Anti-SARS-CoV-2 and cytotoxic activity of two marine alkaloids from green alga Sonder in the Dardanelles

Caulerpa cylindracea Sonder is a green alga belonging to the Caulerpaceae family. This is the first chemical investigation of C. cylindracea in the Dardanelles which resulted in the isolation of four compounds, caulerpin ( 1 ), monomethyl caulerpinate ( 2 ), beta-sitosterol ( 3 ), and palmitic acid...

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Veröffentlicht in:RSC advances 2022-10, Vol.12 (46), p.29983-2999
Hauptverfasser: Erol, Ebru, Orhan, Muge Didem, Avsar, Timucin, Akdemir, Atilla, Okudan, Emine Sukran, Alim Toraman, Gulbahar Ozge, Topcu, Gulacti
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Zusammenfassung:Caulerpa cylindracea Sonder is a green alga belonging to the Caulerpaceae family. This is the first chemical investigation of C. cylindracea in the Dardanelles which resulted in the isolation of four compounds, caulerpin ( 1 ), monomethyl caulerpinate ( 2 ), beta-sitosterol ( 3 ), and palmitic acid ( 4 ). Their structures were elucidated by spectroscopic analyses including 1D- and 2D NMR and mass. The isolated compounds 1 and 2 were tested against the SARS-CoV-2 viral targets spike protein and main protease (3CL) enzyme, and both compounds significantly inhibit the interaction of spike protein and ACE2, while the main protease activity was not significantly reduced. Docking studies suggested that compounds 1 and 2 may bind to the ACE2 binding pocket on spike, and compound 2 may also bind to an allosteric site on spike. As such, these compounds may inhibit the spike-ACE2 complex formation competitively and/or allosterically and have the potential to be used against SARS-CoV-2 virus infection. In addition, compounds 1 and 2 showed at least two-fold higher cytotoxicity against breast cancer cell lines MCF7 and MDA-MB-231 compared to the CCD fibroblast control cell line. Isolated compounds 1 and 2 from Caulerpa cyclindracea inhibit the SARS-CoV-2 spike protein. Modelling studies suggest that the compounds may interfere with the spike-ACE2 interaction directly and also via an interaction with a spike allosteric site.
ISSN:2046-2069
DOI:10.1039/d2ra03358e