Journal of Natural Products · 2019 · 16 citations · 11 references
PharmacyMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryStructure-activity RelationshipsMarine Drug DiscoveryStructure-activity Relationship AnalysisChemical Structure-activity RelationshipsMarine-derived Anticancer CompoundsPurine ChemistryPyrimidine AnalogsPyrimidine AnaloguesPyrimidine ChemistryX-ray Diffraction Analysis
Eleven new pyrimidine nucleosides (1–11) and 12 known analogues (12–23) were isolated from the marine-derived Streptomyces sp. SSA28. All of the new structures were elucidated by extensive NMR spectroscopic analysis and HRESIMS data. The absolute configurations of compound 1 were determined by X-ray diffraction. The configurations of 2–16 were investigated by ECD calculations. Compounds 11–16 showed cytotoxicity against HCT-116 human colon cancer cell lines with IC50 values from 0.39 ± 0.03 to 6.63 ± 0.47 μM.
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New Colorimetric Cytotoxicity Assay for Anticancer-Drug Screening
Philip Skehan, Ritsa Storeng, Dominic A. Scudiero et al. · JNCI Journal of the National Cancer Institute · 1990 · 9.8K citations
Medicine, Oncology, Pharmacology +10