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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½605¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Â-Sitosterol C29H50O ÏàËÆ¶È:93.1% 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 2 . ¦Â-Sitosterol ÏàËÆ¶È:93.1% 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 3 . ¦Â-Sitosterol ÏàËÆ¶È:93.1% 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 4 . ¦Â-sitosterol ÏàËÆ¶È:93.1% 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 5 . ¦Â-sitosterol ÏàËÆ¶È:93.1% Chinese Pharmaceutical Journal 2005 40 1052-1054 Study on chemical constituents of Potentilla discolor XLE Pei-feng, YIN Ting, LIANG Hong, ZHAO Yu-ying Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Â-sitosterol ÏàËÆ¶È:93.1% 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 7 . sitosterol ÏàËÆ¶È:93.1% Chemical Communications 1986 1139-1140 Biosynthesis of Sitosterol in Tissue Cultures of Rabdosia japonica Hara and Ergosterol in Yeast from [2-13C, 2-2H3]Acetate Shujiro Seo, * Ushio Sankawa, Haruo Seto, Atsuko Uomori, Yohko Yoshimura, Yutaka Ebizuka, Hiroshi Noguchi, and Ken'ichi Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-sitosterol ÏàËÆ¶È:93.1% Natural Product Research and Development 2005 17 125-127 Chemical Constituents of Tinospora craveniana LI Hong-bo; HU Jun; CHEN Jian-chao; QIU Ming-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ¦Â-sitosterol ÏàËÆ¶È:93.1% Chinese Traditional and Herbal Drugs 2011 42 25-30 Lignans and flavonoids from rhizome of Drynaria fortunei LIANG Yong-hong, YE Min, HAN Jian, WANG Bao-rong, GUO De-an Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:93.1% Journal of Beijing University of Chemical Technology (Natural Science Edition) 2012 39 40-45 Isolation of the triterpenes from Eriobotrya japonica leaves CHEN Huan CHEN Guang REN HongMei YANG QuanHua YU ChangYuan Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:93.1% Lishizhen Medicine and Materia Medica Research 2012 23 619-620 Ы×Ӳݿ¹¾ú»îÐԳɷֵÄÑо¿ ½ÕðÏ×; ÕÅÏþÁÖ; Åíϼ; ³ÂÕ±¦ Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . cholesterol ÏàËÆ¶È:92.5% Chinese Traditional and Herbal Drugs 2010 41 539-541 ɽʯÁñµÄ»¯Ñ§³É·ÖÑо¿(¢ò) ¸ß¹ã´º;ÌÕÊïºì;ÆáÊ绪;ÕÅ‚Æ;ÀîÇìÐÀ Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ¦Â-sitosterol ÏàËÆ¶È:89.6% 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 14 . ¦Â-sitosterol ÏàËÆ¶È:89.6% 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 15 . stigmast-5-en-3¦Â-ol ÏàËÆ¶È:89.6% 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 16 . stigmasterol ÏàËÆ¶È:89.6% 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 17 . ¦Â-sitosterol ÏàËÆ¶È:89.6% 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 18 . ¦Â-sitosterol ÏàËÆ¶È:89.6% 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 19 . ¦Â-sitosterol ÏàËÆ¶È:89.6% 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 20 . ¦Â-sitosterol ÏàËÆ¶È:89.6% 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 21 . ¦Â-Sitosterol ÏàËÆ¶È:89.6% 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 22 . sitosterol ÏàËÆ¶È:89.6% 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 23 . ¦Â-Sitosterol ÏàËÆ¶È:89.6% 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 24 . compound 5 ÏàËÆ¶È:89.6% 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 25 . compound 1 C29H50O ÏàËÆ¶È:89.6% 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 26 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:89.6% 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 27 . ¦Â-rosasterol C29H50O ÏàËÆ¶È:89.6% 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 28 . ¦Â-sitosterol |

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