dc.contributor.author | Grabarczyk, Małgorzata | en |
dc.contributor.author | Wińska, Katarzyna | en |
dc.contributor.author | Mączka, Wanda | en |
dc.contributor.author | Potaniec, Bartłomiej | en |
dc.contributor.author | Anioł, Mirosław | en |
dc.date.accessioned | 2016-07-21T11:50:20Z | |
dc.date.available | 2016-07-21T11:50:20Z | |
dc.date.issued | 2015-12-17 | en |
dc.identifier.issn | 1730-2366 | en |
dc.identifier.uri | http://hdl.handle.net/11089/18884 | |
dc.description.abstract | It is extremely interesting that this lactone also affects the behavior of ants as well as the development of certain plants (allelopathic activity). However, sometimes there are side effects as in the case of structural analogues of loliolide contributing to extinction of tropical coral. | en |
dc.description.abstract | Niezmiernie interesujący jest fakt, że lakton ten wywiera również wpływ na zachowanie mrówek jak i na rozwój niektórych roślin (aktywność alleplopatyczna). Czasami jednak można zaobserwować również działania niepożądane jak w przypadku analogów strukturalnych loliolidu mających swój udział w wymieraniu raf tropikalnych. | en |
dc.publisher | Wydawnictwo Uniwersytetu Łódzkiego | en |
dc.relation.ispartofseries | Folia Biologica et Oecologica;11 | en |
dc.rights | This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License. | en |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0 | en |
dc.subject | monoterpenoid lactones | en |
dc.subject | loliolide | en |
dc.subject | biological activity fungi | en |
dc.subject | HGT | en |
dc.title | Loliolide – the most ubiquitous lactone | en |
dc.page.number | 1-8 | en |
dc.contributor.authorAffiliation | Grabarczyk, Małgorzata - Department of Chemistry, Wroclaw University of Environmental and Life Sciences, Norwida 25, 50-375 Wrocław, Poland | en |
dc.contributor.authorAffiliation | Wińska, Katarzyna - Department of Chemistry, Wroclaw University of Environmental and Life Sciences, Norwida 25, 50-375 Wrocław, Poland | en |
dc.contributor.authorAffiliation | Mączka, Wanda - Department of Chemistry, Wroclaw University of Environmental and Life Sciences, Norwida 25, 50-375 Wrocław, Poland | en |
dc.contributor.authorAffiliation | Potaniec, Bartłomiej - Department of Chemistry, Wroclaw University of Environmental and Life Sciences, Norwida 25, 50-375 Wrocław, Poland | en |
dc.contributor.authorAffiliation | Anioł, Mirosław - Department of Chemistry, Wroclaw University of Environmental and Life Sciences, Norwida 25, 50-375 Wrocław, Poland | en |
dc.references | Ahmed, A.A., El-Moghazy, S.A., El-Shanawany, M.A. et al. 2004. Polyol monoterpenes and sesquiterpene lactones from the Pacific Northwest plant Artemisia suksdorfii. Journal of Natural Products, 67: 1705‒1710. doi: 10.1021/np049954j | en |
dc.references | Ali, M.S. 2012. A Bird’s-eye View on Chemistry of Marine Algae from Karachi Coast of North Arabian Sea (Pakistan). Journal of Scientific Research in Pharmacy, 1: 1‒5. | en |
dc.references | Ali, M.S., Pervez, M.K., Saleem, M. et al. 2003. Dichotenone-A and -B: two new enones from the marine brown alga Dictyota dichotoma (Hudson) Lamour. Natural Product Research, 17: 301‒306. | en |
dc.references | Borkosky, S., Valdes, D.A., Bardon, A. et al. 1996. Sesquiterpene lactones and other constituents of Eirmocephala megaphylla and Cyrtocymura cincta. Phytochemistry, 42: 1637‒1639. doi: 10.1016/0031-9422(96)82943-8 | en |
