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First Assessment in Humans of the Safety, Tolerability, Pharmacokinetics, and Ex Vivo Pharmacodynamic Antimalarial Activity of the New Artemisinin Derivative Artemisone

Antimicrobial Agents and Chemotherapy, 2008-09, Vol.52 (9), p.3085-3091

2008

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Simple In Vitro Assay for Determining the Sensitivity of Plasmodium vivax Isolates from Fresh Human Blood to Antimalarials in Areas where P. vivax Is Endemic

Antimicrobial Agents and Chemotherapy, 2003-01, Vol.47 (1), p.170-173

2003

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Phenoxypropoxybiguanides, Prodrugs of DHFR−Inhibiting Diaminotriazine Antimalarials

Journal of medicinal chemistry, 2001-11, Vol.44 (23), p.3925-3931

2001

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Antimalarial pharmacodynamics and pharmacokinetics of a third-generation antifolate—JPC2056—in cynomolgus monkeys using an in vivo–in vitro model

Journal of antimicrobial chemotherapy, 2007-10, Vol.60 (4), p.811-818

2007

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Chloroquine bioassay using malaria microcultures

The American journal of tropical medicine and hygiene, 1993-10, Vol.49 (4), p.460

1993

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Plasma chloroquine concentrations in young and older malaria patients treated with chloroquine

Acta tropica, 1997-09, Vol.66 (3), p.155-161

1997

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New quinoline di-Mannich base compounds with greater antimalarial activity than chloroquine, amodiaquine, or pyronaridine

Antimicrobial Agents and Chemotherapy, 1997-06, Vol.41 (6), p.1369-1374

1997

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Structure-activity relationship analysis of substituted 4-quinolinamines, antagonists of immunostimulatory CpG-oligodeoxynucleotides

Bioorganic & medicinal chemistry letters, 1999-07, Vol.9 (13), p.1819-1824

1999

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Chloroquine bioassay of plasma specimens obtained from soldiers on chloroquine plus doxycycline for malaria prophylaxis

International journal for parasitology, 1996-11, Vol.26 (11), p.1325-1329

1996

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In vivo-in vitro model to assess chloroquine activity in monkeys

Chemotherapy (Basel), 1995, Vol.41 (2), p.134

1995

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Artemisone-A Highly Active Antimalarial Drug of the Artemisinin Class

Angewandte Chemie (International ed.), 2006-03, Vol.45 (13), p.2082-2088

2006

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Mutations in Plasmodium falciparum cytochrome b that are associated with Atovaquone resistance are located at a putative drug-binding site

Antimicrobial agents and chemotherapy, 2000-08, Vol.44 (8), p.2100-2108

2000

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First Assessment in Humans of the Safety, Tolerability, Pharmacokinetics, and Ex Vivo Pharmacodynamic Antimalarial Activity of the New Artemisinin Derivative Artemisone

Simple In Vitro Assay for Determining the Sensitivity of Plasmodium vivax Isolates from Fresh Human Blood to Antimalarials in Areas where P. vivax Is Endemic

Phenoxypropoxybiguanides, Prodrugs of DHFR−Inhibiting Diaminotriazine Antimalarials

Antimalarial pharmacodynamics and pharmacokinetics of a third-generation antifolate—JPC2056—in cynomolgus monkeys using an in vivo–in vitro model

Chloroquine bioassay using malaria microcultures

Plasma chloroquine concentrations in young and older malaria patients treated with chloroquine

New quinoline di-Mannich base compounds with greater antimalarial activity than chloroquine, amodiaquine, or pyronaridine

Structure-activity relationship analysis of substituted 4-quinolinamines, antagonists of immunostimulatory CpG-oligodeoxynucleotides

Chloroquine bioassay of plasma specimens obtained from soldiers on chloroquine plus doxycycline for malaria prophylaxis

In vivo-in vitro model to assess chloroquine activity in monkeys

Artemisone-A Highly Active Antimalarial Drug of the Artemisinin Class

Mutations in Plasmodium falciparum cytochrome b that are associated with Atovaquone resistance are located at a putative drug-binding site

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