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15.42,
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19.35,
22.62,
23.09,
23.39,
28.08,
29.10,
29.40,
29.75,
29.80,
30.94,
31.48,
32.08,
32.18,
35.31,
35.75,
35.98,
38.52,
38.67,
38.69,
42.16,
44.15,
71.19,
113.28,
119.57,
140.74,
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·çÖ®»êÁézd: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-03-22 21:57:55
·çÖ®»êÁézd(¶¹¸ç´ú·¢): ½ð±Ò+5, лл 2013-06-15 08:26:52
1 .     hypoglauterpenic acid
    ÏàËÆ¶È:73.3%
Acta Botanica Yunnanica          1993          15(1)          92-96
THE OLEANANE TYPE TRITERPENES FROM THE ROOT OF TRIPTERYGIUM HYPOGLAUCUM
ZHANG Xian-Min,WU Da-Gang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

2 .     ulmudiol
C30H50O2     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          2006          54(6)          775-778
New Triterpenoids Isolated from the Root Bark of Ulmus pumila L.
Dong WANG,Mingyu XIA,and Zheng CUI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     kansenol
C30H48O2     ÏàËÆ¶È:66.6%
Journal of Natural Products          2003          66          630-633
Euphane and Tirucallane Triterpenes from the Roots of Euphorbia kansui and Their in Vitro Effects on the Cell Division of Xenopus
Li-Yan Wang, Nai-Li Wang, Xin-Sheng Yao, Syohei Miyata, and Susumu Kitanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

4 .     2¦Á,3¦Â-dihydroxyfriedelane
    ÏàËÆ¶È:66.6%
Journal of Natural Products          2001          64          1273-1277
Synthetic Secofriedelane and Friedelane Derivatives as Inhibitors of Human Lymphocyte Proliferation and Growth of Human Cancer Cell Lines in Vitro
Cristina Moiteiro,F¨¢tima Justino, Regina Tavares,M. J. Marcelo-Curto, M. Helena Flor¨ºncio,Maria Sao Jos¨¦Nascimento, Madalena Pedro, F¨¢tima Cerqueira, and Madalena M. M. Pinto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     glut-5-ene-3-one
    ÏàËÆ¶È:66.6%
Planta Medica          1994          60          594-596
Biologically Active Compounds from the Euphorbiaceae; 2. Two Triterpenoids of Euphorbia cyparissias
Sevil Oks¨¹z. Roberto R. Gil,Heebyung Chai,JohnM. Pezzuto, GeoffreyA. Cordell,and Ayhan Ulubelen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     glutin-5-ene
    ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1995          43          198-203
NMR Spectra of Triterpenoids. III. Oleanenes and Migrated Oleanenes
Hiroyuki AGETA,Yoko ARAI,Hideki SUZUKI,Tamiko KIYOTANI and Miyoe KITABAYASHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

7 .     adian-5-ene
    ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1994          42          39-44
NMR Spectra of Triterpenoids. II. Hopenes and Migrated Hopenes
Hiroyuki AGETA,Kenji SHIOJIMA,Yoko ARAI,Hideki SUZUKI and Tamiko KIYOTANI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     glutinol
    ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1994          42          608-610
Triterpenoid Constituents of Ficus thunbergii
Junichi KITAJIMA,Masanobu ARAI and Yasuko TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

9 .     compound 4b
    ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1989          37          1673-1675
FERN CONSTITUENTS : THREE FERNENOIC ACIDS AND ONE ADIANENOIC ACID ISOLATED FROM RHIZOMES OF MICROSORIUM BRACHYLEPIS AND M. NORMALE
Kazuo MASUDA,Rumiko KAMAYA,Susumu IKEGAMI,Yukio IKESHIMA and Hiroyuki AGETA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

10 .     adian-5-en-25-ol
C30H50O     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1997          45          639-642
Fern Constituents : Adiantum cuneatum. II. Six New Triterpenoids, Neohop-18-en-12¦Á-ol, 13-Epineohop-18-en-12¦Á-ol, Neohop-13(18)-en-19¦Á-ol, Fern-7-en-25-ol, Fern-9(11)-en-25-ol, and Adian-5-en-25-ol
Kenji SHIOJIMA,Yoko ARAI,Takahisa NAKANE and Hiroyuki AGETA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