dc.references | Chen, Y., Tao, Y., Lian, X. et al. 2010. Chemical constituents of Angiopteris esculenta including two new natural lactones. Food Chemistry, 122: 1173‒1175. doi: 10.1016/j.foodchem.2010.03.111 ThomsonISI: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000278582400035&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=b7bc2757938ac7a7a821505f8243d9f3 | en |
dc.references | Cheng, S.Y., Huang, K.J., Wang, S.K. et al. 2010. Antiviral and anti-inflammatory metabolites from the soft coral Sinularia capillosa. Journal of Natural Products, 73: 771‒775. doi: 10.1021/np9008078 ThomsonISI: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000276950000053&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=b7bc2757938ac7a7a821505f8243d9f3 | en |
dc.references | Da Costa, N.C., Yang, Y., Kowalczyk, J. et al. 2008. The analysis of volatiles and nonvolatiles in Yerba Maté Tea (Ilex Paraguariensis). In: I. Blank, M. Wüst, C. Yeretzian (Eds.). Expression of Multidisciplinary Flavour Science, Interlaken, Switzerland: 494‒487. | en |
dc.references | El Hattab, M., Culioli, G., Valls, R., et al. 2008. Apo-fucoxanthinoids and loliolide from the brown alga Cladostephus spongiosus f. verticillatus (Heterokonta, Sphacelariales). Biochemical Systematics and Ecology, 36: 447‒451. doi: 10.1016/j.bse.2007.08.016 ThomsonISI: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000255793000019&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=b7bc2757938ac7a7a821505f8243d9f3 | en |
dc.references | Elkhayat, E. 2009. Cytotoxic and antibacterial constituents from the roots of Sonchus oleraceus L. growing in Egypt. Pharmacognosy Magazine, 5: 324‒328. doi: 10.4103/0973-1296.58154 | en |
dc.references | Erosa-Rejón, G., Peña-Rodríguez, L.M. & Sterner O. 2009. Secondary Metabolites from Heliotropium angiospermum. Journal of Mexican Chemical Society, 53: 44‒47. | en |
dc.references | Fernandez, I., Pedro, J.R. & Polo, E. 1995. Sesquiterpene lactones from Centaurea alba and C. conifera. Phytochemistry, 38: 655‒657. doi: 10.1016/0031-9422(94)00688-P | en |
dc.references | Fujita, E., Saeki, Y., Ochiart, M. et al. 1972. Investigation of the Neutral Constituents of Lythrum Salicaria L. Bulletin of the Institute for Chemical Research, 50, 327‒331. | en |
dc.references | Fukushima, T., Tanaka, M., Gohbara, M. et al. 1998. Phytotoxicity of three lactones from Nigrospora sacchari, Phytochemistry, 48: 625‒630. doi: 10.1016/S0031-9422(97)01023-6 | en |
dc.references | Garg, S.N. & Agarwal, S.K. 1994. A new monoterpene lactone and chemical composition of essential oil of Brucea jawanica leaves. Journal of Essential Oil Research, 6: 145‒148. | en |
dc.references | Geng, C. & Liu, X. 2008. New Macrocyclic Diamide from Rauvolfia Yunnanensis Tsiang. Chemical Research in Chinese Universities, 24: 303‒305. doi: 10.1016/S1005-9040(08)60065-3 ThomsonISI: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000257176100013&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=b7bc2757938ac7a7a821505f8243d9f3 | en |
dc.references | Grayson, D.H. 1997. Monoterpenoids. Natural Product Reports, 14: 477‒522. doi: 10.1039/np9971400477 | en |
dc.references | Grayson, D.H. 2000. Monoterpenoids. Natural Product Reports, 17: 385‒419. doi: 10.1039/a804437f | en |
dc.references | Grayson, D.H. 1996. Monoterpenoids. Natural Product Reports, 13: 195‒225. doi: 10.1039/np9961300195 | en |
