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12.16,19.15,19.25,19.74,20.04,21.73,23.66,24.88,26.63,28.90,32.45,32.56,32.71,34.61,36.87,37.24,38.16,40.59,43.02,43.27,46.63,51.13,56.83,57.58,71.64,121.51,142.27
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
28 .     ¦Â-sitosterol
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