Among infectious diseases, malaria is common in many parts of the world. Standard alkaloids such as quinine and chloroquine are becoming less and less effective because malaria parasites are developing resistance to such drugs. There is a critical and urgent need, therefore, for development of antimalarial vaccines and new antimalarial non-alkloidal drugs to treat this increasingly widespread international health problem. Ancient Chinese folk medicine has led relatively recently to discovery of sesquiterpene 1,2,4-trixane artemisnin (qinghaosu) representing a new class of non- alkaloidal, clinically useful antimalarial drugs. Although this trioxane antimalaria and its first-generation derivatives have many desirable features (e.g. fast action against even cerebral malaria, useful in combination chemotherapy with standard alkoloidal antimalarials like mefloguine), they have also some disadvantage (e.g. frequent recrudescendences when used alone, short half-lives). Therefore, design and synthesis of the next generation of simpler, inexpensive and therapeutically more desirable peroxide-containing antimalarials is appropriate. Based on the fundamental new knowledge we have generated about the various chemical intermediates involved in the molecular mechanism of action of potent antimalarial peroxides like artemisinin, we now propose the following research goals: (1) to design prepare and evaluate new mechanism-based antimalarial peroxides; (2) to design, prepare and evaluate structurally simple, inexpensive, potent, third-generation peroxidic antimalarials incorporating pharmacologically advantageous substituents and therefore having good chemotherapeutic properties; (3) to design, prepare and evaluate dimeric peroxides as new anti-infective and antitumor drugs; (4)as models for hemin-trixane adducts, to prepare amino acid adducts with the putative alkylating agents (e.g. epoxides, diketones) formed during ferrous ion activation of artemisnin and related antimalarial peroxides; (5) to design, prepare and evaluate new gametocytocidal peroxides for breaking the cycle of malaria transmission from man to mosquito (i.e. chemoprevention of malaria). A medicicinal chemists, we are in a unique position to make fundamental advances in molecular parasitology specifically concerning mechanism of action and improved therapeutic aspect of easily prepared and relatively inexpensive new endoperoxide antimalarial drugs.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI034885-07
Application #
6137183
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Program Officer
Gottlieb, Michael
Project Start
1994-01-01
Project End
2000-12-31
Budget Start
2000-01-01
Budget End
2000-12-31
Support Year
7
Fiscal Year
2000
Total Cost
$312,968
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
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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
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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
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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