11 .     20-Epibryonolic acid
C30H48O3     ÏàËÆ¶È:66.6%
Phytochemistry          1996          42          559-560
20-Epibryonolic acid, phytosterols and ellagic acid from Coriaria intermedia
Yuan-Shiun Chang, Ming-Shiung Lin, Reuy-Ling Jiang, Shun-Chueh Huang, Li-Kang Ho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

12 .     koetjapic acid
C30H46O4     ÏàËÆ¶È:66.6%
Journal of Natural Products          1992          Vol 55          654
Plant Anticancer Agents, L. Cytotoxic Triterpenes from Sandoricum koetjape Stems
Norito Kaneda, John M. Pezzuto, A. Douglas Kinghorn, Norman R. Farnsworth, Thawatchai Santisuk, Patoomratana Tuchinda, Jinda Udchachon, Vichai Reutrakul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     bauerenyl acetate
    ÏàËÆ¶È:66.6%
Phytochemistry          1994          37          1517-1575
13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features
Shashi B. Mahato, Asish P. Kundu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

14 .     compound 379
    ÏàËÆ¶È:66.6%
Phytochemistry          1994          37          1517-1575
13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features
Shashi B. Mahato, Asish P. Kundu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

15 .     trichadenic acid B
    ÏàËÆ¶È:66.6%
Phytochemistry          1992          31          223-225
30-Norfriedelane triterpenes from the stem bark ofCaloncoba glauca
Rosa M. Giner-Pons, Alexander I. Gray, Catherine Lavaud, Georges Massiot, Simon Gibbons, Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

16 .     glutenol
    ÏàËÆ¶È:66.6%
Indian Journal of Chemistry          2009          48B          83-87
New antifungal triterpenoid saponin from Launaea pinnatifida Cass.
Yadava,R N; Chakravarti,N
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

17 .     dulcioic acid
    ÏàËÆ¶È:66.6%
Phytochemistry          1981          20          171-173
Triterpenoids of Scoparia dulcis
Shashi B. Mahato, Manik C. Das, Niranjan P. Sahu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

18 .     ½µÏã´¼
    ÏàËÆ¶È:66.6%
Chinese Traditional and Herbal Drugs          2006          37          338-340
Chemical constituents in Ixeridium gramineum
LIU Jun-xi; WEI Xiao-ning; LU Run-hua; SHI Yan-ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

19 .     adian-5-ene
    ÏàËÆ¶È:66.6%
Natural Product Research and Development          1991          3(2)          74-85
STUDYING PROGRESS ON THE STRUCTURES OF PENTACYCLIC TRITERPENOIDS WITH A PENTATOMIC RING E
Lou Hongxiang; Li Xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

20 .     6-Deoxoblepharodol
C30H44O4     ÏàËÆ¶È:66.6%
Tetrahedron          2005          61          2513-2519
New phenolic triterpenes from Maytenus blepharodes. Semisynthesis of 6-deoxoblepharodol from pristimerin
F¨¦lix M. Rodr¨ªguez, Manuel R. L¨®pez, Ignacio A. Jim¨¦nez, Laila Moujir, Angel G. Ravelo, Isabel L. Bazzocchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

21 .     pachysandiol A
    ÏàËÆ¶È:66.6%
Korean Journal of Pharmacognosy          2010          41          97-102
Inhibition of IL-6 Production in TNF- Stimulated MG-63 by the Triterpenoids Isolated from Aucuba japonica
Jin, Qinglong; Jin, Hong-Guang; Shin, Ji-Eun; Choi, Eun-Jin; Woo, Eun-Rhan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

22 .     compound 40
C30H50O4     ÏàËÆ¶È:66.6%
Heterocycles          2012          85          1117-1139
Synthesis and Biological Evaluation of Oleanolic Acid Derivatives as Novel Inhibitors of Protein Tyrosine Phosphatase 1B
Hui Li, Hui Zou, Lixin Gao, Ting Liu, Fan Yang, Jingya Li, Jia Li,* Wen-Wei Qiu,* and Jie Tang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

23 .     Friedelane-2¦Á,3¦Â-diols
C30H52O2     ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          2011          46          995-996
Triterpene from Armillaria mellea
Wen Juan Guo and Shun Xing Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

