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13C NMR (CD3OD) ¦Ä 153.07, 134.52, 133.91, 129.84, 128.57, 104.08, 77.02, 76.48, 74.39,69.99, 62.25, 61.24, 55.67
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rootulysses: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-05-05 19:49:05
1 .     syringin
    ÏàËÆ¶È:81.2%
China Journal of Chinese Materia Medica          2008          33          1032-1035
Studies on chemical constituents of Saussurea laniceps
DAWA Zhuoma, ZHOU Yan, BAI Yang, GESANG Suolang, XIE Ping, DING Lisheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     cis-syringin
    ÏàËÆ¶È:78.5%
Acta Pharmaceutica Sinica          2007          Vol 42          757-761
The chemical constituents of Polygala hongkongensis Hemsl
WU Jian-feng;; CHEN Si-bao; CHEN Shi-lin; TU Peng-fei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     syringin
    ÏàËÆ¶È:75%
Acta Pharmaceutica Sinica          1999          Vol 34          839-841
STUDIES ON CHEMICAL CONSTITUENTS FROM ACANTHOPANAX SENTICOSUS (RUPR.ET MAXIM.) HARMS
Wu Lijun(Wu LJ); Ruan Lijun(Ruan LJ); Zheng Jian(Zheng J); Wang Feifei(Wang FF); Ding Fuli(Ding FL) and Gong Haiping(Gong HP)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     glucoacetosyringone
    ÏàËÆ¶È:69.2%
Bioorganic & Medicinal Chemistry          2010          18          7052-7057
Chalcone glycosides isolated from aerial parts of Brassica rapa L. ¡®hidabeni¡¯ suppress antigen-stimulated degranulation in rat basophilic leukemia RBL-2H3 cells
Tomohiro Itoh, Masayuki Ninomiya, Yoshinori Nozawa, Mamoru Koketsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     4-ôǼ׻ù-2,6-¼×Ñõ»ù±½·Ó-1-O-¦Â-D-ÆÏÌÑÌÇÜÕ
    ÏàËÆ¶È:69.2%
China Journal of Chinese Materia Medica          2012          37          1782-1787
Phenolic components from Petasites tricholobus
ZHANG Yong; GUO Fujiang; ZENG Peng; JIA Qi; LI Yiming; ZHU Weiliang; CHEN Kaixian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     compound 2
    ÏàËÆ¶È:64.2%
Chemical & Pharmaceutical Bulletin          1988          36          2726-2729
TANGHENOSIDES I AND II FROM CHUAN-DANGSHEN, THE ROOT OF CODONOPSIS TANGSHEN OLIV.
Kenji Mizutani,Masamichi Yuda,Osamu Tanaka,Yuh-ichiro Saruwatari,Ming-Ru Jia,Yi-Kui Ling and Xui-Feng Pu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     4-Allyl-2,6-dimethoxyphenyl glucoside
    ÏàËÆ¶È:64.2%
Archives of Pharmacal Research          2007          30          1067-1074
Lignan and terpene constituents from the aerial parts of saussurea pulchella
Sang Un Choi, Min Cheol Yang, Kyu Ha Lee, Ki Hyun Kim and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     2,6-dimethoxy-4-hydroxyphenol-1-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:64.2%
Journal of Shenyang Pharmaceutical University          2009          26          530-535
Chemical constituents from stem of Cratoxylon cochinchinensis Bl.
YU Hai-yang, WANG Nai-li, ZHANG Xue, JIN San-lin, YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     syringin
    ÏàËÆ¶È:61.5%
China Journal of Chinese Materia Medica          2008          33          1641-1643
Study on Chemical Constituents from Juniperus sabina L.
ZHAO Jun, YAN Ming, HUANG Yi, LIU Tao, ZHAO Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Ã«ÁøÜÕ
    ÏàËÆ¶È:61.5%
Chinese Traditional and Herbal Drugs          2010          41          867-870
´óѪÌٵĻ¯Ñ§³É·ÖÑо¿(¢ò)
³ÂÖÇÏÉ;¸ßÎÄÔ¶;Áõá·ÁÕ;ÕÅÌú¾ü
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     ¶¡ÏãËáÆÏÌÑÌÇÜÕ
C15H20O10     ÏàËÆ¶È:61.5%
Chinese Traditional and Herbal Drugs          2010          41          867-870
´óѪÌٵĻ¯Ñ§³É·ÖÑо¿(¢ò)
³ÂÖÇÏÉ;¸ßÎÄÔ¶;Áõá·ÁÕ;ÕÅÌú¾ü
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     syringin
    ÏàËÆ¶È:61.5%
Chinese Pharmaceutical Journal          2008          43          1461-1463
Study on Chemical Constituents from Juniperus sabina L.
