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250350663: ½ð±Ò+6, ¡ï¡ï¡ïºÜÓаïÖú 2014-05-17 13:36:27
250350663(À±±ÊvСдú·¢): ½ð±Ò+4, ´ú·¢½±Àø½ð±Ò£¬³æÓÑÓ¦ÖúÍê±ÏÈ«¶î·¢·Å½ð±Ò 2014-05-22 00:12:31
1 .     daucosterol linoleate
    ÏàËÆ¶È:69.0%
Chinese Pharmaceutical Journal          2007          42          661-663
Studies on Chemical Constituents of Paeonia veitchii L.
WANG Rui, CHOU Gui-xin, ZHU En-yuan, WANG Zheng-tao, BI Kai-shun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     skimmiarepin C
    ÏàËÆ¶È:67.8%
Natural Product Research          2004          18          117-122
A new insecticidal protolimonoid from Aegle Marmelos
J.K.R. Radhika Samarasekera; Bhupinder P. S. Khambay; K. Patrick Hemalal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Citruslanosteroside
C56H100O7     ÏàËÆ¶È:67.8%
Natural Product Research          2010          24          610-620
Phytochemical investigation of the fruit peels of Citrus reticulata Blanco
M. Aasim Khan; M. Ali; Prawez Alam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     ligustrin B
    ÏàËÆ¶È:67.2%
Phytochemistry          1997          46          977-979
Acylated triterpenoids from Ligustrum ovalifolium
Koichi Machida, Toshio Yamaguchi, Yoshiko Kamiya, Masao Kikuchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     12,6'-dioctanoyl ginsenoside Rh2 (D-Rh2)
    ÏàËÆ¶È:67.2%
Bioorganic & Medicinal Chemistry Letters          2012          22          1082-1085
Structural modification of ginsenoside Rh2 by fatty acid esterification and its detoxification property in antitumor
Gong-Qing Wei, Yi-Nan Zheng, Wei Li, Wen-Cong Liu, Ting Lin, Wei-Yun Zhang, Hai-Feng Chen,Jin-Zhang Zeng, Xiao-Kun Zhang, Quan-Cheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     daucosterol-6'-linoleate
    ÏàËÆ¶È:67.2%
Journal of Shenyang Pharmaceutical University          2008          25          883-885
Chemical constituents from the seeds of Castanea mollissima Blume(III)
LONG Zhi-min, WU Li-jun, JIANG Bing-ya, SUN Bo-hang, HUANG Jian, GAO Hui-yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Ginsenoside PM1
    ÏàËÆ¶È:65.4%
Molecules          2007          12          2140-2150
Isolation, Synthesis and Structures of Cytotoxic Ginsenoside Derivatives
Jun Lei, Xiang Li, Xiao-jie Gong and Yi-nan Zheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Ginsenoside SM1
    ÏàËÆ¶È:65.4%
Molecules          2007          12          2140-2150
Isolation, Synthesis and Structures of Cytotoxic Ginsenoside Derivatives
Jun Lei, Xiang Li, Xiao-jie Gong and Yi-nan Zheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     Citrusteryl arachidate
C55H98O7     ÏàËÆ¶È:65.4%
Natural Product Research          2010          24          610-620
Phytochemical investigation of the fruit peels of Citrus reticulata Blanco
M. Aasim Khan; M. Ali; Prawez Alam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     7¦Â-tert-Butyldimethylsilyloxysitosteryl-9,10-ditert-butyldimethylsilyloxystearate
C65H126O5Si3     ÏàËÆ¶È:64.4%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     5¦Á-stigmast-9(11)-en-3¦Â-ol-tetraco santrienoic acid ester
    ÏàËÆ¶È:63.6%
China Journal of Chinese Materia Medica          1996          21          666-667
Studies on Chemical Components of Cynomorium songaricum Rupr.
Xu Xiuzhi, Zhang Chengzhong and Li Chong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     skimmiarepin A
    ÏàËÆ¶È:63.6%
Phytochemistry          1994          36          1303-1306
Protolimonoid and lignans from Zanthoxylum petiolare
Mara S.P. Arruda, João B. Fernandes, Paulo C. Vieira, M. Fatima Das G.F. Da Silva, Jose R. Pirani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3-O-Carboxymaleinate of ¦Á,¦Â-amyrin
    ÏàËÆ¶È:63.6%
Bioorganic & Medicinal Chemistry          2011          19          1268-1276
Amyrin esters induce cell death by apoptosis in HL-60 leukemia cells
Francisco W. A. Barros, Paulo N. Bandeira, Daisy J. B. Lima, Assuero S. Meira, Silvana S. de Farias,Maria Rose J. R. Albuquerque, H¨¦lcio S. dos Santos, Telma L. G. Lemos, Manoel Odorico de Morais,Let¨ªcia Veras Costa-Lotufo, Claudia do ¨® Pessoa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     shishicrellastatin A
C56H83Na3O16S3     ÏàËÆ¶È:63.6%
Bioorganic & Medicinal Chemistry          2011          19          6594-6598
Shishicrellastatins, inhibitors of cathepsin B, from the marine sponge Crella (Yvesia) spinulata
Shuhei Murayama, Yasufumi Imae, Kentaro Takada, Jo Kikuchi, Yoichi Nakao, Rob W.M. van Soest, Shigeru Okada, Shigeki Matsunaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     balanoinvolin
    ÏàËÆ¶È:63.6%
Journal of Anhui Agricultural Sciences          2012          40          9641-9643
Study on the Chemical Constituents of Mirabilis himalaica Roots
YANG Pan-pan et al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     ¦Â-sitosterol-3-O-(6'-linolenoyl)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:63.6%
Indian Journal of Chemistry Section B          1997          36B          1038-1043
Triterpenoids and other compounds from Euphorbia esula and E.petiolata
Yan-Ping Shi & Zhong-Jian Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (+/-)-3¦Á,7¦Á,12¦Á-Tris(3-{[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yl]oxycarbonyl}propanoyloxy)-5¦Â-cholan-24-oic aci
C123H196O17     ÏàËÆ¶È:63.3%
Steroids          2013          78          435-453
New propanoyloxy derivatives of 5¦Â-cholan-24-oic acid as drug absorption modifiers
Lenka Coufalov¨¢, Lech Mr¨®zek, Lucie R¨¢rov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Katar¨ªna Kr¨¢l¡¯ov¨¢, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     ligustrin A
    ÏàËÆ¶È:63.1%
Phytochemistry          1997          46          977-979
Acylated triterpenoids from Ligustrum ovalifolium
Koichi Machida, Toshio Yamaguchi, Yoshiko Kamiya, Masao Kikuchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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3Â¥2014-05-17 11:43:00
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