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Artículos de revistas sobre el tema "Laurencia obtusa"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 10 de febrero de 2022

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1

Martin, Julio D., Pascual Caballero, Jose J. Fernandez, Manuel Norte, Ricardo Perez, and Matias L. Rodriguez. "Metabolites from Laurencia obtusa." Phytochemistry 28, no. 12 (1989): 3365–67. http://dx.doi.org/10.1016/0031-9422(89)80348-6.

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2

Imre, Sedat, Hermann Lotter, Hildebert Wagner, and Ronald H. Thomson. "Epoxy-trans-isodihydrorhodophytin, ein neuer Metabolit aus Laurencia obtusa / Epoxy-trans-isodihydrorhodophytin, a New Metabolit from Laurencia obtusa." Zeitschrift für Naturforschung C 42, no. 5 (1987): 507–9. http://dx.doi.org/10.1515/znc-1987-0503.

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Abstract Laurencia obtusa, Red Algae, Rhodomelaceae, Acetylenic Ether Epoxy-trans-isodihydrorhodophytin, a new halogenated acetylenic bicyclic ether, has been isolated from a Laurencia obtusa variety, collected in the Marmara sea. Its structure was determined by spectroscopic methods and X-ray diffraction analysis.
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3

Kumajas, Jenny, and Soenandar Millian Tompunu Tengker. "Identifikasi gula spesifik pada aglutinin dari rumput laut." Fullerene Journal of Chemistry 4, no. 2 (2019): 34. http://dx.doi.org/10.37033/fjc.v4i2.51.

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Aglutinin atau lektin adalah protein atau glikoprotein yang mengikat gula secara spesifik. Substans tersebut dapat mengaglutinasi sel karena permukaan sel terdiri atas gula atau sakarida. Halymenia durvillaei, Laurencia obtusa dan Ulva fasciata mengandung aglutinin. Aglutinasi sel oleh aglutinin dapat dihambat oleh gula tertentu yang merupakan gula spesifiknya. Penelitian ini bertujuan untuk menentukan jenis gula spesifik pada aglutinin dari rumput laut Halymenia durvillaei, Laurencia obtusa dan Ulva fasciata. Penelitian ini menunjukkan bahwa gula spesifik pada agglutinin dari ekstrak Laurenci
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4

Hamouda, Ragaa A., Mervat H. Hussein, and Noura El-Ahmady El-Naggar. "Potential value of red and brown seaweed for sustainable bioethanol production." Bangladesh Journal of Botany 44, no. 4 (2018): 565–70. http://dx.doi.org/10.3329/bjb.v44i4.38571.

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Algae are renewable sources of feedstock for bioethanol that can be grown on non arable lands, non productive water sources and inexpensive culture systems. Red seaweed Laurencia obtusa and brown seaweeds Cystoseira compressa, Colpomenia sinuosa were analysed by determining sugar content by HPLC and converted into suitable fermentable feedstock by NaOH, H2SO4, HCl and H3PO4 at concentrations 1, 2, 3, 4 and 5% at 21°C of 20 minutes. The efficiency of hydrolysis significantly improved by 5% HCl for Laurencia obtusa at 42.84 g sugar/100 g dry biomass. Pretreatment of Cystoseira compressa and Colp
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5

Ayyad, S. N., J. Jakupovic, and M. Abdel-Mogib. "A sesquiterpene ether from Laurencia obtusa." Phytochemistry 36, no. 4 (1994): 1077–78. http://dx.doi.org/10.1016/s0031-9422(00)90495-3.

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6

Bawakid, Nahed O., Walied M. Alarif, Hajer S. Alorfi, et al. "Antimicrobial sesquiterpenoids from Laurencia obtusa Lamouroux." Open Chemistry 15, no. 1 (2017): 219–24. http://dx.doi.org/10.1515/chem-2017-0025.

