Determination of the importance of the stereochemistry of psorospermin in topoisomerase II-induced alkylation of DNA and in vitro and in vivo biological activity
ANIMAL CELL;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ARTICLE;
CONTROLLED STUDY;
DNA ALKYLATION;
DRUG MECHANISM;
DRUG POTENCY;
DRUG POTENTIATION;
DRUG RESISTANCE;
DRUG SENSITIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
GROWTH INHIBITION;
HUMAN;
HUMAN CELL;
IN VITRO STUDY;
IN VIVO STUDY;
MOLECULAR MODEL;
NONHUMAN;
PANCREAS CANCER;
PRIORITY JOURNAL;
SOLID TUMOR;
STEREOCHEMISTRY;
STRUCTURE ANALYSIS;
TUMOR GROWTH;
ANIMALS;
ANTINEOPLASTIC COMBINED CHEMOTHERAPY PROTOCOLS;
BODY WEIGHT;
CELL LINE;
CELL LINE, TUMOR;
DEOXYCYTIDINE;
DNA;
DNA TOPOISOMERASES, TYPE II;
DRUG SCREENING ASSAYS, ANTITUMOR;
EPOXY COMPOUNDS;
INHIBITORY CONCENTRATION 50;
LEUKEMIA;
LYMPHOMA;
MICE;
MICE, NUDE;
MODELS, CHEMICAL;
MODELS, MOLECULAR;
PANCREATIC NEOPLASMS;
STEREOISOMERISM;
TIME FACTORS;
XANTHONES;
Natural products as a source of potential cancer chemotherapeutic and chemopreventive agents
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Molecular details of the structure of a psorospermin-DNA covalent/intercalation complex and associated DNA sequence selectivity
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