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²éѯ½á¹û£º¹²²éµ½5410¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . schleicheol 1 C30H52O2 ÏàËÆ¶È:81.8% Journal of Natural Products 2000 63 72-78 Isolation and Structures of Schleicherastatins 1-7 and Schleicheols 1 and 2 from the Teak Forest Medicinal Tree Schleichera oleosa1 George R. Pettit,Atsushi Numata, Gordon M. Cragg, Delbert L. Herald, Tamie Takada,Chika Iwamoto,Roland Riesen, Jean M. Schmidt, Dennis L. Doubek, and Animesh Goswami Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . schleicheol 2 C30H52O2 ÏàËÆ¶È:78.7% Journal of Natural Products 2000 63 72-78 Isolation and Structures of Schleicherastatins 1-7 and Schleicheols 1 and 2 from the Teak Forest Medicinal Tree Schleichera oleosa1 George R. Pettit,Atsushi Numata, Gordon M. Cragg, Delbert L. Herald, Tamie Takada,Chika Iwamoto,Roland Riesen, Jean M. Schmidt, Dennis L. Doubek, and Animesh Goswami Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 7¦Â-methoxy-sigmast-5-en-3¦Â-ol ÏàËÆ¶È:78.7% China Journal of Chinese Materia Medica 2008 33 1035-1038 Study on Steroids of Cacalia tangutica LIU Qing, LIU Zhenling, TIAN Xuan Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (3¦Â,7¦Á)-7-Methoxystigmast-5-en-3-ol C30H52O2 ÏàËÆ¶È:78.7% Chemistry & Biodiversity 2012 9 567-576 Antifeedant Activity of Fatty Acid Esters and Phytosterols from Echium wildpretii Omar Santana, Matias Reina, Braulio M. Fraga, Jes¨²s Sanz and Azucena Gonza¡älez-Coloma Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (24S)-stigmast-5-en-7¦Â-ethoxy-3¦Â-ol C31H54O2 ÏàËÆ¶È:75.7% Journal of Asian Natural Products Research 2005 7 165-169 Sterols from the pericarp of Sphaerophysa salsula DC GUO-YU LI, JIN-HUI WANG and XIAN LI Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . schleicheol 2 ÏàËÆ¶È:75.7% China Journal of Chinese Materia Medica 2008 33 1566-1569 Studies on chemical constituents from stem bark of Trwia nudiflora WU Shaohua, SHENG Yuemao, CHEN Youwei, YANG Liyuan, LI Shaolan, LI Zhiying Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ¦Â-sitosterol ÏàËÆ¶È:75.7% Natural Product Sciences 1996 2 19-23 Sterols and Sterol Glycosides from the Leaves of Gynura procumbens Sadikun, A.; Aminah, I.; Ismail, N.; Ibrahim, P. Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-sitosterol ÏàËÆ¶È:75.7% 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 9 . ¦Â-rosasterol ÏàËÆ¶È:75.7% Chinese Traditional and Herbal Drugs 2009 40 1704-1707 Chemical constituents of mangrove plant Excoecaria agallocha in Hainan Province XU Jie; DENG Zhi-wei; LIN Wen-han; LI Qing-shan Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Â-sitosterol ÏàËÆ¶È:75.7% Journal of Shenyang Pharmaceutical University 2010 27 615-617 Isolation and identification of chemical constituents from stems of Smilax glabra Roxb. WU Bo, MA Yue-ping, YUAN Jiu-zhi, SUN Qi-shi Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . stigmast-4-ene-3¦Â,6¦Â-diol ÏàËÆ¶È:75.7% Natural Product Research and Development 2009 21 960-962 Study on the Chemical constituents of Callipteris esculenta(Athyriaceae) WANG Zi-juan;ZHAO Qin-shi; PENG Li-yan; CHENG Xiao Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ¦Â-rosaterol C29H50O ÏàËÆ¶È:75.7% Natural Product Research and Development 2004 16 379-382 STUDIES ON THE CHEMICAL COMPOSITIONS OF PTERIS MULTIFIDA POIR HU Hao-bin *; ZHENG Xu-dong Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:75.7% 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 14 . 