scholarly journals Cytotoxic halogenated monoterpenes from Plocamium cartilagineum

2016 ◽  
Vol 31 (3) ◽  
pp. 261-267 ◽  
Author(s):  
Omar M. M. Sabry ◽  
Douglas E. Goeger ◽  
Frederick A. Valeriote ◽  
William H. Gerwick
2001 ◽  
Vol 84 (5) ◽  
pp. 1313-1331 ◽  
Author(s):  
Donqhui Gao ◽  
Roy Okuda ◽  
Viorica Lopez-Avila

Abstract Supercritical fluid extraction (SFE) of the marine red alga Plocamium cartilagineum, which is known to contain complex mixtures of halogenated monoterpenes, was investigated. P. cartilagineum samples were extracted by SFE with carbon dioxide and modified carbon dioxide containing up to 10% methanol at different pressure and temperature conditions to establish the optimum conditions for extraction. These conditions were then used in the extraction of halogenated monoterpenes from 2 different samples of P. cartilagineum: one from Davenport, CA, and the other from Casa Beach (San Diego, CA). Several halogenated monoterpenes isolated by conventional solvent extraction with methanol and purified by column chromatography were used as the reference compounds for the determination of the extraction efficiency in the SFE experients. Plocamium cartilagineum belongs to the red alga family—Plocamiaceae, and has been found to contain a large number of halogenated monoterpenes, whose structures typically contain 1–6 bromine and/or chlorine atoms. P. cartilagineum grows along the Pacific coast from Washington to Chile, the British Isles, Australia, and Spain. Interestingly, P. cartilagineum collected from different geographical areas in the world are all reported to produce halogenated monoterpenes, but of different structural types and halogen substitution patterns. Most of these halogenated monoterpenes have been found to exhibit varied biological activities, including antifungal, antimicrobial, and molluscicidal activity.


2004 ◽  
Vol 59 (9-10) ◽  
pp. 679-683 ◽  
Author(s):  
Rodrigo Palma ◽  
Mario Edding ◽  
Juana Rovirosa ◽  
Aurelio San-Martín ◽  
Victor H. Argandoña

Abstract The effect of different photon flux densities (PFD) and temperatures on the relative growth rate (RGR) and the concentration of three halogenated monoterpenes in samples of Plocamium cartilagineum L.( Dixon), a marine alga (Rhodophyceae), were studied. The highest RGR (22.8 ± 0.04 d-1) was obtained at 15 °C and 41 μmol m-2 s-1 of PFD and the lowest (18.0 ± 0.2 d-1) was obtained at 18 °C and 120 μmol m-2 s-1. The different temperatures and light used in assays did not affect significantly the production of organic compounds. The production of mertensene and violacene was not affected significantly. However, compound 1 reached the highest concentration at 15 °C and 65 μmol m-2 s-1. The relationship between growth and production of monoterpenes of P. cartilagineum and the effect of temperature and the PFD were analyzed.


1985 ◽  
Vol 24 (8) ◽  
pp. 1697-1704 ◽  
Author(s):  
Kevin D. Barrow ◽  
Catherine A. Temple

ChemInform ◽  
2003 ◽  
Vol 34 (10) ◽  
Author(s):  
Ana R. Diaz-Marrero ◽  
Mercedes Cueto ◽  
Enrique Dorta ◽  
Juana Rovirosa ◽  
Aurelio San-Martin ◽  
...  

Tetrahedron ◽  
2002 ◽  
Vol 58 (42) ◽  
pp. 8539-8542 ◽  
Author(s):  
Ana R Dı́az-Marrero ◽  
Mercedes Cueto ◽  
Enrique Dorta ◽  
Juana Rovirosa ◽  
Aurelio San-Martı́n ◽  
...  

Marine Drugs ◽  
2019 ◽  
Vol 17 (4) ◽  
pp. 230 ◽  
Author(s):  
Andrew J. Shilling ◽  
Jacqueline L. von Salm ◽  
Anthony R. Sanchez ◽  
Younghoon Kee ◽  
Charles D. Amsler ◽  
...  

The subtidal red alga Plocamium cartilagineum was collected from the Western Antarctic Peninsula during the 2011 and 2017 austral summers. Bulk collections from specific sites corresponded to chemogroups identified by Young et al. in 2013. One of the chemogroups yielded several known acyclic halogenated monoterpenes (2–5) as well as undescribed compounds of the same class, anverenes B–D (6–8). Examination of another chemogroup yielded an undescribed cyclic halogenated monoterpene anverene E (9) as its major secondary metabolite. Elucidation of structures was achieved through one-dimensional (1D) and 2D nuclear magnetic resonance (NMR) spectroscopy and negative chemical ionization mass spectrometry. Compounds 1–9 show moderate cytotoxicity against cervical cancer (HeLa) cells.


2004 ◽  
Vol 59 (5-6) ◽  
pp. 339-344 ◽  
Author(s):  
Concepcián de Inés ◽  
Victor H. Argandoña ◽  
Juana Rovirosa ◽  
Aurelio San-Martín ◽  
Ana R. Díaz-Marrero ◽  
...  

Nine halogenated monoterpenes isolated from the red alga Plocamium cartilagineum have been evaluated for their cytotoxic effects on the tumor cell lines CT26 (murine colon adenocarcinoma), SW480 (human colon adenocarcinoma), HeLa (human cervical adenocarcinoma) and SkMel28 (human malignant melanoma) with several multidrug resistance mechanisms and the mammalian non-tumor cell line CHO (Chinese hamster ovary cells). The activities of these compounds were compared with those of the insecticide γ-hexachlorocyclohexane (lindane) due to chemical structure similarities. Compounds 1, 2, 3, and 5 exhibited selective cytotoxicity against colon and cervical adenocarcinoma cells. Interestingly, the effect of compound 3 was specific and irreversible to human colon adenocarcinoma SW480 cells, which overexpress the transmembrane P-glycoprotein often related to chemoresistance. None of the anti-tumor doses of these compounds was cytotoxic against CHO cells. Furthermore, analysis of cellular extracts after incubation with the test compounds and rotenone (positive uptake control) demonstrated the intracellular accumulation of 1, 2, 3, and 5.


2010 ◽  
Vol 119 (4) ◽  
pp. 1359-1368 ◽  
Author(s):  
Patrícia Valentão ◽  
Pedro Trindade ◽  
Daniela Gomes ◽  
Paula Guedes de Pinho ◽  
Teresa Mouga ◽  
...  

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