Advanced search
Publication Cover
Natural Product Research
Formerly Natural Product Letters
Volume 33, 2019 - Issue 8
Submit an article Journal homepage
181
Views
7
CrossRef citations to date
0
Altmetric
Research Articles

Structurally diverse diterpenoids from Trigonostemon howii

Yan-Ping LiuKey Laboratory of Tropical Medicinal Plant Chemistry of Ministry of Education, Hainan Normal University, Haikou, P. R. China;Key Laboratory of Southern Medicinal Plants Resources of Haikou City, Hainan Normal University, Haikou, P. R. China
,
Qing WenKey Laboratory of Tropical Medicinal Plant Chemistry of Ministry of Education, Hainan Normal University, Haikou, P. R. China;Key Laboratory of Southern Medicinal Plants Resources of Haikou City, Hainan Normal University, Haikou, P. R. China;College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, P. R. China
,
Shi HuKey Laboratory of Tropical Medicinal Plant Chemistry of Ministry of Education, Hainan Normal University, Haikou, P. R. China;Key Laboratory of Southern Medicinal Plants Resources of Haikou City, Hainan Normal University, Haikou, P. R. China;College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, P. R. China
,
Yan-Lei MaKey Laboratory of Tropical Medicinal Plant Chemistry of Ministry of Education, Hainan Normal University, Haikou, P. R. China;Key Laboratory of Southern Medicinal Plants Resources of Haikou City, Hainan Normal University, Haikou, P. R. China;College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, P. R. China
,
Zhi-Hua JiangKey Laboratory of Tropical Medicinal Plant Chemistry of Ministry of Education, Hainan Normal University, Haikou, P. R. China;Key Laboratory of Southern Medicinal Plants Resources of Haikou City, Hainan Normal University, Haikou, P. R. China;College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, P. R. China
,
Jin-Ying TangKey Laboratory of Tropical Medicinal Plant Chemistry of Ministry of Education, Hainan Normal University, Haikou, P. R. China;Key Laboratory of Southern Medicinal Plants Resources of Haikou City, Hainan Normal University, Haikou, P. R. China;College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, P. R. China
&
Yan-Hui FuKey Laboratory of Tropical Medicinal Plant Chemistry of Ministry of Education, Hainan Normal University, Haikou, P. R. China;Key Laboratory of Southern Medicinal Plants Resources of Haikou City, Hainan Normal University, Haikou, P. R. China;College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, P. R. ChinaCorrespondence[email protected]
 show all
Pages 1169-1174 | Received 09 Feb 2018, Accepted 04 Apr 2018, Published online: 16 Apr 2018

