References
- Alarif WM, Al-Footy KO, Zubair MS, Halid Ph M, Ghandourah MA, Basaif SA, Al-Lihaibi SS, Ayyad SE, Badria FA. 2016. The role of new eudesmane-type sesquiterpenoid and known eudesmane derivatives from the red alga Laurencia obtusa as potential antifungal–antitumour agents. Nat Prod Res. 30:1150–1155.10.1080/14786419.2015.1046378
- Chatter R, Othman RB, Rabhi S, Kladi M, Tarhouni S, Vagias C, Roussis V, Guizani-Tabbane L, Kharrat R. 2011. In vivo and in vitro anti-inflammatory activity of neorogioltriol, a new diterpene extracted from the red algae Laurencia glandulifera. Mar Drugs. 9:1293–1306.10.3390/md9071293
- De Nys R, Wright AD, König GM, Sticher O. 1993. Five new sesquiterpenes from the red alga Laurencia flexilis. J Nat Prod. 56:877–883.10.1021/np50096a011
- Espinel-Ingroff A, Bartlett M, Chaturvedi V, Ghannoum M, Hazen KC, Pfaller MA, Rinaldi M, Walsh TJ. 2001. Optimal susceptibility testing conditions for detection of azole resistance in Aspergillus spp.: NCCLS collaborative evaluation. Antimicrob Agents Chemother. 45:1828–1835.10.1128/AAC.45.6.1828-1835.2001
- Izac RR, Poet SE, Fenical W. 1982. The structure of pacifigorgiol, an ichthyotoxic sesquiterpenoid from the pacific gorgonian coral Pacifigorgia cf. adamsii. Tetrahedron Lett. 23:3743–3746.10.1016/S0040-4039(00)87695-9
- Ji NY, Wang BG. 2014. Nonhalogenated organic molecules from Laurencia algae. Phytochem Rev. 13:653–670.10.1007/s11101-013-9326-0
- Juagdan EG, Kalidindi R, Scheuer P. 1997. Two new chamigrenes from Hawaiian red alga, Laurencia cartilaginea. Tetrahedron. 53:521–528.10.1016/S0040-4020(96)01002-2
- Kamada T, Vairappan CS. 2012. A new bromoallene-producing chemical type of the red alga Laurencia nangii Masuda. Molecules. 17:2119–2125.10.3390/molecules17022119
- Kamada T, Vairappan CS. 2015. New laurene-type sesquiterpene from Bornean Laurencia nangii. Nat Prod Commun. 10:843–844.
- Kladi M, Vagias C, Papazafiri P, Furnari G, Serio D, Roussis V. 2007. New sesquiterpenes from the red alga Laurencia microcladia. Tetrahedron. 63:7606–7611.10.1016/j.tet.2007.05.051
- Levison ME. 2004. Pharmacodynamics of antimicrobial drugs. Infect Dis Clin North Am. 18:451–465.10.1016/j.idc.2004.04.012
- Liu CM, Zhu RL, Liu RH, Li HL, Shan L, Xu XK, Zhang WD. 2009. Cis-clerodane diterpenoids from the liverwort Gottschelia schizopleura and their cytotoxic activity. Planta Med. 75:1597–1601.10.1055/s-0029-1185837
- Makhanu DS, Yokoyama M, Miono T, Maesato T, Maedomari M, Wisespongpand P, Kuniyoshi M. 2006. New sesquiterpenes from the Okinawan red alga Laurencia luzonensis. Bull Fac Sci Univ Ryukyus. 81:115–120.
- Paul VJ, Fenical W. 1980. Palisadins A, B and related monocyclofarnesol-derived sesquiterpenoids from the red marine alga Laurencia palisada. Tetrahedron Lett. 21:2787–2790.10.1016/S0040-4039(00)78607-2
- Suzuki M, Vairappan CS. 2005. Halogenated secondary metabolites from Japanese species of the red algal genus Laurencia (Rhodomelaceae, Ceramiales). Curr Top Phytochemistry. 5:1–38.
- Tan KL, Matsunaga S, Vairappan CS. 2011. Halogenated chamigrenes of red alga Laurencia snackeyi (Weber-van Bosse) Masuda from Sulu-Sulawesi Sea. Biochem Syst Ecol. 39:213–215.10.1016/j.bse.2010.09.017
- Tsukamoto S, Yamashita Y, Ohta T. 2005. New cytotoxic and antibacterial compounds isolated from the sea hare, Aplysia kurodai. Mar Drugs. 3:22–28.10.3390/md302022
- Vairappan CS, Kamada T, Lee WW, Jeon YJ. 2013. Anti-inflammatory activity of halogenated secondary metabolites of Laurencia snackeyi (Weber-van Bosse) Masuda, in LPS-stimulated RAW 264.7 macrophages. J Appl Phycol. 25:1805–1813.10.1007/s10811-013-0023-6
- Wang BG, Gloer JB, Ji NY, Zhao JC. 2013. Halogenated organic molecules of rhodomelaceae origin: chemistry and biology. Chem Rev. 113:3632–3685.10.1021/cr9002215
- Wright AD, König GM, Sticher O. 1991. New sesquiterpenes and C15 acetogenins from the marine red alga Laurencia implicata. J Nat Prod. 54:1025–1033.10.1021/np50076a016