| ²é¿´: 244 | »Ø¸´: 1 | |||
zhaocaiguiÒø³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹
|
|
13C NMR (101 MHz, CDCl3) ¦Ä 200.43,168.61,126.25,73.20,56.06,55.89,53.63,45.83,42.50,39.60,38.58,37.99,37.08,36.10,34.24,33.90,29.72,29.17,28.16,26.11,24.14,23.08,20.97,19.80,19.47,19.03,18.72,12.00,11.96 |
» ²ÂÄãϲ»¶
µ÷¼Á
ÒѾÓÐ20È˻ظ´
0703»¯Ñ§
ÒѾÓÐ32È˻ظ´
286Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
278Çóµ÷¼Á
ÒѾÓÐ24È˻ظ´
²ÄÁÏÀà284µ÷¼Á
ÒѾÓÐ19È˻ظ´
Ò»Ö¾Ô¸0703»¯Ñ§ÕÐ61×îÖÕÅÅÃû62»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
299Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
»úеר˶273ÇëÇóµ÷¼Á
ÒѾÓÐ6È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Ò»Ö¬ÈÜÐÔ»¯ºÏÎïµÄ½á¹¹
ÒѾÓÐ9È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎ£¡
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎ£¡
ÒѾÓÐ5È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×½á¹¹
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎ£¡
ÒѾÓÐ7È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â¼ìË÷Ò»»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â¼ìË÷Ò»»¯ºÏÎï
ÒѾÓÐ4È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×Êý¾Ý½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú3¸öÓÃ΢Æ×½âÎöµÄ½á¹¹
ÒѾÓÐ8È˻ظ´
ÇóÖú¡¡Î¢Æ×Êý¾Ý¿â £Ã£Î£Í£ÒÊý¾Ý²éδ֪»¯ºÏÎï½á¹¹
ÒѾÓÐ6È˻ظ´
wq0616
Ìú¸Ëľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 323 (´óѧÉú)
- ½ð±Ò: 6659.6
- ºì»¨: 8
- Ìû×Ó: 955
- ÔÚÏß: 72.9Сʱ
- ³æºÅ: 2001721
- ×¢²á: 2012-09-14
- ÐÔ±ð: MM
- רҵ: ÖÐÒ©ÅÚÖÆ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhaocaigui: ½ð±Ò+10, ¡ïÓаïÖú 2013-03-28 00:28:24
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhaocaigui: ½ð±Ò+10, ¡ïÓаïÖú 2013-03-28 00:28:24
|
1 . 6-hydroxystigmast-4-en-3-one C29H48O2 ÏàËÆ¶È:96.5% Steroids 2006 71 647-652 Ketosteroids and hydroxyketosteroids, minor metabolites of sugarcane wax Patricia Georges, Muriel Sylvestre, Heinz Ruegger, Paul Bourgeois Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . stigmast-4-en-6¦Â-ol-3-one C29H48O2 ÏàËÆ¶È:96.5% Journal of Asian Natural Products Research 2001 3 299-311 CONSTITUENTS FROM LIMONIA CRENULATA XUE-ME1 NIU, SHENG-HONG LI, LI-YAN PENG,and HAN-DONG SUN,ZHONG-WEN LIN, GAO-XIONG RAO Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . stigmast-4-en-6¦Â-ol-3-one ÏàËÆ¶È:96.5% China Journal of Chinese Materia Medica 2008 33 1566-1568 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 ̼Æ×Ä£Äâͼ 4 . (24R)-6¦Â-hydroxy-24-ethylcholest-4-en-3-one C29H48O2 ÏàËÆ¶È:96.5% Phytochemistry 1998 48 471-474 Chemical constituents of aquatic fern Azolla nilotica Yôko Arai, Tomomi Nakagawa, Mari Hitosugi, Kenji Shiojima, Hiroyuki Ageta, Osama Basher, Abdel-Halim Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . stigmastan-4-en-6¦Â-ol-3-one C29H4802 ÏàËÆ¶È:96.5% Journal of Natural Products 1990 Vol 53 1430 Stigmasterols from Typha latifolia Marina Della Greca, Pietro Monaco, Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 6¦Â-Hydroxy-4-stigmasten-3-one ÏàËÆ¶È:96.5% Natural Product Sciences 2007 13 332-336 Norsesquiterpene and Steroid Constituents of Humulus japonicus Yu, Byung-Chul; Yang, Min-Cheol; Lee, Kyu-Ha; Kim, Ki-Hyun; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (24R)-6¦Â-hydroxy-24-ethylcholest-4-en-3-one ÏàËÆ¶È:96.5% Korean Journal of Pharmacognosy 2007 38(4) 376-381 Isolation of Melanin Biosynthesis Inhibitory Compounds from the Seeds of Plantago asiatica L. Oh, Joon-Seok; Lee, Jong-Gu; Jung, Hee-Wook; Choi, Ji-Young; Choi, Eun-Hyang; Kim, Dong-Chun; Kim, Jeong-Ah; Son, Jong-Keun; Lee, Seung-Ho Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 6¦Â-hydroxy-stigmasta-4-en-3-one ÏàËÆ¶È:96.5% 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 ̼Æ×Ä£Äâͼ 9 . Stigmast-4-en-6¦Â-ol-3-one C29H48O2 ÏàËÆ¶È:96.5% Natural Product Research 2011 Vol. 25, No. 13 1243-1249 Chemical constituents from the roots of Xanthium sibiricum Suqin Kan, Guangying Chen, Changri Han, Zhong Chen, Xinming Song, Ming Ren and