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| 13C NMR (126 MHz, cdcl3) ¦Ä 11.88,12.00,18.79,19.04,19.42,19.85,21.09,23.07,24.32,26.05,28.27,29.14,29.72,31.66,31.91,31.93,33.72,33.95,36.16,36.52,37.26,39.78,42.30,42.33,45.83,50.13,56.05,56.77,71.83,121.75,140.76 |
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²éѯ½á¹û£º¹²²éµ½10321¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Â-sitosterol ÏàËÆ¶È:93.5% 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 2 . ¦Â-sitosterol ÏàËÆ¶È:93.5% Planta Medica 1988 54 33-36 In vitro Fibrinolytic Phytosterols Isolated from the Roots of Spatholobus suberetus Yoshiyasu Fukuyama, Yoshinori Nakano, Geng Pei-Wu, Wang Rui, Junko Sumitomo, Bao Jinxian,and Kazuyuki Nakagawa Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . sitosterol ÏàËÆ¶È:93.5% 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 4 . ¦Â-sitosterol ÏàËÆ¶È:93.5% 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 5 . ¦Â-sitosterol ÏàËÆ¶È:93.5% Chemistry of Natural Compounds 1999 35 672-645 I3C NMR SPECTRA OF STEROL DERIVATIVES,INTERMEDIATES IN THE SYNTHESIS OF ECDY- AND BRASSINOSTEROIDS N. V. Kovganko, Zh. N. Kashkan,and E. V. Borisov Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:93.5% 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 7 . ¦Â-sitosterol ÏàËÆ¶È:93.5% Acta Botanica Boreali-Occidentalia Sinica 2008 28 1246-1249 Chemical Constituents in the Leaves of Alsophila spinulosa CHEN Feng-zheng, XIANG Qing-xiang, LI Shu-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-sitosterol ÏàËÆ¶È:93.5% 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 9 . ¦Â-sitosterol ÏàËÆ¶È:93.5% 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 10 . ¦Â-sitosterol ÏàËÆ¶È:93.5% 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 11 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:93.5% 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 12 . stigmasterol ÏàËÆ¶È:93.5% 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 13 . ¦Â-sitosterol ÏàËÆ¶È:93.5% China Journal of Chinese Materia Medica 2003 28 278-279 ¼Ô¹ûÞ§¹áÖÚ»¯Ñ§³É·ÖµÄÑо¿ Ñî á°, ÕÔÓñÓ¢, ÍÀßÏßÏ Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ¦Â-sitosterol ÏàËÆ¶È:93.5% 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 15 . ¦Â-sitosterol ÏàËÆ¶È:93.5% Journal of Natural Products 1990 Vol 53 1430 Stigmasterols from Typha latifolia Marina Della Greca, Pietro Monaco, Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ¦Â-sitosterol ÏàËÆ¶È:93.5% 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 17 . ¦Â-sitosterol ÏàËÆ¶È:93.5% 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 18 . beta-sitosterol ÏàËÆ¶È:93.5% 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 19 . ¦Â-Sitosterol ÏàËÆ¶È:93.5% 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 20 . sitosterol ÏàËÆ¶È:93.5% 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 21 . ¦Â-Sitosterol C29H50O ÏàËÆ¶È:93.5% 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 22 . ¦Â-Sitosterol ÏàËÆ¶È:93.5% 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 23 . ¦Â-Sitosterol ÏàËÆ¶È:93.5% 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 24 . compound 5 ÏàËÆ¶È:93.5% 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 25 . compound 1 C29H50O ÏàËÆ¶È:93.5% 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 26 . compound 3a ÏàËÆ¶È:93.5% 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 27 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:93.5% 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 