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Natural Product Research
Formerly Natural Product Letters
Volume 38, 2024 - Issue 7
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Research Articles

A new diterpenoid from the leaves and twigs of Croton lachnocarpus Benth

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Pages 1184-1190 | Received 01 Aug 2022, Accepted 05 Oct 2022, Published online: 19 Oct 2022

References

  • Cooper JF, Dues DJ, Spielbauer KK, Machiela E, Senchuk MM, Van Raamsdonk JM. 2015. Delaying aging is neuroprotective in Parkinson’s disease: a genetic analysis in C. elegans models. Npj Parkinson’s Dis. 1:15022.
  • Flora of China Editorial Board of Chinese Academy of Sciences 1996a. Flora of China (Zhongguo Zhiwu Zhi). Vol. 44(2). Beijing: Science Press; p. 123.
  • Flora of China Editorial Board of Chinese Academy of Sciences 1996b. Flora of China (Zhongguo Zhiwu Zhi). Vol. 44(2). Beijing: Science Press; p. 131.
  • Fu RH, Harn HJ, Liu SP, Chen CS, Chang WL, Chen YM, Huang JE, Li RJ, Tsai SY, Hung HS, et al. 2014. n-Butylidenephthalide protects against dopaminergic neuron degeneration and α-synuclein accumulation in Caenorhabditis elegans models of Parkinson’s disease. PLoS One. 9(1):e85305.
  • González-Hunt CP, Leung MCK, Bodhicharla RK, McKeever MG, Arrant AE, Margillo KM, Ryde IT, Cyr DD, Kosmaczewski SG, Hammarlund M, et al. 2014. Exposure to mitochondrial genotoxins and dopaminergic neurodegeneration in Caenorhabditis elegans. PLoS One. 9(12):e114459.
  • Kaletta T, Hengartner MO. 2006. Finding function in novel targets: C. elegans as a model organism. Nat Rev Drug Discov. 5(5):387–398.
  • Kuo PC, Yang ML, Hwang TL, Lai YY, Li YC, Thang TD, Wu TS. 2013. Anti-inflammatory diterpenoids from Croton tonkinensis. J Nat Prod. 76(2):230–236.
  • Lehtonen Š, Jaronen M, Vehviläinen P, Lakso M, Rudgalvyte M, Keksa-Goldsteine V, Wong G, Courtney MJ, Koistinaho J, Goldsteins G. 2016. Inhibition of excessive oxidative protein folding is protective in MPP+ toxicity-induced Parkinson’s disease models. Antioxid Redox Signal. 25(8):485–497.
  • Li CJ, Sun X, Yin WJ, Zhan ZC, Tang Q, Wang WZ, Zhuo XF, Wu ZN, Zhang HP, Li YL, et al. 2021. Crassifolins Q − W: clerodane diterpenoids from Croton crassifolius with anti-inflammatory and anti-angiogenesis activities. Front Chem. 9:733350.
  • Liu CP, Xu JB, Zhao JX, Xu CH, Dong L, Ding J, Yue JM. 2014. Diterpenoids from Croton laui and their cytotoxic and antimicrobial activities. J Nat Prod. 77(4):1013–1020.
  • Mbwambo ZH, Foubert K, Chacha M, Kapingu MC, Magadula JJ, Moshi MM, Lemière F, Goubitz K, Fraanje J, Peschar R, et al. 2009. New furanoditerpenoids from Croton jatrophoides. Planta Med. 75(3):262–267.
  • Palmeira Júniora SF, Conserva LM, Barbosa Filho JM. 2006. Clerodane diterpenes from Croton species: distribution and a compilation of their 13C NMR spectral data. Nat Prod Commun. 1(4):319–344.
  • Pan ZH, Ning DS, Liu JL, Pan B, Li DP. 2014. A new triterpenoid saponin from the root of Croton lachnocarpus Benth. Nat Prod Res. 28(1):48–51.
  • Pan ZH, Ning DS, Wu XD, Huang SS, Li DP, Lv SH. 2015. New clerodane diterpenoids from the twigs and leaves of Croton euryphyllus. Bioorg Med Chem Lett. 25(6):1329–1332.
  • Rajachan OA, Lakornwong W, Pitchuanchom S, Suchaichit NP, Boonmak J, Youngme S, Kanokmedhakul K, Kanokmedhakul S. 2021. ent-clerodane diterpenoids from the stems of Croton krabas. Fitoterapia. 152:104912.
  • Rodríguez B, Jimeno ML. 2004. 1H and 13C NMR spectral assignments and conformational analysis of 14 19-nor-neoclerodane diterpenoids. Magn Reson Chem. 42(7):605–616.
  • Sul YH, Lee MS, Cha EY, Thuong PT, Khoi NM, Song IS. 2013. An ent-kaurane diterpenoid from Croton Tonkinensis induces apoptosis by regulating AMP-activated protein kinase in SK-HEP1 human hepatocellular carcinoma cells. Biol Pharm Bull. 36(1):158–164.
  • Sun YH, Wang MC, Ren QH, Li S, Xu J, Ohizumi Y, Xie CF, Jin DQ, Guo YQ. 2014. Two novel clerodane diterpenenes with NGF-potentiating activities from the twigs of Croton yanhuii. Fitoterapia. 95:229–233.
  • Xu WH, Liu WY, Liang Q. 2018. Chemical constituents from Croton species and their biological activities. Molecules. 23(9):2333.

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