Kabirimine, a New Cyclic Imine from an Okinawan Dinoflagellate.
Idam HermawanMikako HigaPhilipus Uli Basa HutabaratTakeshi FujiwaraKiyotaka AkiyamaAkihiko KanamotoTakahiro HaruyamaNobuyuki KobayashiMasahiro HigashiShoichiro SudaJunichi TanakaPublished in: Marine drugs (2019)
On our quest for new bioactive molecules from marine sources, two cyclic imines (1, 2) were isolated from a dinoflagellate extract, inhibiting the growth of the respiratory syncytial virus (RSV). Compound 1 was identified as a known molecule portimine, while 2 was elucidated to be a new cyclic imine, named kabirimine. The absolute stereochemistry of 1 was determined by crystallographic work and chiral derivatization, whereas the structure of 2 was elucidated by means of spectroscopic analysis and computational study on all the possible isomers. Compound 1 showed potent cytotoxicity (CC50 < 0.097 µM) against HEp2 cells, while 2 exhibited moderate antiviral activity against RSV with IC50 = 4.20 µM (95% CI 3.31-5.33).
Keyphrases
- respiratory syncytial virus
- induced apoptosis
- oxidative stress
- ms ms
- cell cycle arrest
- anti inflammatory
- molecular docking
- high performance liquid chromatography
- liquid chromatography tandem mass spectrometry
- high intensity
- ionic liquid
- drinking water
- simultaneous determination
- respiratory tract
- mass spectrometry
- tandem mass spectrometry
- gas chromatography
- high resolution
- ultra high performance liquid chromatography