7¦Â-methoxystigmast-5-en-3¦Â-ol C30H52O2 ÏàËÆ¶È:75.7% Australian Journal of Chemistry 2000 53 831-834 Epoxide Sesquiterpenes and Steroids from Cremanthodium discoideum Ying Zhu, Qi Xiu Zhu and Zhong Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . stigmas-9(11)-en-3-ol ÏàËÆ¶È:75.7% China Journal of Chinese Materia Medica 2013 38 199-203 Chemical constituents of Rabdosia japonica var. glaucocalyx and their anti-complementary activity YAO Shi, XU Nai-yu, CHU Chun-jun, ZHANG Jian, CHEN Dao-feng Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 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ÃðÑÁ¾úËØA µÄ·ÖÀëºÍ½á¹¹¼ø¶¨ Íõº£Ñà, ÐíºèÕ Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . ¦Â-sitosterol ÏàËÆ¶È:72.7% 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 23 . ¦Â-sitosterol benzoate ÏàËÆ¶È:72.7% Planta Medica 1988 54 223-224 Antihepatotoxic Principles of Sambucus formosana Chun-Nan Lin and Whey-Pin Tome Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 22,23-Dihydrospinasterol ÏàËÆ¶È:72.7% Acta Botanica Yunnanica 1995 17(1) 103-108 CHEMICAL CONSTITUENTS FROM CLERODENDRUM JAPONICUM TIAN Jun, SUN Han-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . topsentinol J C30H52O2 ÏàËÆ¶È:72.7% Chemical & Pharmaceutical Bulletin 1997 45 1435-1438 Topsentinols A-J, New Sterols with Highly Branched Side Chains from Marine Sponge Topsentia sp. Masami ISHIBASHI,Emiko YAMAGISHI and Jun'ichi KOBAYASHI Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . stigmastane-3¦Â,6¦Á-diyl C33H56O4 ÏàËÆ¶È:72.7% Chemical & Pharmaceutical Bulletin 1995 43 1813-1817 Structures of Five Hydroxylated Sterols from the Seeds of Trichosanthes kirilowii MAXIM. Yumiro KIMURA,Toshihiko AKIHISA,Ken YASUKAWA,Michio TAKIDO and Toshitake TAMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . ¦Â-sitosterol ÏàËÆ¶È:72.7% 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 28 . ¦Â-sitosterol ÏàËÆ¶È:72.7% 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 29 . compound 2 ÏàËÆ¶È:72.7% Chemistry of Natural Compounds 1999 35 646-649 13C NMR SPECTRA OF II-SITOSTEROL DERIVATIVES WITH OXIDIZED RINGS A AND B N. V. Kovganko, Zh. N. Kashkan,E. V. Borisov, and E. V. Batura Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:72.7% 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 31 . ¦Â-sitosterol ÏàËÆ¶È:72.7% 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 32 . ¦Â-sitosterol ÏàËÆ¶È:72.7% 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 33 . 7¦Â-Hydroxysitosterol C29H50O2 ÏàËÆ¶È:72.7% Journal of Chinese Pharmaceutical Sciences 2007 16 288-293 Chemical constituents of the flower buds of Tussilago farfara Yu-Feng Liu; Xiu-Wei Yang and Bin Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . 7¦Â-hydroxysitosterol C29H50O2 ÏàËÆ¶È:72.7% Steroids 2005 70 886-895 Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . Stigmast-5-ene-3¦Â,7¦Â-diol ÏàËÆ¶È:72.7% Journal of Asian Natural Products Research 2005 7 165-169 Sterols from the pericarp of Sphaerophysa salsula DC GUO-YU LI, JIN-HUI WANG and XIAN LI Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . lawsaritol A C29H50O2 ÏàËÆ¶È:72.7% 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 37 . ¦Â-sitosterol ÏàËÆ¶È:72.7% 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 38 . (24R)24-ethyl-7¦Á-hydroperoxy-cholest-5-en-3¦Â-ol ÏàËÆ¶È:72.7% Natural Product Research 