dc.references | He, Z., Zhang, A., Ding, L et al. 2010. Chemical composition of the green alga Codium Divaricatum Holmes. Fitoterapia, 81: 1125‒1128. doi: 10.1016/j.fitote.2010.07.011 ThomsonISI: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000285281800029&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=b7bc2757938ac7a7a821505f8243d9f3 | en |
dc.references | Hiraga, Y., Taino, K., Kurokawa, M. et al. 1997. (- )-Loliolide and other germination inhibitory active constituents in Equisetum arvense. Natural Product Letters, 10: 181‒187. doi: 10.1080/10575639708041192 | en |
dc.references | Hodges, R. & Porte, A.L. 1964. The structure of loliolide : A terpene from Lolium perenne. Tetrahedron, 20: 1463‒1467. doi: 10.1016/S0040-4020(01)99140-9 | en |
dc.references | Hunyadi, A., Veres, K., Danko, B. et al. 2012. In vitro anti-diabetic activity and chemical characterization of an apolar fraction of Morus alba leaf water extract. Phytotherapy Research, 27: 847‒851. doi: 10.1002/ptr.4803 ThomsonISI: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000320114500008&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=b7bc2757938ac7a7a821505f8243d9f3 | en |
dc.references | Kimura, J. & Maki, N. 2002. New loliolide derivatives from the brown alga Undaria pinnatifida. Journal of Natural Products, 65: 57‒58. doi: 10.1021/np0103057 | en |
dc.references | Kuniyoshi, M. 1985. Germination inhibitors from the brown alga Sargassum crassifolium (Phaeophyta, Sargassaceae). Botanica Marina, 28: 501‒503. doi: 10.1515/botm.1985.28.11.501 | en |
dc.references | Kuo, Y.H, Lo, J.M. & Chan, Y.F. 2002. Cytotoxic components from the leaves of Schefflera taiwaniana. Journal of the Chinese Chemical Society, 49: 427‒431. | en |
dc.references | Kurokawa, M., Hirose, T., Sugata, Y. et al. 1998. 3- Hydroxy-5,6-epoxy-β-ionone as germination inhibitory active constituent in Athyrium yokoscense. Natural Product Letters, 12: 35‒40. doi: 10.1080/10575639808048868 | en |
dc.references | Machado, F.B., Yamamoto, R.E., Zanoli, K. et al. 2012. Evaluation of the antiproliferative activity of the leaves from Arctium lappa by a bioassay-guided fractionation. Molecules, 17: 1852‒1859. doi: 10.3390/molecules17021852 | en |
dc.references | Molnár, I., Gibson, D.M. & Krasnoff, S.B. 2010. Secondary metabolites from entomopathogenic Hypocrealean fungi. Natural Product Reports, 27: 1241‒1275. doi: 10.1039/c001459c ThomsonISI: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000281109500001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=b7bc2757938ac7a7a821505f8243d9f3 | en |
dc.references | Neergaard, J.S., Rasmussen, H.B., Stafford, G.I. et al. 2010. Serotonin transporter affinity of (−)- loliolide, a monoterpene lactone from Mondia whitei. South African Journal of Botany, 76: 593‒596. doi: 10.1016/j.sajb.2010.02.091 ThomsonISI: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000279986300025&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=b7bc2757938ac7a7a821505f8243d9f3 | en |
dc.references | Okunade, A.L. & Wiemer, D.F. (1985). (‒)- Loliolide, an ant-repellent compound from Xanthoxyllum setulosum. Journal of Natural Products, 48: 472‒473. doi: 10.1021/np50039a020 | en |
dc.references | Pan, L., Sinden, M.R., Kennedy, A.H. et al. 2009. Bioactive constituents of Helianthus tuberosus (Jerusalem artichoke). Phytochemistry Letters, 2: 15‒18. doi: 10.1016/j.phytol.2008.10.003 ThomsonISI: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000264009800003&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=b7bc2757938ac7a7a821505f8243d9f3 | en |
