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11.99,12.03,13.37,14.18,18.72,19.02,19.85,21.11,22.73,23.03,24.21,24.92,25.11,25.98,27.26,28.22,28.35,31.94,32.62,33.85,34.04,34.30,34.77,36.15,36.31,37.01,39.74,41.75,42.56,45.78,51.62,53.64,56.06,56.09,69.53,73.32,73.36,76.74,77.06,77.37,128.90,131.66,173.32,173.46
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1 .     6'-linoleic-¦Â-daucosterol
C30H50O     ÏàËÆ¶È:71.1%
Natural Product Research and Development          2009          21          776-778
Chemical Constituents of the Roots of Ligularia fischeri
DENG Mei-cai; JIAO Wei; DONG Wei-wei; LU Run-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     5,6¦Â-Epoxysitosteryl-9,10-di-tertbutyldimethylsilyloxystearate
C59H112O5Si2     ÏàËÆ¶È:70.8%
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
3 .     7¦Â-Hydroxysitosteryl-9,10-dihydroxystearate
C47H84O5     ÏàËÆ¶È:70.4%
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
4 .     ¦Â-sitosteryl-D-glucoside-6'-palmitate
C51H90O7     ÏàËÆ¶È:70.4%
China Journal of Chinese Materia Medica          2006          31          307-308
Studies on the chemical constituents from stem of Chirta longgangensis var. hongyao
WANG Manyuan, YANG Lan, TU Youyou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     ¦Â-sitosteryl glucoside-3'-O-heptadecoicate
    ÏàËÆ¶È:69.5%
Natural Product Research and Development          1997          9(2)          7-10
STUDIES ON THE CHEMICAL CONSTITUENTS OF THE CULTIVATED DESERTLIVING CISTANCHE (CISTANCHE DESERTICOLA)
Tu Pengfei; He Yanping and Lou Zhicen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     ¦Â-Sitosterol glucoside 6'-O-palmitate
    ÏàËÆ¶È:68.8%
Korean Journal of Pharmacognosy          2008          39(3)          186-193
Phytochemical Studies on Astragalus Root (3);Triterpenoids and Sterols
Jung, Hye-Sil; Lee, Eun-Ju; Lee, Je-Hyun; Kim, Ju-Sun; Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     7¦Â-Hydroxysitosteryl oleate
C47H82O3     ÏàËÆ¶È:68.7%
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
8 .     7¦Â-Hydroxycholesteryl-9,10-di-tertbutyldimethylsilyloxystearate
C57H108O5Si2     ÏàËÆ¶È:68.7%
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
9 .     atroside
C45H78O7     ÏàËÆ¶È:68.1%
Fitoterapia          2001          72          712-714
A new acylated steroid glucoside from Pero skia atriplicifolia
M.S. Alia, M. Saleema, A.W. Erian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     colebrin D
C52H90O8     ÏàËÆ¶È:68.1%
Fitoterapia          2000          71          641-648
New steroids from Clerodendrum colebrookianum
Hui Yang, Jia Wang, Ai-Jun Hou, Yun-Pin Guo,Zhong-Wen Lin, Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (6'-O-palmitoyl)-sitosterol-3-O-¦Â-D-glucoside
    ÏàËÆ¶È:68.1%
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
12 .     24-ethylcholest-5-en-3¦Â-O-¦Â-D-pyranoglucosyl-6'-O-palmitat
    ÏàËÆ¶È:68.1%
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
13 .     Sitosterol-3-O-¦Â-D-glucosl-6'-O-palmitate
    ÏàËÆ¶È:68.1%
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
14 .     32,33,34-trimethyl-bacteriohopan-16-ene 3-O-¦Â-D-glucopyranoside
C44H76O6     ÏàËÆ¶È:68.1%
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
15 .     Klainedoxasterol
C79H146O7     ÏàËÆ¶È:68.1%
Fitoterapia          2013          86          108-114
Lanostane-type triterpenoid and steroid from the stem bark of Klainedoxa gabonensis
Eric Ren¨¦ Sieliatchom Nkanwen, Anar Sahib Gojayev, Hippolyte Kamdem Wabo, Jean Jules Kezetas Bankeu, Muhammad Choudhary Iqbal, Akif Alakbar Guliyev, Pierre Tane
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
2Â¥2013-12-09 20:33:33
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