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liuxiaosa: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2014-04-29 09:16:24
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liuxiaosa: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2014-04-29 09:16:24
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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£º¹²²éµ½2126¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Â-sitosteryl-3'-glucopyranoside-6'-O-palmitate ÏàËÆ¶È:91.3% 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 2 . ¦Â-sitosteryl-3¦Â-glucopyranoside-6'-O-palmitate ÏàËÆ¶È:89.1% Fitoterapia 2004 75 500-504 Cytotoxic constituents from Plumbago zeylanica A.T. Nguyen , H. Malonne , P. Duez , R. Vanhaelen-a,b, b a anhaelen-Fastrea,M. Vanhaelen, J. Fontaine Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ¦Â-sitosteryl glucoside-3'-O-heptadecoicate ÏàËÆ¶È:89.1% 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 ̼Æ×Ä£Äâͼ 4 . ¦Â-sitosterol-3-O-¦Â-D-glucoside-6'-O-eicosanate ÏàËÆ¶È:86.9% 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 5 . ¦Â-sitosteryl-3¦Â-glucopyranoside-6'-O-palmitate ÏàËÆ¶È:86.9% Pharmaceutical Chemistry Journal 2012 46 225-227 Chemical constituents of Ficus odorata P.-W. Tsai, K. A. De Castro-Cruz, C.-C. Shen, C.-T. Chiou, C. Y. Ragasa Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Â-sitosterol-3¦Â-glucopyranoside-6'-palmitate ÏàËÆ¶È:86.9% Journal of Chinese Medicinal Materials 2008 31 222-223 Studies on Chemical Constituents of the Seeds of Allium cepa YUAN Ling, JI Teng-fei, WANG Ai-guo, YANG Jian-bo, SU Ya-lun Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ¦Â-sitosteryl-3¦Â-glucopyranoside-6'-O-palmitate ÏàËÆ¶È:86.9% Chinese Traditional and Herbal Drugs 2013 44 2657-2660 Chemical constituents from Cardamine leucantha ZHENG Cong-cong, SU Yan-fang, CHEN Lei, BI Yan-ping, YANG Fan, XU Jing, YAN Shi-lun Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Sitosteryl oleate C47H82O2 ÏàËÆ¶È:84.7% 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 ̼Æ×Ä£Äâͼ 9 . sitosteryl-9,10-dihydroxystearate C47H84O4 ÏàËÆ¶È:84.7% 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 ̼Æ×Ä£Äâͼ 10 . 5,6¦Â-Epoxysitosteryl-9,10-dihydroxystearate C47H84O5 ÏàËÆ¶È:84.7% 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 ̼Æ×Ä£Äâͼ 11 . ¦Â-Sitosterol glucoside 6'-O-palmitate ÏàËÆ¶È:84.7% 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 ̼Æ×Ä£Äâͼ 12 . compound 1 C61H110O7 ÏàËÆ¶È:84.7% Archives of Pharmacal Research 2007 30 172-176 Isolation of constituents and anti-complement activity from Acer okamotoanum WenYi Jin, Byung-Sun Min, JongPill Lee, Phuong Thien Thuong and Hyeong-Kyu Lee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ¦Â-sitosteryl glucoside-6'-palmitoleoate ÏàËÆ¶È:84.7% Chinese Journal of Applied & Environmental Biology 2000 6 194-196 CHEMICAL CONSTITUENTS FROM RUBUS SETCHUENENSIS HUANG Kexin; ZHANG Xiaorong; WANG Mingkui & DING Lisheng Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ¦Â-sitosterol palmitate C45H80O2 ÏàËÆ¶È:82.6% 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 ̼Æ×Ä£Äâͼ 15 . stigmast-5-en-3¦Â-ol-3-O-¦Â-D-(2'-n-triacontanoyl) glucopyranoside C65H118O7 ÏàËÆ¶È:82.6% 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 16 . ºúÂܲ·ÜÕרéµËáõ¥ ÏàËÆ¶È:82.6% 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 17 . (6R,E)-6-((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-(palmitoyloxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-3-ethyl-2-methylhept-4-enoic acid C45H78O4 ÏàËÆ¶È:82.6% Life Sciences 2013 92 202-210 Antiulcer and antioxidant activities of a new steroid from Morus alba Aftab Ahmad, Gaurav Gupta, Muhammad Afzal, Imran Kazmi, Firoz Anwar Structure 13C NMR ̼Æ×Ä£Äâͼ |

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