dc.references | Parmeswaran, P.S., Naik, C.G., Das, B. et al. 1996. Constituents of the brown alga Padina tetrastromatica (Hauck)-II. Indian Journal of Chemistry B, 35: 463‒467. | en |
dc.references | Pettit, G.R., Herald, C.L., Ode, R.H et al. 1980. The isolation of loliolide from an Indian Ocean Opisthobranch mollusk. Journal of Natural Products, 43: 752‒755. doi: 10.1021/np50012a009 | en |
dc.references | Ragasa, C.Y., Agbayani, V., Hernandez, R.B. et al. 1997. Antimutagenic monoterpene from Malachra fasciata (Malvaciae). Philippine Journal of Science, 126: 183‒189. | en |
dc.references | Ragasa, C.Y., De Luna, R.D., Cruz Jr, W.C. et al. 2005. Monoterpene lactones from the seeds of Nephelium lappaceum. Journal of Natural Products, 68: 1394‒1396. doi: 10.1021/np0580053 | en |
dc.references | Ragasa, C.Y., De Luna, R.D. & Hofilena, J.G. 2005. Antimicrobial terpenoids from Pterocarpus indicus. Natural Product Research, 19: 305‒309. | en |
dc.references | Rasher, D.B., Stout, E.P., Engel, S. et al. 2011. Macroalgal terpenes function as allelopathic agents against reef corals. Proceedings of the National Academy of Sciences, 108: 17727‒17731. ThomsonISI: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000296378100040&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=b7bc2757938ac7a7a821505f8243d9f3 | en |
dc.references | Rocca, J.R., Tumlinson, J.H., Glancey, B.M. et al. 1983. The queen recognition pheromone of Solenopsis invicta, preparation of (E-6-(1- pentenyl)-2H-pyran-2-one. Tetrahedron Letters, 24: 1889‒1892. doi: 10.1016/S0040-4039(00)81798-0 | en |
dc.references | Sarker, S.D., Bright, C., Bartholomew, B. et al. 2000. Calendin, tyrosol and two benzoic acid derivatives from Veronica persica (Scrophulariaceae). Biochemical Systematics and Ecology, 28: 799‒801. doi: 10.1016/S0305-1978(99)00122-2 | en |
dc.references | Valde`s. L.J. 1986. Loliolide from Salvia divinorum. Journal of Natural Products, 49: 171-171. doi: 10.1021/np50043a031 | en |
dc.references | Wong. H.F. & Bron. G.D. 2002. β-Methoxy-γ- methylene-α,β-unsaturated-γ-butyrolactones from Artabotrys hexapetalus. Phytochemistry, 59: 99‒104. doi: 10.1016/S0031-9422(01)00433-2 | en |
dc.references | Xiao. Y., Wang. Y.L., Gao. S.X. et al. 2007. Chemical Composition of Hydrilla Verticillata (L. f.) Royle in Taihu Lake. Chinese Journal of Chemistry, 25: 661‒665. doi: 10.1002/cjoc.200790123 | en |
dc.references | Yang, X., Kang, M.C., Lee, K.W. et al. 2011. Antioxidant activity and cell protective effect of loliolide isolated from Sargassum ringgoldianum subsp. Coreanum. Algae, 26: 201‒208. doi: 10.4490/algae.2011.26.2.201 | en |
dc.references | Zajdel, S.M., Graiko, K., Głowniak, K. et al. 2012. Chemical analysis of Penstemon campanulatus (Cav.) Willd. - antimicrobial activities. Fitoterapia, 83: 373‒376. doi: 10.1016/j.fitote.2011.11.021 ThomsonISI: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000300817000019&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=b7bc2757938ac7a7a821505f8243d9f3 | en |
dc.references | Zhou, B., Kong, C.H., Li, Y.H et al. 2013. Crabgrass (Digitaria sanguinalis) allelochemicals that interfere with crop growth and the soil microbial community. Journal of Agricultural and Food Chemistry, 61: 5310‒5317. doi: 10.1021/jf401605g ThomsonISI: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000320153500016&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=b7bc2757938ac7a7a821505f8243d9f3 | en |
dc.contributor.authorEmail | Grabarczyk, Małgorzata - magrab@onet.pl | en |
dc.identifier.doi | 10.1515/fobio-2015-0001 | en |