ZHAO Jun, YAN Ming, HUANG Yi, LIU Tao, ZHAO Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (1S)-1,5-anhydro-D-glucitol-spiro[1.5]-3-(4-cyanophenyl)-1,4,2-oxathiazole
C14H14N2O6S     ÏàËÆ¶È:61.5%
Bioorganic & Medicinal Chemistry          2009          17          5696-5707
Glucose-based spiro-heterocycles as potent inhibitors of glycogen phosphorylase
Veronika Nagy, Mahmoud Benltifa, S¨¦bastien Vidal, Eszter Berzs¨¦nyi, Cathie Teilhet, Katalin Czifr¨¢k, Gyula Batta, Tibor Docsa, P¨¢l Gergely, L¨¢szl¨® Soms¨¢k, Jean-Pierre Praly
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     prunasin
    ÏàËÆ¶È:61.5%
Natural Product Sciences          2012          18          200-203
Chemical Constituents from the Fruits of Prunus mume
Jin, Qinghao; Lee, Chul; Lee, Jin-Woo; Lee, In-Sun; Lee, Mi-Kyeong; Jeon, Won-Kyung; Hwang, Bang-Yeon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     juniperoside
C18H26O9     ÏàËÆ¶È:60%
Planta Medica          1996          62          88-89
Phenyipropane Glycosides from Jun iperus pharnicea
Glues C'omte, AlbertJ. Ghulia. Joseph Vercauteren,and Daovy P. Allais
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     liriodenrin
C34H46O18     ÏàËÆ¶È:57.1%
Chinese Journal of Natural Medicines          2010          8          199-201
Chemical Constituents from the Aerial Part of Peganum nigellastrum
YANG Fei; CHEN Rong; FENG Lin; LI Hai-Dao; ZHANG Hua; LIANG Jing-Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     syringin
    ÏàËÆ¶È:57.1%
Chinese Pharmaceutical Journal          2009          44          1137-1140
Studies on Chemical Constituents of Acanthopanax brachypus(¢ò)
HU Hao-bin, FAN Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     dihydrosyringin
    ÏàËÆ¶È:57.1%
Chinese Pharmaceutical Journal          2010          45          975-979
Phenolic Components and Flavanones from Dendrobium candidum
LI Yan, WANG Chun-lan, WANG Fang-fei, DONG Hai-ling, GUO Shun-xing, YANG Jun-shan, XIAO Pei-gen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     liriodendrin
    ÏàËÆ¶È:57.1%
Turkish Journal of Chemistry          2009          33          561-568
A novel naphthoquinone glycoside from Rubia peregrina L.
UFUK ÖZGEN, CAVİT KAZAZ, HASAN SEÇEN, İHSAN ÇALIŞ, MAKSUT COŞKUN, PETER J. HOUGHTON
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     liriodendrin
    ÏàËÆ¶È:56.2%
Chemical & Pharmaceutical Bulletin          1985          33          1452-1457
Studies on the Constituents of Cistanchis Herba. V. Isolation and Structures of Two New Phenylpropanoid Glycosides, Cistanosides E and F
HIROMI KOBAYASHI,HIROKO KARASAWA,TOSHIO MIYASE and SEIGO FUKUSHIMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     coniferine
C16H22O8     ÏàËÆ¶È:56.2%
Turkish Journal of Chemistry          2009          33          667-675
Secondary metabolites from Nepeta heliotropifolia
ZÜHAL GÜVENALP, HİLAL ÖZBEK, AYŞE KURUÜZÜM-UZ, CAVİT KAZAZ, L. ÖMÜR DEMİREZER
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     4-(1,2,3-trihydroxypropyl)-2,6-dimethoxyphenyl-1-O-¦Â-D-glucopyranoside
C17H26O11     ÏàËÆ¶È:56.2%
Chinese Traditional and Herbal Drugs          2012          43          1462-1470
Studies on chemical constituents from Aidi Injection
ZHANG Miao-miao; LIU Yan-li; CHEN Zhong; LI Xiao-ran; XU Qiong-ming; YANG Shi-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     viridoside
    ÏàËÆ¶È:53.8%
Phytochemistry          2006          67          2380-2391
Comparative phytochemical characterization of three Rhodiola species
Gad G. Yousef, Mary H. Grace, Diana M. Cheng, Igor V. Belolipov,Ilya Raskin, Mary Ann Lila
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     benzyl alcohol glucoside
C13H18O6     ÏàËÆ¶È:53.8%
Phytochemistry          2002          60          873-882
Cyanogenic allosides and glucosides from Passiflora edulis and Carica papaya
David S. Seigler, Guido F. Pauli, Adolf Nahrstedt, Rosemary Leen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     cirsiumoside
C13H20O9     ÏàËÆ¶È:53.8%
Planta Medica          1990          56          472-474
New Furans from Cirsium chiorolepis
Yue-mao Shen and Quan-zhang Mu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     compound 9a
C20H26O14     ÏàËÆ¶È:53.8%
Journal of Asian Natural Products Research          2009          11          172-176
The synthesis of analogs of shuangkangsu, a novel natural cycloperoxide glucoside from Lonicera japonica Thunb
Yan-Bo Tang, Long-Jiang Huang, Di-Zao Li, Qing-Jian Zhang, Ruo-Yun Chen and De-Quan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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