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16.20,16.44,20.16,20.16,20.27,20.30,24.48,25.47,26.60,26.72,28.29,28.64,28.71,28.75,29.67,31.97,40.88,41.14,44.18,44.45,48.42,50.93,56.38,57.08,65.74,75.03,75.50

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²éѯ½á¹û£º¹²²éµ½1445¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     compound 12
    ÏàËÆ¶È:63.3%
Phytochemistry          1992          31          4263-4274
Cycloartanes and other terpenoids and phenylpropanoids from Monocyclanthus vignei
Hans Achenbach, Dieter Frey
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 5
C27H44O2     ÏàËÆ¶È:62.9%
Tetrahedron Letters          2002          43          1151-1155
Deoxygenation of aliphatic acetate derivatives using electrogenerated organic amalgams
Lizeth M. Fragoso-Luna, Bernardo A. Frontana-Uribe, Jorge C¨¢rdenas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     2¦Á,3¦Â,19¦Á-Trihydroxy-28-norurs-12-ene
C29H48O3     ÏàËÆ¶È:62.0%
Chemical & Pharmaceutical Bulletin          2005          53(10)          1338-1341
Sesquiterpenes, Nortriterpenes and Other Constituents from Ligularia tongolensis
Yi Feng HAN,Jing PAN,Kun GAO,and Zhong Jian JIA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     cycloprotobuxinamine
C29H46N2O5     ÏàËÆ¶È:62.0%
Acta Botanica Sinica          1996          38          483-488
Two New Buxus Alkaloids from Buxus microphylla Sieb. Et Zucc
Du Jiang, QiuMing-hua and Nie Rui-lin L¨¹Yang, Wu Nan and Zheng Qi-tai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     2¦Á,3¦Â,19¦Á-trihydroxy-28-norurs-12-ene
C29H48O3     ÏàËÆ¶È:62.0%
Chemistry Letters          2005          34          892-893
Two New Nortriterpenes from Ligularia tongolensis
Yi Feng Han, Kun Gao and Zhong Jian Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3,5-Epoxy-A-nor-olean-12-en-3-(2-isopropyl)-30-oic Acid
    ÏàËÆ¶È:61.2%
Chemistry of Natural Compounds          2006          42          553-557
SYNTHESIS AND HIGH-RESOLUTION NMR SPECTRA OF A-nor-DERIVATIVES OF 11-DEOXYGLYCYRRHETIC ACID
L. R. Mikhailova, L. A. Baltina, R. M. Kondratenko,. Kunert,L. V. Spirikhin,F. Z. Galin, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     20(¦Á),24(S)-epoxy-3¦Â,6¦Á,25-trihydroxycycloartan-16-one
C30H48O5     ÏàËÆ¶È:60.7%
Journal of Natural Products          2001          64          1179-1182
Secondary Metabolites from the Roots of Astragalus zahlbruckneri
Ihsan Çalis,Hasan Abou Gazar, Sonia Piacente, and Cosimo Pizza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     24S-methylcholestan-1¦Á,3¦Â,25-triol
C28H50O3     ÏàËÆ¶È:60.7%
Steroids          2012          77          433-440
Polyhydroxylated sterols from the Indonesian soft coral Sinularia sp.and their effect on farnesoid X-activated receptor
Masteria Yunovilsa Putra,Giorgio Bavestrello,Carlo Cerrano,Barbara Renga,Claudio D¡¯Amore ,Stefano Fiorucci,Ernesto Fattorusso,Orazio Taglialatela-Scafati
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (24S)-24-ethyl-4¦Â-methyl-5¦Á-cholestan-3¦Â-ol
C30H52O     ÏàËÆ¶È:60.7%
Marine Drugs          2012          10          2448-2466
Preliminary Structure-Activity Relationship on Theonellasterol, a New Chemotype of FXR Antagonist, from the Marine Sponge Theonella swinhoei
Valentina Sepe, Raffaella Ummarino, Maria Valeria D'Auria, Orazio Taglialatela-Scafati, Simona De Marino, Claudio D'Amore, Barbara Renga, Maria Giovanna Chini, Giuseppe Bifulco, Yoichi Nakao, Nobuhiro Fusetani, Stefano Fiorucci and Angela Zampella
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound 59
    ÏàËÆ¶È:60.7%
The Journal of Organic Chemistry          2005          70          1808-1827
Novel Cuticular Hydrocarbons from the Cane Beetle Antitrogus parvuluss4,6,8,10,16-Penta- and 4,6,8,10,16,18-HexamethyldocosanessUnprecedented anti-anti-anti-Stereochemistry in the 4,6,8,10-Methyltetrad
Sharon Chow, Mary T. Fletcher, Lynette K. Lambert, Oliver P. Gallagher, Christopher J. Moore, Bronwen W. Cribb, Peter G. Allsopp, and William Kitching
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Buxruguline D
C29H48N2O3     ÏàËÆ¶È:60.7%
Natural Products and Bioprospecting          2011          1          71-74
Triterpenoid alkaloid derivatives from Buxus rugulosa
Yu-Xin Yan, Lin Zhou, Yun Sun, Jian-Chao Chen, Jia Su, Yan Li, Ming-Hua Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     (22E)-3¦Â,5¦Á,9¦Á-trihydroxy-ergosta-7,22-dien-6-one
C28H44O4     ÏàËÆ¶È:60.7%
Chinese Journal of Marine Drugs          2012          31          7-10
Secondary metabolites of marine fungus zp6 and their antifungal bioactivities
GAO Chang-song; ZHONG Hui-min; CAO Jun-wei; CHEN Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
2Â¥2013-09-14 17:53:51
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mrdone.0907

