Synthetic Efforts Toward P97 AAA+ ATPase and P75 Neurotrophin Receptor Inhibitors

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" Synthetic Efforts Toward P97 AAA+ ATPase and P75 Neurotrophin Receptor Inhibitors "
Carder, Evan J. Gold, Barry

Document Type	:	Latin Dissertation
Language of Document	:	English
Record Number	:	1111327
Doc. No	:	TLpq2498538336
Main Entry	:	Carder, Evan J.
	:	Gold, Barry
Title & Author	:	Synthetic Efforts Toward P97 AAA+ ATPase and P75 Neurotrophin Receptor Inhibitors\ Carder, Evan J.Gold, Barry
College	:	University of Pittsburgh
Date	:	2019
student score	:	2019
Degree	:	Ph.D.
Page No	:	547
Abstract	:	The first chapter presented in this dissertation describes the synthesis of diverse 3-sulfanyl-1,2,4-triazole allosteric p97 AAA+ ATPase inhibitors for structure activity/property relationship (SAR/SPR) investigations. This work supported an iterative medicinal chemistry strategy that led to the systematic development of allosteric p97 inhibitors that demonstrated single-digit nanomolar biochemical potency. We were able to scale-up selected analogues to the gram-scale. Further, we synthesized inhibitors to covalently modify p97, as well as potential p97 protein degraders that utilize the hydrophobic tag (HyT) strategy. The second chapter describes a gram-scale synthesis of known p75 neurotrophin receptor inhibitors LM11A-31 and LM11A-24 without the requirement for chromatography. Subsequent investigation of LM11A-31 key pharmacophore features was evaluated through a molecular docking study and the synthesis of LM11A-31 derivatives for SAR investigations. The pursuit of novel p75NTR inhibitors led to the synthesis of the LM11A-31 and LM11A-24 hybrid analog series as well as the 5-aminooxazole series. The chapter is concluded with efforts toward the 5-aminooxazole series, leading to the development of novel methodology that enabled C-5 regioselective direct amination followed by C-2 direct (het)arylation of 4-cyanooxazole.
Subject	:	Military strategy
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