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AbstractPurification of the organic extract of Laurencia obtusa Lamouroux by column chromatography and preparative thin layer chromatography provided four new compounds: a eudesmane-type sesquiterpenoid [eudesma-4(15),11-diene-5,7-diol (1)], a cuparane-type sesquiterpenoid [10-hydroxycuparaldehyde (2)], and two nor-cuparanes [3-hydroxy-15-nor-cuparan-10β-ol (3) and 2-bromo-3-hydroxy-15-nor-cuparan-10β-ol (4)]. Structural identification was made possible by comparison of spectral data with those reported in the literature. Compounds 3 and 4 are significant as nor-cuparanes are rarely isolated f
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7

Imre, Sedat, Zeynep Aydoğmuş, Hüseyin Güner, Hermann Lotter, and Hildebert Wagner. "Polybrominated Non-Terpenoid C15 Compounds from Laurencia paniculata and Laurencia obtusa." Zeitschrift für Naturforschung C 50, no. 11-12 (1995): 743–47. http://dx.doi.org/10.1515/znc-1995-11-1201.

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Two polybrominated C15-acetogenins (1,2) isolated from a Mediterranean sponge previously and a new polybrominated bicyclic ether with a bromoallenic side chain (3) were isolated from Laurencia paniculata and Laurencia obtusa respectively. The structures of these compounds were elucidated by spectroscopic methods.
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8

Kladi, Maria, Helen Xenaki, Constantinos Vagias, Panagiota Papazafiri, and Vassilios Roussis. "New cytotoxic sesquiterpenes from the red algae Laurencia obtusa and Laurencia microcladia." Tetrahedron 62, no. 1 (2006): 182–89. http://dx.doi.org/10.1016/j.tet.2005.09.113.

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9

Sethi, Poonam, and Nandhagopal Plant K. "ANATOMICAL STUDIES OF LAURENCIA OBTUSA (HUDSON) LAMOUROUX (CERAMIALES) OF RHODOPHYCEAE." Chemistry & Material Sciences Research Journal 2, no. 2 (2020): 42–46. http://dx.doi.org/10.51594/cmsrj.v2i2.86.

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Thallus of Laurencia obtusa of Rhodophyceae was studied and detailed micromorphological evaluation was done. Morphology of the thallus has been studied to aid pharmacognostic and phytochemical evidences to aid in taxonomic species identification. Parameters presented in this paper may be proposed to establish the authenticity of this red alga and can possibly help to differentiate this alga from its other species. Since the collections were made in the month of March, Laurencia was with few gametophytic thalli . The study revealed several interesting anatomical characters and its cellular deta
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10

Iliopoulou, Dimitra, Constantinos Vagias, Catherine Harvala, and Vassilios Roussis. "C15 Acetogenins from the red alga Laurencia obtusa." Phytochemistry 59, no. 1 (2002): 111–16. http://dx.doi.org/10.1016/s0031-9422(01)00407-1.

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11

Perdikaris, Stamatios, Alfonso Mangoni, Laura Grauso, Panagiota Papazafiri, Vassilios Roussis, and Efstathia Ioannou. "Vagiallene, a Rearranged C15 Acetogenin from Laurencia obtusa." Organic Letters 21, no. 9 (2019): 3183–86. http://dx.doi.org/10.1021/acs.orglett.9b00897.

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12

Iliopoulou, Dimitra, Vassilios Roussis, Christophe Pannecouque, Erik De Clercq, and Constantinos Vagias. "Halogenated sesquiterpenes from the red alga Laurencia obtusa." Tetrahedron 58, no. 33 (2002): 6749–55. http://dx.doi.org/10.1016/s0040-4020(02)00687-7.

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13

Kennedy, Derek J., Ian A. Selby, and Ronald H. Thomson. "Chamigrane metabolites from Laurencia obtusa and L. scoparia." Phytochemistry 27, no. 6 (1988): 1761–66. http://dx.doi.org/10.1016/0031-9422(88)80439-4.