24 .     pachysandiol A
    ÏàËÆ¶È:66.6%
Korean Journal of Pharmacognosy          2010          41          97-102
Inhibition of IL-6 Production in TNF-¦Á Stimulated MG-63 by the Triterpenoids Isolated from Aucuba japonica
Qinglong Jin, Hong-Guang Jin, Ji Eun Shin, Eun Jin Choi and Eun-Rhan Woo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

25 .     ÇÇÄ¾ÝÆ´¼
    ÏàËÆ¶È:66.6%
Lishizhen Medicine and Materia Medica Research          2011          22          119-120
¾Å¹ÜѪ»¯Ñ§³É·ÖµÄÑо¿
ÆÑÀ¼Ïã; ԬСºì; ÌÆÌì¾ý; ÁõÑà
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

26 .     5(6)-gluten-3¦Á-ol
    ÏàËÆ¶È:66.6%
Lishizhen Medicine and Materia Medica Research          2012          23          2700-2701
Triterpenes from the Leaves of Garcinia oblongifolia
WANG Ning; TANG Li-chang; YAO Hai-ping; DENG Shi-ming; YANG Xian-hui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

27 .     bauerenyl acetate
C32H52O2     ÏàËÆ¶È:65.6%
Chinese Traditional and Herbal Drugs          2008          39          1299-1301
ÔÆÄÏÈïľ֦Ҷ»¯Ñ§³É·ÖÑо¿
Àǿ;ËÎÆôʾ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

28 .     (1S,4R,5R,8R,9S,12R,13S) 12-(1S-Hydroxyethyl)-13-(3-hydroxypropyl)-5-(1,5-dimethylhexyl)-1,9-epoxy-4,8,13 Trimethyl Tricyclo [7,4,0,0(4),(8)] Tridecane
    ÏàËÆ¶È:65.5%
Molecules          2001          6          M221
(1S, 4R, 5R, 8R, 9S, 12R, 13S) 12-(1S-Hydroxyethyl)-13-(3-hydroxypropyl)-5-(1, 5-dimethylhexyl)-1, 9-epoxy-4, 8, 13 Trimethyl Tricyclo [7, 4, 0, 0(4), (8)] Tridecane
M. Daoubi , A. Benharref and M. Pierrot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

29 .     compound III
C29H42O4     ÏàËÆ¶È:65.5%
Acta Pharmaceutica Sinica          1991          26          341-344
THE STRUCTURE OF TRIPTERYGONE
DM Zhang; DQ Yu and FZ Xie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

30 .     C-friedo-oleana-7,9(11)-diene-3¦Á,29-diol
C30H48O2     ÏàËÆ¶È:65.5%
Chinese Pharmaceutical Journal          2000          35          733-736
Studies on the chemical constituents of unsaponifiable lipids from the seeds of Trichosanthes kirilowii
CHAO Zhi mao, HE Bo, ZHANG Ying, AKIHISA Toshihiro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     karounidiol
C30H48O2     ÏàËÆ¶È:65.5%
Chinese Pharmaceutical Journal          2001          36          157-160
Study on the chemical constituents of unsaponifiable lipids from the seeds of Trichosanthes rosthornii
CHAO Zhi mao, HE Bo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

32 .     glutin-5-en-3-one
    ÏàËÆ¶È:65.5%
Natural Product Research and Development          2000          12(3)          30-33
CHEMICAL CONSTITUENTS FROM THE ROOT OF RHODIOLA PAMIERA
Liu Junling; Re Na; Du Niansheng Wei Feng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

33 .     dehydroulmudiol
C30H48O2     ÏàËÆ¶È:63.3%
Chemical & Pharmaceutical Bulletin          2006          54(6)          775-778
New Triterpenoids Isolated from the Root Bark of Ulmus pumila L.
Dong WANG,Mingyu XIA,and Zheng CUI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

34 .     irregularasulfate
C30H51NO5S     ÏàËÆ¶È:63.3%
Journal of Natural Products          2007          70          1812-1815
Protein Phosphatase Inhibitors Isolated from Spongia irregularis Collected in Papua New Guinea
Gavin Carr,Mikolaj Raszek, Rob Van Soest, Teatulohi Matainaho, Micheal Shopik, Charles F. B. Holmes, and Raymond J. Andersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

35 .     mudanpinoic acid A
C30H46O3     ÏàËÆ¶È:63.3%
Journal of Natural Products          1998          61          343-346
Two Novel Compounds from Paeonia suffruticosa
Hang-Ching Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

