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Mark S Tichenor

Showing results (1-10 of 12) with videos related to

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Natural Product Reports|April 5, 2008
Yatakemycin: total synthesis, DNA alkylation, and biological propertiesMark S Tichenor, Dale L Boger
Journal of the American Chemical Society|July 9, 2004
Total synthesis, structure revision, and absolute configuration of (+)-yatakemycinMark S Tichenor, David B Kastrinsky, Dale L Boger
Journal of Medicinal Chemistry|May 21, 2015
Functional Profiling of 2-Aminopyrimidine Histamine H4 Receptor ModulatorsMark S Tichenor, Robin L Thurmond, Jennifer D Venable, et al.
Journal of the American Chemical Society|December 7, 2006
Asymmetric total synthesis of (+)- and ent-(-)-yatakemycin and duocarmycin SA: evaluation of yatakemycin key partial structures and its unnatural enantiomerMark S Tichenor, John D Trzupek, David B Kastrinsky, et al.
Journal of the American Chemical Society|August 19, 2007
Systematic exploration of the structural features of yatakemycin impacting DNA alkylation and biological activityMark S Tichenor, Karen S MacMillan, John D Trzupek, et al.
ACS Medicinal Chemistry Letters|November 19, 2021
Novel Reagent Space: Identifying Unorderable but Readily Synthesizable Building BlocksMark Seierstad, Mark S Tichenor, Renee L DesJarlais, et al.
Journal of the American Chemical Society|October 24, 2007
Rational design, synthesis, and evaluation of key analogues of CC-1065 and the duocarmycinsMark S Tichenor, Karen S MacMillan, James S Stover, et al.
Bioorganic & Medicinal Chemistry Letters|May 19, 2016
The SAR of brain penetration for a series of heteroaryl urea FAAH inhibitorsJohn M Keith, Mark S Tichenor, Richard L Apodaca, et al.
Bioorganic & Medicinal Chemistry Letters|November 13, 2012
Heteroaryl urea inhibitors of fatty acid amide hydrolase: structure-mutagenicity relationships for arylamine metabolitesMark S Tichenor, John M Keith, William M Jones, et al.
Journal of Medicinal Chemistry|March 6, 2020
Discovery of a Gut-Restricted JAK Inhibitor for the Treatment of Inflammatory Bowel DiseaseKristi A Leonard, Lisa A Madge, Paul J Krawczuk, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Natural Product Reports|April 5, 2008
Yatakemycin: total synthesis, DNA alkylation, and biological propertiesMark S Tichenor, Dale L Boger
Journal of the American Chemical Society|July 9, 2004
Total synthesis, structure revision, and absolute configuration of (+)-yatakemycinMark S Tichenor, David B Kastrinsky, Dale L Boger
Journal of Medicinal Chemistry|May 21, 2015
Functional Profiling of 2-Aminopyrimidine Histamine H4 Receptor ModulatorsMark S Tichenor, Robin L Thurmond, Jennifer D Venable, et al.
Journal of the American Chemical Society|December 7, 2006
Asymmetric total synthesis of (+)- and ent-(-)-yatakemycin and duocarmycin SA: evaluation of yatakemycin key partial structures and its unnatural enantiomerMark S Tichenor, John D Trzupek, David B Kastrinsky, et al.
Journal of the American Chemical Society|August 19, 2007
Systematic exploration of the structural features of yatakemycin impacting DNA alkylation and biological activityMark S Tichenor, Karen S MacMillan, John D Trzupek, et al.
ACS Medicinal Chemistry Letters|November 19, 2021
Novel Reagent Space: Identifying Unorderable but Readily Synthesizable Building BlocksMark Seierstad, Mark S Tichenor, Renee L DesJarlais, et al.
Journal of the American Chemical Society|October 24, 2007
Rational design, synthesis, and evaluation of key analogues of CC-1065 and the duocarmycinsMark S Tichenor, Karen S MacMillan, James S Stover, et al.
Bioorganic & Medicinal Chemistry Letters|May 19, 2016
The SAR of brain penetration for a series of heteroaryl urea FAAH inhibitorsJohn M Keith, Mark S Tichenor, Richard L Apodaca, et al.
Bioorganic & Medicinal Chemistry Letters|November 13, 2012
Heteroaryl urea inhibitors of fatty acid amide hydrolase: structure-mutagenicity relationships for arylamine metabolitesMark S Tichenor, John M Keith, William M Jones, et al.
Journal of Medicinal Chemistry|March 6, 2020
Discovery of a Gut-Restricted JAK Inhibitor for the Treatment of Inflammatory Bowel DiseaseKristi A Leonard, Lisa A Madge, Paul J Krawczuk, et al.
Pageof 2