| ²é¿´: 375 | »Ø¸´: 1 | |||
³¾·â4004½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| 30.2,31.9,40.4,46.3,49.8,51.2,56.6,68.2,113.0,116.1,121.6,130.2,134.0,145.4,148.8,156.4,211.9 |
» ²ÂÄãϲ»¶
08¹¤¿ÆÇóµ÷¼Á290·Ö
ÒѾÓÐ12È˻ظ´
286Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
²ÄÁÏÀà284µ÷¼Á
ÒѾÓÐ24È˻ظ´
¿¼Ñе÷¼Á-²ÄÁÏÀà-284
ÒѾÓÐ14È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
Ò»Ö¾Ô¸985³õÊÔ354·ÖÉúÎïµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸2110£¬»¯Ñ§Ñ§Ë¶310·Ö£¬±¾¿ÆÖصãË«·ÇÇóµ÷¼Á
ÒѾÓÐ13È˻ظ´
353Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
308Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
334Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
׿Խ_ÏÈ·æ
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
ºýÍ¿³æ
- Ó¦Öú: 990 (²©ºó)
- ¹ó±ö: 2.955
- ½ð±Ò: 6796.4
- É¢½ð: 12161
- ºì»¨: 82
- ɳ·¢: 17
- Ìû×Ó: 3017
- ÔÚÏß: 2457Сʱ
- ³æºÅ: 1713223
- ×¢²á: 2012-03-24
- ÐÔ±ð: GG
- רҵ: ÁÙ´²Ò©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
³¾·â4004: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ¶àлÁË£¬ÐÁ¿à 2015-04-18 17:24:44
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
³¾·â4004: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ¶àлÁË£¬ÐÁ¿à 2015-04-18 17:24:44
|
²éѯ½á¹û£º¹²²éµ½233¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 5-hydroxy-7-(4-hydroxy-3-methoxyphenyl)-1-(4-hydroxy-phenyl)-3-heptanone C20H24O5 ÏàËÆ¶È:88.8% Journal of Yunnan College of Traditional Chinese Medicine 2013 36 28-30 Studies on Chemical Constituents of the Rhizomes of Hedychium forrestii Dies GAO Jie-jie, HAO Xiao-jiang, HE Hong-ping, ZHAO Qing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 6-gingerol ÏàËÆ¶È:82.3% Chemical & Pharmaceutical Bulletin 1994 42 1226-1230 Stomachic Principles in Ginger. III. An Anti-ulcer Principle, 6-Gingesulfonic Acid, and Three Monoacyldigalactosylglycerols, Gingerglycolipids A, B, and C, from Zingiberis Rhizoma Originating in Taiwan Masayuki YOSHIKAWA,Shoko YAMAGUCHI,Kumiko KUNIMI,Hisashi MATSUDA,Yasuhiro OKUNO,Johji YAMAHARA and Nobutoshi MURAKAMI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 6-gingerol ÏàËÆ¶È:82.3% Chemical & Pharmaceutical Bulletin 1992 40 2239-2241 6-GINGESULFONIC ACID, A NEW ANTI-ULCER PRINCIPLE, AND GINGERGLYCOLIPIDS A, B AND C, THREE NEW MONOACYLDIGALACTOSYLGLYCEROLS, FROM ZINGIBERIS RHIZOMA ORIGINATING IN TAIWAN Masayuki YOSHIKAWA,Shoko HATAKEYAMA,Kumiko TANIGUCHI,Hisashi MATUDA and Johji YAMAHARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 5-hydroxy-7-(4-hydroxy-3-methoxyphenyl)-1-(4-hydroxyphenyl)heptan-3-one C20H24O5 ÏàËÆ¶È:82.3% Natural Product Research 2007 21 444-450 Microbial metabolism. Part 7 : Curcumin Wimal Herath; Daneel Ferreira; Ikhlas A. Khan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 6-Gingerol ÏàËÆ¶È:82.3% Archives of Pharmacal Research 2008 31 415-418 Cytotoxic components from the dried rhizomes of Zingiber officinaleRoscoe Ju Sin Kim, Sa Im Lee, Hye Won Park, Jae Heon Yang and Tae-Yong Shin, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 3 C20H20O4 ÏàËÆ¶È:82.3% Bulletin of the Korean Chemical Society 2004 25 397-399 Diarylheptanoids from the Roots of Juglans mandshurica Gao Li, Chang-Seob Seo, Seung-Ho Lee, Yurngdong Jahng, Hyeun-Wook Chang, Chong-Soon Lee, Mi-Hee Woo, Jong-Keun Son* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . (5S)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-7-(4-hydroxyphenyl)-3-heptanone C20H24O5 ÏàËÆ¶È:80% Bioorganic & Medicinal Chemistry Letters 2011 21 5363-5369 Diarylheptanoids from Curcuma kwangsiensis and their inhibitory activity on nitric oxide production in lipopolysaccharide-activated macrophages Jun Li, Chun-Ru Liao, Jun-Qi Wei, Li-Xia Chen, Feng Zhao, Feng Qiu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound M12 ÏàËÆ¶È:80% Planta medica 2012 78 1351-1356 Isolation and Identification of Phase 1 Metabolites of Curcuminoids in Rats