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14

Norte, Manuel, José J. Fernández, José Z. Ruano, L. Matías, and Ricardo Pérez Rodríguez. "Graciosin and graciosallene, two bromoethers from Laurencia obtusa." Phytochemistry 27, no. 11 (1988): 3537–39. http://dx.doi.org/10.1016/0031-9422(88)80763-5.

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15

Esselin, Hélène, Sylvain Sutour, Ange Bighelli, and Félix Tomi. "Snyderol derivatives from Laurencia obtusa collected in Corsica." Biochemical Systematics and Ecology 82 (February 2019): 24–26. http://dx.doi.org/10.1016/j.bse.2018.11.002.

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16

Canelón, Dilsia J., Marina Ciancia, Alírica I. Suárez, Reinaldo S. Compagnone, and María C. Matulewicz. "Structure of highly substituted agarans from the red seaweeds Laurencia obtusa and Laurencia filiformis." Carbohydrate Polymers 101 (January 2014): 705–13. http://dx.doi.org/10.1016/j.carbpol.2013.09.089.

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17

Brennan, Mary R., Karen L. Erickson, Donna A. Minott, and Keith O. Pascoe. "Chamigrane metabolites from a Jamaican variety of laurencia obtusa." Phytochemistry 26, no. 4 (1987): 1053–57. http://dx.doi.org/10.1016/s0031-9422(00)82349-3.

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18

Ayyad, Seif-Eldin Nasr, Khalid Omar Al-Footy, Walied Mohamed Alarif, et al. "Bioactive C15 Acetogenins from the Red Alga Laurencia obtusa." CHEMICAL & PHARMACEUTICAL BULLETIN 59, no. 10 (2011): 1294–98. http://dx.doi.org/10.1248/cpb.59.1294.

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19

Öztunç, Aysel, Sedat Imre, Hermann Lotter, and Hildebert Wagner. "Two C15 bromoallenes from the red alga Laurencia obtusa." Phytochemistry 30, no. 1 (1991): 255–57. http://dx.doi.org/10.1016/0031-9422(91)84132-c.

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20

Hagiwara, Hisahiro, Shohei Fujiwara, Chikako Iibachi, Toshio Suzuki, and Takashi Hoshi. "A Synthetic Approach Toward a Brominated Oxocane Labdane Diterpenoid Isolated From Laurencia obtusa." Natural Product Communications 15, no. 3 (2020): 1934578X2091286. http://dx.doi.org/10.1177/1934578x20912866.

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The synthesis of a labdane oxocane epoxy-alcohol is described starting from the Wieland–Miescher ketone derivative via ring closing olefin metathesis of a diene derivative, targeting the total synthesis of a brominated oxocane labdane diterpenoid isolated from Laurencia obtusa.
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21

Pereira, R. C., B. A. P. da Gama, V. L. Teixeira, and Y. Yoneshigue-Valentin. "Ecological roles of natural products of the Brazilian red seaweed Laurencia obtusa." Brazilian Journal of Biology 63, no. 4 (2003): 665–72. http://dx.doi.org/10.1590/s1519-69842003000400013.

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Laboratory and field experiments were performed to assess the ecological roles of natural products produced by the Brazilian red seaweed Laurencia obtusa. Laboratory assays revealed that the natural concentration of the crude organic extract of L. obtusa significantly inhibited feeding by two herbivores: the crab Pachygrapsus transversus and the sea urchin Lytechinus variegatus. It was verified that this chemically defensive action was due to halogenated sesquiterpenoid elatol, found to be the major natural product of this red seaweed. In addition, it was verified that the antifouling property
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22

Bawakid, NahedO, MohamedA Ghandourah, and WaliedM Alarif. "New bioactive C15 acetogenins from the red alga Laurencia obtusa." Pharmacognosy Magazine 15, no. 61 (2019): 199. http://dx.doi.org/10.4103/pm.pm_298_18.