Hong Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 6¦Â-hydroxy-stigmast-4-en-3-one ÏàËÆ¶È:96.5% Chinese Traditional and Herbal Drugs 2007 38 14-17 Chemical constituents of whole herb of Dicliptera chinensis GAO Yu-tao; YANG Xiu-wei; AI Tie-min Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . stigmast-4-en-6¦Â-ol-3-one ÏàËÆ¶È:96.5% Chinese Traditional and Herbal Drugs 2007 38 348-350 Æ¿»¨Ä¾»¯Ñ§³É·ÖµÄÑо¿ ÌÕÊïºì;Å˽£Óî;ÆáÊ绪;ÀîÇìÐÀ;ÕÅ‚Æ Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . stigmast-4-en-6¦Â-ol-3-one C29H48O2 ÏàËÆ¶È:96.5% Chinese Traditional and Herbal Drugs 2005 36 510-511+545 Å£¶ú¶ä»¯Ñ§³É·ÖµÄÑо¿ ²ÌÏ麣,µËµÂɽ,ÂíÔÆ±£,ÂÞÏþ¶« Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . stigmast-4-en-6¦Â-ol-3-one C29H48O2 ÏàËÆ¶È:96.5% Chinese Traditional and Herbal Drugs 2001 32 778-780 Studies on chemical constituents of Cipadessa baccifera LUO Xiao dong; WU Shao hua; MA Yun bao; WU Da gang Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . stigmast-4-en-6¦Â-ol-3-one ÏàËÆ¶È:96.5% Chinese Journal of Natural Medicines 2009 7 425-427 Chemical Constituents from Houttuynia cordata QU Wei; LIANG Jing-Yu; LI Meng-Ran Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Stignast-4-en-6¦Â-3-one ÏàËÆ¶È:96.5% Chinese Journal of Natural Medicines 2010 8 16-20 Chemical Constituents from Helwingia japonica XIA Li-Zi; ZHOU Min; XIAO Yan-Hua; LI Guo-You; CHEN Xiao-Zhen; ZHANG Guo-Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 6¦Â-Hydroxyenone (Stigmast-4-en-6¦Â-ol-3-one) ÏàËÆ¶È:96.5% Pharmazie 2004 59 885-888 Terpenoids and steroids from Lappula anocarpa Yuan-Peng Jin, and Yan-Ping Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (24R)-6¦Â-hydroxy-24-ethyl-cholest-4-en-3-one ÏàËÆ¶È:96.5% Chinese Pharmaceutical Journal 2005 40 255-258 Study on phenolic constituents of Pholidota yunnanensis BI Zhi ming, WANG Zheng tao *, XU Luo shan, XU Guo jun Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . stigmast-4-en-6¦Â-ol-3-one ÏàËÆ¶È:96.5% Chinese Pharmaceutical Journal 2010 45 1615-1617 Chemical Constituents of Tetrastigma planicaule(Hook.) Gagnep. SHAO Jia-chun, HE Cui-hong, LEI Ting, HONGi-hua, CEN Ying-zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 6¦Â-hydroxystigmast-4-en-3-one ÏàËÆ¶È:96.5% Modern Chinese Medicine 2010 12(1) 23-24 Study on the Chemical Constituents of from the Roots of Tripterygium wilfordii Yan Zhen, Tian Yang, Ma Yueping, Fu Xiaochun, Zhang Zhenxue, Wang Jinhui Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 6¦Â-hydroxystigmast-4-en-3-one ÏàËÆ¶È:96.5% Chinese Journal of Medicinal Chemistry 2003 13 211-214 Studies on the chemical constituents of Fructus Ailanthi altissimae ZHAO Chun-chao, WANG Jin-hui, LI Wen, SHA Yi, LI Xian Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . stigmast-4-en-6¦Â-ol-3-one ÏàËÆ¶È:96.5% Journal of Shenyang Pharmaceutical University 2009 26 874-877 Isolation and identification of steroids from the leaves of theMagnolia sieboldii K. Koch WANG Ru-ping, WU Di, GAO Hui-yuan, SUN Bo-hang, HUANG Jian, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . stigmast-4-en-6¦Â-ol-3-one ÏàËÆ¶È:96.5% Journal of Shenyang Pharmaceutical University 2009 26 23-26 Chemical constituents from the involucre of Castanea mollissima Blume JIAO Qi-yang, WU Li-jun, HUANG Jian, SUN Bo-hang, GAO Hui-yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . stigmast-4-en-6¦Â-ol-3-one ÏàËÆ¶È:96.5% Journal of Shenyang Pharmaceutical University 2009 26 357-360 Isolation and identification of chemical constituents from testa of Castanea mollissima Blume LU Chuan, WU Zhao-hua, GAO Hui-yuan, SUN Bo-hang, HUANG Jian, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . (24R)-6¦Â-ôÇ»ù-24-ÒÒ»ù-µ¨çÞ-4-Ï©-3-ͪ ÏàËÆ¶È:96.5% Journal of Shenyang Pharmaceutical University 2007 24 611-614 Chemical constituents of Duchesnea indica Focke XU Wen-dong, LIN Hou-wen, QIU Feng, CHEN Wan-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-03-27 18:35:00














»Ø¸´´ËÂ¥