36 .     3-dehydrohancokinol
C30H48O     ÏàËÆ¶È:63.3%
Chemical & Pharmaceutical Bulletin          1991          39          2271-2276
Stereochemistry of Novel Triterpenes from Cynanchum hancokianum
Hongxiang LOU,Xian LI,Masayuki ONDA,Yaeko KONDA,Mieko URANO,Yoshihiro HARIGAYA,Hiroaki TAKAYANAGI and Haruo OGURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     hancolupenone
    ÏàËÆ¶È:63.3%
Acta Pharmaceutica Sinica          1991          26          584-592
ISOLATION AND STRUCTURE DETERMINATION OF A NEW SAPONIN OF ANEMARRHENA ASPHODELOIDES
D Gou; S Li; Q Chi; WG Sun and ZF Sha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

38 .     hancolupenol octacosanate
C30H50O     ÏàËÆ¶È:63.3%
Acta Pharmaceutica Sinica          1991          26          584-592
ISOLATION AND STRUCTURE DETERMINATION OF A NEW SAPONIN OF ANEMARRHENA ASPHODELOIDES
D Gou; S Li; Q Chi; WG Sun and ZF Sha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

39 .     B-friedoolean-5-en-3¦Â-ol
    ÏàËÆ¶È:63.3%
Natural Product Research          1993          2          57-60
13C NMR Assignments of D:B-Friedoolean-5-en-3¦Â-OL
L. Carvalho; J. Seita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

40 .     glut-5-en-3¦Â-ol
    ÏàËÆ¶È:63.3%
Natural Product Research          2005          19          197-202
Antimicrobial triterpenes from Poulsenia armata miq. standl.
Hesham Rushdey El-Seedi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

41 .     glutinol
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2009          34          1097-1100
Studies on chemical constituents from stems of Cudrania tricuspidata
MA Zhaotang, YANG Xiuwei, ZHONG Guoyue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

42 .     3¦Â-hydroxy-glutin-5-ene
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2009          34          708-711
Studies on chemical constituents from herbs of Usnea longissima
FENG Jie, YANG Xiuwei, SU Siduo, HE Chuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

43 .     glut-5-en-3¦Â-ol
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2007          32          1416-1418
Studies on chemical constituents of Helwingia Chinensis
YANG Juan, LOU Fangming, NIU Yukun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

44 .     glutinol
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2006          31          562-565
Chemical constituents from roots of Ardisia punctata
LI Chun , YUE Dangkun, BU Pengbin, SUN Youfu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

45 .     friedelin
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2006          31          477-479
Studies on chemical constituents in leaves of Mallotus furetianus
LIN Lianbo, FU Xiaowen, AI Chaohui, SHEN Jing, WEI Kun, LI Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

46 .     3¦Â-hydroxy-glutin-5-ene
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2003          28          527-530
Chemical Constituents from the Leaves of Dalbergia hainanensis
ZHANG Peicheng, WU Yan, YU Dequan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

47 .     glutinol
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          1998          23          548-549
Studies on Chemical Constituents of Quercus mongolica Fisch
Yuan Jiuzhi and Sun Qishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

48 .     friedelin
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          1994          19          164-165
Studies on Chemical Constituents of Artemisia roxbugiana Wall
Hu Youhua and Li Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

49 .     celastolide
C30H46O5     ÏàËÆ¶È:63.3%
Phytochemistry          1997          46          535-543
Di- and triterpenoids from Tripterygium hypoglaucum
Hongquan Duan, Kazuyoshi Kawazoe, Masahiko Bando, Masaru Kido, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

50 .     aleuritolic acid
C30H48O3     ÏàËÆ¶È:63.3%
Acta Pharmaceutica Sinica          2007          Vol 42          285-289
Chemical constituents from the roots of Homonoia riparia
YANG Shu-min; LIUXi-kui; QING Chen; WUDa-gang; ZHUDa-yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

51 .     wilforol
    ÏàËÆ¶È:63.3%
Acta Pharmaceutica Sinica          1999          Vol 34          210-213
THE TRITERPENOIDS OF TRIPTERYGIUM WILFORDII
Guo Fujiang (Guo FJ); Fang Peifen (Fang Pf) and Li Yuanchao (Li YC)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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