Published April 30, 2020 | Version v1
Journal article Restricted

Anti-inflammatory quinoline alkaloids from the root bark of Dictamnus dasycarpus

Description

Gao, Peng, Wang, Ling, Zhao, Lin, Zhang, Qing-ying, Zeng, Ke-wu, Zhao, Ming-bo, Jiang, Yong, Tu, Peng-fei, Guo, Xiao-yu (2020): Anti-inflammatory quinoline alkaloids from the root bark of Dictamnus dasycarpus. Phytochemistry (112260) 172: 1-7, DOI: 10.1016/j.phytochem.2020.112260, URL: http://dx.doi.org/10.1016/j.phytochem.2020.112260

Files

Restricted

The record is publicly accessible, but files are restricted. <a href="https://zenodo.org/account/settings/login?next=https://zenodo.org/records/8294080">Log in</a> to check if you have access.

Linked records

Additional details

Identifiers

LSID
urn:lsid:plazi.org:pub:8658FFB1FF9FFFFFF267FFF7CF22DD65

References

  • Mara, S.P., Arruda, M., Fatimadas, G.F., Da Silva, Vieira, Paula C., Pirani, Jose R., 1992. Quinolone alkaloids from zanzboxylum acutifoliuiw. Phytochemistry 31, 3617-3619. http://dx.doi.org/10.1016/0031-9422(92)83738-K.
  • Campbell, W.E., Davidowitz, B., Jackson, G.E., 1990. Quinolinone alkaloids from an Agathosma species. Phytochemistry 29, 1303-1306. https://doi.org/10.1016/0031- 9422(90)85447-n.
  • Chen, I.S., Chen, H.F., Cheng, M.J., Chang, Y.L., Teng, C.M., Tsutomu, I., 2001. Quinoline alkaloids and other constituents of melicope semecarpifolia with antiplatelet aggregation activity. J. Nat. Prod. 64, 1143. https://doi.org/10.1021/np010122k.
  • China Pharmacopoeia Committee, 2015. Pharmacopoeia of the People's Republic of China, vol. I. China Chemical Industry Press, Beijing, pp. 110-111.
  • Coppola, G.M., Kahle, A.D., Shapiro, M.J., 2005. 13C NMR investigation of some hetero- ring substituted 2- and 4-quinolone systems. Magn. Reson. Chem. 17, 242-245. https://doi.org/10.1002/mrc.1270170404.
  • Corral, R.A., Orazi, O.O., Benages, I.A., 1973. New balfourodendron 4-quinolone alkaloids. Tetrahedron 29, 205-211. https://doi.org/10.1016/S0040-4020(01)99397-4.
  • Cuca-Suarez, L.E., Elkin Pattarroyo, M., Lozano, J.M., Monache, F.D., 2009. Biological activity of secondary metabolites from peltostigma guatemalense. Nat. Prod. Res. 23, 370-374. http://dx.doi.org/10.1080/14786410802228439.
  • Cuca-Suarez, L.E., Barrera, E.D.C., Caballero, J.M.A., 2011. Quinoline alkaloids and friedelane-type triterpenes isolated from leaves and wood of Esenbeckia alata kunt (Rutaceae). Quim. Nova 34, 984-986. https://doi.org/10.1590/S0100- 40422011000600013.
  • Du, C.F., Yang, X.X., Tu, P.F., 2005. Studies on chemical constituents in bark of dictamnus dasycarpus. China. J. Chin. Mater. Med. 21, 1663-1666 PMID: 16400943.
  • Fauvel, M.T., Gleye, J., Moulis, C., Blasco, F., Stanislas, E., 1981. Alkaloids and flavonoids of Melicope indica. Phytochemistry 20 (8), 2059-2060. https://doi.org/10.1016/ 0031-9422(81)84078-2.
  • Gao, P., Wang, L., Zhao, L., Zhang, C., Zeng, K.W., Zhao, M.B., Zhang, Q.Y., Jiang, Y., Tu, P.F., Guo, X.Y., 2019. Three new compounds from Dictamnus dasycarpus and their anti-inflammatory activities. J. Asian Nat. Prod. Res. 30, 1-8. https://doi.org/10. 1080/10286020.2019.1620213.
  • Jeong, G.S., Byun, E., Li, B., Lee, D.S., 2010. Neuroprotective effects of constituents of the root bark of Dictamnus dasycarpus in mouse hippocampal cells. Arch Pharm. Res. (Seoul) 33, 1269-1275. https://doi.org/10.1007/s12272-010-0818-9.
