Biodiversity Literature Repository

Submit to community
Liberated Data
Published June 30, 2020 | Version v1
Journal article Restricted

Sesquiterpenoids from the roots of Daphne genkwa Siebold et Zucc. With potential anti-inflammatory activity

Authors/Creators

  • 1. ∗∗ & ∗ & Key Laboratory of Computational Chemistry-Based Natural Antitumor Drug Research & Development, Liaoning Province, School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, 110016, PR China

Description

Guo, Rui, Ren, Qiang, Tang, Ya-Xin, Zhao, Feng, Lin, Bin, Huang, Xiao-Xiao, Song, Shao-jiang (2020): Sesquiterpenoids from the roots of Daphne genkwa Siebold et Zucc. With potential anti-inflammatory activity. Phytochemistry (112348) 174: 1-8, DOI: 10.1016/j.phytochem.2020.112348, URL: http://dx.doi.org/10.1016/j.phytochem.2020.112348

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:FF82A11A3A4FA726FFBFE164FF89160E

Has part
Figure: 10.5281/zenodo.8294977 (DOI)
Figure: 10.5281/zenodo.8294981 (DOI)
Figure: 10.5281/zenodo.8294983 (DOI)
Figure: 10.5281/zenodo.8294985 (DOI)
Figure: 10.5281/zenodo.8294987 (DOI)
Figure: 10.5281/zenodo.8294989 (DOI)
Figure: 10.5281/zenodo.8294991 (DOI)

References

  • Baba, K., Taniguchi, M., Kozawa, M., 1992. A spirobiflavonoid genkwanol B from Daphne genkwa. Phytochemistry 31, 975-980.
  • Blay, G., Bargues, V., Cardona, L., Garcia, B., Pedro, J.R., 2001. Ultrasound-assisted reductive cleavage of eudesmane and guaiane γ- enonelactones. Tetrahedron 58, 9719-9725.
  • Bruhn, T., Schaumloffel, A., Hemberger, Y., Bringmann, G., 2013. SpecDis: quantifying the comparison of calculated and experimental electronic circular dichroism spectra. Chirality 25, 243-249.
  • Faiella, L., Temraz, A., Tommasi, N.D., Braca, A., 2012. Diterpenes, ionol-derived, and flavone glycosides from Podocarpus elongatus. Phytochemistry 76, 172-177.
  • Frisch, M.J., Trucks, G.W., Schlegel, H.B., Scuseria, G.E., Robb, M.A., Cheeseman, J.R., Scalmani, G., Barone, V., Mennucci, B., Petersson, G.A., Nakatsuji, H., Caricato, M., Li, X., Hratchian, H.P., Izmaylov, A.F., Bloino, J., Zheng, G., Sonnenberg, J.L., Hada, M., Ehara, M., Toyota, K., Fukuda, R., Hasegawa, J., Ishida, M., Nakajima, T., Honda, Y., Kitao, O., Nakai, H., Vreven, T., Montgomery, J.A., Peralta, J.E., Ogliaro, F., Bearpark, M., Heyd, J.J., Brothers, E., Kudin, K.N., Staroverov, V.N., Kobayashi, R., Normand, J., Raghavachari, K., Rendell, A., Burant, J.C., Iyengar, S.S., Tomasi, J., Cossi, M., Rega, N., Millam, J.M., Klene, M., Knox, J.E., Cross, J.B., Bakken, V., Adamo, C., Jaramillo, J., Gomperts, R., Stratmann, R.E., Yazyev, O., Austin, A.J., Cammi, R., Pomelli, C., Ochterski, J.W., Martin, R.L., Morokuma, K., Zakrzewski, V.G., Voth, G.A., Salvador, P., Dannenberg, J.J., Dapprich, S., Daniels, A.D., Farkas, O., Foresman, J.B., Ortiz, J.V., Cioslowski, J., Fox, D.J., 2013. Gaussian 09, Revision D.01. Gaussian, Inc, Wallingford, CT.
  • Fu, H.W., Zhang, L., Yi, T., Feng, Y.L., Tian, J.K., 2010. Guaiane type sesquiterpenes and other constituents from Daucus carota L. Biochem. Systemat. Ecol. 38, 309-312.
  • Goto, H., Osawa, E., 1989. Corner flapping: a simple and fast algorithm for exhaustive generation of ring conformations. J. Am. Chem. Soc. 111, 8950-8951.
  • Goto, H., Osawa, E., 2008. An efficient algorithm for searching low-energy conformers of cyclic and acyclic molecules. J. Chem. Soc. Perk. Trans. 2, 187-198.
  • Hallx, I.H., Kasai, R., Wu, R.Y., Tagahara, K., Lee, K.H., 1982. Antitumor agents LV: effects of genkwadaphnin and yuanhuacine on nucleic acid synthesis of P-388 lymphocytic leukemia cells. J. Pharmacol. Sci. 71, 1263-1267.
  • Han, B.S., Kim, K.S., Kim, Y.J., Jung, H.Y., Kang, Y.M., Lee, K.S., Sohn, M.J., Kim, C.H., Kim, K.S., Kim, W.G., 2016. Daphnane diterpenes from Daphne genkwa activate Nurr1 and have a neuroprotective effect in an animal model of Parkinson's disease. J. Nat. Prod. 79, 1604-1609.
  • He, W., Cik, M., Appendino, G., Puyvelde, L., Leysen, J.E., Kimpe, N., 2002. Daphnanetype diterpene orthoesters and their biological activities. Mini Rev. Med. Chem. 2, 185-200.
  • Kim, D.C., Kim, J.A., Min, B.S., Jang, T.S., Na, M., Lee, S.H., 2010. Guaiane sesquiterpenoids isolated from the fruits of Torilis japonica and their cytotoxic activity. Helv. Chim. Acta 93, 692-697.
  • Nawamaki, K., Kuroyanagi, M., 1996. Sesquiterpenoids from Acorus calamus as germination inhibitors. Phytochemistry 43, 1175-1182.
  • Okunishi, T., Umezawa, T., Shimada, M., 2001. Isolation and enzymatic formation of lignans of Daphne genkwa and Daphne odora. J. Wood Sci. 47, 383-388.
  • Park, B.Y., Min, B.S., Oh, S.R., Kim, J.H., Bae, K.H., Lee, H.K., 2006. Isolation of flavonoids, a biscoumarin and an amide from the flower buds of Daphne genkwa and the evaluation of their anti-complement activity. Phytother Res. 20, 610-613.
  • Tezuka, Y., Tasaki, M., Huang, Q., Hatanaka, Y., Kikuchi, T., 2010. 15- Hydroxyacorenone: new acorane-type sesquiterpene from the culture broth of the mycoparasitic fungus Trichoderma harzianum. Liebigs Ann. 12, 2579-2580.
  • Zaki, M.H., Akuta, T., Akaike, T., 2005. Nitric oxide-induced nitrative stress involved in microbial pathogenesis. J. Pharmacol. Sci. 98, 117-129.
  • Zhan, Z.J., Fan, C.Q., Ding, J., Yue, J.M., 2005. Novel diterpenoids with potent inhibitory activity against endothelium cell HMEC and cytotoxic activities from a well-known TCM plant Daphne genkwa. Bioorg. Med. Chem. 13, 645-655.
  • Zheng, W., Gao, X., Gu, Q., Chen, C., Wei, Z., Shi, F., 2007. Antitumor activity of daphnodorins from Daphne genkwa roots. Int. Immunopharm. 7, 128-134.