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1 . daucosterol ÏàËÆ¶È:96.8% Chinese Traditional and Herbal Drugs 2012 43 1285-1288 Study on chemical constituents from Potentilla supina ZHENG Guang-hai; PIAO Hui-shun Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-sitosterol-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:94.1% Korean Journal of Pharmacognosy 1996 27(1) 75-79 Phytochemical Constituents from Aconitum pseudolaeve Var. erectum Kim, Dae-Keun; Kwak, Jong-Hwan; Song, Ki-Won; Kwon, Hack-Cheol; Zee, Ok-Pyo; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . daucosterol ÏàËÆ¶È:94.1% Chinese Traditional and Herbal Drugs 2010 41 1787-1790 ëËὬËÞÝàµÄ»¯Ñ§³É·ÖÑо¿ ÕÅ»Ô;³ÂÖØ;ÀîÏÄ;ÀîЦȻ;ÐíÇíÃ÷;ÑîÊÀÁÖ Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ¦Â-Sitosterol-3-O-¦Â-D-glycoside ÏàËÆ¶È:94.1% Archives of Pharmacal Research 2004 27 1016-1019 A new sesquiterpene lactone from Artemisia rubripes nakai Kyu Ha Lee, Yong Deuk Min, Sang Zin Choi, Hak Cheol Kwon and Ock Ryun Cho, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ¦Â-Sitosterol-3-O-glucoside ÏàËÆ¶È:94.1% Archives of Pharmacal Research 2005 28 39-43 Antitumor and antiinflammatory constituents from celtis sinensis Dae Keun Kim, Jong Pil Lim, Jin Wook Kim, Hee Wook Park and Jae Soon Eun Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Â-sitosterol-3-O-¦Â-D-xylopyranoside C34H58O5 ÏàËÆ¶È:93.9% Chinese Pharmaceutical Journal 1997 32 8-11 Chemical constituents from the seeds of Cuscuta australis Guo Cheng(Guo C), Han Gongyu(Han GY), Su Zhongwu(Su ZW) Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Stigmast-5-en-3-O-¦Â-D-glucoside C35H60O6 ÏàËÆ¶È:91.4% 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 8 . daucosterol ÏàËÆ¶È:91.4% Chinese Traditional and Herbal Drugs 2009 40 98-100 ¶ÀÐв˻¯Ñ§³É·ÖÑо¿ Óà¶«»Ô;Áº¾´îÚ;ÅËÇÚ Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . daucosterol C35H60O4 ÏàËÆ¶È:91.4% Chinese Journal of Natural Medicines 2006 4 257-259 Chemical Constituents of Sibiraea angustata TAO Ting-Ting; SEI Yasuo; WANG Tian-Zhi; BAI Chuan; CHANG Yan-Bo Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Sitosterol-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:91.4% Archives of Pharmacal Research 2002 25 628-635 Phytochemical constituens of Cirsium setidens Nakai and their cytotoxicity against human cancer cell lines Won Bin Lee, Hak Cheol Kwon, Ock Ryun Cho, Kang Choon Lee and Sang Un Choi, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ¦Â-daucosterol ÏàËÆ¶È:91.4% Chinese Pharmaceutical Journal 2011 46 341-343 Chemical Constituents of Lysimachia clethroides Duby YUE Shu-mei, CHEN Bai-quan, YUAN Peng-fei, CUI Wei-heng, KANG Wen-yi* Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . daucosterol ÏàËÆ¶È:91.4% Modern Chinese Medicine 2008 10(3) 10-12 Studies on the chemical constituents of Potentill anserine L. Chu Liang, Wang Libo, Zhang Zhe, Gao Huiyuan, Huang Jian, Sun Bohang, Wu Lijun Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . daucosterol ÏàËÆ¶È:91.4% Chinese Journal of Medicinal Chemistry 2006 16 303-305 The constituents of Veratrum japonicum Loes. f. ZHOU Jian-xia, KANG Lu, SHEN Zheng-wu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . daucosterol C35H60O6 ÏàËÆ¶È:91.4% Journal of Shenyang Pharmaceutical University 2008 25 630-632 Chemical constituents from the fruits of Xanthium sibiricum DAI Ying-hui, CUI Zheng, WANG Dong, LI Jian-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . daucosterol ÏàËÆ¶È:91.4% Natural Product Research and Development 2009 21 784-786 Study on the Chemical Constituents of Fruits of Cannabis Sativa L. SHEN Qian;CAI Guang-ming; HE Gui-xia; DU