| ²é¿´: 712 | »Ø¸´: 4 | ||
| µ±Ç°Ö»ÏÔʾÂú×ãÖ¸¶¨Ìõ¼þµÄ»ØÌû£¬µã»÷ÕâÀï²é¿´±¾»°ÌâµÄËùÓлØÌû | ||
LingerTigerгæ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú лл ÒÑÓÐ1È˲ÎÓë
|
|
|
13C NMR (151 MHz, CD3OD) 45.68, 47.25, 50.00, 52.23, 61.16, 62.80, 71.64, 74.90, 77.98, 78.54, 82.38, 98.38, 100.40, 110.93, 130.20, 147.67, 154.01, 170.43 [ Last edited by ׿Խ_ÏÈ·æ on 2015-6-2 at 13:16 ] |
» ²ÂÄãϲ»¶
±¾¿Æ211£¬293·ÖÇëÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
085400µç×ÓÐÅÏ¢319Çóµ÷¼Á£¨½ÓÊÜ¿çרҵµ÷¼Á£©
ÒѾÓÐ5È˻ظ´
268Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
һ־Ը˫·Ç085502£¬267·Ö£¬¹ýËļ¶Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸085404£¬×Ü·Ö291£¬Ëļ¶Òѹý£¬Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
297Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
26µ÷¼Á 086003
ÒѾÓÐ3È˻ظ´
265Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
271·ÖÇóµ÷¼ÁѧУ
ÒѾÓÐ11È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð»~~
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
Çó΢Æ×°ïæ,лл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý4¸ö
ÒѾÓÐ6È˻ظ´
΢Æ×ÇóÖú3¸ö»¯ºÏÎï
ÒѾÓÐ4È˻ظ´
ÇóÖú [color=Red]΢Æ×[/color] Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×Êý¾ÝÇóÖúлл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´

seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48394.9
- ºì»¨: 52
- Ìû×Ó: 6742
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡

4Â¥2015-06-01 18:30:22
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48394.9
- ºì»¨: 52
- Ìû×Ó: 6742
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
1 . scandoside methyl ester ÏàËÆ¶È:94.4% Chemical & Pharmaceutical Bulletin 1991 39 2049-2052 Isolation of 10-O-Acyl Iridoid Glucosides from a Philippine Medicinal Plant, Oldenlandia corymbosa L. (Rubiaceae) Hideaki OTSUKA,Kayoko YOSHIMURA,Kazuo YAMASAKI and Magdalena C. CANTORIA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (6¦Â)-6-hydroxygeniposide ÏàËÆ¶È:94.4% Helvetica Chimica Acta 2010 93 1751-1757 New Chemical Constituents from Borreria verticillata (Rubiaceae) Vinicius F. Moreira, Rodrigo R. Oliveira, Leda Mathias, Raimundo Braz-Filho and Ivo J. Curcino Vieira Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 6¦Â-hydroxygeniposide C17H24O11 ÏàËÆ¶È:94.4% Chinese Traditional and Herbal Drugs 1995 26 443-444 ·ãÏãÊ÷ƤÖеĻ·Ï©ÃÑÝÆ³É·Ö ½ªÖ¾ºê,ÖÜÈÙºº,ºÓÒ°¹¦ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . scandoside methyl ester C17H24O11 ÏàËÆ¶È:94.4% Turkish Journal of Chemistry 2006 30 515-523 Chemical Constituents of Galium tortumense Z¨¹HAL G¨¹VENALP, NURCAN KILIÇ, CAVİT KAZAZ, YUSUF KAYA, L. ÖM¨¹R DEMİREZER Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 6¦Â-hydrogeniposide ÏàËÆ¶È:94.4% Chinese Pharmaceutical Journal 2014 49 275-278 Chemical Constitutents in the Fruits of Gardenia jasminoides var. radicans Makino QIN Fang-min, MENG Ling-jie, YUAN Hong-e, ZHANG Ying, ZHOU Guang-xiong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . scandoside methyl ester ÏàËÆ¶È:94.4% Journal of Chinese Medicinal Materials 2008 31 522-524 Studies on the Chemical Constituents in Herb of Hedyotis diffusa ZHANG Yong-yong, LUO Jia-bo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . scandoside methyl ester ÏàËÆ¶È:94.4% Lishizhen Medicine and Materia Medica Research 2013 24 1599-1603 »ÆÁ¬½â¶¾ÌÀ»¯Ñ§³É·Ö¼°ÆäÉñ¾Ï¸°û±£»¤×÷ÓÃÑо¿ ÑîÑô, ÕÔº£Óþ, Ëν¨·¼, Íõºê½à, Ñ, ˾ÄÏ, ÁõÇìɽ, ±ß±¦ÁÖ* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 6¦Â-hydroxygeniposide ÏàËÆ¶È:83.3% Planta Medica 1987 53 462-464 The Structural Transformation of Gardenoside and Its Related Iridoid Compounds by Acid and -Glucosidase Masanori Miyagoshi, Sakae Amagaya, and Yukio Ogihara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-06-01 15:40:31
LingerTiger
гæ (³õÈëÎÄ̳)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 338
- ºì»¨: 1
- Ìû×Ó: 21
- ÔÚÏß: 16.2Сʱ
- ³æºÅ: 3628624
- ×¢²á: 2015-01-05
- ÐÔ±ð: GG
- רҵ: ÖÐҩҩЧÎïÖÊ

3Â¥2015-06-01 17:09:26
LingerTiger
гæ (³õÈëÎÄ̳)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 338
- ºì»¨: 1
- Ìû×Ó: 21
- ÔÚÏß: 16.2Сʱ
- ³æºÅ: 3628624
- ×¢²á: 2015-01-05
- ÐÔ±ð: GG
- רҵ: ÖÐҩҩЧÎïÖÊ

5Â¥2015-06-15 14:49:21














»Ø¸´´ËÂ¥