28 . ¦Â-¹ÈçÞ´¼ C29H48O ÏàËÆ¶È:93.5% 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 29 . (24s)-stigmast-5-en-3-ol ÏàËÆ¶È:93.5% 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 30 . (24S)-stigmast-5-en-3¦Â-ol ÏàËÆ¶È:93.5% 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 31 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:93.5% 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 32 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:93.5% 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 33 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:93.5% Chinese Traditional and Herbal Drugs 2010 41 704-707 Âúɽºì»¯Ñ§³É·ÖµÄÑо¿ ¸¶ÏþÀö;ÕÅÁ¢Î°;ÁÖÎĺ²;ÀîÇàɽ Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . ¦Â-sitosterol ÏàËÆ¶È:93.5% 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 35 . ¦Â-rosasterol C29H50O ÏàËÆ¶È:93.5% 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 36 . ¦Â-rosasterol C29H50O ÏàËÆ¶È:93.5% 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 37 . ¦Â-sitosterol ÏàËÆ¶È:93.5% 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 38 . compound 3 ÏàËÆ¶È:93.5% 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 39 . ¦Â-Sitosterol ÏàËÆ¶È:93.5% 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 40 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:93.5% Chinese Pharmaceutical Journal 2004 39 173-175 Studies on the chemical constituents of Caragana rosea CUI Yi-ling, MU Qing, HU Chang-qi Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . ¦Â-sitosterol ÏàËÆ¶È:93.5% 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 42 . ¦Â-sitosterol ÏàËÆ¶È:93.5% 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 43 . ¦Â-sitosterol ÏàËÆ¶È:93.5% Chinese Journal of Medicinal Chemistry 2007 17 390-391 Chemical constituents of Boschniakia himalaica JIN Yin-ping, ZHANG Guo-gang, ZHENG Hong-ting, DU Shu-shan Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . ¦Â-sitosterol ÏàËÆ¶È:93.5% Chinese Journal of Medicinal Chemistry 2009 19 130-134 Chemical constituents of Dillenia kerrii and their activities on antitumor and anti-hypoxia in vitro LI Xia, LI Chang-wei, CUI Cheng-bin, LIMing-ming, FAN Ming Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:93.5% Journal of Shenyang Pharmaceutical University 2007 24 611-614 Chemical constituents of Duchesnea indica Focke XU Wen-dong, LIN Hou-wen, QIU Feng, CHEN Wan-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . stigmasterol ÏàËÆ¶È:93.5% Journal of Shenyang Pharmaceutical University 2007 24 619-622 Isolation and identification of non-alkaloid constituents from Gelsemium elegans Benth. ZHAO Qing-chun, FU Yan-hui, GU O Tao, HU A Wei, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . clionasterol ÏàËÆ¶È:93.5% 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 48 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:93.5% Natural Product Research and Development 2010 22 998-1000 Chemical Constituents and Identification of the Caules of Clematis armandii Franch. and Clematis montana Buch.-Ham. LIU Jing-jing;CHEN Xing; WEI Zhi-qi; LI Bin Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . ¦Â-sitosterol C29H5O ÏàËÆ¶È:93.5% Natural Product Research and Development 2010 22 1006-1008 Chemical Constituents of Ophioglossum thermale Kom. ZHANG Guo-wei; WU Nai-zhu; FAN Qiang; ZHOU Xian-li; HUANG shuai Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . ¦Â-sitosterol ÏàËÆ¶È:93.5% Natural Product Research and Development 2010 22 1018-1020 Chemical Constituents from Fruiting Bodies of Ganoderma lucidum.