| ²é¿´: 258 | »Ø¸´: 1 | |||
guigui2011гæ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖúÒ»¸ö»¯ºÏÎï½á¹¹£¬Ìؼ±
|
|
13C NMR (101 MHz, CDCl3) ¦Ä 156.9,130.89,125.28,125.21,105.91,78.83,52.27,48.79,47.99,47.09,45.27,40.48,36.34,36.11,35.88,35.57,32.88,31.95,30.37,29.91,28.14,26.47,26.05,25.73, 25.46,25.41,24.14,21.12,19.99,19.28,18.01,17.63,13.98 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
0854Çóµ÷¼Á
ÒѾÓÐ27È˻ظ´
²ÄÁÏÏà¹Ø×¨Òµ344Çóµ÷¼ÁË«·Ç¹¤¿ÆÑ§Ð£»ò¿ÎÌâ×é
ÒѾÓÐ27È˻ظ´
300Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
291Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
Ò»Ö¾Ô¸»¦9£¬326ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ12È˻ظ´
ÉúÎïѧµ÷¼Á
ÒѾÓÐ10È˻ظ´
320Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
½ÓÊÜÈκε÷¼Á
ÒѾÓÐ7È˻ظ´
»¯Ñ§070300 Çóµ÷¼Á
ÒѾÓÐ29È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖúÒ»»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ½âÆ×
ÒѾÓÐ20È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÌìȻҩÎﻯѧ»¯ºÏÎï½á¹¹¼ø¶¨¡£¡£¡£¡£¼±Ó㬸ßÐüÉÍ
ÒѾÓÐ13È˻ظ´
µ½µ×ÊÇÖÊÆ×Êý¾ÝµÃµ½»¯ºÏÎï½á¹¹µÄÐÅÏ¢¶à»¹ÊǺ˴Ŷà
ÒѾÓÐ4È˻ظ´
´ó»·ÄÚÖ¬À໯ºÏÎïµÄ½á¹¹½âÎö
ÒѾÓÐ9È˻ظ´
Ôõô²éÒ»¸öÒÑÖª½á¹¹»¯ºÏÎïµÄÈ۵㣿
ÒѾÓÐ9È˻ظ´
ÈçºÎ×öÒ»¸öС·Ö×Ó»¯ºÏÎïÓëµ°°×½á¹¹µÄBinding
ÒѾÓÐ11È˻ظ´
ÇóÖúÈçϵÄÁ½¸ö»¯ºÏÎïÈçºÎͨ¹ýÆ×ͼÐÅÏ¢À´È·Ö¤¾ßÌåÊÇÄĸö½á¹¹£¿ лл
ÒѾÓÐ27È˻ظ´
¡¾ÇóÖú¡¿éÎÆ¤ËغÍÏð»ÆËØÊÇͬһ¸ö»¯ºÏÎï°É£¡¿´½á¹¹Ê½ÊÇÒ»ÑùµÄ°¡£¡Êǹ¹ÐͲîÒìÂð£¿
ÒѾÓÐ6È˻ظ´
¡¾ÇóÖú¡¿¼û¹íµÄÁ½¸ö»¯ºÏÎï½á¹¹½âÎö
ÒѾÓÐ18È˻ظ´
¡¾×ªÌû¡¿¡¾ÇóÖú¡¿£ºNMRÖÐCÐźÅȱʧµÄÀý×Ó£¨È纬ôÊ»ùµÄ¿àÄ¾ËØÀ໯ºÏÎï½á¹¹¼ø¶¨µÄÎÄÏ×£©
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿´ÓÒ»¸öÒ©Æ·µÄ´úºÅÔõô²éÕҸû¯ºÏÎïµÄ»¯Ñ§½á¹¹£¿
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿Ààú½á¹¹Ä£ÐÍ»¯ºÏÎïµÄÑ¡Ôñ
ÒѾÓÐ8È˻ظ´
¡¾ÇóÖú¡¿ÓëÆ¥·¥ËûÍ¡¸Æ½á¹¹ÏàËÆµÄ»¯ºÏÎïÓÐÄÄЩ
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿ÇóÒ»¸ö»³ö»¯ºÏÎï½á¹¹Ê½À´¼ìË÷ÎÄÏ×µÄÍøÕ¾
ÒѾÓÐ20È˻ظ´
superspace
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 195 (¸ßÖÐÉú)
- ½ð±Ò: 18748.9
- É¢½ð: 53
- ºì»¨: 7
- Ìû×Ó: 1402
- ÔÚÏß: 197.3Сʱ
- ³æºÅ: 970186
- ×¢²á: 2010-03-13
- רҵ: Éç»áÐÄÀíѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
guigui2011: ½ð±Ò+8, ¡ïÓаïÖú 2012-12-24 13:13:01
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
guigui2011: ½ð±Ò+8, ¡ïÓаïÖú 2012-12-24 13:13:01
|
ÕâÊÇÄãÇóÖúµÄ»¯ºÏÎïÔÚÏàËÆ¶È80%ÒÔÉÏµÄÆ¥ÅäÐÅÏ¢ 1 . nerifoliene C31H50O ÏàËÆ¶È:90.9% Natural Product Research 2004 18 33-37 A new tetracyclic triterpene from the latex of Euphorbia Nerifolia Uppuluri V. Mallavadhani; K. V. S. Satyanarayana; Anita Mahapatra; A. V. S. Sudhakar Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . cycloartenol ÏàËÆ¶È:87.8% Planta Medica 1981 42 268-274 Structure of Methyl Adenophorate and Triphyllol,Triterpenoids of Adenophora triphylla var. japonica Roots Chohachi Konno,Takashi Saito, Yoshiteru Oshima, Hiroshi Hikino and Chizuko Kabuto Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . cycloartenol ÏàËÆ¶È:87.8% Natural Product Research 2004 18 33-37 A new tetracyclic triterpene from the latex of Euphorbia Nerifolia Uppuluri V. Mallavadhani; K. V. S. Satyanarayana; Anita Mahapatra; A. V. S. Sudhakar Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . cycloartenol ÏàËÆ¶È:87.8% China Journal of Chinese Materia Medica 2005 30 671-674 Study on chemical constituents in rhizome