| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 10595137 | Bioorganic & Medicinal Chemistry Letters | 2013 | 7 Pages | 
Abstract
												Non-nucleoside inhibitors of HIV-1 reverse transcriptase (HIV-RT) are reported that feature extension into the entrance channel near Glu138. Complexes of the parent anilinylpyrimidine 1 and the morpholinoethoxy analog 2j with HIV-RT have received crystallographic characterization confirming the designs. Measurement of aqueous solubilities of 2j, 2k, the parent triazene 2a, and other NNRTIs demonstrate profound benefits for addition of the morpholinyl substituent.
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											Authors
												Mariela Bollini, Kathleen M. Frey, José A. Cisneros, Krasimir A. Spasov, Kalyan Das, Joseph D. Bauman, Eddy Arnold, Karen S. Anderson, William L. Jorgensen, 
											