| ²é¿´: 346 | »Ø¸´: 1 | ||
Ó¸ÒÇÚ·Ü½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬·Ç³£¸Ðл£¡ ÒÑÓÐ1È˲ÎÓë
|
|
ÈܼÁ£ºDMSO(ÈܼÁ·åÒѾȥµô) ̼Æ×£º42.25,60.24,78.74,95.23,102.05,115.37,128.56,129.11,129.19,155.33,157.94,158.28,159.74,197.36 |
» ²ÂÄãϲ»¶
»úе¹¤³Ì264ѧ˶Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
264Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
22408 266Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ43È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬¼±Çó£¬ds-3
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¡¸Ð¼¤£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ6È˻ظ´
·Ç³£¸Ðл£¡Î¢Æ×ÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú¡¢¡¢¡¢Ð»Ð»´óÉñ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾ÝÒ»¸ö
ÒѾÓÐ3È˻ظ´
ÒѾÅÅÐòºÃµÄ̼»¯Ñ§Î»ÒÆÖµ£¬°ïæ΢Æ×²é»¯ºÏÎ¶àлÁË
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö΢Æ×Êý¾Ý
ÒѾÓÐ5È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
΢¹Û½á¹¹ ¶Ô ÆäÁ¦Ñ§ÐÔÄܵÄÓ°Ïì µÄÎÊÌ⣬·Ç³£¸Ðл¡£¼±£¡
ÒѾÓÐ5È˻ظ´

1225823858zj
½ð³æ (ÕýʽдÊÖ)
Ïë·ÉµÄ·çóÝ
- Ó¦Öú: 29 (СѧÉú)
- ½ð±Ò: 1182.5
- É¢½ð: 8
- ºì»¨: 12
- Ìû×Ó: 506
- ÔÚÏß: 244.1Сʱ
- ³æºÅ: 1421137
- ×¢²á: 2011-09-28
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ó¸ÒÇÚ·Ü: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-26 16:40:16
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ó¸ÒÇÚ·Ü: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-26 16:40:16
|
²éѯ½á¹û£º¹²²éµ½96¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (¡À) 5,7,4'-trihydroxy-8-methoxyflavanone C8H6O5 ÏàËÆ¶È:100% Shoyakugaku Zasshi 1986 40 432-433 Studies on the Constituents of Scutellaria Species (VIII) : On the Flavonoid Constituents of "Ban Zhi Lian," the Whole Herb of Scutellaria rivularis WALL (2) TOMIMORI TSUYOSHI, MIYAICHI YUKINORI, IMOTO YOSHITAKA, KIZU HARUHISA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 5,7,4'-Trihydroxy-8-methoxyflavanone C16H14O6 ÏàËÆ¶È:87.5% Chemistry of Natural Compounds 2002 38 473-519 PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES V. M. Malikov and M. P. Yuldashev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 5,7,4'-Trihydroxy-6-methoxyflavanone C16H14O6 ÏàËÆ¶È:87.5% Chemistry of Natural Compounds 2002 38 473-519 PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES V. M. Malikov and M. P. Yuldashev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 2(S)-5,7-¶þôÇ»ù-6-¼×Ñõ»ù¶þÇâ»ÆÍª ÏàËÆ¶È:85.7% China Journal of Chinese Materia Medica 2011 36 3270-3275 Study on chemical constituents of Scutelliaria regeliana WANG, Jinlan, ZHAO, Baoying, XU, Hongmei, ZHAO, Ming, TANG, Wanxia, ZHANG, Shujun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 2(S)-5,7,4'-ÈýôÇ»ù-6-¼×Ñõ»ù¶þÇâ»ÆÍª ÏàËÆ¶È:85.7% China Journal of Chinese Materia Medica 2011 36 3270-3275 Study on chemical constituents of Scutelliaria regeliana WANG, Jinlan, ZHAO, Baoying, XU, Hongmei, ZHAO, Ming, TANG, Wanxia, ZHANG, Shujun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 5,7-dihydroxy-6-methoxy-2-(4'-hydroxyphenyl)-2,3-dihydroxy-4H-1-benzopyran-4-one ÏàËÆ¶È:81.2% Journal of the Indian Chemical Society 2002 79 169-175 Stibenoids and flavonoids from the orchids Coelogyne uniflora,Ione paleacea and Acrochoene punctata P.L.Majumder,S.Chakraborty and S.Sen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 5,4'-dihydroxy-6,7-dimethoxyflavanone C17H16O6 ÏàËÆ¶È:80% Journal of Natural Products 1992 Vol 55 357 Isolation of Potential Cancer Chemopreventive Agents from Eriodictyon californicum Yong-Long Liu, David K. Ho, John M. Cassady, Vanessa M. Cook, William M. Baird Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . dihydrooroxylin A ÏàËÆ¶È:75% Journal of Shenyang Pharmaceutical University 2003 20 181-183 Isolation and identif ication of the chemical constituents of roots of Scutellaria amoena C. H. Wright XIAO Li-he, WANG Hong-yan, SONG Shao-jiang, ZHANG Guang-ping, SONG Hai-xiu, XU Sui-xu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . dihydroroxylin A ÏàËÆ¶È:75% Chinese Joumal of Experimental Traditional Medical Fomulae 2011 17 78-81 Triterpenoids from Gardenia jasminoides FU Xiao-mei , WANG Zheng-tao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 5,6,7,4'-tetrahydroxyflavanone C15H12O6 ÏàËÆ¶È:71.4% Applied Biochemistry and Biotechnology 2014 173 67−73 Improved Oxidation of Naringenin to Carthamidin and Isocarthamidin by Rhodotorula marina Anna Madej, Jarosław Popło¨½ski, Ewa Huszcza Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-06-26 11:21:30














»Ø¸´´ËÂ¥
10