Gouregine, an α -Gem-Dimethyltetradehydrocularine Alkaloid, and Other Aporphinoid Alkaloids from the Bark of Guatteria olivacea (Annonaceae) and Their In Vitro Cytotoxic Activities

• Published in: Molecules (Basel, Switzerland) Vol. 29; no. 16; p. 3834
• Main Authors: Costa, Emmanoel V, Freitas, José Guilherme C, Manickchand, Steve Pereira, Araújo, Morgana de S, Silva, Valdenizia R, Santos, Luciano de S, Koolen, Hector Henrique Ferreira, Silva, Felipe M A da, Soares, Milena Botelho Pereira, Bezerra, Daniel P
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 13.08.2024; MDPI
• Subjects: 7,7-dimethylaporhine alkaloids; Alkaloids - chemistry; Alkaloids - isolation & purification; Alkaloids - pharmacology; Antineoplastic Agents, Phytogenic - chemistry; Antineoplastic Agents, Phytogenic - pharmacology; Aporphines - chemistry; Aporphines - isolation & purification; Aporphines - pharmacology; Carbon; Cell Line, Tumor; Cell Survival - drug effects; Chromatography; Guatteria - chemistry; Guatteria olivacea; Humans; in vitro cytotoxic activity; Leaves; Molecular Structure; Phytochemicals; Plant Bark - chemistry; Plant Extracts - chemistry; Plant Extracts - pharmacology; Spectrum analysis; 7,7-dimethylaporhine alkaloids; Guatteria olivacea; in vitro cytotoxic activity
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules29163834

R.E. Fries is an Amazonian species known as 'envira-bobó' and 'envira-fofa' and is common in the states of Amazonas, Acre, and Pará. Recently, the essential oil from the leaves of this species has shown promising antitumor activity both in vitro and in vivo. The presence of isoquinoline-derived alkaloids, including aporphinoids and tetrahydroprotoberberine alkaloids, has also been previously reported. In our ongoing search for bioactive compounds from Annonaceae Amazonian plants, the bark of was investigated via classical chromatography techniques, which revealed nine compounds, eight isoquinoline-derived alkaloids, a rare alkaloid with a -gem-dimethyltetradehydrocularine structure known as gouregine, seven known aporphinoid alkaloids: isopiline, -methylisopiline, melosmine, 9-hydroxyiguattescine, dihydromelosmine, lysicamine, and guattouregidine, and one known pimaradiene diterpene: acanthoic acid. All the isolated compounds were described for the first time in the bark of and their structures were elucidated by extensive analyses of their 1D and 2D NMR spectra in combination with MS data. The NMR data of the alkaloids isopiline, -methylisopiline, melosmine, dihydromelosmine, and guattouregidine were revised due to incomplete data in the literature and some ambiguities. The in vitro cytotoxic activities of the isolated compounds were evaluated against human cancer (HepG2, KG-1a, and HCT116) and noncancerous (MRC-5) cell lines via the Alamar blue assay after 72 h of incubation. Among the compounds evaluated against human cancer cell lines, the most active was the oxoaporphine alkaloid lysicamine, which has strong activity against HCT116 cells, with an IC value of 6.64 µg/mL (22.79 µmol/L). Melosmine had a moderate effect on HCT116 cells, with an IC value of 16.77 µg/mL (49.70 µmol/L), whereas acanthoic acid had moderate effects on HepG2 and HCT116 cells, with IC values of 14.63 µg/mL (48.37 µmol/L) and 21.25 µg/mL (70.25 µmol/L), respectively.