Because of the high incidence of malaria and cancer in many parts of the world, effective and safe new chemotherapies of these human diseases are urgently needed. Toward developing such practical new chemotherapeutic drugs, we are blending chemical insight and synthesis skills with biological testing initially in vitro and then in vivo to establish efficacy and safety. This blending of fundamental chemistry and pharmacology research with practical pre-clinical development of new drugs candidates highlights our ongoing research program at Hopkins on trioxanes for chemotherapy of malaria and cancer. Based on the fundamental new knowledge we have generated about the molecular mechanism of action of potent anti-infective peroxides like the natural trioxane artemisinin, we propose the following, five diverse research goals for the next five years: (1) to design, prepare and evaluate structurally simple, inexpensive, potent, and safe next-generation antimalarial trioxanes; (2) to design, prepare and evaluate dimetric peroxides as new anti-infective and especially antitumor drug candidates; (4) to invent new synthetic methods for efficiently and inexpensive constructing chemotherapeutic antimalarial peroxides; (5) to design, prepare and evaluate new antimalarial endoperoxide analogs in which the peroxide groups is replaced by other heteroatoms. As medicinal chemists, we are a unique position to make fundamental advances in molecular parasitology specifically concerning mechanism of action and unproved therapeutic aspects of easily prepared and relatively inexpensive new endoperoxide antimalarial and antitumor drugs.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
2R01AI034885-08
Application #
6258018
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Program Officer
Gottlieb, Michael
Project Start
1994-01-01
Project End
2005-12-31
Budget Start
2001-01-01
Budget End
2001-12-31
Support Year
8
Fiscal Year
2001
Total Cost
$382,328
Indirect Cost
Name
Johns Hopkins University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Conyers, Ryan C; Mazzone, Jennifer R; Tripathi, Abhai K et al. (2015) Antimalarial chemotherapy: orally curative artemisinin-derived trioxane dimer esters. Bioorg Med Chem Lett 25:245-8
Roy, Sujayita; He, Ran; Kapoor, Arun et al. (2015) Inhibition of human cytomegalovirus replication by artemisinins: effects mediated through cell cycle modulation. Antimicrob Agents Chemother 59:3870-9
Cai, Hongyi; Kapoor, Arun; He, Ran et al. (2014) In vitro combination of anti-cytomegalovirus compounds acting through different targets: role of the slope parameter and insights into mechanisms of Action. Antimicrob Agents Chemother 58:986-94
He, Ran; Forman, Michael; Mott, Bryan T et al. (2013) Unique and highly selective anticytomegalovirus activities of artemisinin-derived dimer diphenyl phosphate stem from combination of dimer unit and a diphenyl phosphate moiety. Antimicrob Agents Chemother 57:4208-14
Slack, Rachel D; Mott, Bryan T; Woodard, Lauren E et al. (2012) Malaria-infected mice are completely cured by one 6 mg/kg oral dose of a new monomeric trioxane sulfide combined with mefloquine. J Med Chem 55:291-6
He, Ran; Park, Kyoungsook; Cai, Hongyi et al. (2012) Artemisinin-derived dimer diphenyl phosphate is an irreversible inhibitor of human cytomegalovirus replication. Antimicrob Agents Chemother 56:3508-15
Jacobine, Alexander M; Mazzone, Jennifer R; Slack, Rachel D et al. (2012) Malaria-infected mice live until at least day 30 after a new artemisinin-derived thioacetal thiocarbonate combined with mefloquine are administered together in a single, low, oral dose. J Med Chem 55:7892-9
He, Ran; Mott, Bryan T; Rosenthal, Andrew S et al. (2011) An artemisinin-derived dimer has highly potent anti-cytomegalovirus (CMV) and anti-cancer activities. PLoS One 6:e24334
Moon, Deuk Kyu; Tripathi, Abhai; Sullivan, David et al. (2011) A single, low, oral dose of a 5-carbon-linked trioxane dimer orthoester plus mefloquine cures malaria-infected mice. Bioorg Med Chem Lett 21:2773-5
Jacobine, Alexander M; Posner, Gary H (2011) Three-component, one-flask synthesis of rhodanines (thiazolidinones). J Org Chem 76:8121-5

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