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shaoyan415

гæ (СÓÐÃûÆø)

[ÇóÖú] GS3---CÆ×ÇóÖú ÒÑÓÐ2È˲ÎÓë

13C NMR (126 MHz, Pyr) ¦Ä 16.60,16.65,17.37,19.65,19.70,19.78,20.20,20.33,22.49,23.47,27.86,28.71,28.95,33.07,35.36,36.92,38.97,39.25,39.27,47.44,48.58,49.78,49.93,50.08,52.17,52.64,54.64,56.92,69.34,72.25,77.47,79.73,141.76154.48,160.37,161.32,199.71,199.90
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yangyinhe

ÖÁ×ðľ³æ (ÖøÃûдÊÖ)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
shaoyan415: ½ð±Ò+6, ¡ï¡ï¡ïºÜÓаïÖú, ллÄú£¬Ì«¸ÐлÁË 2015-03-16 19:06:50
1 .     ganodermacetal
C33H50O7     ÏàËÆ¶È:63.1%
Phytochemistry Letters          2012          5          576-580
Toxic lanostane triterpenes from the basidiomycete Ganoderma amboinense
Sheng-Xiang Yang, Zhao-Cheng Yu, Qiang-Qiang Lu, Wen-Quan Shi, Hartmut Laatsch, Jin-Ming Gao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

2 .     Ganodermacetal
    ÏàËÆ¶È:63.1%
Molecules          2014          19          17478-17535
A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp.
Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

3 .     21¦Â, 22¦Á-O-diangeloyl camelliagenin D
C40H60O8     ÏàËÆ¶È:61.5%
Phytochemistry          2002          59          825-832
Triterpenoid saponins and acylated prosapogenins from Harpullia austro-caledonica
Laurence Voutquenne, C¨¦cile Kokougan, Catherine Lavaud,Isabelle Pouny, Marc Litaudon
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

4 .     21¦Â,22¦Á-O-diangeloyl-protoaesciyenin
C40H6208     ÏàËÆ¶È:60.5%
Phytochemistry          1998          48          1229-1232
Harpuloside a triterpenoid saponin from Harpullia ramiflora
C. Dizes, F. Gerald, C. Lavaud, R. Ellas, R. Faure, G. Massiot, G. Balansard
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

5 .     Cumingianoside R
C37H64O10     ÏàËÆ¶È:60.5%
Phytochemistry          2011          72          2205-2211
Triterpenes and a triterpene glucoside from Dysoxylum cumingianum
Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

6 .     11¦Á,12¦Á-epoxy-3-O-¦Â-D-xylopyranosylolean-28,13¦Â-olide
C35H54O8     ÏàËÆ¶È:60.5%
Journal of Asian Natural Products Research          2012          14          333-341
New triterpenoid saponins from Patrinia scabiosifolia
Liang Gao,Lin Zhang,Li-Ming Wang,Jiang-Yun Liu,Pei-Lie Cai and Shi-Lin Yang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

7 .     3¦Â-hydroxyurs-12,19-dien-28-¦Â-D-glucopyranoside
    ÏàËÆ¶È:60.5%
Chinese Traditional and Herbal Drugs          2010          41          1048-1052
Chemical constituents of charred Sanguisorbae Radix(¢ò)
XIA Hong-min; ZHONG Ying; SUN Jing-yong; SUN Li-li; AN Kun; WANG Ju
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

8 .     compound K
C36H62NaO8     ÏàËÆ¶È:60.5%
Natural Product Research and Development          2014          26          1552-1556,1567
Chenmical Constituents of Enzymatic Hydrolysate of Total Ginsenoside Extract of Panax quinquefolium
JIN Jian-ming, LI You-hua, ZHANG Hai-lun, LIANG Chao-ning, TANG Shuang yan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

9 .     22-angeloyl-21-epoxyangeloylbarringto-genol C
C40H62O8     ÏàËÆ¶È:60%
Planta Medica          2005          71          1068-1070
Two New Triterpenes from the Husks of Xanthoceras sorbifolia
Zhan-Lin Li , Xian Li , Lin-Hao Li , Ning Li , Ming Yu , Da-Li Meng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

