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CDCl3:48.84,49.05,49.27,49.48,49.70,49.91,50.12,55.91,66.35,77.24,109.68,114.51,114.89,115.04,115.84,123.21,126.17,126.74,130.07,132.39,145.92,146.01,147.02,148.24,159.11,170.06,170.24
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chenjjun1982: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, xiexie 2015-06-18 18:03:54
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1 .     9'-O-de-p-hydroxybenzoyl derivative of quiquesetinerviusin A
C27H26O8     ÏàËÆ¶È:55.5%
Phytochemistry Letters          2012          5          696-699
The first record of neolignans from the marine phanerogam Posidonia oceanica
Fatma Bitam, Maria Letizia Ciavatta, Emiliano Manzo, Guido Villani, Margherita Gavagnin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     7-O-trans-caffeoylvanilloloside
C23H26O11     ÏàËÆ¶È:51.8%
Phytochemistry          2008          69          1208-1214
Phenolic and iridoid glycosides from Strychnos axillaris
Atsuko Itoh, Yasuhiro Tanaka, Naotaka Nagakura, Toru Akita, Toyoyuki Nishi, Takao Tanahashi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     (-)-trans-9-acetyl-4,9'-di-O-methyl-3'-de-O-methyldehydrodiconiferyl alcohol
C23H26O7     ÏàËÆ¶È:51.8%
Journal of Natural Products          2002          65          1278-1282
New Chemical Constituents of Euphorbia quinquecostata and Absolute Configuration Assignment by a Convenient Mosher Ester Procedure Carried Out in NMR Tubes
Bao-Ning Su,Eun Jung Park, Zakaria H. Mbwambo, Bernard D. Santarsiero, Andrew D. Mesecar,Harry H. S. Fong, John M.Pezzuto,and A. Douglas Kinghorn
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     trans-3-[4-[[6-[(E)-2-Carboxy-ethenyl]-3-(3,4-di-hydroxyphenyl)-2,3-dihydro-2-(1,4-benzodioxin)]oxy]-3-hydroxyphenyl]-(E)-2-propenoic acid
C26H19O10     ÏàËÆ¶È:51.8%
Canadian Journal of Chemistry          2008          86          821-830
Biotransformation of caffeic acid by Momordica charantia peroxidase
Xiang Wan, Haili Liu, Xuefeng Huang, Jianguang Luo, and Lingyi Kong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     5-[4-[2-(Benzoxazol-2-yl-butylamino)ethoxy]benzyl]-3-(2,2,2-triphenylmethyl)thiazolidine-2,4-dione
    ÏàËÆ¶È:51.8%
Archives of Pharmacal Research          2004          27          1099-1105
Synthesis and biological activity of Benzoxazole containing thiazolidinedione derivatives
Raok Jeon and SoYeon Park
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     salvianolic acid C
    ÏàËÆ¶È:51.8%
Chinese Pharmaceutical Journal          2014          49          22-25
Water-soluble Constituents of Clerodendranthus spicatus
SUN Zhao-cui, ZHENG Qing-xia, WU Hai-feng, MA Guo-xu, XU Xu-dong*, YANG Jun-shan(
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     compound NT7
    ÏàËÆ¶È:51.8%
Natural Product Communications          2010          5          755-762
Computer-aided Structure Elucidation of Neolignans
Mara B. Costantin, Marcelo J. P. Ferreira, Gilberto V. Rodrigues and Vicente P. Emerenciano
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     Schisphenlignan I
C22H24O7     ÏàËÆ¶È:51.8%
Fitoterapia          2013          86          171-177
Six new lignans from the leaves and stems of Schisandra sphenanthera
Cheng-Qin Liang, Jing Hu, Rong-Hua Luo, Yi-Ming Shi, Shan-Zhai Shang, Zhong-Hua Gao, Rui-Rui Wang, Yong-Tang Zheng, Wen-Yong Xiong, Hong-Bin Zhang, Wei-Lie Xiao, Han-Dong Sun
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     butesuperin A
    ÏàËÆ¶È:51.8%
Chinese Pharmaceutical Journal          2011          46          1389-1393
Study on Chemical Constituents in Stems of Pueraria lobata
ZHANG, De-wu, DAI, Sheng-jun, YU, Qun-ying, LI, Gui-hai
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     (7R,8S)-9-acetyl-dehydrodiconiferyl alcohol
C22H24O7     ÏàËÆ¶È:51.8%
Journal of Ethnopharmacology          2014          153          737−743
Lignans from the stems of Clematis armandii (¡°Chuan-Mu-Tong¡±) and their anti-neuroinflammatory activities
Juan Xiong, Van-Binh Bui, Xin-Hua Liu, Zhi-Lai Hong, Guo-Xun Yang, Jin-Feng Hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     compound 32
C36H30F6O8     ÏàËÆ¶È:51.7%
Journal of the American Chemical Society          2009          131          1745-1752
Explorations into Neolignan Biosynthesis: Concise Total Syntheses of Helicterin B, Helisorin, and Helisterculin A from a Common Intermediate
2Â¥2015-06-17 15:31:21
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