| ²é¿´: 430 | »Ø¸´: 1 | ||
183clj3648гæ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖúÒ»¸ö»¯ºÏÎïµÄάÆÕÊý¾Ý£¬Ð»Ð»£¡£¡£¡
|
|
±àºÅ£ºdxh-11-4-7-4-4-4 ÈܼÁ£ºCDCl3 ̼Æ×Êý¾Ý£º15.6,15.7,16.8,17.4,18.3,21.3,23.3,23.4,26.0,27.3,28.1,30.6,32.8,35.2,36.9,38.0,38.8,39.4,39.4,40.0,42.0,47.7,54.0,55.2,69.9,76.8,77.0,77.2,79.0,125.0,138.7·Ç³£¸Ðл£¡£¡£¡ |
» ²ÂÄãϲ»¶
285Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600²ÄÁÏÓ뻯¹¤301·ÖÇóµ÷¼ÁԺУ
ÒѾÓÐ19È˻ظ´
277¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ11È˻ظ´
277Çóµ÷¼Á ÊýÒ»104·Ö
ÒѾÓÐ13È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
336Çóµ÷¼Á£¬Ò»Ö¾Ô¸Öпƴó
ÒѾÓÐ6È˻ظ´
071000ÉúÎïѧ£¬Ò»Ö¾Ô¸ÉîÛÚ´óѧ296·Ö£¬Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ19È˻ظ´
274Çóµ÷¼ÁÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
άÆÕÊý¾Ý ÇóÖú
ÒѾÓÐ4È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄάÆÕÊý¾Ý
ÒѾÓÐ3È˻ظ´
άÆÕÊý¾ÝÇóÖú£¡Êý¾ÝºÜ¼òµ¥£¡
ÒѾÓÐ3È˻ظ´
ÇóάÆÕÊý¾Ý£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
άÆÕÊý¾ÝÇóÖú£¡Âé·³´ó¼ÒÁË£¡
ÒѾÓÐ3È˻ظ´
°ïæ²é¼¸¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý£¬Ê®·Ö¸Ðл~~
ÒѾÓÐ6È˻ظ´
άÆÕÊý¾ÝÇóÖú£¡
ÒѾÓÐ4È˻ظ´
Çó΢ÆÕ½âÎö»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
Çó΢ÆÕ½âÎö»¯ºÏÎï½á¹¹£¨¹²4¸ö£©
ÒѾÓÐ5È˻ظ´
Çó΢ÆÕ½âÎö»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïάÆÕÊý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú3¸ö΢ÆÕÊý¾Ý
ÒѾÓÐ5È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïάÆÕÊý¾Ý
ÒѾÓÐ6È˻ظ´
ËÓÐpudnµÄÕʺţ¬°ïæÏÂÔØÁ½¸ö´úÂ룬ллÁË
ÒѾÓÐ3È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄάÆÕCÆ×Êý¾Ý~~~~ллÁË~~~~~
ÒѾÓÐ3È˻ظ´
ÎÛȾÎïÇ¨ÒÆ×ª»¯¹ý³Ì£¬´ó¼Ò°ï°ïæ°¡
ÒѾÓÐ19È˻ظ´
ÓÐËù²»Îª
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 304 (´óѧÉú)
- ½ð±Ò: 9684.2
- É¢½ð: 16
- ºì»¨: 14
- Ìû×Ó: 1106
- ÔÚÏß: 814.3Сʱ
- ³æºÅ: 481441
- ×¢²á: 2007-12-17
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
183clj3648: ½ð±Ò+8, ¡ïÓаïÖú, ллÄã 2013-12-03 15:30:38
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
183clj3648: ½ð±Ò+8, ¡ïÓаïÖú, ллÄã 2013-12-03 15:30:38
|
²éѯ½á¹û£º¹²²éµ½12228¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 3¦Â,28-bis(dimethylcarbamoxy)urs-12-ene C31H48O5 ÏàËÆ¶È:90.3% Phytochemistry 2002 59 479-488 Microbial transformation of cadina-4,10(15)-dien-3-one,aromadendr-1(10)-en-9-one and methyl ursolate by Mucor plumbeus ATCC 4740 Dwight O. Collins, Peter L.D. Ruddock, Jessica Chiverton de Grasse,William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . erythrodiol C30H50O2 ÏàËÆ¶È:90.3% Acta Botanica Yunnanica 1995 17 108-110 CHEMICAL CONSTITUENTS FROM PTEROCEPHALUS BRETSCHNEIDRI TIANJun, WUFeng-E, QIU Ming-Hua, NIE Rui-Lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 3¦Â,28-dihydroxyurs-12-ene C34H54O4 ÏàËÆ¶È:90.3% Natural Product Research 2005 19 197-202 Antimicrobial triterpenes from Poulsenia armata miq. standl. Hesham Rushdey El-Seedi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 3¦Â,28-dihydroxy-ursane C30H50O2 ÏàËÆ¶È:90.3% China Journal of Chinese Materia Medica 2005 30 1926-1932 Studies on triterpenoid constituents from Rabdosia japonica var. galaucocalyx Wang Fudong, DING Lan, WANG Hanqing Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . vuaol ÏàËÆ¶È:90.3% China Journal of Chinese Materia Medica 2000 25 225-226 Studies on Chemical Components of Gentiana tizuensis