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12.00,12.11,12.13,19.00,19.16,19.97,21.35,23.19,25.83,28.61,29.26,29.84,31.74,34.09,36.23,36.58,37.07,37.27,39.79,42.10,43.00,45,95,48.58,51.00,54.97,55.64,56.57,71.64,74.06,82.03,120.87,121.62
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
16 .     Nymphasterol
C29H48O     ÏàËÆ¶È:75.7%
Medicinal Chemistry Research          2012          21          783-787
Nymphasterol, a new steroid from Nymphaea stellata
Amita Verma , Bahar Ahmed ,Rucha Upadhyay,Neetu Soni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     compound 8(24R)
    ÏàËÆ¶È:75.7%
Shoyakugaku Zasshi          1992          46          302-309
Chemical Components of a Commercial Crude Drug "Byakken" (Ampelopsis Radix)
KATO TAKESHI, SUYAMA TETSUO, YAMANE FUJITOSHI, MORITA YUTAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     compound 8(24S)
    ÏàËÆ¶È:75.7%
Shoyakugaku Zasshi          1992          46          302-309
Chemical Components of a Commercial Crude Drug "Byakken" (Ampelopsis Radix)
KATO TAKESHI, SUYAMA TETSUO, YAMANE FUJITOSHI, MORITA YUTAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:75.7%
Chinese Traditional and Herbal Drugs          2012          43          2356-2360
Chemical constituents from sporophore of Hericium coralloides (¢ñ)
ZHANG Peng; BAO Hai-ying; Tolgor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     ¦Â-Sitosterol
C29H50O     ÏàËÆ¶È:75.7%
Journal of Chinese Medicinal Materials          2006          29          1182-1184
Studies on the Chemical Constituents of Hypogeal Part from Limonium bicolor
WEI You-xia, WANG Jun-xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     compound 3
    ÏàËÆ¶È:75.7%
Chinese Journal of Antibiotics          1998          23          401-463
¶¾Á¦³æÃ¹EB-82 ÃðÑÁ¾ú·¢½Í²úÎïµÄÓÐЧ³É·ÖÑо¿¢ñ. ÃðÑÁ¾úËØA µÄ·ÖÀëºÍ½á¹¹¼ø¶¨
Íõº£Ñà, ÐíºèÕÂ
Structure      13C NMR   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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
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