Nucleoside alkaloids with anti-platelet aggregation activity from the rhizomes of Ligusticum striatum

References

• Abou-Hussein DR, Badr JM, Youssef DT. 2014. Dragmacidoside: a new nucleoside from the Red Sea sponge Dragmacidon coccinea. Nat Prod Res. 28(15):1134–1141.10.1080/14786419.2014.915828
   PubMed Web of Science ®Google Scholar
• Cai X, Chen Z, Pan X, Xia L, Chen P, Yang Y, Hu H, Zhang J, Li K, Ge J, et al. 2014. Inhibition of angiogenesis, fibrosis and thrombosis by tetramethylpyrazine: mechanisms contributing to the SDF-1/CXCR4 axis. PLoS One. 9(2):e88176.10.1371/journal.pone.0088176
   PubMed Web of Science ®Google Scholar
• Chang XL, Jiang ZY, Ma YB, Zhang XM, Tsim KW, Chen JJ. 2009. Two new compounds from the roots of Ligusticum chuanxiong. J Asian Nat Prod Res. 11(9):805–810.10.1080/10286020903071068
   PubMed Web of Science ®Google Scholar
• Chen L, Liu T, Wang Q, Liu J. 2017. Anti-inflammatory effect of combined tetramethylpyrazine, resveratrol and curcumin in vivo. BMC Complement Altern Med. 17(1):767.10.1186/s12906-017-1739-7
   Google Scholar
• Downey AM, Richter C, Pohl R, Mahrwald R, Hocek M. 2015. Direct one-pot synthesis of nucleosides from unprotected or 5- O -monoprotected d -ribose. Org Lett. 17(18):4604–4607.10.1021/acs.orglett.5b02332
   PubMed Web of Science ®Google Scholar
• Guan D, Su Y, Li Y, Wu C, Meng Y, Peng X, Cui Y. 2015. Tetramethylpyrazine inhibits CoCl2-induced neurotoxicity through enhancement of Nrf2/GCLc/GSH and suppression of HIF1α/NOX2/ROS pathways. J Neurochem. 134(3):551–565.10.1111/jnc.2015.134.issue-3
   PubMed Web of Science ®Google Scholar
• Han B, Zhang X, Feng ZM, Jiang JS, Li L, Yang YN, Zhang PC. 2016. Ligubenzocycloheptanone A, a novel tricyclic butenolide with a 6/7/5 Skeleton from Ligusticum chuanxiong. Sci Rep. 6(1):28783.10.1038/srep28783
   PubMedGoogle Scholar
• Hu J, Jia X, Fang X, Li P, He C, Chen M. 2016. Ultrasonic extraction, antioxidant and anticancer activities of novel polysaccharides from Chuanxiong rhizome. Int J Biol Macromol. 85:277–284.10.1016/j.ijbiomac.2015.12.046
   PubMed Web of Science ®Google Scholar
• Jia Y, Wang Z, Zang A, Jiao S, Chen S, Fu Y. 2016. Tetramethylpyrazine inhibits tumor growth of lung cancer through disrupting angiogenesis via BMP/Smad/Id-1 signaling. Int J Oncol. 48(5):2079–2086.10.3892/ijo.2016.3443
   PubMed Web of Science ®Google Scholar
• Kao TK, Ou YC, Kuo JS, Chen WY, Liao SL, Wu CW, Chen CJ, Ling NN, Zhang YH, Peng WH. 2006. Neuroprotection by tetramethylpyrazine against ischemic brain injury in rats. Neurochem Int. 48(3):166–176.10.1016/j.neuint.2005.10.008
   PubMed Web of Science ®Google Scholar
• Kim M, Kim SO, Lee M, Lee JH, Jung WS, Moon SK, Kim YS, Cho KH, Ko CN, Lee EH. 2014. Tetramethylpyrazine, a natural alkaloid, attenuates pro-inflammatory mediators induced by amyloid β and interferon-γ in rat brain microglia. Eur J Pharmacol. 740:504–511.10.1016/j.ejphar.2014.06.037
   PubMed Web of Science ®Google Scholar
• Li SL, Chan SS, Lin G, Ling L, Yan R, Chung HS, Tam YK. 2003. Simultaneous analysis of seventeen chemical ingredients of Ligusticum chuanxiong by on-line high performance liquid chromatography-diode array detector-mass spectrometry. Planta Med. 69:445–451.