Franch. (I) XU Xiuzhi, TIAN Xuan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . obtusol C30H50O2 ÏàËÆ¶È:90.3% Phytochemistry 1999 52 1111-1115 Two triterpenoids from the leaves of Plumeria obtusa Bina S. Siddiqui, Firdous, Sabira Begum Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . obtusalin ÏàËÆ¶È:90.3% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . obtusalin C29H48O ÏàËÆ¶È:90.3% Phytochemistry 1989 28 3143-3147 Pentacyclic triterpenoids from the leaves of Plumeria obtusa Salimuzzaman Siddiqui,Bina Shaheen Siddiqui,Akhtar Naeed,Sabira Begum Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . obtusalin ÏàËÆ¶È:90.3% China Journal of Chinese Materia Medica 2010 35 315-322 Terpenoids of Heteroplexis micocephala and their bioactivities FAN Xiaona; LIN Sheng; ZHU Chenggen; HU Jinfeng; LIU Yang; CHEN Xiaoguang; CHEN Naihong; WANG Wenjie; SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . uvaol ÏàËÆ¶È:90.3% Chinese Traditional and Herbal Drugs 2009 40 24-27 ²ÚÁúµ¨µØÉϲ¿·Ö»¯Ñ§³É·ÖÑо¿ Õž´Ó¨;ÍõÊÀÊ¢;ËÎÆäÁá;¸ßÖ¾¸Õ;ÕÔΰ½Ü Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . Ðܹû´¼ ÏàËÆ¶È:90.3% Chinese Traditional and Herbal Drugs 2009 40 1554-1555 ÞµÀó»¯Ñ§³É·ÖÑо¿ ÕÅ·å;ÕÅ¿¡Çå;¿×ÁîÒå Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . uvaol C30H50O2 ÏàËÆ¶È:90.3% Chinese Traditional and Herbal Drugs 2008 39 182-184 Ò»Ö¦»Æ»¨»¯Ñ§³É·ÖµÄÑо¿ ѦÏþϼ;ÖÙºÆ;Ò¦ÇìÇ¿ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 3¦Â,28-¶þôÇ»ù-12-ϩһÎÚËÕÍé ÏàËÆ¶È:90.3% Chinese Traditional and Herbal Drugs 2006 37 824-826 ͨ³ÇÒÆÖ²Ã«ºíÇÊÈﻨµÄ»¯Ñ§³É·ÖÑо¿ ÀîË®Çå;ÑîÇÉÈÝ;ÍõÏþÃ÷;×Þ¹ú°²;ÁõìÍÎÄ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . uvaol ÏàËÆ¶È:90.3% Chinese Traditional and Herbal Drugs 2002 33 888-889 ËÄ´¨Áúµ¨µÄÈýÝÆ³É·Ö Nam joon-young,ÁõÏòǰ,ÕųÐìÇ,³Êç¼§,Àî¼Ãîç,½²ýä¨ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 3¦Â,28-dihydroxyursane ÏàËÆ¶È:90.3% Chinese Pharmaceutical Journal 2011 46 504-506 Study on Triterpenoid Constituents in the Leaves of Paulownia fortunei ZHANG De-li, LI Xiao-qiang, LI Chong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . uvaol ÏàËÆ¶È:90.3% Modern Chinese Medicine 2006 8(6) 18-20 Studies on the Chemical Constituents of Ledum palustre L. Qiu Guihua, Zuo Wenjian, Wang Jinhui, L i Xian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 12-ursine-3,28-diol ÏàËÆ¶È:90.3% Natural Product Research and Development 2008 20 821-823 Studies on the Chemical Constituents of Ilex cornuta ZHANG Jie; YU Rong; WU Xia; YE Yun-hua; ZHOU Ya-wei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . betulin ÏàËÆ¶È:90.3% 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 -------------------------------------------------------------------------------- 19 . 27-hydroxy-¦Á-amyranol ÏàËÆ¶È:90.3% Natural Product Research and Development 2006 18 772-774 Studies on Chemical Constituents of Periploca omeiensis ZHANG Yuan-hu; CHEN Dong-lin; WANG Feng-peng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . uvaol ÏàËÆ¶È:90.3% Food Chemistry 2006 98 285-290 Annurcoic acid: A new antioxidant ursane triterpene from fruits of cv. Annurca apple Brigida D¡¯Abrosca, Antonio Fiorentino, Pietro Monaco, Palma Oriano, Severina Pacifico Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-12-03 15:17:28














»Ø¸´´ËÂ¥