of Pinellia ternata HE Ping, LI Shuai, WANG Su-juan, YANG Yong-chun, SHI Jian-gong Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . cycloartenol C30H50O ÏàËÆ¶È:87.8% China Journal of Chinese Materia Medica 2001 26 610-612 Studies on Chemical Constituents of Fragaria ananassa Duch RUAN Jinlan, CHEN Jingbo, ZHAO Xiaoya, SUN Nanjun, John M Cassady, Gary D Stoner Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . cycloartenol ÏàËÆ¶È:87.8% Phytochemistry 1996 41 1191-1195 Antibacterial hydroperoxysterols from Xanthosoma robustum Takeshi Kato, Barbara Frei, Michael Heinrich, Otto Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . cycloartenol C30H50O ÏàËÆ¶È:87.8% Chinese Journal of Natural Medicines 2008 6 271-274 Chemical Constituents from the Roots and Stems of Ervatamia hainanensis JIN Li; LU Jia; JIN Yong-Sheng; YANG Xiang-Nan; CHEN Hai-Sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . cycloartenol ÏàËÆ¶È:87.8% Chinese Pharmaceutical Journal 2010 45 1535-1538 Studies on Chemical Constituents of Stamen Nelumbinis CHEN Yan-yan, TANG Yu-ping, DUAN Jin-ao, GUO Sheng, WU Qi-cheng, SHANG Er-xin Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 17a ÏàËÆ¶È:84.8% Chemical & Pharmaceutical Bulletin 2004 52 1382-1384 Chemical Constituents of Malagasy Liverworts, Part II: Mastigophoric Acid Methyl Ester of Biogenetic Interest from Mastigophora diclados (Lepicoleaceae Subf. Mastigophoroideae) Liva Harinantenaina and Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . cycloaudenol ÏàËÆ¶È:84.8% Chinese Traditional and Herbal Drugs 1998 29 433-435 Studies on the Triterpenes from Xiaolangdu (Euphorbia prolifera) Zhang Jun; Yang Chengjin; Wu Dagang (The First Affiliated Hospital of Kuming Medical College; Kunming ); Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . cycloartane-24-methylene-3¦Â,25-diol ÏàËÆ¶È:81.8% Natural Product Research 2001 15 363-369 Cycloartane Triterpenes from Euphorbia tuckeyana U. Maria-Jos¨¦; Ferreira; Filipa C. Pinto; Jos¨¦ R. Ascenso Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 24-methylenecycloartanol C31H52O ÏàËÆ¶È:81.8% China Journal of Chinese Materia Medica 2006 31 1072-1075 Chemical constituents from herb of Alternanthera philoxeroides FANG Jinbo, DUNG Hongquan, ZHANG Yanwen, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 24-methylenecycloartanol C31H52O ÏàËÆ¶È:81.8% Journal of Natural Products 1992 Vol 55 644 Separation of 24-Methylenecycloartanol from Cycloartenol Via a Chemical Method Shoei-Sheng Lee, Liang-Hwa Young, K. C. Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 25-hydroperoxycyrloart-23 -en-3¦Â-ol C30H50O3 ÏàËÆ¶È:81.8% Journal of Natural Products 1995 Vol 58 1920-1924 Hydroperoxycycloartanes from Tillandsia recurvata Gabriela M. Cabrera, Alicia M. Seldes Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 25-hydroperoxycycloart-23-en-3¦Â-ol ÏàËÆ¶È:81.8% Phytochemistry 1996 41 1191-1195 Antibacterial hydroperoxysterols from Xanthosoma robustum Takeshi Kato, Barbara Frei, Michael Heinrich, Otto Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ¦Â-amyrin ÏàËÆ¶È:81.8% Korean Journal of Pharmacognosy 2008 39(1) 37-42 Phytocheical Studies on Paeoniae Radix (3);Triterpenoids