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Lindsey C. Aschenbach
Lindsey C. Aschenbach
Virginia Commonwealth University
Naltrexone
Chemistry
Antagonist
Opioid receptor
Stereochemistry
5
Papers
105
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Design, Synthesis, and Biological Evaluation of 14-Heteroaromatic-Substituted Naltrexone Derivatives: Pharmacological Profile Switch from Mu Opioid Receptor Selectivity to Mu/Kappa Opioid Receptor Dual Selectivity
2013
Journal of Medicinal Chemistry
Yunyun Yuan
Saheem A. Zaidi
Orgil Elbegdorj
Lindsey C. Aschenbach
Guo Li
David L. Stevens
Krista L. Scoggins
William L. Dewey
Dana E. Selley
Yan Zhang
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Citations (24)
Design, Synthesis, and Biological Evaluation of 6α- and 6β-N-Heterocyclic Substituted Naltrexamine Derivatives as μ Opioid Receptor Selective Antagonists
2009
Journal of Medicinal Chemistry
Guo Li
Lindsey C. Aschenbach
Jianyang Chen
Michael P. Cassidy
David L. Stevens
Bichoy H. Gabra
Dana E. Selley
William L. Dewey
Richard B. Westkaemper
Yan Zhang
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Citations (58)
14-O-Heterocyclic-substituted naltrexone derivatives as non-peptide mu opioid receptor selective antagonists: design, synthesis, and biological studies.
2009
Bioorganic & Medicinal Chemistry Letters
Guo Li
Lindsey C. Aschenbach
Hengjun He
Dana E. Selley
Yan Zhang
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Citations (21)
Corrections to Design, Synthesis, and Biological Evaluation of 6α- and 6β- N -Heterocyclic Substituted Naltrexamine Derivatives as μ Opioid Receptor Selective Antagonists
2009
Journal of Medicinal Chemistry
Guo Li
Lindsey C. Aschenbach
Jianyang Chen
Michael P. Cassidy
David L. Stevens
Bichoy H. Gabra
Dana E. Selley
William L. Dewey
Richard B. Westkaemper
Yan Zhang
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Citations (2)
SELECTIVE NON-PEPTIDE MU-OPIOID RECEPTOR ANTAGONIST: DESIGN, SYNTHESIS AND BIOLOGICAL STUDIES
2008
Lindsey C. Aschenbach
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