References

  • Chen AH , Liu QL , Ma YL , Jiang ZH , Tang JY , Liu YP , Chen GY , Fu YH , Xu W . 2017. A new monoterpenoid indole alkaloid from Ochrosia elliptica . Nat Prod Res. 31:1490–1494.10.1080/14786419.2016.1277349
  • Craveiro AA , Silveira ER . 1982. Two cleistanthane type diterpenes from Croton sonderianus . Phytochemistry. 21:2571–2574.10.1016/0031-9422(82)85259-X
  • Dong SH , Liu HB , Xu CH , Ding J , Yue JM . 2011. Constituents of Trigonostemon heterophyllus . J Nat Prod. 74:2576–2581.10.1021/np200772n
  • Dong SH , Zhang CR , Xu CH , Ding J , Yue JM . 2011. Daphnane-type diterpenoids from Trigonostemon howii . J Nat Prod. 74:1255–1261.10.1021/np200231u
  • Duan H , Kawazoe K , Bando M , Kido M , Takaishi Y . 1997. Di-and triterpenoids from Tripterygium hypoglaucum . Phytochemistry. 46:535–543.10.1016/S0031-9422(97)00288-4
  • Fu YH , Zhang Y , He HP , Hou L , Di YT , Li SL , Luo XD , Hao XJ . 2012. Strynuxlines A and B, alkaloids with an unprecedented carbon skeleton from Strychnos nux-vomica . J Nat Prod. 75:1987–1990.10.1021/np300339r
  • Fu YH , Di YT , He HP , Li SL , Zhang Y , Hao XJ . 2014. Angustifonines A and B, cytotoxic bisindole alkaloids from Bousigonia angustifolia . J Nat Prod. 77:57–62.10.1021/np4005823
  • Jayasuriya H , Zink DL , Singh SB , Borris RP , Nanakorn W , Beck HT , Balick MJ , Goetz MA , Slayton L , Gregory L , Zakson-Aiken M . 2000. Structure and stereochemistry of rediocide A, A highly modified daphnane from Trigonostemon reidioides exhibiting potent insecticidal activity. J Am Chem Soc. 122:4998–4999.10.1021/ja994074q
  • Jiang ZH , Liu YP , Huang ZH , Wang TT , Feng XY , Yue H , Guo W , Fu YH . 2017. Cytotoxic dihydrobenzofuran neolignans from Mappianthus iodoies . Bioorg Chem. 75:260–264.10.1016/j.bioorg.2017.10.003
  • Kaemchantuek P , Chokchaisiri R , Prabpai S , Kongsaeree P , Chunglok W , Utaipan T , Chamulitrat W , Suksamrarn A . 2017. Terpenoids with potent antimycobacterial activity against Mycobacterium tuberculosis from Trigonostemon reidioides roots. Tetrahedron. 73:1594–1601.10.1016/j.tet.2017.02.006
  • Kimbu SF , Keumedjio F , Sondengam LB , Connolly JD . 1991. Two dinorditerpenoids from Ricinodendron heudelotii . Phytochemistry. 30:619–621.10.1016/0031-9422(91)83738-7
  • Li BT , Gilbert MG . 2008. Chinese flora. Beijing: Science. 11:272–174.
  • Liu QL , Chen AH , Tang JY , Ma YL , Jiang ZH , Liu YP , Chen GY , Fu YH , Xu W . 2017. A new indole alkaloid with anti-inflammatory activity from Nauclea officinalis . Nat Prod Res. 31:2107–2112.10.1080/14786419.2016.1277351
  • Ma YL , Liu YP , Zhang C , Zhao WH , Shi S , He DN , Zhang P , Liu XH , Han TT , Fu YH . 2018. Carbazole alkaloids from Clausena hainanensis with their potential antiproliferative activities. Bioorg Chem. 76:359–364.10.1016/j.bioorg.2017.12.016
  • Mosmann T . 1983. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 65:55–63.10.1016/0022-1759(83)90303-4
  • Reed LJ , Muench H . 1938. A simple method of estimating fifty percent end points. Am J Hyg. 27:493–497.
  • Takaishi Y , Wariishi N , Tateishi H , Kawazoe K , Miyagi K , Li K , Duan H . 1997. Phenolic diterpenes from Tripterygium wilfordii var. regelii . Phytochemistry. 45:979–984.10.1016/S0031-9422(96)00861-8
  • Tan CJ , Di YT , Wang YH , Zhang Y , Si YK , Zhang Q , Gao S , Hu XJ , Fang X , Li SF , Hao XJ . 2010. Three new indole alkaloids from Trigonostemon lii . Organic Lett. 12:2370–2373.10.1021/ol100715x
  • Tang GH , He HP , Gu YC , Di YT , Wang YH , Li SF , Li SL , Zhang Y , Hao XJ . 2012. 3, 4-seco-diterpenoids from Trigonostemon flavidus . Tetrahedron. 68:9679–9684.10.1016/j.tet.2012.09.052
  • Tang GH , Zhang Y , Gu YC , Li SF , Di YT , Wang YH , Yang CX , Zuo GY , Li SL , He HP , Hao XJ . 2012. Trigoflavidols A–C, degraded diterpenoids with antimicrobial activity, from Trigonostemon flavidus. J Nat Prod. 75:996–1000.10.1021/np3001128
  • Tang GH , Zhang Y , Yuan CM , Li Y , Gu YC , Di YT , Wang YH , Zuo GY , Li SF , Li SL , et al . 2012. Trigohowilols A–G, degraded diterpenoids from the stems of Trigonostemon howii . J Nat Prod. 75:1962–1966.10.1021/np3006315
  • Wu CY , Liao Y , Yang ZG , Yang XW , Shen XL , Li RT , Xu G . 2014. Cytotoxic diterpenoids from Salvia yunnanensis . Phytochemistry. 106:171–177.

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:

Order Reprints Request Corporate Permissions

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:

Request Academic Permissions

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.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.