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13C NMR (101 MHz, CDCl3) ¦Ä 140.76, 138.34, 129.27, 121.73, 71.82, 56.87, 56.77, 56.05, 55.95, 51.25, 50.16, 50.13, 45.83, 42.31, 42.22, 40.52, 39.78, 39.69, 37.26, 36.52, 36.16, 33.95, 31.91, 31.67, 29.72, 29.14, 28.94, 28.26, 26.05, 25.43, 24.38, 24.32, 23.07, 21.23, 21.11, 21.09, 19.84, 19.42, 19.04, 18.99, 18.79, 12.27, 12.06, 11.99, 11.87,
»¯ºÏÎï2
13C NMR (101 MHz, CDCl3) ¦Ä 64.42, 34.44, 31.94, 29.71, 29.67, 29.49, 29.38, 29.27, 29.17, 28.66, 25.95, 25.05, 22.70, 14.14
»¯ºÏÎï3
¦Ä 171.03, 152.73, 131.45, 124.46, 107.47, 80.92, 55.95, 50.84, 49.42, 47.81, 45.24, 40.47, 38.77, 37.89, 37.13, 35.33, 34.10, 31.36, 28.88, 27.98, 27.05, 25.73, 24.93, 23.71, 21.38, 21.35, 18.16, 17.73, 16.51, 16.29, 15.89, 15.64,
»¯ºÏÎï4
13C NMR (101 MHz, CDCl3) ¦Ä 182.91, 164.08, 154.98, 153.12, 152.29, 152.12, 149.31, 130.32, 123.75, 120.11, 111.15, 108.74, 105.75, 104.08, 93.35, 60.90, 56.12, 56.10,
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jiangchunyong: ½ð±Ò+1, лл 2013-03-18 22:20:07
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1 .     daucosterol+stigmasterol-3-O-glucopyranoside
    ÏàËÆ¶È:78.4%
Chinese Traditional and Herbal Drugs          2004          35          608-611
Studies on chemical constituents of Indigofera carlesii
SU Yan-fang; ZHANG Xin-xin; YANG Jing; GUO Zeng-jun; L¨¹ Ju-xian; GUO De-an
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

2 .     N-(Cholest-5-en-3¦Â-yl)-3¦Â-hydroxyandrost-5-ene-17¦Â-carboxamide
C47H75NO2     ÏàËÆ¶È:72.3%
Steroids          2009          74          88-94
Steroids linked with amide bond¡ªExtended cholesterol
Ivan Černý, Miloš Bud¨§š¨ªnský, Vladim¨ªr Pouzar, Pavel Drašar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

3 .     glucoraphenin
    ÏàËÆ¶È:70.2%
Natural Product Research and Development          2010          22          58-59
Studies on the Chemical Constituents of Cirsium henryi
ZHANG Yue; RUAN Han-li; ZHANG Yong-hui; PI Hui-fang; WU Ji-zhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     ¦Â-sitosterol ¦Â-D-glucopyranoside tetraacetate
    ÏàËÆ¶È:68.0%
Planta Medica          1993          59          369-372
A New Oleanolic Acid Derivative from Securinega tinctoria
LuisM. Carvalho and J. Seita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

5 .     Sitosterol-3-O-12',13'-epoxy-9'-oxo-(10'E)-octadecenoate
C47H78O4     ÏàËÆ¶È:68.0%
Journal of Asian Natural Products Research          2003          5          215-221
THE CHEMICAL CONSTITUENTS OF MUNRONIA HENRYI
SHU-HUA QI, DA-GANG WU, YUN-BAO MA and XIAO-DONG LUO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

6 .     stigmast-5-en-3-O-¦Â-D-glucopyranoside tetraacetate
C43H68O10     ÏàËÆ¶È:68.0%
Natural Product Sciences          1999          5          124-126
Sterols and Sterol Glycosides from Cuscuta Reflexa
Anis, E.; Mustafa, G.; Ahmed, S.; Nisarullah, Nisarullah; Malik, A.; Afza, N.; Badar, Y.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

7 .     ¦Â-sitosterol-¦Â-D-ghcopyranoside
    ÏàËÆ¶È:68.0%
Phytochemistry          1991          30          1026-1029
A butyrolactone lignan disaccharide from Flacourtia ramontchi  
V. Satyanarayana, G.L.David Krupadanam, G. Srimannarayana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

8 .     compound 3a
    ÏàËÆ¶È:68.0%
Phytochemistry          1990          29          2351-2355
Sterol glucosides from Prunella vulgaris
Hisashi Kojima,Noriko Sato,Akiko Hatano,Haruo Ogura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

9 .     Stigmast-5-en-3-O-¦Â-D-glucoside tetraacetate
    ÏàËÆ¶È:68.0%
Magnetic Resonance in Chemistry          2001          39          399-405
Complete 1H and 13C NMR assignments of stigma-5-en-3-O-¦Â-glucoside and its acetyl derivative
Shaheen Faizi, Muhammad Ali, Rubeena Saleem, Irfanullah and Sarah Bibi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

10 .     ¦Â-sitosterol-3-O-¦Â-D-glucoside-6'-O-eicosanate
    ÏàËÆ¶È:68.0%
Chinese Traditional and Herbal Drugs          2002          33          6-8
New steroid glycoside derivatives from Stelmatocrypton khasianum
New steroid glycoside derivatives from Stelmatocrypton khasianum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

11 .     (cis)-2-(4-{2-[(ethoxycarbonyl)amino]ethoxy}benzyl)cyclohexyl (3¦Â,22E)-stigmasta-5,22-dien-3-yl butanedioate
    ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

12 .     lanoscopariol
C46H80O3     ÏàËÆ¶È:65.9%
Journal of Natural Products          1996          59          181-184
New 9¦Â-Lanostane-Type Triterpenic and 13, 14-seco-Steroidal Esters from the Roots of Artemisia scoparia
Surendra Kumar Sharma and Mohammad Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

13 .     Sitosteryl oleate
C47H82O2     ÏàËÆ¶È:65.9%
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

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

14 .     ¦Â-sitosteryl-D-glucoside-6'-palmitate
C51H90O7     ÏàËÆ¶È:65.9%
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

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

15 .     compound 3
    ÏàËÆ¶È:65.9%
Natural Product Sciences          1996          2          19-23
Sterols and Sterol Glycosides from the Leaves of Gynura procumbens
Sadikun, A.; Aminah, I.; Ismail, N.; Ibrahim, P.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-03-18 17:47:25
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