Publication Cover
Natural Product Research
Formerly Natural Product Letters
Volume 36, 2022 - Issue 8
240
Views
0
CrossRef citations to date
0
Altmetric
Research Articles

Isolation of a new monoterpenoid glycoside from Anhua dark tea based on an NMR-guided method and its cytotoxic activity against MDA-MB-231 and SH-SY5Y cell lines

, ORCID Icon, , , , , , , & show all
Pages 2015-2020 | Received 23 Aug 2020, Accepted 16 Oct 2020, Published online: 04 Nov 2020

References

  • Deng KZ, Xiong Y, Gao WY. 2009. Chemical constituents of Lobelia chinensis. Chin Tradit Herbal Drugs. 40(8):1198–1201.
  • Fan W, Tezuka Y, Ni KM, Kadota S. 2001. Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis. Chem Pharm Bull (Tokyo). 49(4):396–401.
  • Ha TJ, Lee JH, Hwang SW, Lee J, Kang NS, Park KY, Suh DY, Park KH, Yang MS. 2006. Two acylglycerylgalactosides and a new sesquiterpene galactoside from the flowers of Hemisteptia lyrata Bunge. Agric Chem Biotechnol. 49(1):16–20.
  • Han F, Li YT, Ma L, Liu TF, Wu YW, Xu R, Song AH, Yin R. 2016. A rapid and sensitive UHPLC-FT-ICR MS/MS method for identification of chemical constituents in Rhodiola crenulata extract, rat plasma and rat brain after oral administration. Talanta. 160:183–193.
  • Kawagishi H, Murakami H, Sakai S, Inoue S. 2006. Carnitine-esters from the mushroom Suillus laricinus. Phytochemistry. 67(24):2676–2680.
  • Lehbili M, Magid AA, Kabouche A, Voutquenne-Nazabadioko L, Morjani H, Harakat D, Kabouche Z. 2018. Triterpenoid saponins from Scabiosa stellata collected in North-eastern Algeria. Phytochemistry. 150:40–49.
  • Lia ZJ, Wan CP, Cai L, Li SQ, Zheng X, Qi Y, Dong JW, Yin TP, Zhou ZX, Tan NH, Ding ZT. 2015. Terpenoids with cytotoxic activity from the branches and leaves of Pyrus pashia. Phytochem Lett. 13:246–251.
  • Liu JY, Fan YH, Kim D, Zhong T, Yi P, Fan CC, Wang AD, Yang XS, Lee S, Ren XH, et al. 2019. Neuroprotective effect of catechins derivatives isolated from Anhua dark tea on NMDA-induced excitotoxicity in SH-SY5Y cells. Fitoterapia. 137:104240.
  • Liu JY, Liu D, Zhang H, Ren XH, Xu YN. 2017. Research progress on chemical constituents of Anhua dark tea and their activities. Chin Tradit Herbal Drugs. 48(7):1449–1457.
  • Liu JY, Zhong T, Yi P, Fan CC, Zhang Z, Liang GY, Xu YN, Fan YH. 2020. A new epigallocatechin gallate derivative isolated from Anhua dark tea sensitizes the chemosensitivity of gefitinib via the suppression of PI3K/mTOR and epithelial-mesenchymal transition. Fitoterapia. 143:104590.
  • Lv HP, Zhang YJ, Zhi L, Liang YR. 2013. Processing and chemical constituents of Pu-erh tea: a review. Food Res Int. 53(2):608–618.
  • Manns D. 1995. Linalool and cineole type glucosides from Cunila spicata. Phytochemistry. 39(5):1115–1118.
  • Moon JH, Watanabe N, Sakata K, Yagi A, Ina K, Luo SJ. 1994. Trans- and cis-linalool 3,6-oxide 6-O-beta-D-xylopyranosyl-beta-D-glucopyranosides isolated as aroma precursors from leaves for oolong tea. Biosci Biotechnol Biochem. 58(9):1742–1744.
  • Sakurai K, Takahashi K, Yoshida T. 1983. Two new m-cresol derivatives and a new terpene alcohol from peppermint oil. Agric Biol Chem. 47(6):1249–1256.
  • Wang AD, Bao Y, Liu D, Wang X, Li MC, Liu JY, Xu YN. 2018. Isolation and structure determination of new saponins from Pulsatilla cernua based on an NMR-guided method and their anti-proliferative activities. Phytochem Lett. 27:9–14.
  • Wang W, Chen W, Yang YS, Liu TX, Yang HY, Xin ZH. 2015. New phenolic compounds from Coreopsis tinctoria Nutt. and their antioxidant and angiotensin I-converting enzyme inhibitory activities. J Agric Food Chem. 63(1):200–207.
  • Yang Z, Wu YQ, Zhou H, Cao XJ, Jiang XH, Wang KW, Wu SH. 2015. A novel strategy for screening new natural products by a combination of reversed-phase liquid chromatography fractionation and 13C NMR pattern recognition: the discovery of new anticancer flavone dimers from Dysosma versipellis (Hance). RSC Adv. 5(95):77553–77564.
  • Yu Y, Gao H, Dai Y, Wang Y, Chen HR, Yao XS. 2010. Monoterpenoids from the fruit of Gardenia jasminoides. HCA. 93(4):763–771.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.