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wzbman

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16.6,56.6,56.6,61.1,62.7,71.6,74.9,77.9,78.0,78.8,80.3,102.6,105.8,105.8,138.5,154.3
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wzbman(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+15, ok 2015-05-06 13:18:56
1 .     nikoenoside
C16H24O9     ÏàËÆ¶È:81.2%
Chemical & Pharmaceutical Bulletin          2003          51(1)          62-67
Medicinal Foodstuffs. XXXI. Structures of New Aromatic Constituents and Inhibitors of Degranulation in RBL-2H3 Cells from a Japanese Folk Medicine, the Stem Bark of Acer nikoense
Toshio MORIKAWA, Jing TAO, Kazuho UEDA, Hisashi MATSUDA, and Masayuki YOSHIKAWA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     Sulfatricalysine B
C16H24O12S     ÏàËÆ¶È:68.7%
Chemical & Pharmaceutical Bulletin          2011          59(1)          72-77
Tricalysionoside A, a Megastigmane Gentiobioside, Sulfatricalysines A-F, and Tricalysiosides X-Z, ent-Kaurane Glucosides, from the Leaves of Tricalysia dubia
Junko SHITAMOTO, Sachiko SUGIMOTO, Katsuyoshi MATSUNAMI, Hideaki OTSUKA,Takakazu SHINZATO, and Yoshio TAKEDA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     nikoenoside
C16H24O9     ÏàËÆ¶È:68.7%
Journal of Tropical and Subtropical Botany          2014          22          185-189
Chemical Constituents Study on the Leaves of Mangifera indica L
ZHANG Yi, ZHANG Yu, LIU Li-li, LIU Er-wei, GE Dan-dan, WANG Tao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     elentheroside E
C34H46O18     ÏàËÆ¶È:68.7%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     syringin
    ÏàËÆ¶È:64.7%
Journal of Asian Natural Products Research          2002          4          43-46
PHENOLIC GLUCOSIDES FROM OXYTROPIS MYRIOPHYLLA
JIANG-HAI LU, YI LIU, GUANG-ZHONG TU and YU-YING ZHAO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     2-(methoxy)-2-(3,5-dimethoxy 4-hydroxyphenyl)-ethane-1,2-diol 1-O-¦Â-D-glucopyranoside
C17H26O10     ÏàËÆ¶È:64.7%
Natural Product Communications          2011          6          205-208
Secondary Metabolites from the Roots of Paronychia chionaea
Sibel Avunduk, Özgen Alankuş-Çalişkan, Tomofumi Miyamoto, Chiaki Tanaka and Marie-Aleth Lacaille-Dubois
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     Juniperoside XI
C17H26O10     ÏàËÆ¶È:64.7%
Journal of Natural Medicines          2013          67          359-368
New glycosides of acetophenone derivatives and phenylpropanoids from Juniperus occidentalis
Yuka Inatomi, Hiroko Murata, Akira Inada, Tsutomu Nakanishi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     3,4,5-trimethoxyphenol-1-O-¦Â-D-xylopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
C20H30O13     ÏàËÆ¶È:64.7%
Journal of Yunnan University          2013          35          673-677
The chemical constituents from Pittosporum podocarpum Gagnep (II)
LUO Lei, ZHANG Lv-li, LI Zu-qiang, WANG Ji-hua, WU Yun-fei, MA Guo-yi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     3-hydroxy-5-methoxyphenol-2-O-¦Â-apiofuranosyl-(1¡ú2)-¦Â-glucopyranoside
    ÏàËÆ¶È:62.5%
Journal of Natural Products          2001          64          1179-1182
Secondary Metabolites from the Roots of Astragalus zahlbruckneri
Ihsan Çalis,Hasan Abou Gazar, Sonia Piacente, and Cosimo Pizza
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     juniperoside
C18H26O9     ÏàËÆ¶È:62.5%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-05-03 11:53:17
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