1994 5 7-14 Hydroperoxysterols in Arum italicum Marina Della Greca; Antonio Fiorentino; Antonio Molinaro; Pietro Monaco; Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . stigmast-5-ene-3¦Â,26-diol C29H50O2 ÏàËÆ¶È:72.7% Natural Product Research 2006 20 665-670 Potent tyrosinase inhibitors from Trifolium balansae Temine Şabudak; Mahmut Tareq Hassan Khan; M Iqbal Choudhary; Sevil Oksuz Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . ¦Â-sitosterol ÏàËÆ¶È:72.7% 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 41 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:72.7% 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 42 . stigmasterol ÏàËÆ¶È:72.7% 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 43 . 7¦Â-hydroxysitosterol ÏàËÆ¶È:72.7% China Journal of Chinese Materia Medica 2008 33 1566-1570 Studies on chemical constituents from stem bark of Trwia nudiflora WU Shaohua, SHENG Yuemao, CHEN Youwei, YANG Liyuan, LI Shaolan, LI Zhiying Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . schleicherastatin 1 C30H52O3 ÏàËÆ¶È:72.7% China Journal of Chinese Materia Medica 2008 33 1035-1038 Study on Steroids of Cacalia tangutica LIU Qing, LIU Zhenling, TIAN Xuan Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . stigmast-9(11)-en-3-ol ÏàËÆ¶È:72.7% China Journal of Chinese Materia Medica 2006 31 1689-1691 Chemical constituents in root of Zanthoxylum nitidum HU Jiang, ZHANG Weidong, LIU Runhui, ZHANG Chuan, SHEN Yunheng, XU Xike, LIANG Mingjin, LI Huiliang Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . ¦Â-sitosterol ÏàËÆ¶È:72.7% 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 47 . ¦Â-sitosterol ÏàËÆ¶È:72.7% 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 48 . ¦Â-sitosterol ÏàËÆ¶È:72.7% China Journal of Chinese Materia Medica 1997 22 293-295 Separation and Identification of the Compounds from A chyranthes biden tata Bl W ei Song, L iang Hong, Zhao Yuying and Zhang Ruyi Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 5¦Á-stigmast-9(11)-en-3¦Â-ol C29H50O ÏàËÆ¶È:72.7% China Journal of Chinese Materia Medica 1996 21 666-667 Studies on Chemical Components of Cynomorium songaricum Rupr. Xu Xiuzhi, Zhang Chengzhong and Li Chong Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . 7¦Â-hydroxysitosterol C29H50O2 ÏàËÆ¶È:72.7% Journal of Natural Products 1987 Vol 50 881 Sterols and Steryl Glycosides from Urtica dioica Neera Chaurasia, Max Wichtl Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . ¦Â-sitosterol ÏàËÆ¶È:72.7% 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 52 . 7¦Â-hydroxysitosterol ÏàËÆ¶È:72.7% 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 53 . ¦Â-sitosterol ÏàËÆ¶È:72.7% 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 54 . stigmast-7-en-3¦Â-ol ÏàËÆ¶È:72.7% Acta Pharmaceutica Sinica 2000 Vol 35 29-31 STRUCTURE IDENTIFICATION OF VULGARSAPONIN A Tian Jing; Xiao Zhiyan; Chen Yayan; Zhao Yuying and Wang Zhuju Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . ¦Â-sitosterol ÏàËÆ¶È:72.7% 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 56 . beta-sitosterol ÏàËÆ¶È:72.7% 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 57 . ¦Â-sitosterol ÏàËÆ¶È:72.7% Natural Product Sciences 2003 9 270-272 Constituents of Euphorbia milii YunChoi, Hye-Sook; Jin, Jing-Ling; Hong, Sung-Won; Lee, Yong-Yook; Lee, Jo-Hyung Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . ¦Â-sitosterol ÏàËÆ¶È:72.7% Natural Product Sciences 