Published September 30, 2020 | Version v1

Mexicanolide-type limonoids from the twigs and leaves of Cipadessa baccifera

  • 1. ∗ & Key Laboratory of Tropical Plant Resources and Sustainable Use, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Menglun, 666303, PR China & University of Chinese Academy of Sciences, Beijing, 100049, PR China & Department of Ecogenomics and Systems Biology, University of Vienna, Althanstrasse 14, Vienna, 1090, Austria

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Cao, Dong-Hua, Liao, Shang-Gao, Sun, Peng, Xiao, Yi-Dian, Xiao, Chun-Fen, Hu, Hua-Bin, Weckwerth, Wolfram, Xu, You-Kai (2020): Mexicanolide-type limonoids from the twigs and leaves of Cipadessa baccifera. Phytochemistry (112449) 177: 1-10, DOI: 10.1016/j.phytochem.2020.112449, URL: http://dx.doi.org/10.1016/j.phytochem.2020.112449

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urn:lsid:plazi.org:pub:F342FFED210D403DFFFA7C0F2E39D809

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Figure: 10.5281/zenodo.8295925 (DOI)
Figure: 10.5281/zenodo.8295927 (DOI)
Figure: 10.5281/zenodo.8295929 (DOI)

References

  • Bandi, A.K.R., Lee, D.U., 2012. Secondary metabolites of plants from the genus Cipadessa: chemistry and biological activity. Chem. Biodivers. 9, 1403-1421.
  • Chen, S.K., Chen, B.Y., Li, H., 1997. Chinese Flora (Zhongguo Zhiwu Zhi), vol. 43. Science Press, Beijing, pp. 60.
  • Ellman, G.L., Courtney, K.D., Andres Jr., V., Featherstone, R.M., 1961. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem. Pharmacol. 7, 88-95.
  • Gan, L.S., Wang, X.N., Wu, Y., Yue, J.M., 2007. Tetranortriterpenoids from Cipadessa baccifera. J. Nat. Prod. 70, 1344-1347.
  • Harada, N., Nakanishi, K., 1983. Circular Dichroic Spectroscopy-Exciton Coupling in Organic Stereochemistry. University Science Books (Mill Valley).
  • Jiangsu New Medical College, 1977. Dictionary of Chinese Materia Medica. Shanghai Science and Technology Press, Shanghai 2, pp. 2183.
  • Leite, A.C., Fernandes, J.B., da Silva, M., Vieira, P.C., 2005. Limonoids from Cipadessa fruticosa. Z. Naturforsch. B Chem. Sci.: Biosci. 60, 351-355.
  • Li, G.J., Dong, Q.E., Ma, L., Huang, Y., Zhu, M.L., Ji, Y.P., Wang, Q.H., Mo, M.H., Zhang, K.Q., 2014. Management of Meloidogyne incognita on tomato with endophytic bacteria and fresh residue of Wasabia japonica. J. Appl. Microbiol. 117, 1159-1167.
  • Li, M.Y., Yang, X.B., Pan, J.Y., Feng, G., Xiao, Q., Sinkkonen, J., Satyanandamurty, T., Wu, J., 2009. Granatumins A-G, limonoids from the seeds of a krishna mangrove, Xylocarpus granatum. J. Nat. Prod. 72, 2110-2114.
  • Liao, S.G., Chen, H.D., Yue, J.M., 2009. Plant orthoesters. Chem. Rev. 109, 1092-1140.
  • Lightner, D.A., Gurst, J.E., 2000. Organic Conformational Analysis and Stereochemistry from Circular Dichroism Spectroscopy. Wiley, New York.
  • Malarvannan, S., Giridharan, R., Sekar, S., Prabavathy, V., Nair, S., 2009. Ovicidal activity of crude extracts of few traditional plants against Helicoverpa armigera (Hubner) (Noctuidae: Lepidoptera). J. Biopestic. 2, 64-71.
  • Mootoo, B.S., Ramsewak, R., Khan, A., Tinto, W.F., Reynolds, W.F., McLean, S., Yu, M., 1996. Tetranortriterpenoids from Ruagea glabra. J. Nat. Prod. 59, 544-547.
  • Pennington, T.D., Styles, B.T., 1975. A generic monograph of the Meliaceae. Blumea 22, 419-540.
  • Pescitelli, G., Bruhn, T., 2016. Good computational practice in the assignment of absolute configurations by TDDFT calculations of ECD spectra. Chirality 28, 466-474.
  • Ram, A.J., Bhakshu, L.M., Raju, R.V., 2004. In vitro antimicrobial activity of certain medicinal plants from eastern ghats, India, used for skin diseases. J. Ethnopharmacol. 90, 353-357.
  • Rao, M.M., Krishna, E.M., Gupta, P.S., Singh, P.P., 1978. New tetranortriterpenoid isolated from heartwood of Soymida febrifuga. Indian J. Chem. B 16, 823-825.
  • Reed, L., Muench, H., 1938. A simple method for determining 50 per cent endpoints. Am. J. Hyg. 27, 493-497.
  • Siva, B., Poornima, B., Venkanna, A., Prasad, K.R., Sridhar, B., Nayak, V.L., Ramakrishna, S., Babu, K.S., 2014. Methyl angolensate and mexicanolide-type limonoids from the seeds of Cipadessa baccifera. Phytochemistry 98, 174-182.
  • Siva, B., Venkanna, A., Poornima, B., Divya, R.S., Boustie, J., Bastien, S., Jain, N., Usha, R.P., Suresh, B.K., 2017. New seco-limonoids from Cipadessa baccifera: isolation, structure determination, synthesis and their antiproliferative activities. Fitoterapia 117, 34.
  • Sun, D.M., An, F.L., Wei, S.S., Zhang, Y.Q., Wang, X.B., Luo, J., Kong, L.Y., 2018. Cipadessains A-K, eleven limonoids from the fruits of Cipadessa cinerascens. RSC Adv. 8 (19), 10437-10445.
  • Tan, Q.G., Luo, X.D., 2011. Meliaceous limonoids: chemistry and biological activities. Chem. Rev. 111, 7437-7522.
  • Wang, H.Y., Wang, J.S., Shan, S.M., Wang, X.B., Luo, J., Yang, M.H., Kong, L.Y., 2013. Chemical constituents from Trichilia connaroides and their nitric oxide production and α -glucosidase inhibitory activities. Planta Med. 79, 1767-1774.
  • Yu, J.H., Wang, G.C., Han, Y.S., Wu, Y., Wainberg, M.A., Yue, J.M., 2015. Limonoids with anti-HIV activity from Cipadessa cinerascens. J. Nat. Prod. 78, 1243-1252.
  • Yu, J.H., Zhou, B., Dalal, S., Liu, Q.F., Cassera, M.B., Yue, J.M., 2018. Cipaferoids A-C, three limonoids represent two different scaffolds from Cipadessa baccifera. Chin. J. Chem. 36, 124-128.
  • Zheng, G.W., Luo, S.H., Li, S.F., Hua, J., Li, W.Q., Li, S.H., 2018. Specialized metabolites from Ageratina adenophora and their inhibitory activities against pathogenic fungi. Phytochemistry 148, 57-62.