   PubMed Web of Science ®Google Scholar
• Li W, Tang Y, Chen Y, Duan JA. 2012. Advances in the chemical analysis and biological activities of chuanxiong. Molecules. 17(9):10614–10651.10.3390/molecules170910614
   PubMed Web of Science ®Google Scholar
• Liang SD, Xu CS, Zhou T, Liu HQ, Gao Y, Li GL. 2005. Tetramethylpyrazine inhibits ATP-activated currents in rat dorsal root ganglion neurons. Brain Res. 1040(1–2):92–97.10.1016/j.brainres.2005.01.076
   PubMed Web of Science ®Google Scholar
• Pu ZH, Meng CW, Zhou YX, Peng C, Du JC, Xiong L. 2016. Study on chemical constituents of Ligusticum chuanxiong. J Chin Med Mater. 39:2531–2533.
   Google Scholar
• Ran X, Ma L, Peng C, Zhang H, Qin LP. 2011. Ligusticum chuanxiong Hort: a review of chemistry and pharmacology. Pharm Biol. 49(11):1180–1189.10.3109/13880209.2011.576346
   PubMed Web of Science ®Google Scholar
• Seki T, Morimura S, Tabata S, Tang Y, Shigematsu T, Kida K. 2008. Antioxidant activity of vinegar produced from distilled residues of the Japanese liquor shochu. J Agric Food Chem. 56(10):3785–3790.10.1021/jf073040w
   PubMed Web of Science ®Google Scholar
• Sun JF, Wu Y, Yang B, Liu Y. 2015. Chemical constituents of marine sponge Halichondria sp. from South China Sea. Chem Nat Compd. 51(5):975–977.10.1007/s10600-015-1467-5
   Web of Science ®Google Scholar
• Suzuki T, Tanaka S, Yamada I, Koashi Y, Yamada K, Chida N. 2000. Total synthesis of spicamycin amino nucleoside. Org Lett. 2(8):1137–1140.10.1021/ol005715 l
   PubMed Web of Science ®Google Scholar
• Suzuki T, Suzuki ST, Yamada I, Koashi Y, Yamada K, Chida N. 2002. Total synthesis of spicamycin. J Org Chem. 67(9):2874–2880.10.1021/jo010925c
   PubMed Web of Science ®Google Scholar
• Szlenkier M, Kamel K, Boryski J. 2016. Regioselective mitsunobu reaction of partially protected uridine. Nucleosides Nucleotides Nucleic Acids. 35(8):410–425.10.1080/15257770.2016.1188943
   PubMed Web of Science ®Google Scholar
• Wei W, Xu W, Yang XW. 2017. Two new phthalide dimers from the rhizomes of Ligusticum chuanxiong. J Asian Nat Prod Res. 19(7):704–711.10.1080/10286020.2016.1275584
   PubMed Web of Science ®Google Scholar
• Xiong L, Zhou QM, Zou Y, Chen MH, Guo L, Hu GY, Liu ZH, Peng C. 2015. Leonuketal, a spiroketal diterpenoid from Leonurus japonicus. Org Lett. 17(24):6238–6241.10.1021/acs.orglett.5b03227
   PubMed Web of Science ®Google Scholar
• Yang NY, Ren DC, Duan JA, Xu XH, Xie N, Tian LJ. 2009. Ceramides and cerebrosides from Ligusticum chuanxiong Hort. Helv Chim Acta. 92(2):291–297.10.1002/hlca.v92:2
   Web of Science ®Google Scholar
• Yang ML, Kuo PC, Hwang TL, Wu TS. 2011. Anti-inflammatory principles from Cordyceps sinensis. J Nat Prod. 74(9):1996–2000.10.1021/np100902f
   PubMed Web of Science ®Google Scholar
• Yang J, Feng XL, Yu Y, Wang Q, Zou J, Wang CX, Mu ZQ, Yao XS, Gao H. 2016. Novel phthalide derivatives identified from Ligusticum chuanxiong (Chuanxiong). Chin Med. 11(1):1180.10.1186/s13020-016-0080-2
   Google Scholar
• Zhu H, Zhou QM, Peng C, Chen MH, Li XN, Lin DS, Xiong L. 2017. Pocahemiketals A and B, two new hemiketals with unprecedented sesquiterpenoid skeletons from Pogostemon cablin. Fitoterapia. 120:67–71.10.1016/j.fitote.2017.05.013
   PubMed Web of Science ®Google Scholar