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wdzhengqun: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-10-01 19:43:06
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²éѯ½á¹û£º¹²²éµ½15944¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Â-sitosterol ÏàËÆ¶È:100% Zeitschrift f¨¹r Naturforschung C 2003 58 441-445 Feeding Stimulative Activity of Steroidal and Secoiridoid Glucosides and Their Hydrolysed Derivatives toward the Olive Weevil (Dyscerus perforatus) E. Kadowaki, Y. Yoshida, N. Baba, and S. Nakajima Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:100% Molecules 2013 18 1325-1336 Chemical Constituents of Caesalpinia decapetala (Roth) Alston Xiao-Hua Wei, Sheng-Jie Yang, Na Liang, De-Yu Hu, Lin-Hong Jin, Wei Xue and Song Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ¦Â-sitosterol ÏàËÆ¶È:100% Chemistry and Industry of Forest Products 2013 33 133-136 Chemical Constituents from the Branch of Litsea cubeba ( Lour. ) Pers. CHEN Zhan-juan, BI He-ping, FAN Chao-jun, BAO Chang-yu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . campesterol ÏàËÆ¶È:100% Chinese Pharmaceutical Journal 2012 47 500-503 Study on Chemical Constituents of Rosa chinensis Jacq. Flower WANG Xiao-yan; WANG Wen-wen; ZHOU Yong-hui; JIANG Xin-ke; JING Lin-lin; JIA Lu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ¦Â-sitosterol ÏàËÆ¶È:100% Korean Journal of Pharmacognosy 2013 44 1-5 Isolation of Compounds having Inhibitory Activity toward Tyrosinase from Receptaculum Nelumbinis Hyun Woo Cho, Won Seok Jung, Byeong Gwan An, Jung Hee Cho and Su Young Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Â-sitosterol ÏàËÆ¶È:100% Northwest Pharmaceutical Journal 2013 28 241-244 Study on chemical constituents of Arenaria kansuensis Maxim. ¢ô LEI Ning, L¨¹ Yali, DU Shushan, DENG Zhiwei, MA Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ¦Â-sitosterol ÏàËÆ¶È:100% Chinese Joumal of Experimental Traditional Medical Fomulae 2011 17 118-120 Research on Chemical Constituents of Ethyl Acetate Fraction from Li Nationality Medicine Elaeagnus gonyanthes Caulis et Folium WEI Na, WANG Yong, LI Pei-pei, LI Hong-fu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Phytochemistry 2004 65 2463-2470 Biosynthesis of the irregular monoterpene artemisia ketone, the sesquiterpene germacrene D and other isoprenoids in Tanacetum vulgare L. (Asteraceae) Dirk Umlauf, Josef Zapp, Hans Becker, Klaus Peter Adam Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . sitosterol ÏàËÆ¶È:96.5% Chemical & Pharmaceutical Bulletin 1979 27 38-42 Carbon-13 Nuclear Magnetic Resonance of 24-Substituted Steroids NAOYUKI KOIZUMI,YOSHINORI FUJIMOTO,TORU TAKESHITA and NOBUO IKEKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Chemistry of Natural Compounds 2000 36 595-598 13C NMR SPECTRA OF FUNCTIONALLY SUBSTITUTED 3 ¦Â-CHLORODERIVATIVES OF CHOLESTEROL AND ¦Â -SITOSTEROL N. V. Kovganko, Zh. N. Kashkan, and E. V. Borisov Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:96.5% Acta Botanica Boreali-Occidentalia Sinica 2004 24 1292-1294 Chemical constituents from Saussurea polycolea LI Yu-lin, WANG Hong-lun, SUO You-rui Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Acta Botanica Sinica 1999 41 107-110 Chemical constituents of the Anemone tomentosa Root Wang Jun-Ru, Peng Shu-Lin, Wang Ming-Kui, Feng Jun-Tao, Ding Li-Sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Journal of Chinese Pharmaceutical Sciences 1999 8 237-240 Chemical Constituents of Stelmatocrypton khasianum Zhang Qingying; Zhao Yuying; Ma Libin; Cheng Tieming Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Journal of