Advanced search
Publication Cover
Journal of Asian Natural Products Research Volume 12, 2010 - Issue 1
Submit an article Journal homepage
148
Views
16
CrossRef citations to date
0
Altmetric
Original Article

New grayanol diterpenoid and new phenolic glucoside from the flowers of Pieris formosa

Original article

Wei-Guang Wang The College of Life Science and Technology, Kunming University of Science and Technology, Kunming, 650224, China
,
Hong-Mei Li The College of Life Science and Technology, Kunming University of Science and Technology, Kunming, 650224, China
,
Hai-Zhou Li The College of Life Science and Technology, Kunming University of Science and Technology, Kunming, 650224, China
,
Zhao-Yuan Wu The College of Life Science and Technology, Kunming University of Science and Technology, Kunming, 650224, China
&
Rong-Tao Li The College of Life Science and Technology, Kunming University of Science and Technology, Kunming, 650224, ChinaCorrespondence[email protected]
Pages 70-75 | Received 18 Aug 2009, Accepted 23 Oct 2009, Published online: 01 Feb 2010

Citations (16)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (2)

Yan-Ping Li, Yan-Hong Li, Jin-Dong Zhong & Rong-Tao Li. (2013) Antioxidant phenolic glycoside and flavonoids from Pieris japonica . Journal of Asian Natural Products Research 15:8, pages 875-879.
Read now
Zhi-Run Zhang, Jin-Dong Zhong, Hong-Mei Li, Hai-Zhou Li, Rong-Tao Li & Xu-Liang Deng. (2012) Two new grayanane diterpenoids from the flowers of Rhododendron molle . Journal of Asian Natural Products Research 14:8, pages 764-768.
Read now

Articles from other publishers (14)

Guijuan Zheng, Pengfei Jin, Lang Huang, Qihua Zhang, Lingkui Meng & Guangmin Yao. (2020) Structurally diverse diterpenoids from Pieris japonica as potent analgesics. Bioorganic Chemistry 99, pages 103794.
Crossref
Chun-Huan Li, Xi-Tao Yan, An-Ling Zhang & Jin-Ming Gao. (2017) Structural Diversity and Biological Activity of the Genus Pieris Terpenoids . Journal of Agricultural and Food Chemistry 65:46, pages 9934-9949.
Crossref
Zhi Wang, Haiyan Zha, Xuedong Yang, Licui Hu, Wenfeng Zheng & Lizhen Xu. (2017) Two new hemiterpene glycosides and one new phenolic glycoside from the roots of Securidaca inappendiculata Hassk. Phytochemistry Letters 21, pages 74-77.
Crossref
Chun-Huan Li, Shi-Hong Luo, Sheng-Hong Li & Jin-Ming Gao. (2017) New Antifeedant Grayanane Diterpenoids from the Flowers of Pieris formosa. Molecules 22:9, pages 1431.
Crossref
Xuan-Qin Chen, Ling-Huan Gao, Yan-Ping Li, Hong-Mei Li, Dan Liu, Xia-Li Liao & Rong-Tao Li. (2017) Highly Oxygenated Grayanane Diterpenoids from Flowers of Pieris japonica and Structure–Activity Relationships of Antifeedant Activity against Pieris brassicae . Journal of Agricultural and Food Chemistry 65:22, pages 4456-4463.
Crossref
Ya‐Zhu Zhu, Yan‐Hong Li, Dan Liu, Ling‐Huan Gao, Hong‐Mei Li & Rong‐Tao Li. (2015) Isolation and Characterization of Secondary Metabolites from Rhododendron microphyton . Helvetica Chimica Acta 98:8, pages 1132-1140.
Crossref
Yong Li, Yun-Bao Liu & Shi-Shan Yu. (2013) Grayanoids from the Ericaceae family: structures, biological activities and mechanism of action. Phytochemistry Reviews 12:2, pages 305-325.
Crossref
Wei‐Guang Wang, Zhao‐Yuan Wu, Rui Chen, Hai‐Zhou Li, Hong‐Mei Li, Yuan‐Dan Li, Rong‐Tao Li & Huai‐Rong Luo. (2013) Pierisformotoxins A – D, Polyesterified Grayanane Diterpenoids from Pieris formosa and Their cAMP‐Decreasing Activities . Chemistry & Biodiversity 10:6, pages 1061-1071.
Crossref
Cheng Zhou, Xiaolei Li, Hongmei Li & Rongtao Li. (2012) Chemical constituents from the leaves of Craibiodendron yunnanense. Biochemical Systematics and Ecology 45, pages 179-182.
Crossref
Hai-Zhou Li, He-Jiao Song, Hong-Mei Li, Yu-Yin Pan & Rong-Tao Li. (2012) Characterization of phenolic compounds from Rhododendron alutaceum. Archives of Pharmacal Research 35:11, pages 1887-1893.
Crossref
Zhao-Yuan Wu, Hai-Zhou Li, Wei-Guang Wang, Xiao-Lei Li & Rong-Tao Li. (2012) Secopieristoxins A and B, two unusual diterpenoids with a new 9,10-secograyanane skeleton from the fruits of Pieris formosa. Phytochemistry Letters 5:1, pages 87-90.
Crossref
Zhao‐Yuan Wu, Hong‐Mei Li, Yuan‐Dan Li, Hai‐Zhou Li & Rong‐Tao Li. (2011) Highly Acylated 3,4‐Secograyanane Diterpenoids from the Fruits of Pieris formosa . Helvetica Chimica Acta 94:7, pages 1283-1289.
Crossref
Zhao‐Yuan Wu, Hai‐Zhou Li, Wei‐Guang Wang, Hong‐Mei Li, Rui Chen, Rong‐Tao Li & Huai‐Rong Luo. (2011) Lyonin A, a New 9,10‐Secograyanotoxin from Lyonia ovalifolia . Chemistry & Biodiversity 8:6, pages 1182-1187.
Crossref
Zhao-Yuan Wu, Yuan-Dan Li, Gui-Sheng Wu, Huai-Rong Luo, Hong-Mei Li & Rong-Tao Li. (2011) Three New Highly Acylated 3,4-seco-Grayanane Diterpenoids from the Fruits of Pieris formosa. CHEMICAL & PHARMACEUTICAL BULLETIN 59:4, pages 492-495.
Crossref

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.