The rhizome of Drynaria rigidula has been traditionally claimed to have anti-infective properties. A phytochemical study conducted on the rhizome successfully isolated two new aromatic glycosides as well as three known terpenoids, two benzoic acid derivatives and two known flavonoid glycosides. The rhizome methanol extract and its fractions were tested against Mycobacterium tuberculosis, Plasmodium falciparum, herpes simplex virus and KB-oral cancer cell; insignificant activity was found.
NugrahaA.S., KellerP.A. (2011) Revealing indigenous Indonesian traditional medicine: anti-infective agents. Natural Product Communications, 6, 1953–1966.
2.
BenzingD.H. (1990) Vascular epiphytes: General biology and related biota.Cambridge University Press, Cambridge, 1–354.
3.
KhanA., HaqueE., Mukhlesur RahmanM., MosaddikA., RahmanM., SultanaN. (2007) Isolation of antibacterial constituent from rhizome of Drynaria quercifolia and its sub-acute toxicological studies. Daru-Journal of Faculty of Pharmacy, Tehran University of Medical Science, 15, 205–211.
4.
LiuS., XiaoZ., FengR. (1994) A flavanol glycoside from Drynaria propinqua. Phytochemistry, 35, 1595–1596.
5.
RameshN., ViswanathanM.B., SaraswathyA., BalakrishnaK., BrindhaP., LakshmanaperumalsamyP. (2001) Phytochemical and antimicrobial studies on Drynaria quercifolia. Fitoterapia, 72, 934–936.
6.
WangX.L., WangN.L., GaoH., ZhangG., QinL., WongM.S., YaoX.S. (2010) Phenylpropanoid and flavonoids from osteoprotective fraction of Drynaria fortunei. Natural Product Research, 24, 1206–1213.
7.
WangX.L., WangN.L., ZhangY., GaoH., PangW.Y., WongM.S., ZhangG., QinL., YaoX.S. (2008) Effects of eleven flavonoids from the osteoprotective fraction of Drynaria fortunei (Kunze) J. SM. on osteoblastic proliferation using an osteoblast-like cell line. Chemical and Pharmaceutical Bulletin, 56, 46–51.
8.
GiesenW., WulffraatS., ZierenM., ScholtenL. (2006) Mangrove guidebook for Southeast Asia.FAO and Wetlands International, Bangkok, 1–769.
9.
AgetaH., ShiojimaK., AraiY., SuzukiH., KiyotaniT. (1994) NMR spectra of triterpenoids. II. Hopenes and migrated hopenes. Chemical and Pharmaceutical Bulletin, 42, 39–44.
10.
AgetaH., ShiojimaK., SuzukiH., NakamuraS. (1993) NMR spectra of triterpenoids. I. Conformation of the side chain of hopane and isohopane, and their derivatives. Chemical and Pharmaceutical Bulletin, 41, 1939–1943.
11.
BalamuruganR., StalinA., IgnacimuthuS. (2012) Molecular docking of γ-sitosterol with some targets related to diabetes. European Journal of Medicinal Chemistry, 47, 38–43.
12.
LinS.S.C., LuT.M., ChaoP.C., LaiY.Y., TsaiH.T., ChenC.S., LeeY.P., ChenS.C., ChouM.C., YangC.C. (2011) In vivo cytokine modulatory effects of cinnamaldehyde, the major constituent of leaf essential oil from Cinnamomum osmophloeum Kaneh. Phytotherapy Research, 25, 1511–1518.
13.
RaoG.V., RaoP.S. (1985) A new flavonol glycoside from the flowers of Crotalaria verrucosa. Fitoterapia, 56, 175–177.
14.
DuusJ., GotfredsenC.H., BockK. (2000) Carbohydrate structural determination by NMR spectroscopy: modern methods and limitations. Chemical Reviews, 100, 4589–614.
15.
DesjardinsR.S., CanfeldC.J., HaynesJ.D., ChulayJ.D. (1979) Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique. Antimicrobial Agents and Chemotherapy, 16, 710–718.
16.
HaritakunR., SappanM., SuvannakadR., TasanathaiK., IsakaM. (2010) An antimycobacterial cyclodepsipeptide from the entomopathogenic fungus Ophiocordyceps communis BCC 16475. Journal of Natural Products, 73, 75–78.