Chinese Pharmaceutical Sciences 2005 14 75-78 Chemical Constituents of Hedysarum gmelinii LIU Yi; MA Xiao-xia; CHEN Hu-biao; TU Guang-zhong; HE Jiu-ming; and ZHAO Yu-ying Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Journal of Asian Natural Products Research 2002 4 73-79 A NEW COMPOUND FROM GASTRODIA ELATA BLUME YONG-QING XIAO, LI LI, XIAO-LIN YOU, BAO-LIN BIAN, XIN-MIAO LIANG and YI-TAO WANG Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . lawsaritol A C29H50O2 ÏàËÆ¶È:96.5% Natural Product Research 1994 4 195-201 Isolation and Characterization of a Dihydroxysterol from Lawsonia inermis Sarita Gupta; Mohammad Ali; M. Sarwar Alam; Masatake Niwa; Tatsuko Sakai Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Natural Product Research 2006 20 860-865 A new dihydroisocoumarin from the rhizomes of Notopterygium forbesii Yan-Hui Li; Fan Luo; Shu-Lin Peng; Jian Liang; Li-Sheng Ding Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:96.5% Natural Product Research 2008 22 1085-1093 Isolation of antibacterial diterpenoids from Cryptomeria japonica bark Wen-Hsin Li; Shang-Tzen Chang; Shan-Chwen Chang; Hui-Ting Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . stigmasterol ÏàËÆ¶È:96.5% Chemical & Pharmaceutical Bulletin 1998 46 1408-1411 New Sterols and Triterpenoids of Ficus pumila Fruit Junichi KITAJIMA,Kaoru KIMIZUKA and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . ¦Â-sitosterol ÏàËÆ¶È:96.5% China Journal of Chinese Materia Medica 2002 27 843-845 Studies on Chemical Constituents in the Root of Hedysarum polybotrys HAI Liqian, LIANG Hong, ZHAO Yuying, DU Niansheng Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Acta Pharmaceutica Sinica 2002 Vol 37 196-198 STUDIES ON FLAVONIOD CONSTITUENTS OF HEDYSARUM MULTIJUGUM WANG Wei; CHEN Hu-biao; WANG Wen-ming; ZHAO Yu-ying Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Natural Product Sciences 2000 6 135-138 Antioxidative Constituents from the Seeds of Cuscuta chinensis Kwon, Yong-Soo; Chang, Bok-Sim; Kim, Chang-Min Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . beta-sitosterol ÏàËÆ¶È:96.5% Natural Product Sciences 2002 8 137-140 The Constituents of the Aerial Part of Gastrodia elata Blume Liu, Xiang Qian; Baek, Wan-Sook; Ahn, Duk-Kyun; Choi, Ho-Young; Yook, Chang-Soo Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . ¦Â-Sitosterol ÏàËÆ¶È:96.5% Natural Product Sciences 2007 13 332-336 Norsesquiterpene and Steroid Constituents of Humulus japonicus Yu, Byung-Chul; Yang, Min-Cheol; Lee, Kyu-Ha; Kim, Ki-Hyun; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . lawsaritol C29H50O ÏàËÆ¶È:96.5% Phytochemistry 1992 31 2558-2560 24¦Â-Ethylcholest-4-en-3¦Â-ol from the roots of Lawsonia inermis M. Sarwar Alam, Masatake Niwa, Tatsuko Sakai, Sarita Gupta, Mohd. Ali Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . ¦Â-Sitosterol C29H50O ÏàËÆ¶È:96.5% Korean Journal of Pharmacognosy 2008 39(4) 357-364 Chemical Constituents of Saposhnikovia divaricata Kim, So-Jun; Chin, Young-Won; Yoon, Kee-Dong; Ryu, Min-Youl; Yang, Min-Hye; Lee, Je-Hyun; Kim, Jin-Woong Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . ¦Â-Sitosterol ÏàËÆ¶È:96.5% 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 28 . ¦Â-Sitosterol ÏàËÆ¶È:96.5% 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 29 . compound 5 ÏàËÆ¶È:96.5% Korean Journal of Pharmacognosy 2000 31(3) 300-305 Chemical Components of Evodia daniellii Ju, Hei-Kyoung; Hwang, Bang-Yeon; Ahn, Byong-Tae; Kim, Mi-Jeong; Choi, Woo-Hoi; Cho, Bong-Jn; Ro, Jai-Seup; Lee, Kyong-Soon Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . compound 1 C29H50O