Journal of Medicinal Chemistry, ISSN 0022-2623, 07/2018, Volume 61, Issue 13, pp. 5664 - 5678
The dependence of drug potency on diastereomeric configurations is a key facet. Using a novel general divergent synthetic route for a three-chiral center...
CHEMISTRY, MEDICINAL | INHIBITION | TRANSFER-RNA SYNTHETASE | STRUCTURAL BASIS | MEFLOQUINE | PROVIDES | METABOLITE | Plasmodium falciparum - enzymology | Antimalarials - metabolism | Stereoisomerism | Models, Molecular | Plasmodium falciparum - drug effects | Antimalarials - pharmacology | Isocoumarins - pharmacology | Antimalarials - chemistry | Lysine-tRNA Ligase - metabolism | Protein Conformation | Lysine-tRNA Ligase - chemistry | Drug Evaluation, Preclinical | Isocoumarins - metabolism | Isocoumarins - chemistry
CHEMISTRY, MEDICINAL | INHIBITION | TRANSFER-RNA SYNTHETASE | STRUCTURAL BASIS | MEFLOQUINE | PROVIDES | METABOLITE | Plasmodium falciparum - enzymology | Antimalarials - metabolism | Stereoisomerism | Models, Molecular | Plasmodium falciparum - drug effects | Antimalarials - pharmacology | Isocoumarins - pharmacology | Antimalarials - chemistry | Lysine-tRNA Ligase - metabolism | Protein Conformation | Lysine-tRNA Ligase - chemistry | Drug Evaluation, Preclinical | Isocoumarins - metabolism | Isocoumarins - chemistry
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