| ²é¿´: 194 | »Ø¸´: 1 | ||||
gaoaicai123½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú
|
| 11.6,13.8,16.2,22.8,24.2,26.7,27.4,30.6,32.8,34.9,36.4,37.4,41.4,41.7,42.4,51.7,67.9,68.9,72.3,76.8,77.1,77.3,128.2,129.4,131.7,133.3,172.7,176.8 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
22408 266Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ43È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏ¿ÆÑ§Ó빤³Ì320Çóµ÷¼Á£¬080500
ÒѾÓÐ9È˻ظ´
0703»¯Ñ§µ÷¼Á 348·Ö
ÒѾÓÐ10È˻ظ´
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
gaoaicai123: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-07-18 15:29:02
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
gaoaicai123: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-07-18 15:29:02
|
°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½1302¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . lactone ring-opened monacolin K ÏàËÆ¶È:89.2% Mycosystema 2011 30 636-643 The bioactive metabolites of Aspergillus versicolor F62 isolated from Haliclona simulans DONG Shi-Hao GONG Ting ZHU Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . monacolin K ÏàËÆ¶È:71.4% The Journal of Antibiotics 1985 38 444-448 BIOSYNTHESIS OF ML-236B (COMPACTIN) AND MONACOLIN K AKIRA ENDO, YOSHINORI NEGISHI, TAKASHI IWASHITA, KOSEI MIZUKAWA, MASAHIRO HIRAMA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ÍÑˮĪÄÉ¿ÉÁÖ K ÏàËÆ¶È:67.8% Chinese Traditional and Herbal Drugs 2007 38 650-652 Chemical constituents of Xuezhikang Capsula MA Xue-min; GUO Shu-ren; DUAN Zhen-wen; WANG Xiang-yun Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . lovastatin C24H36O5 ÏàËÆ¶È:67.8% Chinese Traditional and Herbal Drugs 1999 30(3) 172-174 ºìÇúÖнµÑªÖ¬»îÐԳɷֵÄÑо¿ 嵺×Ãù,ËκéÌÎ,³ÂÀÚ,Ñî¸ù½ð,¹ùÌÎ Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Âå·¥ËûÍ¡ ÏàËÆ¶È:67.8% Mycosystema 2011 30 636-643 The bioactive metabolites of Aspergillus versicolor F62 isolated from Haliclona simulans DONG Shi-Hao GONG Ting ZHU Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 14-deoxy-14,18-cyclo-20-hydroxyecdysone C27H42O6 ÏàËÆ¶È:64.2% Steroids 2002 67 127-135 Photochemical transformation of 20-hydroxyecdysone: production of monomeric and dimeric ecdysteroid analogues Juraj Harmatha, Miloš Budĕš¨ªnsky, Karel Vok¨¢ĕ Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Compound 8 ÏàËÆ¶È:64.2% Magnetic Resonance in Chemistry 2009 47 71-83 Complete assignment of 1H and 13C NMR data of pravastatin derivatives (pages 71¨C83) Markus Bacher, Karl Baumann, Hermann Knapp, Andrea Steck and Sigrid Teibl Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound ÏàËÆ¶È:64.2% Zeitschrift f¨¹r Naturforschung C 2003 58 62-64 Production and Purification of Statins from Pleurotus ostreatus (Basidiomycetes) Strains J. Alarc¨®n, S. ¨¢guila, P. Arancibia-Avila, O. Fuentes, E. Zamorano-Ponce, and M. Hern¨¢ndez Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ML-236B ÏàËÆ¶È:64.2% The Journal of Antibiotics 1985 38 444-448 BIOSYNTHESIS OF ML-236B (COMPACTIN) AND MONACOLIN K AKIRA ENDO, YOSHINORI NEGISHI, TAKASHI IWASHITA, KOSEI MIZUKAWA, MASAHIRO HIRAMA Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (1S,2S,4aR,6R,8S,8aS,4'R,6'R,2''S)-6'-[2-[1,2,4a,5,6,7,8,8a-octahydro-6-hydroxy-2-methyl-8-[(2'-metnyl-1''-oxobutyl)oxy]-1-naphthalenyl]ethyl]tetrahydro-4'-hydroxy-2H-pyran-2'-one C23H36O6 ÏàËÆ¶È:64.2% Journal of Medicinal Chemistry 1992 35 3388-3393 The synthesis and biological evaluation of dihydroeptastatin, a novel inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase Elisabeth A. Bone, Alan H. Davidson, Christopher N. Lewis, Richard S. Todd Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compactin ÏàËÆ¶È:64.2% Chinese Journal of Antibiotics 1996 21 241-248 ΢ÉúÎïÀ´Ô´µÄµ¨¹Ì´¼ÉúÎïºÏ³ÉøÒÖÖÆ¼ÁÑо¿¢ó. ¿¹ÉúËØSIPI-8915ת»¯²úÎïµÄÑо¿ ¹¨±þÓÀ, ³ÂÈðÓ¢, ½ª, ½¡, Ö챦Ȫ Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Lovastatin C24H36O5 ÏàËÆ¶È:64.2% World Journal of Microbiology and Biotechnology 2005 21 1067-1075 Antimicrobial butyrolactone I derivatives from the Ecuadorian soil fungus Aspergillus terreus Thorn.var terreus M.E. Cazar, G. Schmeda-Hirschmann, and L. Astudillo Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Taxuyunnanine X C31H40O11 ÏàËÆ¶È:62.0% Tetrahedron 2003 59 37-45 Novel taxoids from the Chinese yew Taxus yunnanensis Sheng-Hong Li, Hong-Jie Zhang, Xue-Mei Niu, Ping Yao, Han-Dong Sun, Harry H.S Fong Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (24S,25S)-3¦Á,7¦Á,12¦Á,24-tetrahydroxy-5¦Â-cholestan-27-oyltaurine ÏàËÆ¶È:62.0% Steroids 2012 77 1510-1521 A novel varanic acid epimer ¨C (24R,25S)-3¦Á,7¦Á,12¦Á,24-tetrahydroxy-5¦Â-cholestan-27-oic acid ¨C is a major biliary bile acid in two varanid lizards and the Gila monster Lee R. Hagey, Shoujiro Ogawa, Narimi Kato, Rika Satoh (n¨¦e Okihara), Mizuho Une, Kuniko Mitamura, Shigeo Ikegawa, Alan F. Hofmann, Takashi Iida Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . aconicarchamine B C31H41NO7 ÏàËÆ¶È:62.0% Helvetica Chimica Acta 2011 94 122-126 Two New C20-Diterpenoid Alkaloids from Aconitum carmichaelii Yong Shen, Ai-Xue Zuo, Zhi-Yong Jiang, Xue-Mei Zhang, Hong-Ling Wang and Ji-Jun Chen Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-07-14 10:16:15














»Ø¸´´ËÂ¥