Li, Jun; Liu, Yue; Wei, Jun-Qi; Wang, Kun; Chen, Li-Xia; Yao, Xin-Sheng; Qiu, Feng: Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound M13 ÏàËÆ¶È:80% Planta medica 2012 78 1351-1356 Isolation and Identification of Phase 1 Metabolites of Curcuminoids in Rats Li, Jun; Liu, Yue; Wei, Jun-Qi; Wang, Kun; Chen, Li-Xia; Yao, Xin-Sheng; Qiu, Feng: Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 6-Gingerol ÏàËÆ¶È:76.4% Journal of Chinese Pharmaceutical Sciences 2007 16 24-26 Studies on the chemical constituents of the active fraction of Gui-Zhi decoction Shuo Zhou; Hong Liang; Shao-Qing Cai; and Yu-Ying Zhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 4-Gingerol ÏàËÆ¶È:76.4% Archives of Pharmacal Research 2008 31 415-418 Cytotoxic components from the dried rhizomes of Zingiber officinaleRoscoe Ju Sin Kim, Sa Im Lee, Hye Won Park, Jae Heon Yang and Tae-Yong Shin, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (5R)-5-hydroxy-1-(4-hydroxyphenyl)-7-(4-hydroxy-3-methoxyphenyl)-3-heptanone ÏàËÆ¶È:75% Food Chemistry 2010 119 513-517 New diarylheptanoids from the rhizome of Alpinia officinarum Hance Ning An, Hong-wu Zhang, Li-zhen Xu, Shi-lin Yang, Zhong-mei Zou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . diarylheptanoid 5-hydroxy-7-(4-hydroxy-3-methoxyphenyl)-1-phenyl-3-heptanone ÏàËÆ¶È:75% Journal of the Korean Society for Applied Biological Chemistry 2009 52 367-370 Anti-Helicobacter pylori Diarylheptanoid Identified in the Rhizome of Alpinia officinarum Haeng-Byung Lee, Hyun-Kyung Lee, Jun-Ran Kim, and Young-Joon Ahn* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 8-Gingerol ÏàËÆ¶È:73.6% Archives of Pharmacal Research 2008 31 415-418 Cytotoxic components from the dried rhizomes of Zingiber officinaleRoscoe Ju Sin Kim, Sa Im Lee, Hye Won Park, Jae Heon Yang and Tae-Yong Shin, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . (5R)-5-hydroxy-1-(4-hydroxy-phenyl)-7-(4-hydroxy-3-methoxyphenyl)-3-heptanone ÏàËÆ¶È:73.6% Natural Product Communications 2010 5 1687 - 1708 Naturally Occurring Diarylheptanoids Haining Lv and Gaimei She Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (5R)-5-hydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxy-3-methoxyphenyl)-3-heptanone C20H24O6 ÏàËÆ¶È:73.6% Journal of Yunnan College of Traditional Chinese Medicine 2013 36 28-30 Studies on Chemical Constituents of the Rhizomes of Hedychium forrestii Dies GAO Jie-jie, HAO Xiao-jiang, HE Hong-ping, ZHAO Qing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . K005[5-hydroxy-7-(4''-hydroxy-3''-methoxyphenyl)-1-phenyl-3-heptanone] ÏàËÆ¶È:72.2% Korean Journal of Pharmacognosy 2000 31(1) 57-62 Isolation of COX-2 Inhibitors from Alpinia officinarum Kim, Ju-Sun; Son, Kun-Ho; Kim, Hyun-Pyo; Chang, Hyeun-Wook; Kang, Sam-Sik Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 4-methoxy-2-oxatricyclo[13.2.2.13,7]eicosa-1(18),3,5,7(20),15(19),16-hexaen-12-one ÏàËÆ¶È:72.2% European Journal of Organic Chemistry 2007 2007 1338-1344 A Versatile Synthesis of Cyclic Diphenyl Ether-Type Diarylheptanoids: Acerogenins, (¡À)-Galeon, and (¡À)-Pterocarine Byeong-Seon Jeong, Qian Wang, Jong-Keun Son and Yurngdong Jahng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . [12]-gingerol C23H38O4 ÏàËÆ¶È:72.2% Food Chemistry 2014 165 191-197 Influence of side chain structure changes on antioxidant potency of the [6]-gingerol related compounds Dong-Liang Lu, Xiu-Zhuang Li, Fang Dai , Yan-Fei Kang, Yan Li, Meng-Meng Ma, Xiao-Rong Ren,Gao-Wei Du, Xiao-Ling Jin, Bo Zhou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . octahydrocurcumin ÏàËÆ¶È:70.5% Chemical & Pharmaceutical Bulletin 1987 35 3298-3304 Diarylheptanoids from the Rhizomes of Curcuma xanthorrhiza and Alpinia officinarum SHIN-ICHI UEHARA,ICHIRO YASUDA,KAZUYUKI AKIYAMA,HIROSHI MORITA,KOICHI TAKEYA and HIDEJI ITOKAWA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-04-18 17:06:43













»Ø¸´´ËÂ¥