Fang-lu Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . daucosterol ÏàËÆ¶È:91.4% Natural Product Research and Development 2008 20 60-62 Chemical Constituents from the Defatted Seeds of Linum usitatissimum L. SHI Gao-feng; SUN Hao-ran;ZHAO Yan-fang; CHEN Xue-fu; QI Zhi-guo Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . daucosterol ÏàËÆ¶È:91.4% Natural Product Research and Development 2005 17 743-745 Compounds from the Root Bark of Paeonia suffruticosa SHENG Xi-feng;XU Kang-ping; TANG Ling; TAN Gui-shan Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . daucosterol C35H60O6 ÏàËÆ¶È:91.4% Natural Product Research and Development 1998 10(3) 15-19 CHEMICAL STUDY OF RABDOSIA COETSA Wang Jianzhong; Wang Fengpeng Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . ¦Â-Sitosterol Glucoside ÏàËÆ¶È:91.4% Journal of Agricultural and Food Chemistry 2010 58 180-186 Bioactive Compounds from Sour Orange Inhibit Colon Cancer Cell Proliferation and Induce Cell Cycle Arrest G. K. Jayaprakasha, Y. Jadegoud, G. A. Nagana Gowda and Bhimanagouda S. Patil Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . daucosterol ÏàËÆ¶È:91.4% Chinese Traditional and Herbal Drugs 2012 43 1905-1909 Resource chemical constituents from sarcocarp of Ziziphus jujuba var. spinosa GUO Sheng; DUAN Jin-ao; ZHAO Jin-long; QIAN Ye-fei; TANG Yu-ping; QIAN Da-wei Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ¦Â-ºúÂܲ·ÜÕ ÏàËÆ¶È:91.4% China Journal of Chinese Materia Medica 2012 37 1408-1411 ¦Á-glucosidase inhibitory active constituents contained in nutshell of Trapa acornis CHEN Baiquan; ZHANG Qian; WANG Wei; HUANG Huan; KANG Wenyi Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 7¦Â-hydroxysitosterol-3-O-¦Â-D-glucoside ÏàËÆ¶È:91.4% Lishizhen Medicine and Materia Medica Research 2012 23 1-2 Chemical Constituents from Angiopteris Fokiensis WEN Xiao-qiong; HU Ying; ZENG Xiao-jun; ZHANG Lei; CEN Ying-zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . ¦Â-Sitosterol ¦Â-D-glucopyranoside ÏàËÆ¶È:91.1% Korean Journal of Pharmacognosy 2007 38(4) 354-357 Isolation of Two Steroids and a Triterpenoid from the Roots of Potentilla discolor Park, Hee-Juhn; Lee, Kyung-Tae; Park, Jong-Hee Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . daucosterol ÏàËÆ¶È:91.1% Chinese Traditional and Herbal Drugs 2010 41 533-536 Â黯¸ùµÄ»¯Ñ§³É·ÖÑо¿ ÌÕ»ªÃ÷;ÍõÁ¥Êé;´ÞÕ¼³¼;ÕÔ´óÇì;ÁõÓÀºê Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . daucosterol ÏàËÆ¶È:90.9% Phytochemistry 2005 66 2381-2387 Phenolic and terpenoid compounds from Chione venosa (SW.) URBAN var. venosa (Bois Band¨¦) Angelika Lendl, Ingrid Werner, Sabine Glasl, Christa Kletter, Pavel Mucaji,Armin Presser, Gottfried Reznicek, Johann Jurenitsch, David W. Taylor Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . Sitosterol-3-O-¦Â-glucoside ÏàËÆ¶È:90.9% Chemistry of Natural Compounds 2007 43 614-615 FLAVONOIDS FROM Trifolium resupinatum VAR. microcephalum Emel Isik, Temine Sabudak, and Sevi Oksuz Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . sitosterol-3-O-¦Â-D-glicopiranos¨ªdeo ÏàËÆ¶È:90.6% Qu¨ªmica Nova 2008 31 744-750 Chemical constituents and antiedematogenic activity of Peltodon radicans (Lamiaceae) Costa, Habdel Nasser Rocha da; Santos, Maria Cristina dos; Alcântara, Antônio Flavio de Carvalho; Silva, Marilda Conceição; França, Roberta Cabral; Pil¨®-Veloso, Dorila Structure 13C NMR ̼Æ×Ä£Äâͼ |

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dongmings
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3Â¥2013-05-07 08:49:53
wm0629
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dongmings
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6Â¥2013-05-08 10:52:27
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