Published October 31, 2022
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Anti-neuroinflammatory 3-hydroxycoumaronochromones and isoflavanones enantiomers from the fruits of Ficus altissima Blume
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- 1. ** & * & School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, 510006, China
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Yao, Jiaming, Qin, Qiuyi, Wang, Yihai, Zeng, Jia, Xu, Jingwen, He, Xiangjiu (2022): Anti-neuroinflammatory 3-hydroxycoumaronochromones and isoflavanones enantiomers from the fruits of Ficus altissima Blume. Phytochemistry (113313) 202: 1-8, DOI: 10.1016/j.phytochem.2022.113313, URL: http://dx.doi.org/10.1016/j.phytochem.2022.113313
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- urn:lsid:plazi.org:pub:C33DFFCA312EFFD4A85DFFF2FFF64029
References
- Boyd, A., Byrne, S., Middleton, R.J., Banati, R.B., Liu, G.J., 2021. Control of neuroinflammation through radiation-induced microglial changes. Cells 10, 2381. https://doi.org/10.3390/cells10092381.
- Chalifoux, A.M., Boles, G.C., Berden, G., Oomens, J., Armentrout, P.B., 2018. Experimental and theoretical investigations of infrared multiple photon dissociation spectra of arginine complexes with Zn(2+ ) and Cd(2). Phys. Chem. Chem. Phys. 20, 20712-20725. https://doi.org/10.1039/C8CP03484B.
- Cheng, J., Yi, X., Wang, Y., Huang, X., He, X., 2017. Phenolics from the roots of hairy fig (Ficus hirta Vahl.) exert prominent anti-inflammatory activity. J. Funct.Foods 31, 79-88. https://doi.org/10.1016/j.jff.2017.01.035.
- Dai, J., Shen, D., Yoshida, W., Parrish, S., Williams, P., 2012. Isoflavonoids from Ficus benjamina and their inhibitory activity on BACE1. Planta Med. 78, 1357-1362. https://doi.org/10.1055/s-0032-1315001.
- Dai, L., Yang, H., Zhao, X., Wang, L., 2021. Identification of cis conformation natural rubber and proteins in Ficus altissima Blume latex. Plant Physiol. Biochem. (Amsterdam, Neth.) 167, 376-384. https://doi.org/10.1016/j.plaphy.2021.08.015.
- Kittakoop, P., 2014. α -Glucosidase inhibitory activities of isoflavanones, isoflavones, and pterocarpans from Mucuna pruriens. Planta Med. 80, 604-608. https://doi.org/ 10.1055/s-0034-1368427.
- Deng, Y.T., Liang, G., Shi, Y., Li, H.L., Zhang, J., Mao, X.M., Fu, Q.R., Peng, W.X., Chen, Q.X., Shen, D.Y., 2016. Condensed tannins from Ficus altissima leaves: structural, antioxidant, and antityrosinase properties. Process Biochem. 51, 1092-1099. https://doi.org/10.1016/j.procbio.2016.04.022.
- Dheen, S.T., Kaur, C., Ling, E.A., 2007. Microglial activation and its implications in the brain diseases. Curr. Med. Chem. 14, 1189-1197. https://doi.org/10.2174/ 092986707780597961.
- DuBois, J., Sneden, A., 1996. Ferreirinol, a new 3-hydroxyisoflavanone from Swartzia polyphylla. J. Nat. Prod. 59, 902-903. https://doi.org/10.1021/np960122y.
- Fan, J.R., Kuang, Y., Dong, Z.Y., Yi, Y., Zhou, Y.X., Li, B., Qiao, X., Ye, M., 2020. Prenylated phenolic compounds from the aerial parts of Glycyrrhiza uralensis as PTP1B and α -glucosidase inhibitors. J. Nat. Prod. 83, 814-824. https://doi.org/ 10.1021/acs.jnatprod. 9b00262.
- Grimblat, N., Zanardi, M.M., Sarotti, A.M., 2015. Beyond DP4: an improved probability for the stereochemical assignment of isomeric compounds using quantum chemical calculations of NMR shifts. J. Org. Chem. 80, 12526-12534. https://doi.org/ 10.1021/acs.joc.5b02396.
