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1 .     cineracipadesin A
C32H40O10     ÏàËÆ¶È:54.5%
Journal of Natural Products          2009          72          714-718
Tetranortriterpenoids from the Leaves of Cipadessa cinerascens
Xin Fang, Ying-Tong Di, Chun-Shun Li, Zhao-Liang Geng, Zhen Zhang, Yu Zhang,Yang Lu, Qi-Tai Zheng,Shi-Yin Yang,and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     14,18-di-O-acetylwithaphysalin C
C32H42O7     ÏàËÆ¶È:54.5%
Helvetica Chimica Acta          2007          Vol. 90          1406
Cytotoxic Withaphysalins from Physalis minima
Lei Ma, Xian-Wen Gan, Qing-Ping He, Hai-Yun Bai, Mohammad Arfan, Feng-Chang Lou, and Li-Hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     21¦Â-acetoxy-serrat-14-en-3-one
    ÏàËÆ¶È:54.5%
Phytochemistry          1994          37          209-211
Serratenes from the stem bark of Picea Jezoensis carr. hondoensis
Reiko Tanaka, Rie Tsuboi, Shunyo Matsunaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     2¦Â,3¦Â-dihydroxy-30-norolean-12,20(29)-diene-23,28-dioic acid 28-O-¦Â-D-glucopyranosyl ester
C35H52O11     ÏàËÆ¶È:54.2%
Journal of Agricultural and Food Chemistry          1998          46          1797-1804
Studies on the Constituents of Amaranthus caudatus Leaves:  Isolation and Structure Elucidation of New Triterpenoid Saponins and Ionol-Derived Glycosides
Luca Rastrelli, Rita Aquino, Susana Abdo, Maria Proto, Francesco De Simone, and Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     Shearinine I
C37H45NO7     ÏàËÆ¶È:54.0%
Tetrahedron          2007          63          435-444
Shearinines D¨CK, new indole triterpenoids from an endophytic Penicillium sp. (strain HKI0459) with blocking activity on large-conductance calcium-activated potassium channels
Minjuan Xu, Guido Gessner, Ingrid Groth, Corinna Lange, Arnulf Christner, Torsten Bruhn, Zhiwei Deng, Xiang Li, Stefan H. Heinemann, Susanne Grabley, Gerhard Bringmann, Isabel Sattler, Wenhan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     jinfushanoside B
C36H56O9     ÏàËÆ¶È:52.7%
Planta Medica          2005          71          983-986
Four New Cucurbitane Glycosides from Hemsleya jinfushanensis
Jian-Chao Chen, Xue-Mei Niu , Zhong-Rong Li , Ming-Hua Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3¦Â-hydroxyurs-12,19-dien-28-¦Â-D-glucopyranoside
    ÏàËÆ¶È:52.7%
Chinese Traditional and Herbal Drugs          2010          41          1048-1052
Chemical constituents of charred Sanguisorbae Radix(¢ò)
XIA Hong-min; ZHONG Ying; SUN Jing-yong; SUN Li-li; AN Kun; WANG Ju
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     isocystoseirone diacetate
C31H42O8     ÏàËÆ¶È:51.5%
Journal of Natural Products          2004          67          495-499
Novel Meroditerpenes from the Brown Alga Cystoseira sp.
Guillermo Navarro, Jos J. Fernndez, and Manuel Norte
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     amphidinolide H4
    ÏàËÆ¶È:51.5%
Journal of Natural Products          2007          70          1676-1679
Amphidinolides B6 and B7, Cytotoxic Macrolides from a Symbiotic Dinoflagellate Amphidinium Species
Keiko Oguchi, Masashi Tsuda, Rie Iwamoto, Yumiko Okamoto, Taeko Endo,Jun¡¯ichi Kobayashi, Tomoko Ozawa, and Atsunori Masuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     castanopsinin C
C50H64O19     ÏàËÆ¶È:51.5%
Chemical & Pharmaceutical Bulletin          1988          36          1646-1663
Tannins and Related Compounds. LXVII. : Isolation and Characterization of Castanopsinins A-H, Novel Ellagitannins Containing a Triterpenoid Glycoside Core, from Castanopsis cuspidata var. sieboldii NAKAI. (3)
MASAYUKI AGETA,GEN-ICHIRO NONAKA and ITSUO NISHIOKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     3¦Â-Acetoxyolean-12-en-28,30-dioic acid
    ÏàËÆ¶È:51.5%
Chemistry of Natural Compounds          1992          28          1-23
13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES
A. I. Kalinovskii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     21¦Â-Hydroxyserrat-14-en
    ÏàËÆ¶È:51.5%
Chemistry of Natural Compounds          1992          28          575-579
POLYFUNCTIONAL TRITERPENOIDS FROM THE BARK OF YEDDO SPRUCE
G. F. Chernenko, I. Yu. Bagryanskaya,Yu. V. Gatilov, G. E. Sal'nikov,E. N. Shmidt, and V. I. Mamatyuk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     rubiarbonol A 7-acetate
C32H52O5     ÏàËÆ¶È:51.5%
Journal of Natural Products          2011          74          2069-2080
Biologically Active Arborinane-Type Triterpenoids and Anthraquinones from Rubia yunnanensis
Jun-Ting Fan, Bin Kuang, Guang-Zhi Zeng, Si-Meng Zhao, Chang-Jiu Ji, Yu-Mei Zhang,and Ning-Hua Tan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 21
    ÏàËÆ¶È:51.5%
Phytochemistry          1984          23          2893-2898
Further triterpenoids and 13C NMR spectra of oleanane derivatives from Phytolacca acinosa
S. Harkar, T.K. Razdan, E.S. Waight
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     amphidinolide H4
C36H63NO10     ÏàËÆ¶È:51.5%
The Journal of Organic Chemistry          2002          67          6585-6592
Amphidinolides H2−H5, G2, and G3, New Cytotoxic 26-and 27-Membered Macrolides from Dinoflagellate Amphidinium sp.
Jun'ichi Kobayashi, Kazutaka Shimbo, Masaaki Sato, and Masashi Tsuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     15G256¦Ä
C33H46N4O10     ÏàËÆ¶È:51.5%
The Journal of Antibiotics          1998          51          303-316
Cell Wall Active Antifungal Compounds Produced by the Marine Fungus Hypoxylon oceanicum LL-15G256 II. Isolation and Structure Determination
GERHARD SCHLINGMANN, LISA MILNE, DAVID R. WILLIAMS, GUY T. CARTER
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     compound C-OCH3
    ÏàËÆ¶È:51.5%
Journal of Agricultural and Food Chemistry          1977          25          1197-1201
Paspalum staggers: isolation and identification of tremorgenic metabolites from sclerotia of Claviceps paspali
Richard J. Cole, Joe W. Dorner, John A. Lansden, Richard H. Cox, Countney Pape, Barry Cunfer, Stephen S. Nicholson, David M. Bedell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     nobiliside A
C35H50O8     ÏàËÆ¶È:51.4%
Planta Medica          2006          72          932-935
Nobilisides A- C, Three New Triterpene Glycosides from the Sea Cucumber Holothuria nobilis
Jun Wu , Yang-Hua Yi , Hai-Feng Tang , Hou-Ming Wu ,Zhen-Rong Zou , Hou-Wen Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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