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13.9,14.3,19.4,19.4,20.0,20.3,22.8,28.1,28.5,29.5,30.3,32.2,36.6,41.4,41.7,43.0,47.6,50.7,52.6,54.7,64.2,64.9,68.8,69.0,75.3,79.4,84.5,116.5,123.9,124.7,133.8,134.1,145.6,170.7,174.6,185.6,195.4,206.7
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xzhfood: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-12 08:17:55
²éѯ½á¹û£º¹²²éµ½139¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     charantoside II
C38H62O9     ÏàËÆ¶È:57.8%
Journal of Natural Products          2007          70          1233-1239
Cucurbitane-Type Triterpenoids from the Fruits of Momordica charantia and Their Cancer Chemopreventive Effects
Toshihiro Akihisa,Naoki Higo,Harukuni Tokuda,Motohiko Ukiya, Hiroyuki Akazawa, Yuichi Tochigi,Yumiko Kimura, Takashi Suzuki, and Hoyoku Nishino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3¦Á-(3'-butylcarboxyacetoxy)oxepanoquercinic acid C
C38H60O8     ÏàËÆ¶È:57.8%
Fitoterapia          2009          80          263-266
Antibacterial triterpenes from the threatened wood-decay fungus Fomitopsis rosea
Milena Popova, Boryana Trusheva, Melania Gyosheva, Iva Tsvetkova, Vassya Bankova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     2¦Á,3¦Â,23-Triacetoxy-11¦Â-methoxy-urs-12-en-28-oate
C38H58O9     ÏàËÆ¶È:57.8%
Phytochemistry          1993          32          466-468
Triterpenoids from the resin of Shorea robusta
Rai K. Hota, Maringanti Bapuji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     4'-deoxy-3-O-a-tetrahydrofuranylneospiramycin I
    ÏàËÆ¶È:57.8%
The Journal of Antibiotics          1984          37          738-749
CHEMICAL MODIFICATION OF SPIRAMYCINS II. SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF 4'-DEOXY DERIVATIVES OF NEOSPIRAMYCIN I AND THEIR 12-(Z)-ISOMERS
HIROSHI SANG, MICHI INOUE, SATOSHI OMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     19(R)-n-Butanoxy-5¦Â,19-epoxycucurbita-6,23-diene-3¦Â,25-diol 3-O-¦Â-glucopyranoside
C40H66O9     ÏàËÆ¶È:57.5%
Molecules          2009          14          4804-4813
New Cucurbitane Triterpenoids and Steroidal Glycoside from Momordica charantia
Jie-Qing Liu, Jian-Chao Chen, Cui-Fang Wang and Ming-Hua Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     4'-O-b-tetrahydropyranylneospiramycin I
    ÏàËÆ¶È:56.4%
The Journal of Antibiotics          1983          36          1336-1344
CHEMICAL MODIFICATION OF SPIRAMYCINS I. SYNTHESIS OF THE ACETAL DERIVATIVES OF NEOSPIRAMYCIN I
HIROSHI SANO, MICHI INOUE, KINYA YAMASHITA, RYO OKACHI, SATOSHI OMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     quadranoside I
C36H58O10     ÏàËÆ¶È:55.2%
Journal of Natural Products          2000          63          496-500
Quadranosides I-V, New Triterpene Glucosides from the Seeds of Combretum quadrangulare
I Ketut Adnyana, Yasuhiro Tezuka, Arjun H. Banskota, Quanbo Xiong, Kim Qui Tran, and Shigetoshi Kadota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Quadranoside I
    ÏàËÆ¶È:55.2%
Molecules          2008          13          2717-2728
Bioactive Pentacyclic Triterpenes from the Stems of Combretum laxum
Eder Bisoli, Walmir S. Garcez, Lidilhone Hamerski, Caroline Tieppo and Fernanda R. Garcez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound y1
    ÏàËÆ¶È:55.2%
Acta Pharmaceutica Sinica          1995          30          27-33
NEW TRTEKPENOIDAL SAPOGENINS FROM THE ROOTS OF GLYCYRRHIZA YUNNANENSIS
JF Hu; ZL Ye and FJ Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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