| ²é¿´: 905 | »Ø¸´: 4 | ||||
ÀîÂüÂüÕÅ½Ü½ð³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý²éѯ
|
|
¹òÇó΢Æ×Êý¾Ý£ºÎ¢Ì¼Æ×ÇóÖúC£¨ßÁà¤) 21.5,21.7,28.4,29.9,31.3,35.2,35.4,35.5,36.6,39.7,40.4,44.4,44.9,70.6,72.2 ¼±Çó£¬Ð»Ð»¸÷λ¡£Ó¦¸ÃÊDZ¶°ëÝÆÀ໯ºÏÎï¡£ |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸Ö£ÖÝ´óѧ085600Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á Ò»Ö¾Ô¸Î÷ÄϽ»Í¨´óѧ085701»·¾³¹¤³Ì 282·Ö
ÒѾÓÐ7È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
²ÄÁÏר˶283Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
£¨µ÷¼Á£©Ò»Ö¾Ô¸±¨¿¼¹þ¶û±õ¹¤Òµ´óѧ0857×ÊÔ´Óë»·¾³×¨Òµ378·Ö¿¼Éú
ÒѾÓÐ3È˻ظ´
±¾¿Æ211£¬293·ÖÇëÇóµ÷¼Á
ÒѾÓÐ9È˻ظ´
315Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
308Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
301Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
Çó΢Æ×Êý¾Ý¿â¼ìË÷2¸öÎå»·ÈýÝÆ»¯ºÏÎï
ÒѾÓÐ4È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻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 ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÀîÂüÂüÕŽÜ: ½ð±Ò+30, ¡ïÓаïÖú 2013-11-14 19:22:05
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÀîÂüÂüÕŽÜ: ½ð±Ò+30, ¡ïÓаïÖú 2013-11-14 19:22:05
|
²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´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£º¹²²éµ½516¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 2 C15H26O3 ÏàËÆ¶È:80% Journal of Asian Natural Products Research 2009 11 539-547 Constituents from the seeds of Brucea javanica with inhibitory activity of Tobacco mosaic virus Qi-Jian Chena, Ming-An Ouyangab, Qing-Wei Tanb, Zheng-Kun Zhanga,Zu-Jian Wua and Qi-Ying Lina Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 17 ÏàËÆ¶È:80% Phytochemistry 1990 29 757-763 Rearranged caryophyllenes by biotransformation with Chaetomium cochliodes Wolf-Rainer Abraham,Ludger Ernst,Hans-Adolf Arfmann Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (1S,4R,5R,8S,9S)-clovane-5,9,12-triol C15H26O3 ÏàËÆ¶È:73.3% Journal of Natural Products 2006 69(10) 1429-1434 Microbial Transformation and Butyrylcholinesterase Inhibitory Activity of (− -Caryophyllene Oxide and Its DerivativesMuhammad Iqbal Choudhary, Zafar A. Siddiqui, Sarfraz A. Nawaz, and Atta-ur-Rahman Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . foliachinenol E C15H26O3 ÏàËÆ¶È:73.3% Chemical & Pharmaceutical Bulletin 2011 59(8) 1020-1028 Chemical Structures and Hepatoprotective Effects of Constituents from the Leaves of Salacia chinensis Seikou NAKAMURA,Yi ZHANG,Hisashi MATSUDA, Kiyofumi NINOMIYA, Osamu MURAOKA, and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3b,4,4a,5,6,7,7a,8-Octahydro-3a,8-dihydroxy-4,6,6-trimethyl-3H-indeno[5',6': 1,3]cyclopropa[1,2-c]furan-3(3aH)-one 8a and 4a,5,6,7,7a,8-hexahydro-4-hydroxy-6,6,8-trimethyl-4H-indeno-[5,6-c]furan-1-carboxylic acid C15H22O4 ÏàËÆ¶È:73.3% Journal of the Chemical Society, Perkin Transactions 1 2000 745-751 Secondary mould metabolites. Part 58. Modifications in basic conditions and Michael additions of the protoilludane