| ²é¿´: 229 | »Ø¸´: 1 | ||
н´77Òø³æ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý
|
| GJ-V-4-2 13C NMR (75 MHz, MeOD) ¦Ä 20.35, 26.55, 26.72, 34.79, 40.95, 63.00, 69.99, 71.39, 71.80,74.24,75.44, 78.26,78.39, 78.51, 96.03,105.01,129.41,130.57,134.00, 135.18,170.23, |
» ²ÂÄãϲ»¶
287Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
274Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
308Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
±¾¿ÆÖ£ÖÝ´óѧ£¬Ò»Ö¾Ô¸»ª¶«Ê¦·¶´óѧ282Çóµ÷¼Á
ÒѾÓÐ24È˻ظ´
»¯Ñ§308·ÖÇóµ÷¼Á
ÒѾÓÐ18È˻ظ´
Çó²ÄÁϵ÷¼Á£¬Ò»Ö¾Ô¸Ö£ÖÝ´óѧ289·Ö
ÒѾÓÐ19È˻ظ´
277Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
266Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
É격
ÒѾÓÐ8È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý ÖØ½±
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
audreygc
Ìú¸Ëľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 236 (´óѧÉú)
- ½ð±Ò: 5115.1
- ºì»¨: 5
- Ìû×Ó: 519
- ÔÚÏß: 131Сʱ
- ³æºÅ: 1978000
- ×¢²á: 2012-09-05
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
²éѯ½á¹û£º¹²²éµ½413¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . jasminoside R C22H34O12 ÏàËÆ¶È:95.4% Bioorganic & Medicinal Chemistry Letters 2013 23 1127-1131 Chemical constituents from the fruit of Gardenia jasminoides and their inhibitory effects on nitric oxide production Kaifeng Peng, Liguo Yang, Shizhe Zhao, Lixia Chen, Feng Zhao, Feng Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . jasminoside R C22H34O12 ÏàËÆ¶È:95.4% Chemistry & Biodiversity 2012 9 1490-1499 Melanogenesis Inhibitory Activity of Monoterpene Glycosides from Gardeniae Fructus Toshihiro Akihisa, Kensuke Watanabe, Ayako Yamamoto, Jie Zhang, Masahiro Matsumoto and Makoto Fukatsu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Jasminoside J C16H24O7 ÏàËÆ¶È:76.1% Helvetica Chimica Acta 2010 93 763-771 Monoterpenoids from the Fruit of Gardenia jasminoides Yang Yu, Hao Gao, Yi Dai, Ying Wang, He-Ru Chen and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . jasminoside S C22H36O12 ÏàËÆ¶È:68.1% Bioorganic & Medicinal Chemistry Letters 2013 23 1127-1131 Chemical constituents from the fruit of Gardenia jasminoides and their inhibitory effects on nitric oxide production Kaifeng Peng, Liguo Yang, Shizhe Zhao, Lixia Chen, Feng Zhao, Feng Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . ¦Â-gentiobiosyl 2,6,6-trimethylcyclohex-1-ene-1-carboxylate C22H36O12 ÏàËÆ¶È:68.1% Chemistry & Biodiversity 2012 9 1490-1499 Melanogenesis Inhibitory Activity of Monoterpene Glycosides from Gardeniae Fructus Toshihiro Akihisa, Kensuke Watanabe, Ayako Yamamoto, Jie Zhang, Masahiro Matsumoto and Makoto Fukatsu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 1-O-trans-cinnamoyl-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranose ÏàËÆ¶È:66.6% Phytochemistry 1996 43 481-485 Coumarins from Metrodorea flavida Ana Cristina S. Baetas, Mara S. P. Arruda, Adolfo H. M¨¹ller, Alberto C. Arruda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 2-phenylpropionyl 6-O-¦Â-D-glucopyranosyl-¦Â-D-glucopyranoside ÏàËÆ¶È:66.6% Phytochemistry 1987 26 2983-2989 Glycosylation of 2-phenylpropionic acid and its ethyl ester in suspension cultures of Nicotiana tabacum,Dioscoreophyllum cumminsii and Aconitum japonicum Tsutomu Furuya,Masashi Ushiyama,Yoshihisa Asada,Takafumi Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . Jasminoside M C21H34O11 