10 .     sutherlandioside B
C36H60O10     ÏàËÆ¶È:57.8%
Journal of Natural Products          2008          71(10)          1749-1753
Cycloartane Glycosides from Sutherlandia frutescens
Xiang Fu, Xing-Cong Li, Troy J. Smillie, Paulo Carvalho, Wilfred Mabusela, James Syce, Quinton Johnson, William Folk, Mitchell A. Avery, and Ikhlas A. Khan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-03-16 18:44:29
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

seuseasoar

ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
shaoyan415: ½ð±Ò+4, ¡ï¡ï¡ïºÜÓаïÖú, ллÄú¡£ 2015-03-16 19:07:09
1 .     ganodermacetal
C33H50O7     ÏàËÆ¶È:63.1%
Phytochemistry Letters          2012          5          576-580
Toxic lanostane triterpenes from the basidiomycete Ganoderma amboinense
Sheng-Xiang Yang, Zhao-Cheng Yu, Qiang-Qiang Lu, Wen-Quan Shi, Hartmut Laatsch, Jin-Ming Gao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     Ganodermacetal
    ÏàËÆ¶È:63.1%
Molecules          2014          19          17478-17535
A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp.
Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     21¦Â, 22¦Á-O-diangeloyl camelliagenin D
C40H60O8     ÏàËÆ¶È:61.5%
Phytochemistry          2002          59          825-832
Triterpenoid saponins and acylated prosapogenins from Harpullia austro-caledonica
Laurence Voutquenne, C¨¦cile Kokougan, Catherine Lavaud,Isabelle Pouny, Marc Litaudon
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     21¦Â,22¦Á-O-diangeloyl-protoaesciyenin
C40H6208     ÏàËÆ¶È:60.5%
Phytochemistry          1998          48          1229-1232
Harpuloside a triterpenoid saponin from Harpullia ramiflora
C. Dizes, F. Gerald, C. Lavaud, R. Ellas, R. Faure, G. Massiot, G. Balansard
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     Cumingianoside R
C37H64O10     ÏàËÆ¶È:60.5%
Phytochemistry          2011          72          2205-2211
Triterpenes and a triterpene glucoside from Dysoxylum cumingianum
Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     11¦Á,12¦Á-epoxy-3-O-¦Â-D-xylopyranosylolean-28,13¦Â-olide
C35H54O8     ÏàËÆ¶È:60.5%
Journal of Asian Natural Products Research          2012          14          333-341
New triterpenoid saponins from Patrinia scabiosifolia
Liang Gao,Lin Zhang,Li-Ming Wang,Jiang-Yun Liu,Pei-Lie Cai and Shi-Lin Yang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     3¦Â-hydroxyurs-12,19-dien-28-¦Â-D-glucopyranoside
    ÏàËÆ¶È:60.5%
Chinese Traditional and Herbal Drugs          2010          41          1048-1052
Chemical constituents of charred Sanguisorbae Radix(¢ò)
XIA Hong-min; ZHONG Ying; SUN Jing-yong; SUN Li-li; AN Kun; WANG Ju
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     compound K
C36H62NaO8     ÏàËÆ¶È:60.5%
Natural Product Research and Development          2014          26          1552-1556,1567
Chenmical Constituents of Enzymatic Hydrolysate of Total Ginsenoside Extract of Panax quinquefolium
JIN Jian-ming, LI You-hua, ZHANG Hai-lun, LIANG Chao-ning, TANG Shuang yan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     22-angeloyl-21-epoxyangeloylbarringto-genol C
C40H62O8     ÏàËÆ¶È:60%
Planta Medica          2005          71          1068-1070
Two New Triterpenes from the Husks of Xanthoceras sorbifolia
Zhan-Lin Li , Xian Li , Lin-Hao Li , Ning Li , Ming Yu , Da-Li Meng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     datiscoside C
    ÏàËÆ¶È:60%
Journal of the Chemical Society, Perkin Transactions 1          1983                   1333-1347
New cytotoxic principles from Datisca glomerata
