Publication Cover
Natural Product Research
Formerly Natural Product Letters
Volume 32, 2018 - Issue 15
234
Views
6
CrossRef citations to date
0
Altmetric
Research Article

Oxidatively rearranged cycloartane triterpenoids from the seeds of Pseudolarix amabilis

, , , , , , , , & show all
Pages 1817-1823 | Received 10 Aug 2017, Accepted 03 Nov 2017, Published online: 24 Nov 2017

References

  • Arthur HR, Ko PDS, Tai CH. 1974. Triterpenes of lithocarpus species. Phytochemistry. 13(11):2551–2557.10.1016/S0031-9422(00)86935-6
  • Barf T, Vallgårda J, Emond R, Häggström C, Kurz G, Nygren A, Larwood V, Mosialou E, Axelsson K, Olsson R, et al. 2002. Arylsulfonamidothiazoles as a new class of potential antidiabetic drugs. Discovery of potent and selective inhibitors of the 11beta-hydroxysteroid dehydrogenase type 1. J Med Chem. 45(18):3813–3815.10.1021/jm025530f
  • Bühler H, Perschel FH, Hierholzer K. 1991. Inhibition of rat renal 11β-hydroxysteroid dehydrogenase by steroidal compounds and triterpenoids; structure/function relationship. Biochim Biophys Acta. 1075(3):206–212.10.1016/0304-4165(91)90268-L
  • Chen GF, Li ZL, Pan DJ. 1993. The isolation and structural elucidation of four novel triterpene lactones, pseudolarolides A, B, C, and D, from Pseudolarix kaempferi. J Nat Prod. 56(7):1114–1122.10.1021/np50097a015
  • [CLSI] Clinical and Laboratory Standards Institute. 2009. Performance standards for antimicrobial disk susceptibility tests; approved standard M02–A10. 10th ed. Wayne (PA): Clinical and Laboratory Standards Institute.
  • He WJ, Chu HB, Zhang YM, Han HJ, Yan H, Zeng GZ, Fu ZH, Olubanke O, Tan NH. 2011. Antimicrobial, cytotoxic lignans and terpenoids from the twigs of pseudolarix kaempferi. Planta Med. 77(17):1924–1931.10.1055/s-0031-1280020
  • Li EG, Clark AM, Hufford CD. 1995. Antifungal evaluation of pseudolaric acid B, a major constituent of Pseudolarix kaempferi. J Nat Prod. 58(1):57–67.10.1021/np50115a007
  • Li XC, Miao AD, Zhang HF, Wang L, Li Q, Liu YJ, Wei YC. 2014. Research progress of Pseudolarix amabilis. Modern J Integrated Traditional Chin Western Med. 29:3301–3304 (in Chinese).
  • Liu P, Guo HZ, Wang WX, Zhang J, Li N, Han J, Zhou JP, Hu YC, Zhang T, Liu ZM, et al. 2007. Cytotoxic diterpenoids from the bark of pseudolarix kaempferi and their structure−activity relationships. J Nat Prod. 70(4):533–537.10.1021/np060439q
  • Liu P, Sun JH, Xu M, Guo H, Guo HZ, Kang J, Han J, Wang BR, Guo DA. 2011. Characterization of diterpenoids in the bark of Pseudolarix kaempferi by HPLC-ESI/MSn. Acta Pharmaceutica Sinica. 46:213–220.
  • Novy P, Kloucek P, Rondevaldova J, Havlik J, Kourimska L, Kokoska L. 2014. Thymoquinone vapor significantly affects the results of Staphylococcus aureus, sensitivity tests using the standard broth microdilution method. Fitoterapia. 94:102–107.10.1016/j.fitote.2014.01.024
  • Tan JM, Qiu YH, Tan XQ, Tan CH. 2011. Three New peroxy triterpene lactones from Pseudolarix kaempferi. Helv Chim Acta. 94(9):1697–1702.10.1002/hlca.v94.9
  • Wei XZ, Hu YX, Lin JX, Wang XP. 1999. The biology and conservation of Pseudolarix amabilis (nelson) rehd. J Wuhan Botanical Res. 17:73–77.
  • Wu XD, He J, Shen Y, Dong LB, Pan ZH, Xu G, Gong X, Song LD, Leng Y, Li Y, et al. 2012. Pseudoferic acids A-C, three novel triterpenoids from the root bark of Pseudolarix kaempferi. Tetrahedron Lett. 53(7):800–803.10.1016/j.tetlet.2011.12.004
  • Yang SP, Yue JM. 2001. Two novel cytotoxic and antimicrobial triterpenoids from Pseudolarix kaempferi. Bioorg Med Chem Lett. 11(24):3119–3122.10.1016/S0960-894X(01)00633-3
  • Yang SP, Wu Y, Yue JM. 2002. Five new diterpenoids from Pseudolarix kaempferi. J Nat Prod. 65(7):1041–1044.10.1021/np0200010
  • Yang SP, Wang Y, Wu Y, Yue JM. 2004. Chemical constituents from Pseudolarix kaempferi. Nat Prod Res. 18(5):439–446.10.1080/14786410310001643911
  • Yang SP, Cai YJ, Zhang BL, Tong LJ, Xie H, Wu Y, Lin LP, Ding J, Yue JM. 2008. Structural modification of an angiogenesis inhibitor discovered from traditional Chinese medicine and a structure–activity relationship study. J Med Chem. 51(1):77–85.10.1021/jm070906 g

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.