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Ñà¿Ê¸ß·É: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-18 19:44:30
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²éѯ½á¹û£º¹²²éµ½34964¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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:96.6% 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:96.6% 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 . clionasterol ÏàËÆ¶È:96.6% 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 5 . ¦Â-Sitosterol C29H50O ÏàËÆ¶È:96.6% Chemistry of Natural Compounds 2007 43 358-359 TRITERPENE GLYCOSIDES FROM Astragalus AND THEIR GENINS.LXXV. STEROLS AND TRITERPENOIDS FROM Astragalus orbiculatus I. M. Isaev, R. P. Mamedova, M. A. Agzamova, and M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 7 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 8 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:96.6% Acta Bot. Boreal. -Occident. Sin. 2004 24 1292-1294 Chemical constituents from Saussurea polycolea LI Yu-lin, WANG Hong-lun, SUO You-rui Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ¦Â-sitosterol ÏàËÆ¶È:96.6% Acta Bot. Boreal. -Occident. Sin. 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 10 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 11 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:96.6% Acta Botanica Sinica 2003 45 1003-1007 Two New Triterpenes from Neonauclea sessilifolia KANG Wen-Yi, LI Guo-Hong, HAO Xiao-Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 13 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 14 . ¦Â-sitosterol ÏàËÆ¶È:96.6% Guihaia 2007 27 140-142 Chemical constituents from leaves of Livistona chinensis LIU Zhi-Ping; CUI Jian-Guo ; LIU Hong-Xing; HUANG Chu-Sheng; ZHONG Zhen-Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ¦Â-Sitosterol ÏàËÆ¶È:96.6% Journal of Asian Natural Products Research 2008 10 281-283 Artemisterol, a new steryl ester from the whole plant of Artemisia apiacea Sung-Jin Lee Hye Min Kim, Jeong Min Lee, Hee Seung Park and Sanghyun Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 17 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 18 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 19 . stigmast-5-en-3¦Â-ol ÏàËÆ¶È:96.6% Natural Product Research 2008 22 942-949 Bioactivities and chemical constituents of a Vietnamese medicinal plant Che Vang, Jasminum subtriplinerve Blume (Oleaceae) Dai Hue Ngan; Ho Thi Cam Hoai; Le Mai Huong; Poul Erik Hansen; Ole Vang Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:96.6% 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 21 . stigmasterol ÏàËÆ¶È:96.6% 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 22 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 23 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 24 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 25 . ¦Â-sitosterol ÏàËÆ¶È:96.6% Fitoterapia 2005 76 433-438 A new dihydroxysterol from the marine phytoplankton Diacronema sp. Am¨¦lia P. Rauter, Manuela M. Filipe, Carla Prata,João P. Noronha, Maria A.M. Sampayo,Jorge Justino,Jaime Bermejo Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . sitosterol ÏàËÆ¶È:96.6% 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 27 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 28 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 29 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 30 . beta-sitosterol ÏàËÆ¶È:96.6% 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 31 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 32 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:96.6% Natural Product Sciences 2007 13 317-321 Phytochemical Study of Lotus ornithopodioloides L. Abdel-Kader, Maged S.; Basudan, Omer A.; Alqasoumi, Saleh I.; Abou-Shoer, Mohamed I. Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . ¦Â-Sitosterol ÏàËÆ¶È:96.6% 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 34 . ¦Â-Sitosterol ÏàËÆ¶È:96.6% Natural Product Sciences 2007 13 394-397 Chemical Constituents of the Moss Hylocomium splendens Kang, Shin-Jung; Jovel, Eduardo; Hong, Seong-Su; Hwang, Bang-Yeon; Liu, Patty; Lee, Meng-Hsin; Lee, Meng-Chun; Lee, Kyung-Soon; Towers, George Hugh Neil Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . sitosterol ÏàËÆ¶È:96.6% 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 36 . ¦Â-Sitosterol C29H50O ÏàËÆ¶È:96.6% 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 37 . ¦Â-Sitosterol ÏàËÆ¶È:96.6% 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 38 . ¦Â-Sitosterol ÏàËÆ¶È:96.6% 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 39 . compound 5 ÏàËÆ¶È:96.6% 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 40 . compound 1 C29H50O ÏàËÆ¶È:96.6% 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 41 . compound 3a ÏàËÆ¶È:96.6% 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 42 . ¦Â-sitosterol ÏàËÆ¶È:96.6% Korean Journal of Pharmacognosy 1981 12(1) 12-24 Revision of 13C NMR Assignments of ¦Â-sitosterol and ¦Â-sitosteryl-3-O-¦Â-D-glucopyranoside Isolated from Plantago asiatica Seed Chang, Il-Moo; YunChoi, Hye-Sook; Yamasaki, Kazuo Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:96.6% 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 44 . ¦Â-¹ÈçÞ´¼ C29H48O ÏàËÆ¶È:96.6% 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 45 . (24s)-stigmast-5-en-3-ol ÏàËÆ¶È:96.6% 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 46 . (24S)-stigmast-5-en-3¦Â-ol ÏàËÆ¶È:96.6% 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 47 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:96.6% 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 48 . sitosterol ÏàËÆ¶È:96.6% Phytochemistry 1990 29 2351-2355 Sterol glucosides from Prunella vulgaris Hisashi Kojima,Noriko Sato,Akiko Hatano,Haruo Ogura Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . Stosterol ÏàËÆ¶È:96.6% Natural Product Research 2010 24 34-39 A new analogue of fatty alcohol from Tamarix hampeana L. Ahmet Aykaç; Yurdanur Akg¨¹l Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:96.6% 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 51 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:96.6% Chinese Traditional and Herbal Drugs 2010 41 704-707 Âúɽºì»¯Ñ§³É·ÖµÄÑо¿ ¸¶ÏþÀö;ÕÅÁ¢Î°;ÁÖÎĺ²;ÀîÇàɽ Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . ¦Â-sitosterol ÏàËÆ¶È:96.6% 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 |
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