- Lapˇcik, O., 2007. Isoflavonoids in non-leguminous taxa: a rarity or a rule? Phytochemistry 68, 2909-2916. https://doi.org/10.1016/j. phytochem.2007.08.006.
- Luo, H., Wang, Y., Qin, Q., Wang, Y., Xu, J., He, X., 2021. Anti-inflammatory naphthoates and anthraquinones from the roots of Morinda officinalis. Bioorg. Chem. 110, 104800 https://doi.org/10.1016/j.bioorg.2021.104800.
- Mai, Y., Wang, Z., Wang, Y., Xu, J., He, X., 2020. Anti-neuroinflammatory triterpenoids from the seeds of Quercus serrata Thunb. Fitoterapia 142, 104523. https://doi.org/ 10.1016/j.fitote.2020.104523.
- Osawa, K., Yasuda, H., Maruyama, T., Morita, H., Takeya, K., Itokawa, H., 1992. Isoflavanones from the heartwood of Swartzia polyphylla and their antibacterial activity against cariogenic bacteria. Chem. Pharm. Bull. 40, 2970-2974. https://doi. org/10.1248/cpb.40.2970.
- Seo, Y.H., Jeon, J.H., Jeong, M., Ryu, S.M., Jeon, W.K., Jang, D.S., Shim, S.H., Lee, D., Choi, J.H., Lee, J., 2018. Chemical constituents of Apios americana tubers and their inhibitory activities on nitric oxide production in lipopolysaccharide-stimulated RAW 264.7 macrophages. J. Nat. Prod. 81, 1598-1603. https://doi.org/10.1021/ acs.jnatprod. 8b00182.
- Slade, D., Ferreira, D., Marais, J.P.J., 2005. Circular dichroism, a powerful tool for the assessment of absolute configuration of flavonoids. Phytochemistry 66, 2177-2215. https://doi.org/10.1016/j.phytochem.2005.02.002.
- Smith, S.G., Goodman, J.M., 2010. Assigning stereochemistry to single diastereoisomers by GIAO NMR calculation: the DP4 probability. J. Am. Chem. Soc. 132, 12946-12959. https://doi.org/10.1021/ja105035r.
- Wang, Y., Lei, Y., Huang, Y., Wang, Z., Xu, J., He, X., 2020. Jasmonates from Chinese acorns (Quercus serrata var. brevipetiolata) exert pronounced anti-neuroinflammatory activities. Bioorg. Chem. 103, 104143 https://doi.org/10.1016/j. bioorg.2020.104143.
- Xiang, L., Wang, Y., Yi, X., He, X., 2018. Anti-inflammatory steroidal glycosides from the berries of Solanum nigrum L. (European black nightshade). Phytochemistry 148, 87-96. https://doi.org/10.1016/j.phytochem.2018.01.019.
- Xu, X., Huang, Y., Xu, J., He, X., Wang, Y., 2020. Anti-neuroinflammatory and antioxidant phenols from mulberry fruit (Morus alba L.). J. Funct.Foods 68, 103914. https://doi.org/10.1016/j.jff.2020.103914.
- Yao, J., Wang, Z., Wang, R., Wang, Y., Xu, J., He, X., 2021. Anti-proliferative and anti-inflammatory prenylated isoflavones and coumaronochromones from the fruits of Ficus altissima. Bioorg. Chem. 113, 104996 https://doi.org/10.1016/j. bioorg.2021.104996.
- Zhang, D.L., Feng, Y.H., Liang, Z.Y., Lin, Q., Xu, J., 2012. Chemical composition of essential oil from fruit of Ficus altissima. Adv. Mater. Res. 554-556, 1125-1128. https://doi.org/10.4028/www.scientific.net/AMR.554-556.1125.
- Zhao, M., Duan, J.A., Che, C.T., 2007. Isoflavanones and their O -glycosides from Desmodium styracifolium. Phytochemistry 68, 1471-1479. https://doi.org/10.1016/j. phytochem.2007.02.015.
- Zheng, X., Kadir, A., Zheng, G., Jin, P., Qin, D., Maitinuer, M., Aisa, H., Yao, G., 2020. Antiproliferative abietane quinone diterpenoids from the roots of Salvia deserta. Bioorg. Chem. 104, 104261 https://doi.org/10.1016/j.bioorg.2020.104261.