ÏàËÆ¶È:96.5% Korean Journal of Pharmacognosy 1998 29(4) 277-282 Isolation of Anti-Herpes Simplex Virus Type 1(HSV-1) Component from Thujae orientalis Semen Kang, Eun-Jung; Kang, Bong-Joo; Park, Kap-Joo; Ko, Byoung-Seob; Kim, Ho-Kyoung Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . compound 3a ÏàËÆ¶È:96.5% Korean Journal of Pharmacognosy 1996 27(4) 389-396 Constituents of Spiraea prunifolia var. simpliciflora Lee, Eun-Hee; Chung, Soon-Ok; Kim, Chong-Won; Woo, Mi-Hee Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:96.5% Chinese Journal of Marine Drugs 2006 25(1) 21-24 Studies on chemical constituents of the marine sponge Craniell a australiensis from the South China Sea KUANG Xia, ZHANG Hong-jun, SUN Jing-bo, WANG Zeng-lei, LIN Hou-wen Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . ¦Â-¹ÈçÞ´¼ C29H48O ÏàËÆ¶È:96.5% Chinese Journal of Marine Drugs 2006 25(3) 15-17 Study on the chemical constituents of Ipomoea Pescaprae( L.) Sweet(I) WANG Qing-Ji, WANG You-Shao, HE Lei, ZHANG Si Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . (24s)-stigmast-5-en-3-ol ÏàËÆ¶È:96.5% Chinese Journal of Marine Drugs 2004 23(2) 15-17 Studies on chemical constituents of the marine sponge Spheciospongia vagabunda from the South China Sea (I) MA Wei-jie, XIAO Ding-jun, DENG Song-zhi Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . (24S)-stigmast-5-en-3¦Â-ol ÏàËÆ¶È:96.5% Chinese Journal of Marine Drugs 2002 21(2) 1-4 Studies on the chemical constituents of the marine sponge Clathria fasciculate from the South China Sea XIAO Ding-jun, DENG Song-zhi, ZENG Long-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:96.5% Chinese Journal of Marine Drugs 2002 21(1) 1-4 Sterol con stituents from marine brown alga ishige okamurai TANG Hai-feng, YI Yang-hua, YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . sitosterol ÏàËÆ¶È:96.5% Phytochemistry 1990 29 2351-2355 Sterol glucosides from Prunella vulgaris Hisashi Kojima,Noriko Sato,Akiko Hatano,Haruo Ogura Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:96.5% Chinese Traditional and Herbal Drugs 2010 41 206-208 ÷×»¨¶Å¾éÒ¶µÄ»¯Ñ§³É·ÖÑо¿ ÖÜÏÈÀñ; ÇØ³¤ºì; ÷Ө; »ÆË§; °¢Æ¼ Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Chinese Traditional and Herbal Drugs 2009 40 1015-1018 Chemical constituents in Tridax procumbens XU Run-sheng; YUAN Ke; YIN Ming-wen; FANG Lei-jie; MAO Nong-nong Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . ¦Â-stosterol ÏàËÆ¶È:96.5% Chinese Traditional and Herbal Drugs 2008 39 1622-1624 ¶ÀһζµÄ»¯Ñ§³É·ÖÑо¿ É£ÓýÀè;ºÂÑÓ¾ü;ÑîËÉËÉ Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . ¦Â-rosasterol C29H50O ÏàËÆ¶È:96.5% Chinese Traditional and Herbal Drugs 2006 37 666-668 Å·ÑÇÐý¸²»¨ÖÐÈýÝÆºÍçÞÌ廯ºÏÎïµÄ·ÖÀëºÍ½á¹¹¼ø¶¨ ÎâÒ»±ø;ÍõÔÆÖ¾;²é½¨Åî;ÑîË«¸ï;ʯÏþΰ;ÕŵÕȺ Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . ¦Â-rosasterol C29H50O ÏàËÆ¶È:96.5% Chinese Traditional and Herbal Drugs 1996 27 389-391 Studies on the Chemical Constituents of Dyers Woad(Isatis tinctoria) Li Ling; Yang Genjin; Dong Tongyi; et al(Address£ºLi Ling£®College of Pharmacy; Second Military Medical University; Sanghai); Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Chinese Traditional and Herbal Drugs 2010 41 1932-1936 Chemical constituents of anti-oxidative activities from seeds of Jatropha curcas LI Ling; LI Xiao-fan; WU Hui-xing; LI Rong; WANG Nai-li Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Chinese Journal of Natural Medicines 2009 7 293-296 Chemical Constituents from Thalictrum fortunei ZHANG Xian-Tao; ZHANG Lei-Hong; WANG Ying; LI Yan; WANG Yu-Sheng; YE Wen-Cai Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . compound 