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2Â¥: Originally posted by wangkaibo123 at 2013-09-14 17:53:51
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mrdone.0907

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3Â¥: Originally posted by mrdone.0907 at 2013-09-14 19:14:56
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16.20,16.44,20.16,20.16,20.27,20.30,24.48,25.47,26.60,26.72,28.29,28.64,28.71,28.75,29.67,31.97,40.88,41.14,44.18,44.45,48.42,50.93,56.38,57.08,65.74,75.03,75.50,77.96,80.36
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wangkaibo123

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kerry

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mrdone.0907: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ×î½ü±È½Ï棬»Ø¸´µÄÓÐЩ³Ù 2013-09-17 15:44:26
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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

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²éѯ½á¹û£º¹²²éµ½2189¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     cycloprotobuxinamine
C29H46N2O5     ÏàËÆ¶È:65.5%
Acta Botanica Sinica          1996          38          483-488
Two New Buxus Alkaloids from Buxus microphylla Sieb. Et Zucc
Du Jiang, QiuMing-hua and Nie Rui-lin L¨¹Yang, Wu Nan and Zheng Qi-tai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     neomyrrhaol
C30H52O4     ÏàËÆ¶È:63.3%
Planta Medica          2009          75          351-355
Isolation and Biological Activities of Neomyrrhaol and Other Terpenes from the Resin of Commiphora myrrha
Shu-Lan Su,Jin-Ao Duan,Yu-Ping Tang, Xu Zhang1, Li Yu, Feng-Rong Jiang,Wei Zhou1, Dan Luo,An-Wei Ding
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3¦Â,22¦Á-dihydroxy-lanosta-8,24E-diene-25-peroxide
C30H50O4     ÏàËÆ¶È:63.3%
Chinese Chemical Letters          2000          11          45-48
Triterpenoids from Fuscoporia obliqua
Jian HE, Xiao zhang FENG, Bin ZHAO, Yang LU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     fuscoporianol B
C30H50O4     ÏàËÆ¶È:63.3%
Journal of Asian Natural Products Research          2001          3          55-61
Three New Triterpenoids from Fuscoporia Obliqua
JJAN HE, XIAO-ZHANG FENG, YANG LU and BIN ZHAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     ¦Â-kudinlactone
C30H46O5     ÏàËÆ¶È:63.3%
Phytochemistry          1996          43          443-445
Triterpenoid glycosides from Ilex kudincha
Ming-An Ouyang, Han-Qing Wang, Zi-Li Chen, Chong-Ren Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     ¦Â-Kudinlactone
C30H46O5     ÏàËÆ¶È:63.3%
Phytochemistry          1996          41          871-877
Triterpenes and triterpenoid glycosides from the leaves of Ilex kudincha
Ming-An Ouyang, Chong-Ren Yang, Zi-Li Chen, Han-Qing Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     compound 12
    ÏàËÆ¶È:63.3%
Phytochemistry          1992          31          4263-4274
Cycloartanes and other terpenoids and phenylpropanoids from Monocyclanthus vignei
Hans Achenbach, Dieter Frey
