| ²é¿´: 347 | »Ø¸´: 1 | |||
ÏëÒªÈëµÀµÄ³æÄ¾³æ (СÓÐÃûÆø)
|
[ÇóÖú]
III-c ÒÑÓÐ1È˲ÎÓë
|
|
190.41, 177.33, 165.31, 165.02, 162.81, 138.75, 128.57, 128.47, 125.96, 104.73, 96.20, 93.28, 79.04, 78.79, 77.60, 77.34, 77.08, 56.21, 55.49, 49.77, 49.00, 48.80, 48.66, 48.63, 48.49, 48.46, ÈܼÁ ¼×´¼£ºÂÈ·Â |
» ²ÂÄãϲ»¶
һ־Ը³¶«´óѧ071000ÉúÎïѧѧ˶³õÊÔ·ÖÊý276Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸¹þ¹¤´ó 085600 277 12²Ä¿Æ»ùÇóµ÷¼Á
ÒѾÓÐ33È˻ظ´
Ò»Ö¾Ô¸Öйú¿ÆÑ§ÔºÉϺ£ÓлúËù£¬Óлú»¯Ñ§356·ÖÕÒµ÷¼Á
ÒѾÓÐ12È˻ظ´
071000ÉúÎïѧ£¬Ò»Ö¾Ô¸ÉîÛÚ´óѧ296·Ö£¬Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
0854µ÷¼Á
ÒѾÓÐ12È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ37È˻ظ´
271Çóµ÷¼Á
ÒѾÓÐ23È˻ظ´
²ÄÁÏÏà¹Ø×¨Òµ344Çóµ÷¼ÁË«·Ç¹¤¿ÆÑ§Ð£»ò¿ÎÌâ×é
ÒѾÓÐ11È˻ظ´
»¯¹¤Ñ§Ë¶294·Ö£¬Çóµ¼Ê¦ÊÕÁô
ÒѾÓÐ14È˻ظ´
2026 WRÇà°Î
ÒѾÓÐ5È˻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 ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÏëÒªÈëµÀµÄ³æ: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-10 16:32:42
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÏëÒªÈëµÀµÄ³æ: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-10 16:32:42
|
. alpinetin C16H15O4 ÏàËÆ¶È:55.5% Phytochemistry 1981 20 2503-2506 Phenolic compounds from the rhizomes of Alpinia speciosa Hideji Itokawa, Makoto Morita, Susumu Mihashi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . alpinetin C16H14O4 ÏàËÆ¶È:55.5% Chinese Traditional and Herbal Drugs 2008 39 1147-1149 ½µÏãÖлÆÍªÀ໯ѧ³É·ÖÑо¿ ¹ùÀö±ù;ÍõÀÙ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . alpinetin and ÏàËÆ¶È:55.5% Natural Product Research 2012 26 2089-2094 Antitumor constituents from the leaves of Carya cathayensis Xu-Dong Cao , Zhi-Shan Ding , Fu-Sheng Jiang, Xing-Hong Ding, Jian-Zhen Chen, Su-Hong Chen & Gui-Yuan Lv Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 5-methoxy-7-hydroxyflavonone ÏàËÆ¶È:55.5% 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 5 . compound 9 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1984 32 362-365 NOVEL C-3/C-3''-BIFLAVANONES FROM STELLERA CHAMAEJASME L. GuoQuan Liu,Hiroshi Tatematsu,Mikio Kurokawa,Masatake Niwa and Yoshimasa Hirata Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 5-hydroxy-7-methoxy-8-methylflavanone ÏàËÆ¶È:50% Natural Product Research and Development 2008 20 827-829 Study on the Chemical Constituents of Baeckea frutescens CHEN Jia-yuan; YA Qi-kang; LU Wen-jie; LIU Bu-ming Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 5-hydroxy-7-methoxy-8-methylflavanone ÏàËÆ¶È:50% European Journal of Organic Chemistry 1999 1999 2309-2314 Biomimetic Synthesis of the Flavanone Leridol, Revision of the Structure of the Natural Product Guy Solladi¨¦, Nicolai Gehrold and Jean Maignan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 5,7-Dimethoxyflavanone C17H16O4 ÏàËÆ¶È:50% Synthesis 2014 46 465-474 Mild and Efficient One-Pot Synthesis of Diverse Flavanone Derivatives via an Organocatalyzed Mannich-Type Reaction Vuppalapati, Srinivasu V. N.; Xia, Likai; Edayadulla, Naushad; Lee, Yong Rok Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . (¡À)-7-O-methylcryptostrobin ÏàËÆ¶È:50% Australian Journal of Chemistry 1982 35 1851-1858 The crystal structure of (S)-(¨C)-6-Bromo-5,7-dihydroxy-8-methyl-2-phenyl-2,3-dihydro-4H-1-benzopyran-4-one [(¨C)-6-bromocryptostrobin] and a 13C N.M.R. study of (¡À)-cryptostrobin and related substances. Revision of the structures of the natural products (¡À LT Byrne, JR Cannon, DH Gawad, BS Joshi, BW Skelton and RFWAH Toia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . alpinetin ÏàËÆ¶È:50% Central South Pharmacy 2013 11 1-3 Chemical constituents in the green peel of Juglans Mandshurica Maxim. LI Jing, XU Kang-ping, ZOU Hui, LONG Hong-ping, ZOU Zhen-xing, KUANG Jun-wei, TAN Gui-shan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . pinostrobin ÏàËÆ¶È:50% Natural Product Research and Development 2014 26 1038-1042 Chemical Constituents of Flavones Part from the Stems and Leaves of Alpinia oxyphylla Miq£® LI Hong-fu, TAN Yin-feng, WANG Yong, WEI Na, LI Yong-hui, ZHANG Jun-qing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . pinostrobin C16H14O4 ÏàËÆ¶È:50% Journal of the Chemical Society of Pakistan 2012 34 1204−1212 Isolation, Structure Elucidation and Antioxidant Screening of Secondary Metabolites from Rhynchosia pseudo-cajan TAUHEEDA RIAZ, MUHAMMAD ATHAR ABBASI*, NAHEED RIAZ, AZIZ-UR-REHMAN, MUHAMMAD SALEEM, KHALID MOHAMMED KHAN, AND MUHAMMAD AJAIB Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-03-10 15:56:44













»Ø¸´´ËÂ¥