(¢ò) CHEN Man; ZHANG Mi; SUN Shi; XIA Bing; ZHANG Han-qing Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:93.5% Natural Product Research and Development 2009 21 963-965 Study on the Chemical Constituents of Heterostemma alatum Wight ZHUANG Peng-yu;FU Wen-wei; TAN Chang-heng; YANG Shu-min; LIU Fei; WANG Zhe-xing; ZHU Da-yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:93.5% Natural Product Research and Development 2007 19 244-246 Chemical Constituents of Vitex quinata CHENG Wei-xian; CHEN Hong-yan; ZHANG Yi-ping; QIN Xiu-lin; GU Kun Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . ¦Â-stitosterol C29H50O ÏàËÆ¶È:93.5% Natural Product Research and Development 2001 13(2) 11-13 THE STUDIES OF CHEMICAL COMPONENTS OF CLAUSENA DUNNIANA CUI Shu ya;CHENG Dong liang; TIAN Jun; WU Feng e Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . daucosterol C35H60O6 ÏàËÆ¶È:93.5% 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 55 . ¦Â-sitosterol ÏàËÆ¶È:93.5% Journal of the Chinese Chemical Society 1998 45 103-110 Chemical Constituents of Neolitsea parvigemma and Neolitsea Konishii ê?¿Ë½B(Keh-Shaw Chen);?ˆ·¼˜s(Fang-Rong Chang);ÙZÒËè¡(Yi-Chen Chia);…ÇÌìÙp(Tian-Shung Wu);…ÇÓÀ²ý(Yang-Chang Wu) Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . ¦Â-Sitosterol ÏàËÆ¶È:93.5% Journal of the Chinese Chemical Society 2000 47 373-380 The Constituents of Lindera glauca Yuh-Chwen Chang, Fang-Rong Chang and Yang-Chang Wu* Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:93.5% Zeitschrift f¨¹r Naturforschung C 2004 59 15-18 Chemical Constituents of Euphorbia marschalliana Boiss. A. R. Jassbi, S. Zamanizadehnajari, and S. Tahara Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:93.5% Turkish Journal of Chemistry 2009 33 667-675 Secondary metabolites from Nepeta heliotropifolia Z¨¹HAL G¨¹VENALP, HİLAL ÖZBEK, AYŞE KURU¨¹Z¨¹M-UZ, CAVİT KAZAZ, L. ÖM¨¹R DEMİREZER Structure 13C NMR ̼Æ×Ä£Äâͼ 59 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:93.5% Turkish Journal of Chemistry 2009 33 813-823 Antioxidant and anticholinesterase constituents of Salvia poculata UFUK KOLAK, IŞIL HACIBEKİROĞLU, MEHMET ÖZT¨¹RK, FEVZİ ÖZGÖKÇE, G¨¹LAÇTI TOPÇU, AYHAN ULUBELEN Structure 13C NMR ̼Æ×Ä£Äâͼ 60 . ¦Â-sitosterol ÏàËÆ¶È:93.5% Turkish Journal of Chemistry 2006 30 15-20 Phytochemical Studies on the Underground Parts of Asperula taurina subsp. caucasica UFUK ÖZGEN, CAVİT KAZAZ, HASAN SEÇEN, MAKSUT COŞKUN Structure 13C NMR ̼Æ×Ä£Äâͼ 61 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:93.5% Turkish Journal of Chemistry 2006 30 515-523 Chemical Constituents of Galium tortumense Z¨¹HAL G¨¹VENALP, NURCAN KILIÇ, CAVİT KAZAZ, YUSUF KAYA, L. ÖM¨¹R DEMİREZER Structure 13C NMR ̼Æ×Ä£Äâͼ 62 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:93.5% Turkish Journal of Chemistry 2005 29 177-186 Terpenoids and Steroids from the Roots of Salvia blepharochlaena UFUK KOLAK, G¨¹LAÇTI TOPÇU, SEHER BİRTEKSÖZ, G¨¹LTEN ÖT¨¹K, AYHAN ULUBELEN Structure 13C NMR ̼Æ×Ä£Äâͼ 63 . ¦Â-sitosterol ÏàËÆ¶È:93.5% Korean Journal of Pharmacognosy 2011 42 117-126 Phytochemical Studies on Rehmanniae Radix Preparata Lee, Joo-Young; Lee, Eun-Ju; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 64 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:93.5% Asian Journal of Traditional Medicines 2009 4 85-91 Flavonol glycosides and triterpenes from the leaves of Uncaria rhynchophylla (Miq.) Jacks. 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