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Volumn 1, Issue 2, 2005, Pages 159-171
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Growth inhibition of drug-resistant species of Plasmodium falciparum by domain structured N1,N2-derivatized hydrazines: denticity effects, redox switches, and reductant-driven redox-cycling.
a
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Author keywords
[No Author keywords available]
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Indexed keywords
HYDRAZINE DERIVATIVE;
IRON;
LIGAND;
ANIMAL;
ARTICLE;
CHEMICAL STRUCTURE;
CHEMISTRY;
CYCLIZATION;
DRUG EFFECT;
DRUG RESISTANCE;
DRUG SENSITIVITY;
ELECTRON;
GROWTH, DEVELOPMENT AND AGING;
OXIDATION REDUCTION REACTION;
PLASMODIUM FALCIPARUM;
SPECIES DIFFERENCE;
STEREOISOMERISM;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
ANIMALS;
CYCLIZATION;
DRUG RESISTANCE;
ELECTRONS;
HYDRAZINES;
IRON;
LIGANDS;
MOLECULAR STRUCTURE;
OXIDATION-REDUCTION;
PARASITIC SENSITIVITY TESTS;
PLASMODIUM FALCIPARUM;
RESEARCH SUPPORT, NON-U.S. GOV'T;
SPECIES SPECIFICITY;
STEREOISOMERISM;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 33846087472
PISSN: 15734064
EISSN: None
Source Type: Journal
DOI: 10.2174/1573406053175265 Document Type: Article |
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Times cited : (2)
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References (0)
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