| ²é¿´: 225 | »Ø¸´: 1 | ||||
hejiangboľ³æ (ÖøÃûдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×²éѯ
|
|
ÈܼÁ£º¼×´¼ ÏàËÆ¶È£º90%ÒÔÉÏ ºË´ÅÊý¾Ý£º 19.20.9,21.1,22.5,22.5,22.7,35.6,42.3,44.1,46.1,46.1,55.7,69.2,73.1,75.6 |
» ²ÂÄãϲ»¶
284Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
266Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
±¾¿ÆÉúÎïÐÅϢѧ£¬×Ü·Ö362 Çó07 08µ÷¼Á
ÒѾÓÐ3È˻ظ´
283Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
333Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
286Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ7È˻ظ´
297Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
312Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
085602»¯Ñ§¹¤³Ì268·Ö¶×µ÷¼Á
ÒѾÓÐ9È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
Çó΢ÆÕ½âÎö»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
Çó΢Æ×¼ìË÷»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾Ý¡£Ç󻯺ÏÎï½âÎö
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
¼±¼±¼±¡£¡£¡£¡£ÇóÖú΢Æ×Êý¾Ý£¨50%ÏàËÆ¶È¾ÍOKÁË£©£¬²»Ê¤¸Ðл£¡
ÒѾÓÐ8È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÖú΢Æ×²éѯ½âÆ×
ÒѾÓÐ5È˻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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hejiangbo: ½ð±Ò+10 2013-11-04 22:51:29
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hejiangbo: ½ð±Ò+10 2013-11-04 22:51:29
|
ôÓÐ90ÒÔÉϰ¡ 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£º¹²²éµ½245¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . cryptomeridiol ÏàËÆ¶È:66.6% Journal of Asian Natural Products Research 2007 9 277-283 Sesquiterpenoids from Hedychium yunnanense and Porana discifera, and the structural revision of two sesquiterpenoids from Laggera pterodonta W.-M. ZHU, Q. ZHAO, S.-L. LI and X.-J. HAO Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . isodonsesquitin A C15H28O2 ÏàËÆ¶È:66.6% Phytochemistry 1993 34 1176-1178 Terpenoids from Isodon grandifolia var. Atuntzensis Wu Shun-Hua, Zhang Hong-Jie, Lin Zhong-Wen, Sun Han-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Cryptomeridiol C15H28O2 ÏàËÆ¶È:66.6% Zeitschrift f¨¹r Naturforschung B 2007 62b 267-271 Sesquiterpenes and Phenolic Compounds from Achillea clypeolata Ingrid Werner, Pavel Mucaji, Armin Presser, and Sabine Glasl Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . selin-11-en-4¦Á-ol C15H26O ÏàËÆ¶È:66.6% Indian Journal of Chemistry Section B 2005 44B 1922-1926 Composition of a new chemotype of Tanacetum nubigenum Chanotiya,C S; Sammal,S S; Mathela,C S Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 4¦Á,6¦Á-dihydroxy-5¦Á,11 ¦ÁH-eudesma-12,8¦Â-olide C15H24O4 ÏàËÆ¶È:66.6% Planta Medica 2012 78 1002-1009 Sesquiterpene Lactones from Inula hupehensis Inhibit Nitric Oxide Production in RAW264.7 Macrophages Qin, Jiang-Jiang; Zhu, Jia-Xian; Zeng, Qi; Cheng, Xiang-Rong; Zhang, Shou-De; Jin, Hui-Zi; Zhang, Wei-Dong: Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . longipin-2-ene-1¦Â,7¦Â,9¦Á-15-tetrahydroxy 7,15-acetonide ÏàËÆ¶È:61.1% Phytochemistry 1993 32 1219-1223 Longipinene derivatives from Stevia origanoides Carlos M. Cerda-Garc¨ªa-Rojas, Eugenio S¨¢nchez-Arreola, Pedro Joseph-Nathan, Luisa U. Rom¨¢n, Juan D. Hernandez Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . chrysothol monoacetyl derivative(1c) ÏàËÆ¶È:60% Phytochemistry 2006 67 1547-1553 Constituents of Chrysothamnus viscidiflorus Ahmed A. Ahmed , Mohamed-Elamir F. Hegazy, Nahed M. Hassan,Malgorzata Wojcinska, Joe Karchesy, Paul W. Pare, Tom J. Mabry Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . li-selinen-4-ol ÏàËÆ¶È:60% Planta Medica 1995 61 196-197 Isolation and Identification of 11- Selinen-4¦Á,7¦Â-ol and 10-Aromadendranolin the Essential Oil of Murraya koenigii I. Wa¦Âmuth- Wagner, H.-O. Kalinowski. andH. fork Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 5¦ÁH,7¦ÁH-eudesman-4¦Á,6¦Á,11,12-tetraol C15H28O4 ÏàËÆ¶È:60% Planta Medica 2005 71 706-710 New Sesquiterpene Lactones from Laurus nobilis Leaves as Inhibitors of Nitric Oxide Production Simona De Marino,Nicola Borbone,Franco Zollo,Angela Ianaro,Paola Di Meglio, Maria Iorizzi Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-methyl-5-(2,2,6-trimethyl-6-hydroxy-cyclohexyl)-pentanoic acid ÏàËÆ¶È:60% Planta Medica 2002 68 808-812 Antimicrobial Terpenoids from the Oleoresin of the Peruvian Medicinal Plant Copaifera paupera Benigna M.Tincusi,Ignacio A.Jim¨¦nez,Isabel L.Bazzocchi,Laila M.Moujir,Zulma A.Mamani,Jos¨¦P.Barroso,Angel G.Ravelo,Basilio V.Hern¨¢ndez Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-11-04 22:50:58














»Ø¸´´ËÂ¥