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23

Norte, Manuel, José J. Fernández, and José Z. Ruano. "Three new bromo ethers from the red alga laurencia obtusa." Tetrahedron 45, no. 18 (1989): 5987–94. http://dx.doi.org/10.1016/s0040-4020(01)89125-0.

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24

Iliopoulou, Dimitra, Vassilios Roussis, Christophe Pannecouque, Erik De Clerq, and Constantinos Vagias. "ChemInform Abstract: Halogenated Sesquiterpenes from the Red Alga Laurencia obtusa." ChemInform 33, no. 50 (2010): no. http://dx.doi.org/10.1002/chin.200250157.

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25

Ayyad, Seif-Eldin Nasr, Khalid Omar Al-Footy, Walied Mohamed Alarif, et al. "ChemInform Abstract: Bioactive C15Acetogenins from the Red Alga Laurencia obtusa." ChemInform 43, no. 11 (2012): no. http://dx.doi.org/10.1002/chin.201211213.

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26

Caccamese, Salvatore, Vincenzo Amico, and Placido Neri. "Two New Rearranged Sesquiterpenoids from the Red Alga Laurencia obtusa." Journal of Natural Products 53, no. 5 (1990): 1287–96. http://dx.doi.org/10.1021/np50071a023.

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27

Ayyad, Seif-Eldin Nasr, Khalid Omar Al-Footy, Walied Mohamed Alarif, et al. "Erratum: Bioactive C15 Acetogenins from the Red Alga Laurencia obtusa." CHEMICAL & PHARMACEUTICAL BULLETIN 60, no. 2 (2012): 283. http://dx.doi.org/10.1248/cpb.60.283.

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28

Amico, Vincenzo, Salvatore Caccamese, Placido Neri, Giusy Russo, and Mario Foti. "Brasilane-type sesquiterpenoids from the mediterranean red alga Laurencia obtusa." Phytochemistry 30, no. 6 (1991): 1921–27. http://dx.doi.org/10.1016/0031-9422(91)85041-w.

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29

Blanchfield, Joanne T., Sharon Chow, Paul V. Bernhardt, Colin H. L. Kennard, and William Kitching. "Concerning the Proposed Structure of (+)-Laurobtusol: Spectral Discrepancies with Synthetic, Racemic Stereoisomers." Australian Journal of Chemistry 57, no. 7 (2004): 673. http://dx.doi.org/10.1071/ch04047.

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Laurobtusol, a minor metabolite from Laurencia obtusa, had been assigned constitution 1 and relative stereochemistry, 2. However, several stereoisomers of this novel, cyclopropane-containing system 1 have now been synthesized and spectral correspondence between the synthesized isomers and laurobtusol is lacking.
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30

Esselin, Hélène, Félix Tomi, Ange Bighelli, and Sylvain Sutour. "New Metabolites Isolated from a Laurencia obtusa Population Collected in Corsica." Molecules 23, no. 4 (2018): 720. http://dx.doi.org/10.3390/molecules23040720.

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31

Bawakid, Nahed O., Walied M. Alarif, Ali I. Ismail, Mohamed E. El-Hefnawy, Khalid O. Al-Footy, and Sultan S. Al-Lihaibi. "Bio-active maneonenes and isomaneonene from the red alga Laurencia obtusa." Phytochemistry 143 (November 2017): 180–85. http://dx.doi.org/10.1016/j.phytochem.2017.08.001.

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32

Gerwick, William H., Albert Lopez, Ramon Davila, and Richard Albors. "Two New Chamigrene Sesquiterpenoids from the Tropical Red Alga Laurencia obtusa." Journal of Natural Products 50, no. 6 (1987): 1131–35. http://dx.doi.org/10.1021/np50054a020.