sesquiterpene tsugicoline A; some implications for the biogenesis of other sesquiterpenoids produced by Basidiomycetes Alberto Arnone, Cristiana De Gregorio, Andrea Mele, Gianluca Nasini and Orso Vajna de Pava Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Rumphellclovane B C15H24O3 ÏàËÆ¶È:73.3% Bulletin of the Chemical Society of Japan 2011 84 119-121 Rumphellclovane B, a Novel Clovane Analogue from the Gorgonian Coral Rumphella antipathies Hsu-Ming Chung, Tsong-Long Hwang, Yung-Husan Chen, Jui-Hsin Su, Mei-Chin Lu, Jih-Jung Chen, Jan-Jung Li, Lee-Shing Fang, Wei-Hsien Wang, Ping-Jyun Sung Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 9¦Á-hydroxy-1¦Â-methoxycaryolanol C16H28O2 ÏàËÆ¶È:68.7% Helvetica Chimica Acta 2008 Vol. 91 1894 Four New Compounds from Sinacalia tangutica Ying Zhu, Yan Zhao, Guo-Du Huang, and Wang-Suo Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (1S,3R,3aR,6S,7S,9aR)-decahydro-1-(hydroxymethyl)-1,7-dimethyl-3a,7-methano-3aH-cyclopentacyclooctene C15H26O3 ÏàËÆ¶È:66.6% Chemistry & Biodiversity 2006 Vol. 3 791 Four New Compounds from the Leaves of Acer truncatum Lang-Ping Dong, Hai-Yang Liu, Wei Ni, Jun-Zhu Li, and Chang-Xiang Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 15 ÏàËÆ¶È:66.6% Phytochemistry 2005 66 249-260 Sesquiterpenes from Cupressus macrocarpa foliage Laurence G. Cool Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 9-O-oxoisocaryolane-1-ol C15H24O2 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1994 42 941-946 Constituents of Sindora sumatrana MIQ. II. Five New Sesquiterpenoids from the Dried Pods Henry HEYMANN,Yasuhiro TEZUKA,Tohru KIKUCHI and Sutardjo SUPRIYATNA Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . caryolane-1,9¦Â-diol ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2009 34 2765-2767 Bioactive constituents from whole herbs of Vernonia cinerea (¢ò) ZHU Huaxu, TANG Yuping, MIN Zhida, GONG Zhunan Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-11-13 19:10:46
ÀîÂüÂüÕŽÜ
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 3 (Ó×¶ùÔ°)
- ½ð±Ò: 2832.5
- Ìû×Ó: 420
- ÔÚÏß: 77.4Сʱ
- ³æºÅ: 1616366
- ×¢²á: 2012-02-14
- רҵ: ÖÐÒ©ÖÊÁ¿ÆÀ¼Û
3Â¥2013-11-13 19:45:24
jiangyanqiu
Ìú³æ (СÓÐÃûÆø)
- Ó¦Öú: 1 (Ó×¶ùÔ°)
- ½ð±Ò: 1074.3
- Ìû×Ó: 105
- ÔÚÏß: 50Сʱ
- ³æºÅ: 2555772
- ×¢²á: 2013-07-20
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
4 . caryolane-1,6¦Â-Diol C15H26O2 ÏàËÆ¶È:60% Acta Pharmaceutica Sinica 2012 47 364-366 Sesquiterpenes and an intermediate 1¦Á,6¦Â,11-eudesmanetriol in the biosynthesis of geosmin from Streptomyces sp. YANG Ya-bin; YANG Zhi; YANG Xue-qiong; ZHANG Yong; ZHAO Li-xing; XU Li-hua; DING Zhong-tao Structure 13C NMR ̼Æ×Ä£Äâͼ ¿´Ò»Ï£¬Õâ¸ö¶ÔÂ𣿠|

4Â¥2013-11-13 20:34:13
ÀîÂüÂüÕŽÜ
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 3 (Ó×¶ùÔ°)
- ½ð±Ò: 2832.5
- Ìû×Ó: 420
- ÔÚÏß: 77.4Сʱ
- ³æºÅ: 1616366
- ×¢²á: 2012-02-14
- רҵ: ÖÐÒ©ÖÊÁ¿ÆÀ¼Û
5Â¥2013-11-13 21:17:47














»Ø¸´´ËÂ¥
-Caryophyllene Oxide and Its Derivatives