  • Liu, Y., Zhang, X.J., Kelsang, N., Tu, G.A., Kong, D.X., Lu, J.H., Zhang, Y.T., Liang, H., Tu, P.F., Zhang, Q.Y., 2018. Structurally diverse cytotoxic dimeric chalcones from Oxytropis chiliophylla. J. Nat. Prod. 81, 307-315. https://doi.org/10.1021/acs. jnatprod.7b00736.
  • Lv, M.Y., Xu, P., Tian, Y., Liang, J.Y., Gao, Y.Q., Xu, F.G., Zhang, Z.J., Sun, J.B., 2015. Medicinal uses, phytochemistry and pharmacology of the genus Dictamnus (Rutaceae). J. Ethnopharmacol. 171, 247-263. https://doi.org/10.1016/j.jep.2015. 05.053.
  • Lv, H.N., Wang, S., Zeng, K.W., Li, J., Guo, X.Y., Jiang, Y., Tu, P.F., 2015. Anti-inflammatory coumarin and benzocoumarin derivatives from Murraya alata. J. Nat. Prod. 78, 279-285. https://doi.org/10.1021/np500861u.
  • Poplata, A., Troster, A., Zou, Y.Q., Bach, T., 2016. Recent advances in the synthesis of cyclobutanes by olefin [2 + 2] photocycloaddition reactions. Chem. Rev. 116, 9748-9815. https://doi.org/10.1021/acs.chemrev.5b00723.
  • Shin, H.K., Do, J.C., Son, J.K., 1998. Quinoline alkaloids from the fruits of Evodia officinalis. Planta Med. 64, 764. http://dx.doi.org/10.1055/s-2006-957579.
  • Song, W.W., Zeng, G.Z., Peng, W.W., Chen, K.X., Tan, N.H., 2014. Cytotoxic amides and quinolones from Clausena lansium. Helv. Chim. Acta 97, 298-305. http://dx.doi.org/ 10.1002/hlca.201300323.
  • Souleles, C., 1989. Flavonoids from Dictamnus albus. Planta Med. 55, 402. http://dx.doi. org/10.1016/0031-9422(90)85447-N.
  • Storer, R., Young, D.W., 1973. Constituents of the root of Dictamnus albus L. Tetrahedron 29, 1217-1222. http://dx.doi.org/10.1016/0040-4020(73)80105-X.
  • Sun, J., Qu, W., Wang, P., 2013a. Degraded limonoids and quinoline alkaloids from Dictamnus angustifolius G. Don ex Sweet. and their anti-platelet aggregation activity. Fitoterapia 90, 209-213. http://dx.doi.org/10.1016/j.fitote.2013.07.023.
  • Sun, J., Qu, W., Xiong, Y., 2013b. Quinoline alkaloids and sesquiterpenes from the roots of Dictamnus angustifolius. Biochem. Syst. Ecol. 50, 62-64. http://dx.doi.org/10. 1016/j.bse.2013.03.036.
  • Varamini, P., Javidnia, K., Soltani, M., Mehdipour, A.R., Ghaderi, A., 2009. Cytotoxic activity and cell cycle analysis of quinoline alkaloids isolated from Haplophyllum canaliculatum Boiss. Planta Med. 75, 1509-1516. https://doi.org/10.1055/s-0029- 1185807.
  • Yang, G.H., Chen, D.F., 2008. Alkaloids from the roots of Zanthoxylum nitidum and their antiviral and antifungal effects. Chem. Biodivers. 5, 1718-1722. https://doi.org/10. 1002/cbdv.200890160.
  • Yang, J.L., Liu, L.L., Shi, Y.P., 2011. Limonoids and quinoline alkaloids from Dictamnus dasycarpus. Planta Med. 77, 271-276. https://doi.org/10.1055/s-0030-1250344.
  • Yoon, J.S., Jeong, E.J., Yang, H., Kim, S.H., Sung, S.H., Kim, Y.C., 2012. Inhibitory alkaloids from Dictamnus dasycarpus root barks on lipopolysaccharide-induced nitric oxide production in BV2 cells. J. Enzym. Inhib. Med. Chem. 27, 490-494. https://doi. org/10.3109/14756366.2011.598151.
  • Yu, X.L., Scheller, D., Rademacher, O., Wolff, T., 2003. Selectivity in the photodimerization of 6-alkylcoumarins. J. Org. Chem. 68, 7386-7399. https://doi.org/10. 1021/jo034627m.
  • Zhao, W.M., Wolfender, J.L., Hostettmann, K., Xu, R.S., Qin, G.W., 1998. Antifungal alkaloids and limonoid derivatives from Dictamnus dasycarpus. Phytochemistry 47 (1), 7-11. https://doi.org/10.1016/S0031-9422(97)00541-4.
  • Ziegler, E., Kappe, T., 1965. Synthesen von Heterocyclen, 69. Mitt.: Uber eine Synthese des Indigotins. Monatsh.Chem. 96, 889-895. http://dx.doi.org/10.1007/ BF00905258.