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2010 93 763-771 Monoterpenoids from the Fruit of Gardenia jasminoides Yang Yu, Hao Gao, Yi Dai, Ying Wang, He-Ru Chen and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . Sinapyl alcohol 1,3'-di-O-¦Â-D-glucopyranoside ÏàËÆ¶È:66.6% Pharmazie 2002 57 209-211 Two new steroids from Adenophora stenanthina subsp. xifengensis Zhen-Fu Hou - Yong-Qiang Tu - Yu Li Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . jasminoside I C22H36O12 ÏàËÆ¶È:63.6% Journal of Natural Products 2008 71(6) 995-999 Pyronane Monoterpenoids from the Fruit of Gardenia jasminoides Quan Cheng Chen, UiJoung Youn, Byung-Sun Min, and KiHwan Bae Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . Jasminoside P C22H36O12 ÏàËÆ¶È:63.6% Helvetica Chimica Acta 2010 93 763-771 Monoterpenoids from the Fruit of Gardenia jasminoides Yang Yu, Hao Gao, Yi Dai, Ying Wang, He-Ru Chen and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (1R,3R,4R)-p-menthane-3,8-diol3-O-¦Â-D-gentiobioside ÏàËÆ¶È:63.6% Journal of the Chemical Society, Perkin Transactions 1 1989 1711-1719 Biotransformation of (¨C)-menthol by Eucalyptus perriniana cultured cells Tsutomu Furuya, Yutaka Orihara and Hiromitsu Miyatake Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . nuciferoside C22H38O11 ÏàËÆ¶È:63.6% Biological and Pharmaceutical Bulletin 2010 33 267-272 Selective Cholinesterase Inhibitory Activities of a New Monoterpene Diglycoside and Other Constituents from Nelumbo nucifera Stamens Hyun Ah Jung, Yu Jung Jung, Sook Kyung Hyun, Byung-Sun Min, Dong-Wook Kim, Jee H. Jung, Jae Sue Choi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . Breyniaionoside C C19H34O9 ÏàËÆ¶È:61.9% Chemical & Pharmaceutical Bulletin 2004 52(9) 1086-1090 Terpenic and Phenolic Glycosides from Leaves of Breynia officinalis HEMSL. Hiroyuki MORIKAWA,Ryoji KASAI, Hideaki OTSUKA,Eiji HIRATA,Takakazu SHINZATO,Mitsunori ARAMOTO,and Yoshio TAKEDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . campyloside A C21H25O10N ÏàËÆ¶È:61.9% Phytochemistry 2008 69 2209-2213 Nitrile glucosides and serotobenine from Campylospermum glaucum and Ouratea turnarea Auguste Abouem ¨¤ Zintchem, Dominique Ngono Bikobo, Alex de Th¨¦odore Atchad¨¦,Jos¨¦phine Ngo Mbing, Joseph Gangoue-Pieboji, Raphael Ghogomu Tih, Alain Blond,Dieudonn¨¦ Emmanuel Pegnyemb Bernard Bodo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 6-O-(¦Â-D-glucopyranosyl)-1-O-octanoyl-¦Â-D-glucopyranose C20H36O12 ÏàËÆ¶È:61.9% Journal of Natural Products 2000 63 1182-1183 Novel Glycosides from Noni (Morinda citrifolia) Mingfu Wang, Hiroe Kikuzaki, Yi Jin, Nobuji Nakatani, Nanqun Zhu, Katalin Csiszar, Charles Boyd, Robert T. Rosen, Geetha Ghai, and Chi-Tang Ho Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . dendrantheinoside A C19H34O8 ÏàËÆ¶È:61.9% Planta Medica 1992 58 373-375 Structural Elucidation of endranthemosides A and B:Two New f3-Ionone Glucosides from Dendranthema shiwogiku Hideaki Otsuka, Yasuyuki Takeda,Kazuo Yamasaki, and Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . integrifoside C ÏàËÆ¶È:61.9% Phytochemistry 2000 53 479-484 Eudesmane derivatives from Tessaria integrifolia Masateru Ono, Chikako Masuoka, Yusuke Odake, Yasuyuki Ito, Toshihiro Nohara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . turpinionoside A ÏàËÆ¶È:61.9% Natural Product Sciences 2009 15 192-197 Chemical