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Showing results (261-270 of 318) with videos related to

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Journal of Medicinal Chemistry|April 7, 2020
Lead Optimization of a Pyrrole-Based Dihydroorotate Dehydrogenase Inhibitor Series for the Treatment of MalariaSreekanth Kokkonda, Xiaoyi Deng, Karen L White, et al.
Journal of Medicinal Chemistry|June 18, 2016
Trisubstituted Pyrimidines as Efficacious and Fast-Acting AntimalarialsNeil R Norcross, Beatriz Baragaña, Caroline Wilson, et al.
Cell Chemical Biology|July 31, 2024
Identification of potent and reversible piperidine carboxamides that are species-selective orally active proteasome inhibitors to treat malariaAloysus Lawong, Suraksha Gahalawat, Sneha Ray, et al.
The Journal of Biological Chemistry|August 13, 2010
Novel inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase with anti-malarial activity in the mouse modelMichael L Booker, Cecilia M Bastos, Martin L Kramer, et al.
Biorxiv : the Preprint Server for Biology|August 12, 2025
The Human Chk1 Inhibitor CHIR-124 Shows Multistage Activity Against <i>Plasmodium falciparum</i> via Dual Inhibition of <i>Pf</i>Ark1 and Hemozoin FormationKathryn J Wicht, John G Woodland, Larnelle F Garnie, et al.
Angewandte Chemie (International Ed. in English)|May 3, 2025
The ATM Kinase Inhibitor AZD0156 Is a Potent Inhibitor of Plasmodium Phosphatidylinositol 4-Kinase (PI4Kβ) and Is an Attractive Candidate for Medicinal Chemistry Optimization Against MalariaJohn G Woodland, Dina Coertzen, Kathryn J Wicht, et al.
ACS Chemical Biology|June 13, 2026
The Human Chk1 Inhibitor CHIR-124 Shows Multistage Activity against the Human Malaria Parasite <i>Plasmodium falciparum</i> via Polypharmacological Inhibition of <i>Pf</i>Ark1 and Hemozoin FormationKathryn J Wicht, John G Woodland, Larnelle F Garnie, et al.
Antimicrobial Agents and Chemotherapy|March 23, 2011
Aminoindoles, a novel scaffold with potent activity against Plasmodium falciparumRobert H Barker, Sameer Urgaonkar, Ralph Mazitschek, et al.
Journal of Medicinal Chemistry|June 25, 2024
2,8-Disubstituted-1,5-naphthyridines as Dual Inhibitors of <i>Plasmodium falciparum</i> Phosphatidylinositol-4-kinase and Hemozoin Formation with <i>In Vivo</i> EfficacyGodwin Akpeko Dziwornu, Donald Seanego, Stephen Fienberg, et al.
Science Translational Medicine|September 20, 2019
Antimalarial pantothenamide metabolites target acetyl-coenzyme A biosynthesis in <i>Plasmodium falciparum</i>Joost Schalkwijk, Erik L Allman, Patrick A M Jansen, et al.
Pageof 32

Showing results (261-270 of 318) with videos related to

Sort By:
Pageof 32
Journal of Medicinal Chemistry|April 7, 2020
Lead Optimization of a Pyrrole-Based Dihydroorotate Dehydrogenase Inhibitor Series for the Treatment of MalariaSreekanth Kokkonda, Xiaoyi Deng, Karen L White, et al.
Journal of Medicinal Chemistry|June 18, 2016
Trisubstituted Pyrimidines as Efficacious and Fast-Acting AntimalarialsNeil R Norcross, Beatriz Baragaña, Caroline Wilson, et al.
Cell Chemical Biology|July 31, 2024
Identification of potent and reversible piperidine carboxamides that are species-selective orally active proteasome inhibitors to treat malariaAloysus Lawong, Suraksha Gahalawat, Sneha Ray, et al.
The Journal of Biological Chemistry|August 13, 2010
Novel inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase with anti-malarial activity in the mouse modelMichael L Booker, Cecilia M Bastos, Martin L Kramer, et al.
Biorxiv : the Preprint Server for Biology|August 12, 2025
The Human Chk1 Inhibitor CHIR-124 Shows Multistage Activity Against <i>Plasmodium falciparum</i> via Dual Inhibition of <i>Pf</i>Ark1 and Hemozoin FormationKathryn J Wicht, John G Woodland, Larnelle F Garnie, et al.
Angewandte Chemie (International Ed. in English)|May 3, 2025
The ATM Kinase Inhibitor AZD0156 Is a Potent Inhibitor of Plasmodium Phosphatidylinositol 4-Kinase (PI4Kβ) and Is an Attractive Candidate for Medicinal Chemistry Optimization Against MalariaJohn G Woodland, Dina Coertzen, Kathryn J Wicht, et al.
ACS Chemical Biology|June 13, 2026
The Human Chk1 Inhibitor CHIR-124 Shows Multistage Activity against the Human Malaria Parasite <i>Plasmodium falciparum</i> via Polypharmacological Inhibition of <i>Pf</i>Ark1 and Hemozoin FormationKathryn J Wicht, John G Woodland, Larnelle F Garnie, et al.
Antimicrobial Agents and Chemotherapy|March 23, 2011
Aminoindoles, a novel scaffold with potent activity against Plasmodium falciparumRobert H Barker, Sameer Urgaonkar, Ralph Mazitschek, et al.
Journal of Medicinal Chemistry|June 25, 2024
2,8-Disubstituted-1,5-naphthyridines as Dual Inhibitors of <i>Plasmodium falciparum</i> Phosphatidylinositol-4-kinase and Hemozoin Formation with <i>In Vivo</i> EfficacyGodwin Akpeko Dziwornu, Donald Seanego, Stephen Fienberg, et al.
Science Translational Medicine|September 20, 2019
Antimalarial pantothenamide metabolites target acetyl-coenzyme A biosynthesis in <i>Plasmodium falciparum</i>Joost Schalkwijk, Erik L Allman, Patrick A M Jansen, et al.
Pageof 32