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shaoyan415гæ (СÓÐÃûÆø)
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[ÇóÖú]
GS1--CÆ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
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| 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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ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
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shaoyan415: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ллÄú£¬Ì«¸ÐлÁË 2015-03-17 14:38:37
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shaoyan415: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ллÄú£¬Ì«¸ÐлÁË 2015-03-17 14:38:37
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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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ |
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