glucocorticoid-regulated kinase 1 (SGK1) inhibitorsMarlys Hammond, David G Washburn, H Tram Hoang, et al.Bioorganic & Medicinal Chemistry Letters|November 21, 2009
Improving the developability profile of pyrrolidine progesterone receptor partial agonistsLara S Kallander, David G Washburn, Tram H Hoang, et al.Bioorganic & Medicinal Chemistry Letters|July 27, 2013
The discovery of potent blockers of the canonical transient receptor channels, TRPC3 and TRPC6, based on an anilino-thiazole pharmacophoreDavid G Washburn, Dennis A Holt, Jason Dodson, et al.Bioconjugate Chemistry|February 1, 2021
In Vivo Half-Life Extension of BMP1/TLL Metalloproteinase Inhibitors Using Small-Molecule Human Serum Albumin BindersJulien C Vantourout, Andrew M Mason, Josephine Yuen, et al.Pageof 1