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Research Article

Terpenoidal constituents of Eucalyptus loxophleba ssp. lissophloia

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Pages 823-827 | Received 20 Jun 2011, Accepted 25 Oct 2011, Published online: 03 Apr 2012

References

  • Begum S, Farhat Siddiqui, BS. (1997). Triterpenoids from the leaves of Eucalyptus camaldulensis var. obtusa. J Nat Prod, 60, 20–23.
  • Begum S, Sultana I, Siddiqui BS, Shaheen F, Gilani AH. (2002). Structure and spasmolytic activity of eucalyptanoic acid from Eucalyptus camaldulensis var. obtusa and synthesis of its active derivative from oleanolic acid. J Nat Prod, 65, 1939–1941.
  • Bell SJ, Barton AFM, Stocker LJ. (2001). Agriculture for health and profit in Western Australia: The Western Oil Mallee Project. Ecosyst Health, 7, 116–121.
  • Dayal R. (1990). Two new compounds from ursolic acid lactone. Indian J Chem B Org, 29, 156–157.
  • Ghisalberti EL. (1996). Bioactive acylphloroglucinol derivatives from Eucalyptus species. Phytochemistry, 41, 7–22.
  • Hakki Z, Cao B, Heskes AM, Goodger JQ, Woodrow IE, Williams SJ. (2010). Synthesis of the monoterpenoid esters cypellocarpin C and cuniloside B and evidence for their widespread occurrence in Eucalyptus. Carbohydr Res, 345, 2079–2084.
  • Hongcheng W, Fujimoto Y. (1993). Triterpene esters from Eucalyptus tereticornis. Phytochemitry, 33, 151–153.
  • Ikuta A, Tomiyasu H, Morita Y, Yoshimura K. (2003). Ursane- and oleanane-type triterpenes from Ternstroemia gymnanthera callus tissues. J Nat Prod, 66, 1051–1054.
  • Katai M, Terai T, Meguri H. (1983). Triterpenoids of the bark of Pieris japonica D. DON (Japanese name: Asebi). II. 13C nuclear magnetic resonance of the γ-lactones of ursane- and oleanane-type triterpenoids. Chem Pharm Bull, 31, 1567–1571.
  • Khare M, Srivastava SK, Singh AK. (2002). A new triterpenic acid from Eucalyptus robusta. Indian J Chem, 41B, 440–445.
  • Mikus J, Steverding D. (2000). A simple colorimetric method to screen drug cytotoxicity against Leishmania using the dye Alamar blue. Parasitol Int, 48, 265–269.
  • Moghaddam FM, Farimani MM, Salahvarzi S, Amin G. (2007). Chemical constituents of dichloromethane extract of cultivated Satureja khuzistanica. Evid Based Complement Alternat Med, 4, 95–98.
  • Ordonez-Gutierrez L, Espada-Fernandez R, Auxiliadora DM, Jose TJ, Bolas-Fernandez F, Maria AJ. (2007). In vitro effect of new formulations of amphotericin A on amastigote and promastigotes forms of Leishmania infantum. Int J Antimicrobial Agents, 30, 325–329.
  • Savian AA, Sokolskaya T, Zakharov VF. (1988). 11, 12-Dehydroursolic acid lactone from leaves of Eucalyptus viminalis. Chem Nat Comp, 24, 253–254.
  • Sidana J, Rohilla RK, Roy N, Barrow RA, Foley WJ, Singh IP. (2010). Antibacterial sideroxylonals and loxophlebal A from Eucalyptus loxophleba foliage. Fitoterapia, 81, 878–883.
  • Sidana J, Singh S, Arora SK, Foley WJ, Singh IP. (2011). Formylated phloroglucinols from Eucalyptus loxophleba foliage. Fitoterapia, 82, 1118–1122.
  • Vermeersch M, da Luz RI, Toté K, Timmermans JP, Cos P, Maes L. (2009). In vitro susceptibilities of Leishmania donovani promastigote and amastigote stages to antileishmanial reference drugs: Practical relevance of stage-specific differences. Antimicrob Agents Chemother, 53, 3855–3859.

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