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33

Alarif, Walied, Sultan Al-Lihaibi, Nahed Bawakid, Ahmed Abdel-Lateff, and Hamdan Al-malky. "Rare Acetogenins with Anti-Inflammatory Effect from the Red Alga Laurencia obtusa." Molecules 24, no. 3 (2019): 476. http://dx.doi.org/10.3390/molecules24030476.

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Three new rare C12 acetogenins (enyne derivatives 1–3) were isolated from the organic extract obtained from the red alga Laurencia obtusa, collected from the Red Sea. The chemical structures of the isolated compounds were established by spectroscopical data analyses. Potent anti-inflammatory effect of the isolated metabolites was evidenced by inhibition of the release of inflammatory mediators (e.g., TNF-α, IL-1β and IL-6) by employing Human Peripheral Blood Mononuclear Cells (PBMC).
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34

Esselin, Hélène, Sylvain Sutour, Joana Liberal, et al. "Chemical Composition of Laurencia obtusa Extract and Isolation of a New C15-Acetogenin." Molecules 22, no. 5 (2017): 779. http://dx.doi.org/10.3390/molecules22050779.

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35

Bawakid, Nahed, Walied Alarif, Najla Alburae, et al. "Isolaurenidificin and Bromlaurenidificin, Two New C15-Acetogenins from the Red Alga Laurencia obtusa." Molecules 22, no. 5 (2017): 807. http://dx.doi.org/10.3390/molecules22050807.

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36

Mihopoulos, Nikos, Constantinos Vagias, Emmanuel Mikros, Michael Scoullos, and Vassilios Roussis. "Prevezols A and B: new brominated diterpenes from the red alga Laurencia obtusa." Tetrahedron Letters 42, no. 22 (2001): 3749–52. http://dx.doi.org/10.1016/s0040-4039(01)00538-x.

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37

Dassouki, Zeina, Hiba Mawlawi, Reem Al Monla, Yahya Salma, Achraf Kouzayha, and Hala Gali-Muhtasib. "Antioxidative, cytotoxic, and anti-metastatic potentials of Laurencia obtusa and Ulva lactuca seaweeds." Asian Pacific Journal of Tropical Biomedicine 11, no. 7 (2021): 308. http://dx.doi.org/10.4103/2221-1691.317242.

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38

Pereira, Leonel, Saly F. Gheda, and Paulo J. A. Ribeiro-Claro. "Analysis by Vibrational Spectroscopy of Seaweed Polysaccharides with Potential Use in Food, Pharmaceutical, and Cosmetic Industries." International Journal of Carbohydrate Chemistry 2013 (March 12, 2013): 1–7. http://dx.doi.org/10.1155/2013/537202.

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Polysaccharides present in several seaweeds (Kappaphycus alvarezii, Calliblepharis jubata, and Chondrus crispus—Gigartinales, Rhodophyta; Gelidium corneum and Pterocladiella capillacea—Gelidiales, Rhodophyta; Laurencia obtusa—Ceramiales, Rhodophyta; Himanthalia elongata, Undaria pinnatifida, Saccorhiza polyschides, Sargassum vulgare, and Padina pavonica—Phaeophyceae, Ochrophyta) are analyzed by spectroscopic techniques. The nature of the polysaccharides (with extraction and without any type of extraction) present in these seaweeds was determined with FTIR-ATR and FT-Raman analysis of extracted
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39

Lajili, Sirine, Hiba Hadj Ammar, Zeineb Mzoughi, et al. "Characterization of sulfated polysaccharide from Laurencia obtusa and its apoptotic, gastroprotective and antioxidant activities." International Journal of Biological Macromolecules 126 (April 2019): 326–36. http://dx.doi.org/10.1016/j.ijbiomac.2018.12.089.

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40

Caccamese, Salvatore, Vincenzo Amico, Placido Neri, and Mario Foti. "The structure of laurobtusol, a new rearranged sesquiterpenoid from the mediterranean red alga laurencia obtusa." Tetrahedron 47, no. 48 (1991): 10101–8. http://dx.doi.org/10.1016/s0040-4020(01)96059-4.

