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yaoxue1122

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»¯ºÏÎï  Êý¾Ý15.2,16.3,16.7,16.8,18.2,18.7,21.7,23.9,26.0,26.3,26.8,27.7,30.3,31.8,31.9,35.3,36.7,39.3,39.5,40.3,41.2,43.8,46.8,50.7,56.3,62.3,62.7,69.4,71.5,71.9,72.3,72.3,73.9,74.6,76.4,76.7,77.5,77.8,78.0,78.3,78.6,78.7,79.7,88.6,101.5,103.2,105.3
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kaola0916

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yaoxue1122: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл 2012-04-17 13:33:22
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1 .     (3¦Â,20S,23S)-3((O-6-deoxy-¦Á-L-mannopyranosyl-(1¡ú2)-O-[¦Â-D-glucopyranosyl-(1¡ú3)]-¦Â-D-glucopyranosyl)oxy)-20,23-dihydroxydammar-24-en-21-oic acid 21,23-lactone
C49H78O18     ÏàËÆ¶È:83.3%
Helvetica Chimica Acta          2005          Vol. 88          1126
Six New Triterpene Saponins with a 21,23-Lactone Skeleton from Gynostemma pentaphyllum
Feng Yin, Li-Hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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2 .     compound 2
    ÏàËÆ¶È:83.3%
Acta Pharmaceutica Sinica          1996          31          940-944
ISOLATION AND STRUCTURE ELUCIDATION OF CIRENSENOSIDES O AND P FROM THE LEAVES OF OPLOPANAX ELATUS NAKAL
GS Wang; YP Chen; JD Xu; T Murayama and J Shoji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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3 .     kudzudsaponin A3
    ÏàËÆ¶È:81.2%
Chemical & Pharmaceutical Bulletin          1996          44          1222-1227
Triterpene Saponins from Abrus cantoniensis (Leguminosae). I. Isolatioin and Characterization of Four New Saponins and a New Sapogenol
Hideo MIYAO,Yusuke SAKAI,Takashi TAKESHITA,Junei KINJO and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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4 .     kudzusaponin B1
    ÏàËÆ¶È:81.2%
Chemical & Pharmaceutical Bulletin          1996          44          1970-1972
Oleanene-Type Triterpene Glycosides from Puerariae Radix. III.Three New Saponins from Pueraria thomsonii
Tomonori ARAO,Tomoko IDZU,Junei KINJO,Toshihiro NOHARA and Ryuichi ISOBE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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5 .     kudzusaponin A3
    ÏàËÆ¶È:81.2%
Chemical & Pharmaceutical Bulletin          1994          42          1874-1878
Five New Triterpene Glycosides from Russell Lupine
Junei KINJO,Fumiko KISHIDA,Kazutaka WATANABE,Fumio HASHIMOTO and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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6 .     3-O-¦Â-D-glucopyranosyl, 28-O-[¦Á-L-rhamnosyl (1¡ú2)]-¦Â-D-glucopyranosyl 16-deoxybarrin-gtogenol C
C48H80O18     ÏàËÆ¶È:81.2%
Journal of Asian Natural Products Research          2008          10          260-264
Two new triterpenoid saponins from the carpophore of Xanthoceras sorbifolia Bunge
Wei Li, Xian Li, Jia Yang, Da-Li Meng and Ning Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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7 .     3-O- ¦Á-L-rhamnopyranosyl(1¡ú2)-¦Â-D-galactopyranosyl(1¡ú2)-¦Â-D-glucuronopyranosyl kuzusapogenol A methyl ester
    ÏàËÆ¶È:81.2%
Korean Journal of Pharmacognosy          2002          33(2)          110-115
Isolation of Flavonoids and a Saponin from Echinosophora koreensis
Kim, Ju-Sun; Byun, Ji-Hye; Son, Kun-Ho; Kim, Hyun-Pyo; Chang, Hyeun-Wook; Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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8 .     3-O-¦Â-D-glucopyranosyl-28-O-[¦Â-D-glucopyranosyl(1¡ú2)]-¦Â-D-glucopyranosyl-21¦Â,22¦Á-dihydroxyl-olean-12-ene
C48H80O19     ÏàËÆ¶È:81.2%
Journal of Asian Natural Products Research          2012          14          216-223
Two new oleanane-type pentacyclic triterpenoid saponins from the husks of Xanthoceras sorbifolia Bunge
Hao Cui, Hang Xiao, Xiao-Ku Ran, Ying-Ying Li, De-Qiang Dou & Ting-Guo Kang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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9 .     3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucuronopyranosyl-21-epi-kudzusapogenol A
C48H78O20     ÏàËÆ¶È:80.8%
Journal of Natural Products          2008          71(1)          141-145
Triterpene Glycosides from the Roots of Astragalus flavescens
Sibel Avunduk, Anne-Claire Mitaine-Offer, Özgen Alankus#-Çalis#kan,Tomofumi Miyamoto, Serdar Gökhan S#enol, and Marie-Aleth Lacaille-Dubois
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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10 .     soyasaponin A3 methyl ester
C49H80O19     ÏàËÆ¶È:79.5%
Phytochemistry          1992          31          1339-1342
Triterpenoid saponins from Sophora subprostrata
Shiho Sakamoto, Masanori Kuroyanagi, Akira Ueno, Setsuko Sekita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-04-17 13:19:41
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