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Vicky M Avery

Showing results (161-170 of 220) with videos related to

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Journal of Medicinal Chemistry|September 9, 2014
Blood schizontocidal and gametocytocidal activity of 3-hydroxy-N'-arylidenepropanehydrazonamides: a new class of antiplasmodial compoundsMichael Leven, Jana Held, Sandra Duffy, et al.
Journal of Medicinal Chemistry|December 13, 2018
Hydroxamic Acid Inhibitors Provide Cross-Species Inhibition of Plasmodium M1 and M17 AminopeptidasesNatalie B Vinh, Nyssa Drinkwater, Tess R Malcolm, et al.
Journal of Medicinal Chemistry|May 31, 2008
Clavatadine A, a natural product with selective recognition and irreversible inhibition of factor XIaMalcolm S Buchanan, Anthony R Carroll, Deborah Wessling, et al.
International Journal for Parasitology. Drugs and Drug Resistance|September 30, 2023
Thieno[3,2-b]pyrrole 5-carboxamides as potent and selective inhibitors of Giardia duodenalisChristopher Js Hart, Andrew G Riches, Snigdha Tiash, et al.
ACS Infectious Diseases|August 1, 2024
Enhancing the Intrinsic Antiplasmodial Activity and Improving the Stability and Selectivity of a Tunable Peptide Scaffold Derived from Human Platelet Factor 4Nicole Lawrence, Thomas N G Handley, Simon J de Veer, et al.
Journal of Medicinal Chemistry|June 13, 2012
Antimalarial activity of pyrroloiminoquinones from the Australian marine sponge Zyzzya spRohan A Davis, Malcolm S Buchanan, Sandra Duffy, et al.
European Journal of Medicinal Chemistry|January 26, 2016
Potent dual inhibitors of Plasmodium falciparum M1 and M17 aminopeptidases through optimization of S1 pocket interactionsNyssa Drinkwater, Natalie B Vinh, Shailesh N Mistry, et al.
Journal of Medicinal Chemistry|July 1, 2014
Pyridyl benzamides as a novel class of potent inhibitors for the kinetoplastid Trypanosoma bruceiLori Ferrins, Michelle Gazdik, Raphaël Rahmani, et al.
European Journal of Medicinal Chemistry|September 25, 2018
One-pot, multi-component synthesis and structure-activity relationships of peptoid-based histone deacetylase (HDAC) inhibitors targeting malaria parasitesDaniela Diedrich, Katharina Stenzel, Eva Hesping, et al.
Nature Communications|February 1, 2017
SC83288 is a clinical development candidate for the treatment of severe malariaStefano Pegoraro, Maëlle Duffey, Thomas D Otto, et al.
Pageof 22

Showing results (161-170 of 220) with videos related to

Sort By:
Pageof 22
Journal of Medicinal Chemistry|September 9, 2014
Blood schizontocidal and gametocytocidal activity of 3-hydroxy-N'-arylidenepropanehydrazonamides: a new class of antiplasmodial compoundsMichael Leven, Jana Held, Sandra Duffy, et al.
Journal of Medicinal Chemistry|December 13, 2018
Hydroxamic Acid Inhibitors Provide Cross-Species Inhibition of Plasmodium M1 and M17 AminopeptidasesNatalie B Vinh, Nyssa Drinkwater, Tess R Malcolm, et al.
Journal of Medicinal Chemistry|May 31, 2008
Clavatadine A, a natural product with selective recognition and irreversible inhibition of factor XIaMalcolm S Buchanan, Anthony R Carroll, Deborah Wessling, et al.
International Journal for Parasitology. Drugs and Drug Resistance|September 30, 2023
Thieno[3,2-b]pyrrole 5-carboxamides as potent and selective inhibitors of Giardia duodenalisChristopher Js Hart, Andrew G Riches, Snigdha Tiash, et al.
ACS Infectious Diseases|August 1, 2024
Enhancing the Intrinsic Antiplasmodial Activity and Improving the Stability and Selectivity of a Tunable Peptide Scaffold Derived from Human Platelet Factor 4Nicole Lawrence, Thomas N G Handley, Simon J de Veer, et al.
Journal of Medicinal Chemistry|June 13, 2012
Antimalarial activity of pyrroloiminoquinones from the Australian marine sponge Zyzzya spRohan A Davis, Malcolm S Buchanan, Sandra Duffy, et al.
European Journal of Medicinal Chemistry|January 26, 2016
Potent dual inhibitors of Plasmodium falciparum M1 and M17 aminopeptidases through optimization of S1 pocket interactionsNyssa Drinkwater, Natalie B Vinh, Shailesh N Mistry, et al.
Journal of Medicinal Chemistry|July 1, 2014
Pyridyl benzamides as a novel class of potent inhibitors for the kinetoplastid Trypanosoma bruceiLori Ferrins, Michelle Gazdik, Raphaël Rahmani, et al.
European Journal of Medicinal Chemistry|September 25, 2018
One-pot, multi-component synthesis and structure-activity relationships of peptoid-based histone deacetylase (HDAC) inhibitors targeting malaria parasitesDaniela Diedrich, Katharina Stenzel, Eva Hesping, et al.
Nature Communications|February 1, 2017
SC83288 is a clinical development candidate for the treatment of severe malariaStefano Pegoraro, Maëlle Duffey, Thomas D Otto, et al.
Pageof 22