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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½2185¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . stigmast-5-en-3¦Â-ol-3-O-¦Â-D-(2'-n-triacontanoyl) glucopyranoside C65H118O7 ÏàËÆ¶È:83.7% Journal of Asian Natural Products Research 2012 14 301-307 New steroidal glycoside ester and aliphatic acid from the fruits of Lycium chinense Woo-Suk Jung,Ill-Min Chung,Mohd Ali and Ateeque Ahmad Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-sitosteryl-3'-glucopyranoside-6'-O-palmitate ÏàËÆ¶È:82.6% Chinese Herbal Medicines 2014 6 65-69 Chemical Constituents from Barks of Lannea coromandelica Xiao-juan Yun, Huo-ming Shu, Guang-ying Chen, Ming-hui Ji, Jin-yue Ding Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ¦Â-sitosterol-3-O-¦Â-D-glucoside-6'-O-eicosanate ÏàËÆ¶È:80.9% 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 4 . mixture of ¦Â-sitosterol-3-O-¦Â-D-glucoside and stigmasterol-3-O-¦Â-D-glucoside ÏàËÆ¶È:80.9% The Chinese Pharmaceutical Journal 2003 55 109-119 Antiproliferative Constituents from Gynura divaricata subsp. formosana Sheng-Chih Chen*, Li-Ling Hong, Chung-Yang Chang, Chun-Jen Chen, Mei-Hua Hsu, Yuan-Chao Huang, Tai-Hung Huang and Sheng-Chu Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . glucoraphenin ÏàËÆ¶È:79.5% 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 6 . ¦Â-sitosteryl-3-O-¦Â-D-glucopyranoside-2'-O-palmitate C51H90O7 ÏàËÆ¶È:78.5% Phytochemistry 2008 69 2627-2633 Non-cannabinoid constituents from a high potency Cannabis sativa variety Mohamed M. Radwan, Mahmoud A. ElSohly, Desmond Slade, Safwat A. Ahmed, Lisa Wilson,Abir T. El-Alfy, Ikhlas A. Khan, Samir A. Ross Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 24-ethylcholest-5-en-3¦Â-O-¦Â-D-pyranoglucosyl-6'-O-palmitat ÏàËÆ¶È:78.5% 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 ̼Æ×Ä£Äâͼ 8 . ºúÂܲ·ÜÕרéµËáõ¥ ÏàËÆ¶È:78.5% Chinese Pharmaceutical Journal 2008 43 971-973 Studies on Chemical Constituents of Acetyl Acetate Extracted Fraction from Veratrum dahuricum NIE Li-yue TANG Jian~LI Hui-liang JIN Hui-zi ZHANG Wei-dong Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3¦Â-sitosterol laminaribioside ÏàËÆ¶È:78.5% 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 ̼Æ×Ä£Äâͼ 10 . ¦Â-sitosterol-3-O-¦Â-D-glucoside and stigmasterol-3-O-¦Â-D-glucoside ÏàËÆ¶È:78.5% 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 ̼Æ×Ä£Äâͼ 11 . 6'-O-benzoyldaucosterol ÏàËÆ¶È:76.1% China Journal of Chinese Materia Medica 1998 23 419-421 Chemical Constituents of Tet rast igma hemsleyanum Diels. et Gilg Yang Dajian , Liu Hongya , Li Xinzhong , Huang Xiaoping and Qin Jian Structure 13C NMR ̼Æ×Ä£Äâͼ |

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