Published February 29, 2016
| Version v1
Journal article
Restricted
Cytotoxic sesquiterpenes from the endophytic fungus Pseudolagarobasidium acaciicola
Authors/Creators
- 1. Chulabhorn Graduate Institute, Chemical Biology Program, Kamphaeng Phet 6 Road, Laksi, Bangkok 10210, Thailand
Description
Wibowo, Mario, Prachyawarakorn, Vilailak, Aree, Thammarat, Mahidol, Chulabhorn, Ruchirawat, Somsak, Kittakoop, Prasat (2016): Cytotoxic sesquiterpenes from the endophytic fungus Pseudolagarobasidium acaciicola. Phytochemistry 122: 126-138, DOI: 10.1016/j.phytochem.2015.11.016, URL: http://dx.doi.org/10.1016/j.phytochem.2015.11.016
Files
Linked records
Additional details
Identifiers
- LSID
- urn:lsid:plazi.org:pub:324B1F00FFF54229FFFEFFCB946EF451
References
- Beekman, A.C., Wierenga, P.K., Woerdenbag, H.J., Van Uden, W., Pras, N., Konings, A. W.T., El-Feraly, F.S., Galal, A.M., Wikstrom, H.V., 1998. Artemisinin-derived sesquiterpene lactones as potential antitumour compounds: cytotoxic action against bone marrow and tumour cells. Planta Med. 64, 615-619.
- Carmichael, J., DeGraff, W.G., Gazdar, A.F., Minna, J.D., Mitchell, J.B., 1987. Evaluation of a tetrazolium-based semiautomated colorimetric assay: assessment of chemosensitivity testing. Cancer Res. 47, 936-942.
- Chaturvedi, D., Goswami, A., Pratim Saikia, P., Barua, N.C., Rao, P.G., 2010. Artemisinin and its derivatives: a novel class of anti-malarial and anti-cancer agents. Chem. Soc. Rev. 39, 435-454.
- Chokpaiboon, S., Sommit, D., Bunyapaiboonsri, T., Matsubara, K., Pudhom, K., 2011. Antiangiogenic effect of chamigrane endoperoxides from a Thai mangrovederived fungus. J. Nat. Prod. 74, 2290-2294.
- Chokpaiboon, S., Sommit, D., Teerawatananond, T., Muangsin, N., Bunyapaiboonsri, T., Pudhom, K., 2010. Cytotoxic nor-chamigrane and chamigrane endoperoxides from a basidiomycetous fungus. J. Nat. Prod. 73, 1005-1007.
- Chomcheon, P., Sriubolmas, N., Wiyakrutta, S., Ngamrojanavanich, N., Chaichit, N., Mahidol, C., Ruchirawat, S., Kittakoop, P., 2006. Cyclopentenones, scaffolds for organic synthesis produced by the endophytic fungus, mitosporic Dothideomycete sp. LRUB20. J. Nat. Prod. 69, 1351-1353.
- Chomcheon, P., Wiyakrutta, S., Aree, T., Sriubolmas, N., Ngamrojanavanich, N., Mahidol, C., Ruchirawat, S., Kittakoop, P., 2010. Curvularides A-E: antifungal hybrid peptide-polyketides from the endophytic fungus Curvularia geniculata. Chem. Eur. J. 16, 11178-11185.
- Chomcheon, P., Wiyakrutta, S., Sriubolmas, N., Ngamrojanavanich, N., Mahidol, C., Ruchirawat, S., Kittakoop, P., 2009. Metabolites from the endophytic mitosporic Dothideomycete sp. LRUB20. Phytochemistry 70, 121-127.
- Dong, J.Y., Ma, X.Y., Cai, X.Q., Yan, P.C., Yue, L., Lin, C., Shao, W.W., 2013. Sesquiterpenoids from Curcuma wenyujin with anti-influenza viral activities. Phytochemistry 85, 122-128.
- Doyle, A., Griffiths, J.B., 1997. Mammalian Cell Culture: Essential Techniques. John Wiley & Sons, Chichester, UK.
- Hill, R.A., Sutherland, A., 2014. Hot off the press. Nat. Prod. Rep. 31, 1242-1246.
- Kikuchi, T., Uchiyama, E., Ukiya, M., Tabata, K., Kimura, Y., Suzuki, T., Akihisa, T., 2011. Cytotoxic and apoptosis-inducing activities of triterpene acids from Poria cocos. J. Nat. Prod. 74, 137-144.
- Kusari, S., Pandey, S.P., Spiteller, M., 2013. Untapped mutualistic paradigms linking host plant and endophytic fungal production of similar bioactive secondary metabolites. Phytochemistry 91, 81-87.
- Li, H., Huang, H., Shao, C., Huang, H., Jiang, J., Zhu, X., Liu, Y., Liu, L., Lu, Y., Li, M., Lin, Y., She, Z., 2011. Cytotoxic norsesquiterpene peroxides from the endophytic fungus Talaromyces flavus isolated from the mangrove plant Sonneratia apetala. J. Nat. Prod. 74, 1230-1235.
- Liu, D.Z., Dong, Z.J., Wang, F., Liu, J.K., 2010. Two novel norsesquiterpene peroxides from basidiomycete Steccherinum ochraceum. Tetrahedron Lett. 51, 3152-3153.
- Lombardo, M., Sonawane, D.P., Quintavalla, A., Trombini, C., Dhavale, D.D., Taramelli, D., Corbett, Y., Rondinelli, F., Fattorusso, C., Persico, M., Taglialatela- Scafati, O., 2014. Optimized synthesis and antimalarial activity of 1,2-dioxane- 4-carboxamides. Eur. J. Org. Chem. 2014, 1607-1614.
- Najjar, F., Baltas, M., Gorrichon, L., Moreno, Y., Tzedakis, T., Vial, H., Andre-Barres, C., 2003. Synthesis and electrochemical studies of new antimalarial endoperoxides. Eur. J. Org. Chem., 3335-3343
- Parsons, S., Flack, H.D., Wagner, T., 2013. Use of intensity quotients and differences in absolute structure refinement. Acta Cryst. B69, 249-259.
- Ruiz, J., Mallet-Ladeira, S., Maynadier, M., Vial, H., Andre-Barres, C., 2014. Design, synthesis and evaluation of new tricyclic endoperoxides as potential antiplasmodial agents. Org. Biomol. Chem. 12, 5212-5221.
- Senadeera, S.P., Wiyakrutta, S., Mahidol, C., Ruchirawat, S., Kittakoop, P., 2012. A novel tricyclic polyketide and its biosynthetic precursor azaphilone derivatives from the endophytic fungus Dothideomycete sp. Org. Biomol. Chem. 10, 7220-7226.
- Sheldrick, G.M., 2008. A short history of SHELX. Acta Cryst. A64, 112-122.
- Tan, R.X., Zou, W.X., 2001. Endophytes: a rich source of functional metabolites. Nat. Prod. Rep. 18, 448-459.
- Wibowo, M., Prachyawarakorn, V., Aree, T., Wiyakrutta, S., Mahidol, C., Ruchirawat, S., Kittakoop, P., 2014. Tricyclic and spirobicyclic norsesquiterpenes from the endophytic fungus Pseudolagarobasidium acaciicola. Eur. J. Org. Chem. 2014, 3976-3980.