Kim, Ju-Sun; Kim, Yoon-Jung; Lee, So-Young; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 24-methylene cycloartanol ÏàËÆ¶È:81.8% Phytochemistry 1988 27 2813-2815 Triterpenoids of Paeonia japonica callus tissue Akira Ikuta,Hideji Itokawa Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 24-methylene-cycoar tanol C31H52O ÏàËÆ¶È:81.8% Chinese Traditional and Herbal Drugs 2009 40 697-701 èßÁø¿¹Ö×ÁöÝÆÀà³É·ÖÑо¿ Íõ±ó;½ªµÇîÈ;Àî¹úÇ¿;¹Ü»ªÊ« Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 24-methylenecycloartanol ÏàËÆ¶È:81.8% Chinese Traditional and Herbal Drugs 2009 40 1198-1201 Chemical constituents of Lobelia chinensis DENG Ke-zhong; XIONG Ying; GAO Wen-yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 24-methene-cycloartenol ÏàËÆ¶È:81.8% Chinese Traditional and Herbal Drugs 2008 39 497-499 Chemical constituents from roots of Euphorbia songarica LIN Jia AN Ning LIU Chun-yu XU Li-zhen Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 24-ÑǼ׻ù-»·°¢¶ûÍ¢´¼ ÏàËÆ¶È:81.8% Chinese Traditional and Herbal Drugs 2008 39 499-502 ¿ÕÐÄÁ«×Ӳݻ¯Ñ§³É·ÖÑо¿ Âí׿;ÀîÇíÛë;·¶ÎÄǬ;·½Äî²®;ÁõìÍÎÄ Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 24-methylenecycloartanol ÏàËÆ¶È:81.8% Chinese Journal of Natural Medicines 2010 8 101-103 Diterpenes and Triterpenes from the Roots of Euphorbia fischeriana WU Qi-Cheng; TANG Yu-Ping; DING An-Wei; YOU Fen-Qiang; DUAN Jin-Ao Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 24-Methylenecycloartanol ÏàËÆ¶È:81.8% Archives of Pharmacal Research 2010 33 515-521 A new phenylpropane glycoside from the rhizome of Sparganium stoloniferum Seung Young Lee, Sang Un Choi, Jei Hyun Lee, Dong Ung Lee and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 24-methylenecycloartanol ÏàËÆ¶È:81.8% Journal of the Chemical Society, Perkin Transactions 1 1989 1969-1974 Biosynthesis of 24¦Â-ethylsterols in cultured cells of Trichosanthes kirilowii(cucurbitaceae) fed with [1,2-13C2]- and [2-13C2H3]-acetate: reinvestigation of the stereochemistry at C-25 Shujiro Seo, Atsuku Uomori, Yohko Yoshimura, Ken'ichi Takeda, Haruo Seto, Yutaka Ebizuka, Hiroshi Noguchi and Ushio Sankawa Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 24-methylenecycloartenol ÏàËÆ¶È:81.8% Natural Product Research and Development 2010 22 597-599 Steroids and Terpenoids from the Mangrove Acanthus ilicifolius HAI Fang; TANG Xv-li; LI Guo-qiang Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 24-methylenecycloartaol ÏàËÆ¶È:81.8% Natural Product Research and Development 2007 19 365-368 Triterpenoid from Ecdysanthera rosea XU Fu-quan;LIU Hai-yang; TENG Fei; CHEN Chang-xiang; ZHONG Hui-min Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 24-methylenecycloartanol ÏàËÆ¶È:81.8% Natural Product Research and Development 2007 19 240-243 Chemical Constituents of Cibotium barometz WU Qi; YANG Xiu-wei; YANG Shi-hai; ZOU Lei; YAN Jing Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 24-methylenecycloartan-3¦Â-ol C31H52O ÏàËÆ¶È:81.8% Zeitschrift f¨¹r Naturforschung C 2004 59 15-18 Chemical Constituents of Euphorbia marschalliana Boiss. A. R. Jassbi, S. Zamanizadehnajari, and S. Tahara Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2012-12-17 20:27:07













»Ø¸´´ËÂ¥