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41

Salgado, L. T., N. B. Viana, L. R. Andrade, et al. "Intra-cellular storage, transport and exocytosis of halogenated compounds in marine red alga Laurencia obtusa." Journal of Structural Biology 162, no. 2 (2008): 345–55. http://dx.doi.org/10.1016/j.jsb.2008.01.015.

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42

Brito, Inmaculada, Mercedes Cueto, Enrique Dorta, and José Darias. "Bromocyclococanol, a halogenated sesquiterpene with a novel carbon skeleton from the red alga Laurencia obtusa." Tetrahedron Letters 43, no. 14 (2002): 2551–53. http://dx.doi.org/10.1016/s0040-4039(02)00332-5.

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43

Caf, F., Ö. Yilmaz, and N. Şen Özdemir. "Potential of Laurencia obtusa as a substrate for the development of a probiotic Saccharomyces cerevisiae." Cellular and Molecular Biology 63, no. 8 (2017): 71. http://dx.doi.org/10.14715/cmb/2017.63.8.16.

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44

Mihopoulos, Nikos, Constantinos Vagias, Emmanuel Mikros, Michael Scoullos, and Vassilios Roussis. "ChemInform Abstract: Prevezols A and B: New Brominated Diterpenes from the Red Alga Laurencia obtusa." ChemInform 32, no. 36 (2010): no. http://dx.doi.org/10.1002/chin.200136180.

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45

Suzuki, Minoru, Yoshinori Takahashi, Yoshihide Matsuo, Michael D. Guiry, and Michio Masuda. "Scanlonenyne, a novel halogenated C 15 acetogenin from the red alga Laurencia obtusa in Irish waters." Tetrahedron 53, no. 12 (1997): 4271–78. http://dx.doi.org/10.1016/s0040-4020(97)00153-1.

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46

Dorta, Enrique, Ana R. Dı́az-Marrero, Mercedes Cueto, Luis D’Croz, Juan L. Maté, and José Darias. "Chamigrenelactone, a polyoxygenated sesquiterpene with a novel structural type and devoid of halogen from Laurencia obtusa." Tetrahedron Letters 45, no. 38 (2004): 7065–68. http://dx.doi.org/10.1016/j.tetlet.2004.07.125.

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47

CACCAMESE, S., V. AMICO, P. NERI, and M. FOTI. "ChemInform Abstract: Structure of Laurobtusol, a New Rearranged Sesquiterpenoid from the Mediterranean Red Alga Laurencia obtusa." ChemInform 23, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.199212245.

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48

Angawi, Rihab F., Walied M. Alarif, Rehab I. Hamza, Farid A. Badria, and Seif-Eldin N. Ayyad. "ChemInform Abstract: New Cytotoxic Laurene-, Cuparene-, and Laurokamurene-Type Sesquiterpenes from the Red Alga Laurencia obtusa." ChemInform 46, no. 16 (2015): no. http://dx.doi.org/10.1002/chin.201516284.

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49

Alarif, Walied M., Sultan S. Al-Lihaibi, Seif-Eldin N. Ayyad, Mohamed H. Abdel-Rhman, and Farid A. Badria. "Laurene-type sesquiterpenes from the Red Sea red alga Laurencia obtusa as potential antitumor–antimicrobial agents." European Journal of Medicinal Chemistry 55 (September 2012): 462–66. http://dx.doi.org/10.1016/j.ejmech.2012.06.060.

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50

Barot, Megha, Nirmal Kumar JI, and Rita N. Kumar. "Bioactive compounds and antifungal activity of three different seaweed species Ulva lactuca, Sargassum tenerrimum and Laurencia obtusa collected from Okha coast, Western India." Journal of Coastal Life Medicine 4, no. 4 (2016): 284–89. http://dx.doi.org/10.12980/jclm.4.2016j5-185.

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