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CÆ×Êý¾Ý£º12.14,12.26,12.31,12.58,17.96,19.09,19.33,19.42,19.57,20.17,21.09,21.39,21.59,23.10,24.34,25.34,25.97,28.27,29.21,29.75,31.86,31.90,33.85,35.98,
36.69,37.32,38.81,42.34,45.65,50.10,51.09,55.94,56.67,61.58,70.57,73.94,77.21,77.26,77.45,101.32,121.64
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1 .     ¦Â-sitosterol
    ÏàËÆ¶È:82.9%
China Journal of Chinese Materia Medica          2002          27          752-754
Studies on the Chemical Constituents in Radix Astilbes Chinensis
SUN Hongxiang, YE Yiping, YANG Ke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     32,33,34-trimethyl-bacteriohopan-16-ene 3-O-¦Â-D-glucopyranoside
C44H76O6     ÏàËÆ¶È:81.8%
Journal of Ethnopharmacology          2011          135          78-87
Chemical constituents from the stem bark of Symplocos paniculata Thunb. with antimicrobial, analgesic and anti-inflammatory activities
Ruchi Badoni Semwal, Deepak Kumar Semwal, Ravindra Semwal, Randhir Singh, Mohan Singh Maniyari Rawat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     ¦Â-sitosterol-3-O-¦Â-D-glucoside and stigmasterol-3-O-¦Â-D-glucoside
    ÏàËÆ¶È:80.4%
The Chinese Pharmaceutical Journal          2000          52          261-273
Studies on Anti-inflammatory Constituents of Leucas Mollissima WALL. var. Chinensis Benth
¹Åؑͥ(Chen-Ting Ku), ê?„ÙÖÇ(Sheng-Chih Chen), ÍõÀ^ƽ(Jih-Pyang Wang), …ǽðžI(Jin-Bin Wu), ¹ù„ÙÖú(Sheng-Chu Kuo)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     3¦Â-sitosterol laminaribioside
    ÏàËÆ¶È:78.0%
Natural Product Research and Development          2010          22          940-944
Chemical Constituents from Melastoma dodecandrum
YANG Dan;MA Qing-yun; LIU Yu-qing; DING Zhong-tao; ZHOU Jun; ZHAO You-xing;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     ¦Â-sitosteryl-3-O-¦Â-D-glucopyr-anoside-2'-O-palmitate
C51H90O7     ÏàËÆ¶È:76.1%
Natural Product Research and Development          2014          26          197-201
Chemical Constituents from the Roots of Nothapodytes pittosporoides
BAI Yong-hua, SONG Qi-shi*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     iyengaroside-B
    ÏàËÆ¶È:75.6%
Natural Product Research          2002          16          407-413
Steroid and Antibacterial Steroidal Glycosides from Marine Green Alga Codium Iyengarii Borgesen
Muhammad Shaiq Ali; Muhammad Saleem; Raghav Yamdagni; Muhammad Ashfaq Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     ¦Â-sitosteroldiglucoside
C41H70O11     ÏàËÆ¶È:75.6%
Phytochemistry          1999          52          917-921
Two saponins from Pteleopsis hylodendron
F.N. Ngounou, Atta-ur-Rahman, M. Iqbal Choudhary, Shahid Malik, Seema Zareen, Riaz Ali, D. Lontsi, B.L. Sondengam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (6'-O-palmitoyl)-sitosterol-3-O-¦Â-D-glucoside
    ÏàËÆ¶È:75.6%
Journal of Natural Products          1987          Vol 50          881
Sterols and Steryl Glycosides from Urtica dioica
Neera Chaurasia, Max Wichtl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     Sitosterol-3-O-¦Â-D-glucosl-6'-O-palmitate
    ÏàËÆ¶È:75.6%
Phytochemical Analysis          1992          3          38-41
Characterization of acylated steryl glycosides from Euryale ferox by nuclear magnetic resonance spectroscopy
Zhao Haoru and Zhao Shoushun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     24-Ethylcholesterol-acetate
    ÏàËÆ¶È:75.6%
Steroids          1989          53          625-638
Sterols of some Clerodendrum species(verbenaceae): Occurrence of the 24¦Á- and 24¦Â-epimers of 24-ethylsterols lacking a ¦¤25-bond
Toshihiro Akihisa, Yuzuru Matsubara, Parthasarathi Ghosh, Swapnadip Thakur, Toshitake Tamura, Taro Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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