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xianlu

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15.409,16.868,18.229,19.151,20.933,21.072,24.451,26.509,27.28,27.824,27.967,28.252,29.271,29.973,30.354,31.072,35.642,37.074,37.087,38.893,44.11,44.233,44.257,48.689,49.391,50.372,50.404,53.381,53.421,71.946,71.957,75.635,78.938,134.192,134.229,134.462,134.483

[ Last edited by PSA on 2013-6-21 at 11:12 ]
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²éѯ½á¹û£º¹²²éµ½696¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     compound 4a
C40H55NO5     ÏàËÆ¶È:70.2%
Phytochemistry          1993          32          1239-1244
Triterpenes of Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     24Z-ethylidenelanost-8-en-3¦Â-ol
C31H54O     ÏàËÆ¶È:67.5%
Phytochemistry          1994          37          201-203
Lanostane triterpenes from the bark of Neolitsea sericea
Mahesh C. Sharma, Tatsuro Ohira, Mitsuyoshi Yatagai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     21,22:24,25-di-O-isopropylidene derivative
C36H60O5     ÏàËÆ¶È:67.5%
Tetrahedron          2013          69          3536-3542
Terresterol, a polyoxygenated lanostanoid, isolated from the oomycete Saprolegnia terrestris, and its innate immune-promoting activity
Haruhisa Kikuchi, Yuichi Sato, Shoichiro Kurata, Yasuhiro Katou, Yoshiteru Oshima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     pisosterol
C33H54O4     ÏàËÆ¶È:67.5%
Australian Journal of Chemistry          1989          42          995-1001
The Structure and Absolute Stereochemistry of Pisosterol, the Principal Triterpenoid From Fruitbodies of the Fungus Pisolithus tinctorius
M Gill, MJ Kiefel, BW Skelton and AH White
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     Inonotsuoxide A diacetate
C34H54O5     ÏàËÆ¶È:67.5%
Bioorganic & Medicinal Chemistry          2007          15          257-264
Structure determination of inonotsuoxides A and B and in vivo anti-tumor promoting activity of inotodiol from the sclerotia of Inonotus obliquus
Tomoko Nakata, Takeshi Yamada, Sayaka Taji, Hirofumi Ohishi, Shun-ichi Wada, Harukuni Tokuda, Kazuo Sakuma, Reiko Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3¦Â-acetoxy-25-methoxylanost¦Á-8,23-diene
C33H54O3     ÏàËÆ¶È:64.8%
Phytochemistry          2005          66          495-501
Cytotoxic triterpenes from the aerial roots of Ficus microcarpa
Yi-Ming Chiang, Jang-Yang Chang, Ching-Chuan Kuo,Chi-Yen Chang, Yueh-Hsiung Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     25-methylpisolactone
C32H52O3     ÏàËÆ¶È:64.8%
Phytochemistry          1997          45          499-504
Triterpenoids from Pisolithus tinctorius isolates and ectomycorrhizas
Alfred Baumert, Brigitte Schumann, Andrea Porzel, J¨¹rgen Schmidt, Dieter Strack
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 2a
C39H53NO5     ÏàËÆ¶È:64.8%
Phytochemistry          1993          32          1239-1244
Triterpenes of Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     3¦Â-(2-Methoxy-oxalyloxy)-24-methylene-5¦Á-lanost-8-en-21-oic acid
C34H52O6     ÏàËÆ¶È:64.8%
Journal of Asian Natural Products Research          2013          15          253-257
Two new triterpenoids from the fungus Perenniporia maackiae
Hua Guo, Jing Si, Zheng-Hui Li, Tao Feng, Ze-Jun Dong, Yu-Cheng Dai & Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     3-O-iso-butylmalonyl-12¦Â-acetoxy-3¦Á,25-dihydroxy-(20S,24R)-epoxydammarane
C39H64O8     ÏàËÆ¶È:63.1%
Bioorganic & Medicinal Chemistry          2010          18          2964-2975
Papyriferic acid derivatives as reversal agents of multidrug resistance in cancer cells
Juan Xiong, Masatoshi Taniguchi, Yoshiki Kashiwada, Michiko Sekiya, Takashi Yamagishi, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     3¦Â-(E)-cinnamoyleuphorbol
    ÏàËÆ¶È:63.1%
Journal of the Brazilian Chemical Society          2011          22          1880-1887
Molluscicidal Activity of Compounds Isolated from Euphorbia conspicua N. E. Br.
Rosalina C. S. Mata, Dina I. M. D. de Mendonça, Liliana Vieira, Aldenir F. dos Santos, Luciana A. da Silva, Jorge F. Gaspar, C¨¦lia Martins, Jos¨¦ Rueff and Antônio E. G. Sant¡¯Ana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     acetylated derivative of methyl 3¦Á-hydroxy-24-oxotirucalla-8,25-dien-21-oate
C33H50O5     ÏàËÆ¶È:62.1%
Phytochemistry          2006          67          1309-1315
Tirucallane triterpenes from the roots of Ozoroa insignis
Yonghong Liu , Pedro Abreu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3¦Á,25-dihydroxy-24-(2-hydroxyethyl)-tirucall-8-en-21-oic acid
C32H54O5     ÏàËÆ¶È:62.1%
Phytochemistry          2006          67          1309-1315
Tirucallane triterpenes from the roots of Ozoroa insignis
Yonghong Liu , Pedro Abreu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     euphorbol acetate
C33H54O2     ÏàËÆ¶È:62.1%
Journal of Natural Products          2002          65          158-162
Eupha-7,9(11),24-trien-3â-ol (¡°Antiquol C¡±) and Other Triterpenes from Euphorbia antiquorum Latex and Their Inhibitory Effects on Epstein-Barr Virus Activation
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