3 ÏàËÆ¶È:96.5% Archives of Pharmacal Research 1998 21 357-360 Isolation of 3- O -(4'-Hydroxybenzyl)-¦Â-sitosterol and 4-[4'-(4¡å-Hydroxybenzyloxy)benzyloxy]benzyl methyl ether from fresh tubers of Gastrodia elata Hye Sook Yun-Choi, Mi Kyung Pyo and Kyung Mi Park Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . ¦Â-Sitosterol ÏàËÆ¶È:96.5% Archives of Pharmacal Research 2006 29 617-623 Chemical constituents of the root of Dystaenia takeshimana and their anti-inflammatory activity Ju Sun Kim, Jin Cheul Kim, Sang Hee Shim, Eun Ju Lee and Wen Yi Jin, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . ¦Â-Sitosterol ÏàËÆ¶È:96.5% Archives of Pharmacal Research 2008 31 10-16 Phytochemical investigation of Tiarella polyphylla Guanghai Shen, Sei-Ryang Oh, Byung-Sun Min, Joongku Lee and Kyung Seop Ahn, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . sitosterol (24R) ÏàËÆ¶È:96.5% 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 49 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Chinese Pharmaceutical Journal 2006 41 1533-1535 Study on Constituents of Tilia mongolica Leaves and Wood MA Yun-xiang, TIAN Fu-li, WANG Jing-yuan, FANG Li, DU Yu-ying Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . ¦Â-sitosterol ÏàËÆ¶È:96.5% 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 51 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:96.5% Chinese Journal of Medicinal Chemistry 2001 11 51-62 Study Progress on the Chiral Separation YIN Guo, LIU Zhen-hua, ZENG Shan-shan, ZHU Guo-hong Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Chinese Journal of Medicinal Chemistry 2006 16 303-305 The constituents of Veratrum japonicum Loes. f. 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ZHAO Qing-chun, FU Yan-hui, GU O Tao, HU A Wei, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . clionasterol ÏàËÆ¶È:96.5% Journal of Chemistry 2008 46 456-461 Isolation and structural characterization of triterpenes from Celastrus hindii Benth Trịnh Thị Thủy Quyen, Nguyễn Huy Cường, Phạm Thị Ninh, Trần Văn Sung Structure 13C NMR ̼Æ×Ä£Äâͼ 59 . ¦Â-sitosterol C29H5O ÏàËÆ¶È:96.5% Natural Product Research and Development 2010 22 1006-1008 Chemical Constituents of Ophioglossum thermale Kom. 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B-sitosterol ÏàËÆ¶È:96.5% Journal of Beijing Medical University 2000 32 226-228 Chemical constituents from Rubus alceaefolius Poir GAN Lu; WANG Bin; LIANG Hong; ZHAO Yu Ying; JIANG Feng Chi Structure 13C NMR ̼Æ×Ä£Äâͼ 97 . ¦Â-Sitosterol ÏàËÆ¶È:96.5% Journal of Chinese Pharmaceutical Sciences 2012 21 183-186 Isolation of metabolic products from the fungus Nectria sp.HLS206 that is associated with the marine sponge Gelliodes carnosa collected from the South China Sea Rui-Shan Wang; Ting Gong; Ping Zhu; Ke-Di Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ 98 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Guihaia 2012 32 548-550 Study on chemical constituents of Abies yuanbaoshanensis HE Rui-Jie; FANG Hong; WU Ying-Rui Structure 13C NMR ̼Æ×Ä£Äâͼ 99 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:96.5% Chinese Traditional and Herbal Drugs 2012 43 636-639 Chemical constituents in roots of Pandanus tectorius LIU Jia-wei; PENG Li-hua; XIAN Mei-ting; CHENG Jin-le; CHEN Wei-wen Structure 13C NMR ̼Æ×Ä£Äâͼ 100 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:96.5% Lishizhen Medicine and Materia Medica Research 2007 18 2202-2203 Studies on the Fat-soluble Chemical Constituents of Carex siderosticta YANG Bo JI Ying YIN Xue-zhi ZHAO Ping Structure 13C NMR ̼Æ×Ä£Äâͼ |
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