Hiroshi Sasamori, K. Sambi Reddy, Michael P. Kirkup, Jeffrey Shabanowitz, David G. Lynn, Sidney M. Hecht, Kwamena A. Woode, Robert F. Bryan, James Campbell, William S. Lynn, Ernst Egert and George M. Sheldrick
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     cumingianoside C
    ÏàËÆ¶È:58.5%
Chemical & Pharmaceutical Bulletin          1997          45          202-206
Antitumor Agents. 169. Dysoxylum cumingianum. V. Cumingianosides P and Q, New Cytotoxic Triterpene Glucosides with an Apotirucallane-Type Skeleton from Dysoxylum cumingianum
Toshihiro FUJIOKA,Akio SAKURAI,Kunihide MIHASHI,Yoshiki KASHIWADA,Ih-Sheng CHEN and Kuo-Hsiung LEE
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     sutherlandioside B
C36H60O10     ÏàËÆ¶È:57.8%
Journal of Natural Products          2008          71(10)          1749-1753
Cycloartane Glycosides from Sutherlandia frutescens
Xiang Fu, Xing-Cong Li, Troy J. Smillie, Paulo Carvalho, Wilfred Mabusela, James Syce, Quinton Johnson, William Folk, Mitchell A. Avery, and Ikhlas A. Khan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     compound K
    ÏàËÆ¶È:57.8%
Chemical & Pharmaceutical Bulletin          1982          30          2393-2398
Studies on the Saponins of Ginseng. IV. On the Structure and Enzymatic Hydrolysis of Ginsenoside-Ra1
HARUYO KOIZUMI,SHUICHI SANADA,YOSHITERU IDA and JUNZO SHOJI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     3¦Â-O-(2-deoxy-¦Á-L-arabinohexopyranosyl)-20(29)-lupen-28-oic acid
C37H60O7     ÏàËÆ¶È:57.8%
Chemistry of Natural Compounds          2006          42          706-709
SYNTHESIS OF METHYL ESTERS OF BETULINIC ACID 2-DEOXY-a-GLYCOSIDES AND 28-OXO-19,28-EPOXYOLEANANE
O. B. Flekhter, N. I. Medvedeva, E. V. Tret'yakova,F. Z. Galin, and G. A. Tolstikov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     compound 63
    ÏàËÆ¶È:57.8%
Chemistry of Natural Compounds          1992          28          1-23
13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES
A. I. Kalinovskii
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     compound 7
    ÏàËÆ¶È:57.8%
Chemistry of Natural Compounds          1985          21          605-612
13C NMR SPECTRA OF A NUMBER OF PENTA- AND HEXACYCLIC TRITERPENOIDS DERIVED FROM GLYCYRRHETIC ACID
G. A. Tolstikov, L. M. Khalilov, L. A. Baltina, R. M. Kondratenko, A. A. Panasenko, and E. V. Vasil'eva
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     compound SU1
    ÏàËÆ¶È:57.8%
Phytochemistry Letters          2009          2          123-125
SU3, an oxocycloartane diglucoside from Sutherlandia humilis
Denise K. Olivier, Carl F. Albrecht, Ben-Erik van Wyk, Fanie R. van Heerden
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     cumingianoside M
C38H62O11     ÏàËÆ¶È:57.8%
Chemical & Pharmaceutical Bulletin          1997          45          68-74
Antitumor Agents. 168. Dysoxylum cumingianum. IV. The Structures of Cumingianosides G-O, New Triterpene Glucosides with a 14, 18-Cycloapotirucallane-Type Skeleton from Dysoxylum cumingianum, and Their Cytotoxicity against Human Cancer Cell Lines
Toshihiro FUJIOKA,Akio SAKURAI,Kunihide MIHASHI,Yoshiki KASHIWADA,Ih-Sheng CHEN and Kuo-Hsiung LEE
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     derivative of methyl tormentate
C35H54O7     ÏàËÆ¶È:57.8%
Phytochemistry          1998          48          171-174
Cecropioic acid, a pentacyclic triterpene from Musanga cecropioides
D. Lontsi, B. L. Sondengam, M. T. Martin, B. Bodo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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3Â¥2015-03-16 18:46:07
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