| ²é¿´: 340 | »Ø¸´: 1 | ||
¿ÓµùÒ©»¯Ìú³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬¼±¼±¼±£¡£¡£¡ ÒÑÓÐ1È˲ÎÓë
|
| CÆ×Êý¾Ý£º12.32,17.10,23.14,26.67,28.07,46.65,53.65,79.38,95.72,95.84,105.20,105.56,165.76,165.79,165.95,207.02,211.43 |
» ²ÂÄãϲ»¶
²ÄÁÏ¿ÆÑ§Ó빤³Ì320Çóµ÷¼Á£¬080500
ÒѾÓÐ4È˻ظ´
0703µ÷¼Á£¬Ò»Ö¾Ô¸Ìì½ò´óѧ319·Ö
ÒѾÓÐ17È˻ظ´
Ò»Ö¾Ô¸211£¬0703»¯Ñ§305·ÖÇóµ÷¼Á
ÒѾÓÐ5È˻ظ´
0703»¯Ñ§µ÷¼Á 348·Ö
ÒѾÓÐ6È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
308Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
²ÄÁÏÓ뻯¹¤363ÇóÍÆ¼ö
ÒѾÓÐ11È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ12È˻ظ´
ÉúÎïѧµ÷¼Á ¿Éµ÷¼Áµ½ÉúÎïÓëÒ½Ò©
ÒѾÓÐ3È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú2014.11.14
ÒѾÓÐ9È˻ظ´
΢Æ×ÇóÖú лл´ó¼Ò
ÒѾÓÐ3È˻ظ´
podÊý¾Ý´¦ÀíÇóÖú
ÒѾÓÐ12È˻ظ´
΢Æ×ÇóÖú£¬¶àлÁË
ÒѾÓÐ3È˻ظ´
Çó¼«ÖµÎÊÌâ¡£¼±¼±¼±
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл¸÷λ
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú лл£¡
ÒѾÓÐ3È˻ظ´
Çó΢Æ×°ïæ,лл
ÒѾÓÐ3È˻ظ´
ÇóÖú¦Á-¼×»ù±½ÒÒÏ©Óë¹ýÁ¿±½·ÓÔÚÁòËá¼ÓÈÈÌõ¼þÏ·¢Éúʲô·´Ó¦£¿
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¡¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
¼±Çó΢Æ×¿â²éѯ£¡·Ç³£¸Ðл£¡
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú ¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾ÝÇóÖú ¼±±ÏÒµ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¿ÓµùÒ©»¯: ½ð±Ò+6, ¡ïÓаïÖú 2014-12-29 20:07:28
¿ÓµùÒ©»¯: ½ð±Ò+4, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-14 16:34:10
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¿ÓµùÒ©»¯: ½ð±Ò+6, ¡ïÓаïÖú 2014-12-29 20:07:28
¿ÓµùÒ©»¯: ½ð±Ò+4, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-14 16:34:10
|
²éѯ½á¹û£º¹²²éµ½6¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 2-(2-methylbutyryl)- phloroglucinol 1-O-¦Â-D-glucopyranoside ÏàËÆ¶È:58.8% Chemical & Pharmaceutical Bulletin 2002 50(6) 841-843 Two New Acylated Flavanone Glycosides from the Leaves and Branches of Phyllanthus emblica Ying-Jun ZHANG,Tomomi ABE,Takashi TANAKA,Chong-Ren YANG,and Isao KOUNO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 2 C17H25O9 ÏàËÆ¶È:52.9% Phytochemistry 1989 28 2439-2441 Multifidol and multifidol glucoside from the latex of Jatropha multifida Samlipto Kosasi,Willem G. Van Der Sluis,Rudi Labadie Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 5-[3-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-yl)butyl]-2,2-dimethyl-1,3-dioxane-4,6-dione C16H22O8 ÏàËÆ¶È:52.9% Journal of Heterocyclic Chemistry 2006 43 365-369 1,3-Dipolar cycloadditions of 9-diazofluorenes and diphenyldiazomethane to 2-acyl-2H-1,2,3-diazaphospholes Xiangyun Guo,Li Feng,Quanrui Wang,Zhiming Li and Fenggang Tao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Rhodomyrtoxin C ÏàËÆ¶È:52.9% Phytochemistry 1984 23 1139-1141 Two dibenzofuran derivatives from fruits of Rhodomyrtus macrocarpa Chike A. Igboechi, Robert T. Parfitt, Michael G. Rowan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 1-(2,4,6-Trihydroxyphenyl)-1-decanone C16H24O4 ÏàËÆ¶È:52.9% Bioorganic & Medicinal Chemistry 2005 13 6651-6662 Triketones active against antibiotic-resistant bacteria: Synthesis, structure¨Cactivity relationships, and mode of action John W. van Klink, Lesley Larsen, Nigel B. Perry, Rex T. Weavers, Gregory M. Cook, Phil J. Bremer, Andrew D. MacKenzie, Teruo Kirikae Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 1-(2,4,6-Trihydroxyphenyl)-1-dodecanone C18H28O4 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2005 13 6651-6662 Triketones active against antibiotic-resistant bacteria: Synthesis, structure¨Cactivity relationships, and mode of action John W. van Klink, Lesley Larsen, Nigel B. Perry, Rex T. Weavers, Gregory M. Cook, Phil J. Bremer, Andrew D. MacKenzie, Teruo Kirikae Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-12-29 18:08:28














»Ø¸´´ËÂ¥