| ²é¿´: 406 | »Ø¸´: 1 | |||
kaopumaľ³æ (ÖøÃûдÊÖ)
|
[ÇóÖú]
΢Æ×ÇóÖú £¬Ð»Ð» ÒÑÓÐ1È˲ÎÓë
|
| 22.1,22.5,23.1,31.8,36.8,38.2,44.8,46.1,62.6,71.0,71.5,75.7,77.6,78.2,78.4,85.4,105.7,115.5,129.9,140.0,146.5 |
» ²ÂÄãϲ»¶
283Çóµ÷¼Á 086004¿¼Ó¢¶þÊý¶þ
ÒѾÓÐ17È˻ظ´
352 Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
µ÷¼ÁÇóÖú
ÒѾÓÐ7È˻ظ´
305Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
270Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
366Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
271Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
290µ÷¼ÁÉúÎï0860
ÒѾÓÐ8È˻ظ´
Çóµ÷¼Á£¬Ò»Ö¾Ô¸´óÁ¬Àí¹¤´óѧ354·Ö
ÒѾÓÐ6È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×Êý¾ÝÇóÖúлл
ÒѾÓÐ3È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
Çó´óϺ²é΢Æ×£¬Íò·Ö¸Ðл°¡£¡£¡£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48433.9
- ºì»¨: 52
- Ìû×Ó: 6749
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
kaopuma: ½ð±Ò+8, ¡ïÓаïÖú 2015-03-27 11:48:32
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
kaopuma: ½ð±Ò+8, ¡ïÓаïÖú 2015-03-27 11:48:32
|
1 . dendronobiloside E C21H34O8 ÏàËÆ¶È:66.6% Planta Medica 2002 68 723-729 New Alloaromadendrane,Cadinene and Cyclocopacamphane Type Sesquiterpene Derivatives and Bibenzyls from Dendrobium nobile Qinghua Ye,Weimin Zhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . penstemid ÏàËÆ¶È:66.6% Planta Medica 1983 49 161-163 8-epi-Valerosidate, a New Iridoid Glucoside from Penstemon serrulatus Peter Junior Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 1 ¦Á-Hydroxy-6¦Â-O-¦Â-D-glucosyl-eudesm-3-ene C21H36O7 ÏàËÆ¶È:66.6% Archives of Pharmacal Research 2003 26 132-137 Cerebrosides and terpene glycosides from the root of aster scaber Kwon Hak Cheol, Cho Ock Ryun, Lee Kang Choon and Lee Kang Ro Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 1¦Â,6¦Â-dihydroxy-cis-eudesm-3-ene-6-O-¦Â-D-glucopyranoside C21H36O7 ÏàËÆ¶È:66.6% Molecules 2011 16 9017-9024 A New Eudesmane Sesquiterpene Glucoside from Liriope muscari Fibrous Roots Hai Ming Zhang, Gang Li Wang, Chun Qi Bai, Peng Liu, Zi Mu Liu, Qi Zhi Liu, Yong Yan Wang, Zhi Long Liu, Shu Shan Du and Zhi Wei Deng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 1¦Á,6¦Â-dihydroxy-cis-eudesm-3-ene-6-O-¦Â-D-glucopyranoside C21H36O7 ÏàËÆ¶È:66.6% Molecules 2011 16 9017-9024 A New Eudesmane Sesquiterpene Glucoside from Liriope muscari Fibrous Roots Hai Ming Zhang, Gang Li Wang, Chun Qi Bai, Peng Liu, Zi Mu Liu, Qi Zhi Liu, Yong Yan Wang, Zhi Long Liu, Shu Shan Du and Zhi Wei Deng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (1R,4S,6R)-6-hydroxyfenchan-2-one 6-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside ÏàËÆ¶È:63.6% Phytochemistry 1994 36 55-59 Biotransformation of (+)- and (?)-fenchone by cultured cells of Eucalyptus perriniana Yutaka Orihara, Tsutomu Furuya Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . liriopeoside A C21H36O7 ÏàËÆ¶È:61.9% Journal of Natural Products 2004 67 1761-1763 cis-Eudesmane Sesquiterpene Glycosides from Liriope muscari and Ophiopogon japonicus Zhi-Hong Cheng, Tao Wu, S. W. Annie Bligh, Alan Bashall, and Bo-Yang Yu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ophiopogonoside A C21H38O8 ÏàËÆ¶È:61.9% Journal of Natural Products 2004 67 1761-1763 cis-Eudesmane Sesquiterpene Glycosides from Liriope muscari and Ophiopogon japonicus Zhi-Hong Cheng, Tao Wu, S. W. Annie Bligh, Alan Bashall, and Bo-Yang Yu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . dendronobiloside B C21H38O8 ÏàËÆ¶È:61.9% Journal of Natural Products 2001 64 1196-1200 Three New Sesquiterpene Glycosides from Dendrobium nobile with Immunomodulatory Activity Weimin Zhao,Qinghua Ye,Xiaojian Tan, Hualiang Jiang, Xiaoyu Li, Kaixian Chen, and A. Douglas Kinghorn Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . penstemid ÏàËÆ¶È:61.9% Planta Medica 1987 53 438-439 Catalytic Hydrogenation of Penstemide: lO-Deoxypenstemide, a New Valeriana Type Ester Iridoid Peter Junior, Claudia Dethlefs and Ulrike Jungel Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . penstemid ÏàËÆ¶È:61.9% Planta Medica 1986 52 356-358 Dihydropenstemide from Penstemon confertus and the Preparation of epi-Dihydropenstemide from Penstemide Birgit Gering Peter Junior und Max Wichtl Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . penstemide ÏàËÆ¶È:61.9% Planta Medica 1984 50 417-420 Serruloside and Serrulatoside, two New Iridoid Glycosides from Penstemon serrulatus Peter Junior Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . (1S,4R,6S)-6-hydroxyfenchan-2-one 6-O-¦Â-D-glucopyranoside ÏàËÆ¶È:61.9% Phytochemistry 1994 36 55-59 Biotransformation of (+)- and (− -fenchone by cultured cells of Eucalyptus perrinianaYutaka Orihara, Tsutomu Furuya Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 1a C21H34O7 ÏàËÆ¶È:61.9% Heterocycles 2006 68 2335-2342 Medicinal Foodstuffs. XXXII. Novel Sesquiterpene Glycoside Sulfate, Fukinoside A, with Antiallergic Activity from Japanese Butterbur (Petasites japonicus) Masayuki Yoshikawa,* Toshio Morikawa, Junji Tanaka, and Hiroshi Shimoda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . ent-2-oxo-3¦Â,15,16-trihydroxypima¦Á-8(14)-en-3-O-¦Â-glucopyranoside C26H42O9 ÏàËÆ¶È:61.5% Journal of Natural Products 2004 67 1517-1521 Novel Diterpenoids and Diterpenoid Glycosides from Siegesbeckia orientalis Ying Xiang, Hua Zhang, Cheng-Qi Fan, and Jian-Min Yue Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (1S,4R,6S)-6-hydroxyfenchan-2-one 6-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside ÏàËÆ¶È:59.0% Phytochemistry 1994 36 55-59 Biotransformation of (+)- and (− -fenchone by cultured cells of Eucalyptus perrinianaYutaka Orihara, Tsutomu Furuya Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-03-26 22:17:27













»Ø¸´´ËÂ¥
-fenchone by cultured cells of Eucalyptus perriniana