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Palabras clave – provistas por la editorial

canthin-6-one; Picrolemma huberi; Simaroubaceae; antiplasmodial activity; Sarcococca hookeriana; sarchookloides A–C; steroidal alkaloid; cytotoxicity; Rhodophiala; alkaloids; molecular docking; AChE; BuChE; GC-MS; Mahonia imbricata; Berberidaceae; isoquinoline alkaloid; mahimbrine A; hedgehog signaling; Veratrum californicum; cyclopamine; HPLC-MS; Shh-Light II cells; halogencyclopropane; dichlorocarbene; epoxidation; vindoline; catharanthine; dimer alkaloids; vindoline trimer; Ruta graveolens; photosystem II; Chl a fluorescence; Hill reaction inhibitors; acridone alkaloids; benzylisoquinoline alkaloids; cytochrome P450 monooxygenase; medicinal properties; methyltransferase; Nelumbo nucifera; norcoclaurine synthase; sacred lotus; stereochemistry; Aristotelia chilensis Molina Stuntz; vascular activity; endothelium-independent; indole alkaloid; 8-oxo-9-dihydromakomakine; voltage-dependent calcium channels; Catharanthus roseus; cambial meristematic cells; Aspergillus flavus; terpenoid indole alkaloids; biosynthesis; Buxaceae; Borago officinalis; Crassocephalum; Copper-dependent diamine oxidase; Gynura bicolor; Homospermidine synthase; Lolium perenne; Necic acids; Necine bases; Pyrrolizidine alkaloid biosynthesis; Senecionine; tropane alkaloids; scopolamine; cocaine; calystegine; chemistry; pharmacology; biotechnological production; Erythroxylaceae; Erythroxylum coca; next generation sequencing; traditional medicine; bioprospecting; tropane; late-stage functionalization; sulfinate; DiversinateTM; natural product; medicinal chemistry; papaverine; scaffold; library; biodiscovery; Swinglea glutinosa; dereplication; acridones; phenylacrylamides