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     17,24-epoxy-25-hydroxy-3-oxobaccharan-21-oic acid
C30H48O5     ÏàËÆ¶È:63.3%
The Journal of Organic Chemistry          2004          69          3350-3358
Silvestrol and Episilvestrol, Potential Anticancer Rocaglate Derivatives from Aglaia silvestris
Bang Yeon Hwang, Bao-Ning Su, Heebyung Chai, Qiuwen Mi, Leonardus B. S. Kardono, Johar J. Afriastini, Soedarsono Riswan, Bernard D. Santarsiero, Andrew D. Mesecar, Robert Wild, Craig R. Fairchild, Gregory D. Vite, William C. Rose, Norman R. Farnsworth, Ge
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     colossolactone C
C32H46O6     ÏàËÆ¶È:62.5%
Journal of Natural Products          2001          64          236-239
Colossolactones, New Triterpenoid Metabolites from a Vietnamese Mushroom Ganoderma colossum
Peter Kleinwächter, Ngo Anh,Trinh Tam Kiet,Brigitte Schlegel, Hans-Martin Dahse, Albert Härtl, and Udo Gräfe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     2¦Á,3¦Â,19¦Á-Trihydroxy-28-norurs-12-ene
C29H48O3     ÏàËÆ¶È:62.0%
Chemical & Pharmaceutical Bulletin          2005          53(10)          1338-1341
Sesquiterpenes, Nortriterpenes and Other Constituents from Ligularia tongolensis
Yi Feng HAN,Jing PAN,Kun GAO,and Zhong Jian JIA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     20(¦Á),24(S)-epoxy-3¦Â,6¦Á,25-trihydroxycycloartan-16-one
C30H48O5     ÏàËÆ¶È:62.0%
Journal of Natural Products          2001          64          1179-1182
Secondary Metabolites from the Roots of Astragalus zahlbruckneri
Ihsan Çalis,Hasan Abou Gazar, Sonia Piacente, and Cosimo Pizza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     compound 5
C27H44O2     ÏàËÆ¶È:62.0%
Tetrahedron Letters          2002          43          1151-1155
Deoxygenation of aliphatic acetate derivatives using electrogenerated organic amalgams
Lizeth M. Fragoso-Luna, Bernardo A. Frontana-Uribe, Jorge C¨¢rdenas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     halistanol sulfate
C29H52O12S3Na3     ÏàËÆ¶È:62.0%
Tetrahedron letters          1981          22          1985-1988
Bioactive marine metabolites II. Halistanol sulfate, an antimicrobial novel steroid sulfate from the marine sponge halichondria cf. moorei bergquist
N. Fusetani, S. Matsunaga, S. Konosu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     2¦Á,3¦Â,19¦Á-trihydroxy-28-norurs-12-ene
C29H48O3     ÏàËÆ¶È:62.0%
Chemistry Letters          2005          34          892-893
Two New Nortriterpenes from Ligularia tongolensis
Yi Feng Han, Kun Gao and Zhong Jian Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Buxruguline D
C29H48N2O3     ÏàËÆ¶È:62.0%
Natural Products and Bioprospecting          2011          1          71-74
Triterpenoid alkaloid derivatives from Buxus rugulosa
Yu-Xin Yan, Lin Zhou, Yun Sun, Jian-Chao Chen, Jia Su, Yan Li, Ming-Hua Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
5Â¥2013-09-14 20:04:30
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