نتایج جستجو برای: diterpenoids

تعداد نتایج: 1055  

Journal: :Journal of the Serbian Chemical Society 2006

Journal: :Chemical and Pharmaceutical Bulletin 2011

Journal: :Chemical and Pharmaceutical Bulletin 2003

Journal: :Bioorganic & Medicinal Chemistry 2017

Journal: :Bulletin of the Chemical Society of Japan 1982

2013
Kuan-Hua Chen Chang-Feng Dai Mei-Chin Lu Jan-Jung Li Jih-Jung Chen Yu-Chia Chang Yin-Di Su Wei-Hsien Wang Ping-Jyun Sung

Two new 13-hydroxycembrane diterpenoids, arbolides A (1) and B (2), along with a known trihydroxysteroid, crassarosterol A (3), were isolated from the soft coral Sinularia arborea. The structures of new cembranes 1 and 2 were elucidated by spectroscopic methods. Steroid 3 was found to exhibit cytotoxicity toward K562 and MOLT-4 leukemia.

Journal: :Organic letters 2014
Chenchen Fu Yuanbao Zhang Jun Xuan Chenlong Zhu Bingnan Wang Hanfeng Ding

A concise and efficient approach for the diastereoselective total synthesis of salvileucalin C, as well as their biosynthetically related diterpenoids salvileucalin D, salvipuberulin, isosalvipuberulin, and dugesin B, has been reported for the first time. The key features of the strategy are based on a Beckwith-Dowd ring expansion, a tandem diastereoselective Stille coupling/debromination/desil...

Journal: :Chemical & pharmaceutical bulletin 2009
Shin-Pin Chen Jui-Hsin Su Hsiao-Chien Yeh Atallah Fouad Ahmed Chang-Feng Dai Yang-Chang Wu Jyh-Horng Sheu

A novel skeletal norhumulene (1) and six xeniaphyllane-derived compounds, including norditerpenoids (2, 3) and diterpenoids (4-7), were isolated from the EtOAc extract of the Formosan soft coral Sinularia gibberosa. Their structures were elucidated by spectroscopic analysis. In vitro cytotoxic evaluation of the above metabolites revealed that 2 and 4 showed weak cytotoxicity toward a few cancer...

Journal: :Chemical & pharmaceutical bulletin 2011
Zhao-Yuan Wu Yuan-Dan Li Gui-Sheng Wu Huai-Rong Luo Hong-Mei Li Rong-Tao Li

Phytochemical investigation on the fruits of Pieris formosa resulted in the isolation of three new highly acylated 3,4-seco-grayanane diterpenoids, pierisformotoxins E-G (1-3). Their structures were elucidated on the basis of extensive spectroscopic analysis, including 1D-, 2D-NMR, electrospray ionization-mass spectra (ESI-MS) and high resolution (HR)-MS.

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