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shaoyan415

гæ (СÓÐÃûÆø)

[ÇóÖú] GS1--CÆ×ÇóÖú ÒÑÓÐ1È˲ÎÓë

13C NMR (126 MHz, Pyr) ¦Ä 16.57,16.62,17.04,17.07,17.34,19.59,19.61,19.75,20.18,20.27,21.44,22.47,23.46,27.83,28.70,28.87,33.06,34.80,34.94,35.31,36.87,38.95,39.22,39.25,39.29,46.46,46.68,47.41,48.31,48.52,48.58,49.67,49.76,50.05,51.57,52.14,54.62,56.90,69.31,69.40,72.21,77.10,77.44,79.71,125.91,141.45,141.77,154.30,160.35,161.32,176.13,199.71,199.89,207.45,208.65
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yangyinhe

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shaoyan415: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ллÄú£¬Ì«¸ÐлÁË 2015-03-17 14:38:37
1 .     Ginsenoside PM1
    ÏàËÆ¶È:56.3%
Molecules          2007          12          2140-2150
Isolation, Synthesis and Structures of Cytotoxic Ginsenoside Derivatives
Jun Lei, Xiang Li, Xiao-jie Gong and Yi-nan Zheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     gordonoside D
C53H80O18     ÏàËÆ¶È:54.5%
Journal of Natural Products          2009          72          866-870
Cytotoxic Triterpenoid Glycosides from the Roots of Gordonia chrysandra
Lei Yu, Jing-Zhi Yang, Xiao-Guang Chen, Jian-Gong Shi, and Dong-Ming Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     (1R,3S,5S)-tert-butyl 5-(2-((1S,2S,4aS,4bR,8aS,10aS)-8-(tert-butyldimethylsilyloxy)-1-(2-methoxy-2-oxoethyl)-1,2,4a-trimethyl-6-methylene-3,10-dioxo-1,2,3,4,4a,4b,5,6,8a,9,10,10a-dodecahydrophenanthren-2-yl)ethyl)-3-methyl-8-oxa-6-azabicyclo[3.2.1]octane-
C41H65NO8Si     ÏàËÆ¶È:54.5%
Chemistry-A European Journal          2009          15          6626-6644
Synthetic Studies of the Zoanthamine Alkaloids: The Total Syntheses of Norzoanthamine and Zoanthamine
Fumihiko Yoshimura, Minoru Sasaki, Izumi Hattori, Kei Komatsu, Mio Sakai, Keiji Tanino and Masaaki Miyashita
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     aesculioside IIIc
C56H88O23     ÏàËÆ¶È:53.5%
Phytochemistry          2007          68          2075-2086
Cytotoxic triterpenoid saponins from the fruits of Aesculus pavia L.
Zhizhen Zhang, Shiyou Li
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     pubescenoside D
C53H84O21     ÏàËÆ¶È:52.7%
Chemistry & Biodiversity          2008          Vol. 5          1369
Two New Triterpene Saponins from the Anti-Inflammatory Saponin Fraction of Ilex pubescens Root
Jing-Rong Wang, Hua Zhou, Zhi-Hong Jiang, and Liang Liu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     22-O-acetyl-21-O-(3',4'-di-O-angeloyl)-¦Â-D-fucopyranosylprotoaescigenin 3-O-¦Â-D-glucuronopyranoaside
C54H82O19     ÏàËÆ¶È:52.7%
Chemical & Pharmaceutical Bulletin          1985          33          1043-1048
Studies on the Constituents of Xanthoceras sorbifolia BUNGE. IV. Structures of the Minor Prosapogenins
YINGJIE CHEN,TADAHIRO TAKEDA and YUKIO OGIHARA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     hacquetiasaponin 3
    ÏàËÆ¶È:52.7%
Phytochemistry          1995          39          195-198
Saponins from Hacquetia epipactis
Jan Burczyk, Gottfried Reznicek, Sabine Baumgarten, Martina Hugh-Bloch, Johann Jurenitsch, Harald Schröder, Udo Werz, Ernst Haslinger
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     compound 6
    ÏàËÆ¶È:52.7%
Phytochemistry          1992          31          3177-3181
Saponins from Steganotaenia araliacea
Catherine Lavaud, Georges Massiot, Louisette Le Men-Olivier, Alain Viari, Paul Vigny, Clement Delaude
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     29-norcycloart-5-ene and 5,8-lanostadiene-3¦Â-ol
    ÏàËÆ¶È:52.7%
Zeitschrift f¨¹r Naturforschung C          2004          59          15-18
Chemical Constituents of Euphorbia marschalliana Boiss.
A. R. Jassbi, S. Zamanizadehnajari, and S. Tahara
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     Methyl 1,4-(E)-dihydroxyimino-13-isopropyl-7,10a-dimethylpentacyclo[10.6.2(1,10).0(4,9).0(13,18)]icos-14-ene-7-carboxylate
    ÏàËÆ¶È:51.7%
Bioorganic & Medicinal Chemistry          2014          22          6481-6489
Synthesis and anticancer activity of quinopimaric and maleopimaric acids¡¯ derivatives
Elena V. Tretyakova, Irina E. Smirnova, Oxana B. Kazakova, Genrikh A. Tolstikov, Nadejda P. Yavorskaya, Irina S. Golubeva, Rujena B. Pugacheva, Galina N. Apryshko, Vladimir V. Poroikov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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11 .     Spirosupinanonediol
C30H50O3     ÏàËÆ¶È:51.6%
Chemical Communications          1984                   1128-1129
The Structure of Spirosupinanonediol, a Triterpenoid bearing a Novel Skeletal System from Euphorbia supina
Shunyo Matsunaga, Reiko Morita, Toshimasa Ishida, Masatoshi Inoue, Masataka Shigi, and Akira Miyamae
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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12 .     eryngioside L
C54H84O22     ÏàËÆ¶È:50.9%
Phytochemistry          2008          69          2070-2080
Phenolic compounds and rare polyhydroxylated triterpenoid saponins from Eryngium yuccifolium
Zhizhen Zhang, Shiyou Li,Stacy Ownby, Ping Wang, Wei Yuan, Wanli Zhang, R. Scott Beasley
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-03-16 15:18:23
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