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»¯ºÏÎï1 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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jiangchunyong: ½ð±Ò+1, лл 2013-03-18 22:20:07
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»¯ºÏ1 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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
2Â¥2013-03-18 17:47:25
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