Antileishmanial activity mediated by apoptosis and structure-based target study of peganine hydrochloride dihydrate: An approach for rational drug design
DNA TOPOISOMERASE;
HERBACEOUS AGENT;
PEGANINE HYDROCHLORIDE DIHYDRATE;
PHOSPHATIDYLSERINE;
UNCLASSIFIED DRUG;
ANTIPROTOZOAL ACTIVITY;
APOPTOSIS;
ARTICLE;
CELL STRUCTURE;
CONTROLLED STUDY;
DRUG DESIGN;
DRUG DNA INTERACTION;
DRUG ISOLATION;
DRUG SAFETY;
DRUG STRUCTURE;
DRUG TARGETING;
ENZYME INHIBITION;
LEISHMANIA DONOVANI;
MITOCHONDRIAL MEMBRANE;
MOLECULAR DOCKING;
MOLECULAR DYNAMICS;
MOLECULAR MODEL;
NICK END LABELING;
NONHUMAN;
PEGANUM HARMALA;
PLANT SEED;
STRUCTURE ANALYSIS;
VISCERAL LEISHMANIASIS;
ALKALOIDS;
ANIMALS;
ANTIPROTOZOAL AGENTS;
APOPTOSIS;
DNA TOPOISOMERASES, TYPE I, EUKARYOTIC;
DRUG DESIGN;
LEISHMANIA DONOVANI;
MEMBRANE POTENTIAL, MITOCHONDRIAL;
MODELS, MOLECULAR;
PROTEIN BINDING;
PROTEIN STRUCTURE, TERTIARY;
QUINAZOLINES;
STRUCTURE-ACTIVITY RELATIONSHIP;
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