2004 10 306-309 Triterpenoids from Orostachys japonicus Lee, Sang-Hyun; Paek, Sun-Ha; Kim, Seung-Ki; Kim, Bak-Kwang; Shin, Kuk-Hyun Structure 13C NMR ̼Æ×Ä£Äâͼ 59 . ¦Â-Sitosterol ÏàËÆ¶È:72.7% Natural Product Sciences 2008 14 100-106 Phytochemical Constituents of Schizonepeta tenuifolia Briquet Lee, Il-Kyun; Kim, Min-Ah; Lee, Seung-Young; Hong, Jong-Ki; Lee, Jei-Hyun; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 60 . ¦Â-sitosterol ÏàËÆ¶È:72.7% Natural Product Sciences 2009 15 181-184 Phytochemical Constituents from the Seeds of Lithospermum erythrorhizon Park, Jun-Yeon; Lee, Sul-Lim; Han, Saem; Kim, Hye-Min; Lee, Jeong-Min; Ahn, Young-Hee; Lee, Sook-Young; Lee, Sang-Hyun Structure 13C NMR ̼Æ×Ä£Äâͼ 61 . lawsaritol C29H50O ÏàËÆ¶È:72.7% 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 62 . sitosterol ÏàËÆ¶È:72.7% 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 63 . ¦Â-Sitosterol C29H50O ÏàËÆ¶È:72.7% 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 64 . ¦Â-Sitosterol ÏàËÆ¶È:72.7% 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 65 . ¦Â-Sitosterol ÏàËÆ¶È:72.7% 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 66 . compound 5 ÏàËÆ¶È:72.7% 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 67 . compound 1 C29H50O ÏàËÆ¶È:72.7% 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 68 . compound 3a ÏàËÆ¶È:72.7% 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 69 . stigmast-5-ene-3¦Â,7¦Â-diol ÏàËÆ¶È:72.7% Chemical Research in Chinese Universities 1997 13 378-381 Two New Sterols f rom Adenophora Stenanthina Subsp. Xif engensis HOU Zhen-fu, SHI Yan-ping, MEI Shuang-x i and LI Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 70 . stigmast-5-en-3¦Â,7¦Â-diol ÏàËÆ¶È:72.7% China Journal of Chinese Materia Medica 2011 Vol 36,Issue 7 891-895 Chemical constituents from petroleum ether portion of Abelmoschus esculentus JIA Lu, GUO M ingm ing, LI Dong, JING Lin lin Structure 13C NMR ̼Æ×Ä£Äâͼ 71 . ¦Â-¹ÈçÞ´¼ C29H48O ÏàËÆ¶È:72.7% 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 72 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:72.7% 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 73 . 3¦Â-hydroxy-7¦Á-ethoxy-24¦Â-ethylcholest-5-ene C31H54O2 ÏàËÆ¶È:72.7% Journal of Asian Natural Products Research 2011 Vol. 13, No. 10 920-929 Sesquiterpenoids and other constituents from the flower buds of Tussilago farfara Lei-Lei Liu, Jun-Li Yang and Yan-Ping Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 74 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:72.7% 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 75 . 7¦Â-hydroxysitosterol ÏàËÆ¶È:72.7% Chinese Traditional and Herbal Drugs 2010 41 187-190 Studies on chemical constituents of Oxytropis kansuensis GONG Hong-fei; YANG Ai-mei; LIU Jun-xi; DI Duo-long Structure 13C NMR ̼Æ×Ä£Äâͼ 76 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:72.7% Chinese Traditional and Herbal Drugs 2010 41 704-707 Âúɽºì»¯Ñ§³É·ÖµÄÑо¿ ¸¶ÏþÀö;ÕÅÁ¢Î°;ÁÖÎĺ²;ÀîÇàɽ Structure 13C NMR ̼Æ×Ä£Äâͼ 77 . stigmast-7-en-3¦Â-ol ÏàËÆ¶È:72.7% Chinese Traditional and Herbal Drugs 2009 40 1039-1042 ɽ·¯µÄ»¯Ñ§³É·ÖÑо¿ »ô³¤ºç;Áººè;ÕÅÇìÓ¢;Íõß“;ÕÔÓñÓ¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 78 . 24R-ÒÒ»ù-5¦Á-µ¨çÞ-3¦Â,6¦Á-¶þ´¼ ÏàËÆ¶È:72.7% Chinese Traditional and Herbal Drugs 2004 35 621-622 СľͨµÄ»¯Ñ§³É·ÖÑо¿ (¦©) »ÆÎÄÎä,¿×µÂÔÆ,ÑîÅàÃ÷ Structure 13C NMR ̼Æ×Ä£Äâͼ |

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