Biodiversity Literature Repository

Submit to community
Liberated Data
Published December 31, 2020 | Version v1
Journal article Restricted

Specialized metabolites of the United States lichen Niebla homalea and their antiproliferative activities

Authors/Creators

  • 1. * & Division of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, The Ohio State University, Columbus, OH, 43210, USA

Description

Zhang, Yan, Tan, Choon Yong, Spjut, Richard W., Fuchs, James R., Kinghorn, A. Douglas, Rakotondraibe, Liva Harinantenaina (2020): Specialized metabolites of the United States lichen Niebla homalea and their antiproliferative activities. Phytochemistry (112521) 180: 1-7, DOI: 10.1016/j.phytochem.2020.112521, URL: http://dx.doi.org/10.1016/j.phytochem.2020.112521

Files

Restricted

The record is publicly accessible, but files are restricted. Log in to check if you have access.

Linked records

Additional details

Identifiers

LSID
urn:lsid:plazi.org:pub:4E38C060FFD7FFFCFFE8FF84FF8CC97E
URL
http://publication.plazi.org/id/4E38C060FFD7FFFCFFE8FF84FF8CC97E

Cites
Publication: 10.1063/1.4895198 (DOI)
Publication: 10.3897/mycokeys.73.47287 (DOI)
Has part
Taxonomic treatment: 10.5281/zenodo.8301842 (DOI)
Taxonomic treatment: http://treatment.plazi.org/id/B201B818FFD3FFF9FCDAFAC1FC38C830 (URL)
Dataset: http://table.plazi.org/id/6ED75986FFD6FFFDFF8CFF12FF7CC9A4 (URL)
Figure: 10.5281/zenodo.8301844 (DOI)
Figure: 10.5281/zenodo.8301846 (DOI)
Figure: 10.5281/zenodo.8301848 (DOI)
Figure: 10.5281/zenodo.8301850 (DOI)
Dataset: http://table.plazi.org/id/6ED75986FFD2FFF9FF8CFF12FE9DC9A4 (URL)
Is source of
Dataset: http://www.gbif.org/dataset/0e544916-1788-433e-aa13-645717cc1cd8 (URL)

References

  • Kirk, D.N., Klyne, W., 1976. Chiroptical studies. Part LXXXIX. An empirical analysis of the circular dichroism of hexahydroindanones, bicyclo[4.2.0]octan-7-ones, and their polycyclic analogs. J. Chem. Soc., Perkin Trans. 1, 762-779.
  • Krivoshchekova, O.E., Maximov, O.B., Stepanenko, L.S., Mishchenko, N.P., 1982. Quinones of the lichen Cetraria cucullata. Phytochemistry 21, 193-196.
  • Kuwahara, Y., Zhang, A., Soma, H., Tsuda, A., 2012. Photochemical molecular storage of Cl2, HCl, and COCl2: synthesis of organochlorine compounds, salts, ureas, and polycarbonate with photodecomposed chloroform. Org. Lett. 14, 3376-3379.
  • LaGreca, S., Lumbsch, H., Thorsten, K.M., Wei, X., Han, J.E., Moon, K.H., Kashiwadani, H., Aptroot, A., Leavitt, S.D., 2020. A molecular phylogenetic evaluation of the Ramalina siliquosa complex, with notes on species circumscription and relationships within Ramalina. Lichenol. 52, 197-211.
  • Lai, D., Odimegwu, D.C., Esimone, C., Grunwald, T., Proksch, P., 2013. Phenolic compounds with in vitro activity against respiratory syncytial virus from the Nigerian lichen Ramalina farinacea. Planta Med. 79, 1440-1446.
  • Le, D.H., Takenaka, Y., Hamada, N., Tanahashi, T., 2013. Eremophilane-type sesquiterpenes from cultured lichen mycobionts of Sarcographa tricosa. Phytochemistry 91, 242-248.
  • Le Pogam, P., Boustie, J., 2016. Xanthones of lichen source: a 2016 update. Molecules 21 (3), 294.
  • Li, X.-B., Zhou, Y.-H., Zhu, R.-X., Chang, W.-Q., Yuan, H.-Q., Gao, W., Zhang, L.-L., Zhao, Z.-T., Lou, H.-X., 2015. Identification and biological evaluation of secondary metabolites from the endolichenic fungus Aspergillus versicolor. Chem. Biodivers. 12, 575-592.
  • Lubbe, M., Guetlein, J.-P., Reinke, H., Langer, P., 2008. Regioselective synthesis of polyketide-type phenols by formal [3+3]-cyclocondensations of 1,3-bis(silyloxy)- 1,3-butadienes with 3-oxo-orthoesters. Synlett 2671-2673.
  • Mie, R., Din, L.B., Samsudin, M.W., Ahmad, A., 2014. Secondary metabolite isolated from Ramalina dumeticola and its application for silver nanoparticles production. AIP Conf. Proc. 1614, 213-217. https://doi.org/10.1063/1.4895198.
  • Moroney, S.E., Ronaldson, K.J., Wilkins, A.L., Green, T.G.A., James, P.W., 1981. Depsidone constituents from the quintaria group of Nephroma species. Phytochemistry 20, 787-789.
  • Nguyen, D.M.T., Do, L.M.T., Nguyen, V.T., Chavasiri, W., Mortier, J., Nguyen, P.P.K., 2017. Phenolic compounds from the lichen Lobaria orientali s. J. Nat. Prod. 80, 261-268.
  • Snatzke, G., 1968. Circular dichroism and optical rotatory dispersion. Principles and application to the investigation of the stereochemistry of natural products. Angew. Chem., Int. Ed. Engl. 7, 14-25.
  • Spjut, R.W., 1996. Niebla and Vermilacinia (Ramalinaceae) from California and Baja California Sida, Botanica Miscellany: 14. Botanical Research Institute of Texas, Inc, pp. 207-pp.
  • Spjut, R.W., Simon, A., Guissard, M., Magain, N., S´erusiaux, E., n.d.. The fruticose genera in the Ramalinaceae (Ascomycota, Lecanoromycetes): their diversity and evolutionary history. MycoKeys 73, 1-68. doi:10.3897/mycokeys.73.47287. In press.
  • Tabacchi, R., Tsoupras, G., Huneck, S., 1987. Lichen substances. No. 148. Steroids and nortriterpenoids from lichens. J. Hattori Bot. Lab. 63, 351-355.
  • Tan, C.Y., Wang, F., Anaya-Eugenio, G.D., Gallucci, J.C., Goughenour, K.D., Rappleye, C. A., Spjut, R.W., Carcache de Blanco, E.J., Kinghorn, A.D., Rakotondraibe, L.H., 2019. α- Pyrone and sterol constituents of Penicillium aurantiacobrunneum, a fungal associate of the lichen Niebla homalea. J. Nat. Prod. 82, 2529-2536.
  • Wilkins, A.L., Bremer, J., Ralph, J., Holland, P.T., Ronaldson, K.J., Jager, P.M., Bird, P. W., 1989. A one- and two-dimensional carbon-13 and proton NMR study of some triterpenes of the hopane, stictane and flavicene groups. Aust. J. Chem. 42, 243-257.
  • Yu, X., Guo, Q., Su, G., Yang, A., Hu, Z., Qu, C., Wan, Z., Li, R., Tu, P., Chai, X., 2016. Usnic acid derivatives with cytotoxic and antifungal activities from the lichen Usnea longissima. J. Nat. Prod. 79, 1373-1380.