Constituents from Artemisia iwayomogi Increase the Function of Osteoblastic MC3T3-E1 Cells Ding, Yan; Liang, Chun; Choi, Eun-Mi; Ra, Jeong-Chan; Kim, Young-Ho Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . dendranthemoside A ÏàËÆ¶È:61.9% Phytochemistry 1996 42 723-727 Glycosides of megastigmane and of the simple alcohols from Alangium premnifolium Hidehiko Kijima, Hideaki Otsuka, Toshinori Ide, Choei Ogimi, Eiji Hirata, Anki Takushi, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . dendranthemoside A C19H34O8 ÏàËÆ¶È:61.9% Phytochemistry 1994 35 1331-1334 Alangionosides A and B, ionol glycosides from leaves of Alangium premnifolium Hideaki Otsuka, Kenji Kamada, Choei Ogimi, Eiji Hirata, Anki Takushi, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . everlastoside F C17H28O12 ÏàËÆ¶È:61.9% Chemical & Pharmaceutical Bulletin 2009 57 853-859 Medicinal Flowers. XXX. Eight New Glycosides, Everlastosides F¡ªM, from the Flowers of Helichrysum arenarium Toshio Morikawa, Li-Bo Wang, Kiyofumi Ninomiya, Seikou Nakamura, Hisashi Matsuda, Osamu Muraoka, Li-Jun Wu and Masayuki Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . (2S)-2-phenylpropionyl 6-O-¦Â-D-xylopyranosyl-¦Â-D-glucopyranoside ÏàËÆ¶È:61.9% Phytochemistry 1989 28 483-487 Biotransformation of 2-phenylpropionic acid in root culture of Panax ginseng Tsutomu Furuya,Masashi Ushiyama,Yoshihisa Asada,Takafumi Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . compound 1 ÏàËÆ¶È:61.9% Phytochemistry 1990 29 1179-1181 Amygdalin acyl derivatives,cyanogenic glycosides from the seeds of Merremia dissecta Adolf Nahrstedt,Essam Abdel Sattar,Soheir M.H. El-Zalabani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . Jasminoside O C21H34O11 ÏàËÆ¶È:61.9% Helvetica Chimica Acta 2010 93 763-771 Monoterpenoids from the Fruit of Gardenia jasminoides Yang Yu, Hao Gao, Yi Dai, Ying Wang, He-Ru Chen and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . 6-O-(¦Â-D-glucopyranosyl)-1-O-decanoyl-¦Â-D-glucopyranose C22H40O12 ÏàËÆ¶È:61.9% Phytochemistry Letters 2010 3 238-241 Identification of novel fatty acid glucosides from the tropical fruit Morinda citrifolia L. Hye-Kyeong Kim, Min-Kyong Kwon, Jin-Nam Kim, Chang-Kwon Kim, Yeon-Ju Lee, Hee Jae Shin, Joongku Lee, Hyi-Seung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . D-amygdalin C20H27NO11 ÏàËÆ¶È:61.9% Chinese Traditional and Herbal Drugs 2002 33 101-104 Isomers of amygdalin in BUYANG HUANWU TANG and its production WU Jun; TU Peng fei; ZHAO Yu ying Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . compound BYB-16 C20H27NO11 ÏàËÆ¶È:61.9% Chinese Traditional and Herbal Drugs 2002 33 101-104 Isomers of amygdalin in BUYANG HUANWU TANG and its production WU Jun; TU Peng fei; ZHAO Yu ying Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . amygdalin ÏàËÆ¶È:61.9% Natural Product Research and Development 2004 16 496-499 GLYCOSIDES FROM THE STEMS OF PHOTINIA PARVIFOLIA ZHANG Dong-ming; LI Yuan; YU Shi-shan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . poacynose C18H24O11 ÏàËÆ¶È:61.9% Journal of Natural Medicines 2012 66 39-48 Promoting the effect of chemical constituents from the flowers of Poacynumhendersonii on adipogenesis in 3T3-L1 cells Toshio Morikawa, Katsuya Imura, Sohachiro Miyake, Kiyofumi Ninomiya and Hisashi Matsuda, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-03-28 09:29:00














»Ø¸´´ËÂ¥