| ²é¿´: 255 | »Ø¸´: 1 | ||
kengkengsee½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬¸Ðл£¡
|
|
ÈܼÁ£ºë®´úÂȷ ̼Æ×Ðźţº16.41,16.69,17.85,22.52,23.95,34.06,34.88,37.85,41.50,52.32,67.53,75.28,106.33,148.18 |
» ²ÂÄãϲ»¶
0703µ÷¼Á£¬Ò»Ö¾Ô¸Ìì½ò´óѧ319·Ö
ÒѾÓÐ18È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
334·Ö»úеר˶Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
±¾¿ÆÖ£ÖÝ´óѧ£¬Ò»Ö¾Ô¸»ª¶«Ê¦·¶´óѧ282Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
305·ÖÇóµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ21È˻ظ´
»¯¹¤Ñ§Ë¶ 285Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
328Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ9È˻ظ´
081700ѧ˶£¬323·Ö£¬Ò»Ö¾Ô¸Öйúº£Ñó´óѧÇóµ÷¼ÁѧУ
ÒѾÓÐ18È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
»¯ºÏÎï΢Æ×ÇóÖú лл
ÒѾÓÐ9È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¡¼±£¡£¡£¡ÏÈлл°¡£¡
ÒѾÓÐ3È˻ظ´
¼±£¡Î¢Æ×ÇóÖú£¡ÏÈлл°¡£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬¸ø30J
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¡¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý YC-8
ÒѾÓÐ7È˻ظ´
ÇóÖúһ΢Æ×Êý¾Ý 15 лл£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
Çó΢Æ×Êý¾Ý лл
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾ÝÇóÖú ¼±±ÏÒµ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×²é½á¹¹ лл
ÒѾÓÐ3È˻ظ´
ÇóÈË΢Æ×²éѯ£¬¼±£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
kengkengsee: ½ð±Ò+5, ¡ïÓаïÖú 2013-10-16 10:24:43
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
kengkengsee: ½ð±Ò+5, ¡ïÓаïÖú 2013-10-16 10:24:43
|
²éѯ½á¹û£º¹²²éµ½146¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . compound 8 ÏàËÆ¶È:66.6% Planta Medica 1999 65 153-156 Sesquiterpene Lactone Glycosides from Arnica longifolia Claus M.Passreiter,Massimo De Carlo,and A.Steigel Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 1¦Â-Hydroxy-6,7¦Á-dihydroxyeudesm-4(15)-ene C15H26O3 ÏàËÆ¶È:66.6% Journal of Natural Products 2011 74 937-942 Estrogenic Activity of Chemical Constituents from Tephrosia candida Mohamed-Elamir F. Hegazy, Abou El-Hamd H. Mohamed, Ali M. El-Halawany, Pierre C. Djemgou, Abdelaaty A. Shahat, and Paul W. Par¨¦ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (3a¦Â,4a¦Á,8a¦Â,9a¦Â)-3a,4,4a,5,6,7,8,8a,9,9a-Decahydro-8a-methyl-5-methylenenaphtho[2,3-b]furan-2(3H)-one C14H20O2 ÏàËÆ¶È:64.2% Journal of the Chemical Society, Perkin Transactions 1 1993 239-247 Total synthesis of three eudesman-12,8-olides, (¡À)-isoalantolactone, (¡À)-dihydrocallitrisin and (¡À)-septuplinolide; structure revision of septuplinolide Masahiro Tada, Hirokazu Yamada, Akira Kanamori and Kazuhiro Chiba Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 7 C17H32O6S2 ÏàËÆ¶È:60% Journal of Natural Products 2001 64 348-349 Synthesis of (+)-Cyclozonarone and the Absolute Configuration of Naturally Occurring (-)-Cyclozonarone Manuel Cort¨¦s, Jaime A. Valderrama, Mauricio Cuellar, Ver¨®nica Armstrong, and Marcelo Preite Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 9¦Á-hydroxy-calarene C15H24O ÏàËÆ¶È:60% Phytochemistry 1992 31 3749-3755 Microbial oxidation of tricyclic sesquiterpenoids containing a dimethylcyclopropane ring Wolf-Rainer Abraham, Klaus Kieslich, Burkhard Stumpf, Ludger Ernst Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 2¦Á-methyldiplopterol ÏàËÆ¶È:60% Magnetic Resonance in Chemistry 2010 48 951-954 NMR spectral assignment of 2- and 3¦Â-methylhopanes and evidence for boat conformation in D ring of 17(H), 21(H)-hopanes (pages 951¨C954) Geir Kildahl-Andersen, Hans Peter Nytoft and Jon Eigill Johansen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (-)-juneol ÏàËÆ¶È:60% Journal of Oleo Science 2004 53 343-348 Eudesmane-Type Sesquiterpenoids in the Volatile Oil from Bursera graveolens Chiyoki YUKAWA, Hisakatsu IWABUCHI, Sadao KOMEMUSHI, Akiyoshi SAWABE Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (-)-Caryophyllene-6,7,12-triol C15H26O3 ÏàËÆ¶È:60% Flavour and Fragrance Journal 2010 25 161-170 Microbial transformation of isopinocampheol and caryophyllene oxide Yoshiaki Noma, Toshihiro Hashimoto, Shinya Uehara and Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . Faurinol-2 ÏàËÆ¶È:57.1% Phytochemistry 1983 22 1505-1506 A structure of faurinone, a sesquiterpene ketone isolated from valeriana officinalis R. Bos, H. Hendriks, J. Kloosterman, G. Sipma Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . ¦Â-sitosterol C15H26O ÏàËÆ¶È:57.1% Chinese Traditional and Herbal Drugs 2006 37 678-679 ÏãÁÛëާ»¯Ñ§³É·ÖµÄÑо¿(¢ò) ÉòÖ¾±õ;ÂíÓ¢Àö;½ðÕÜÐÛ;ÕŵÂÁ¬ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . compound 28 C14H20O2 ÏàËÆ¶È:57.1% Journal of the Chemical Society, Perkin Transactions 1 1993 239-247 Total synthesis of three eudesman-12,8-olides, (¡À)-isoalantolactone, (¡À)-dihydrocallitrisin and (¡À)-septuplinolide; structure revision of septuplinolide Masahiro Tada, Hirokazu Yamada, Akira Kanamori and Kazuhiro Chiba Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . lythgoe-Inhoffen diol ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry 2010 18 4119-4137 Vitamin D receptor agonist/histone deacetylase inhibitor molecular hybrids Marc Lamblin, Basel Dabbas, Russell Spingarn, Rodrigo Mendoza-Sanchez, Tian-Tian Wang, Beum-Soo An, Dao Chao Huang, Richard Kremer, John H. White, James L. Gleason Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (1S,2R)-2-chlorocyclopropanecarboxylic acid (1S,2R,5S)-5-isopropyl-2-methylcyclohexyl ester C14H23O2Cl ÏàËÆ¶È:57.1% Journal of the American Chemical Society 2002 124 10396-10415 Callipeltoside A: Total Synthesis, Assignment of the Absolute and Relative Configuration, and Evaluation of Synthetic Analogues Barry M. Trost, Janet L. Gunzner, Olivier Dirat, and Young H. Rhee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 3-methyl-3-(4-methyl-3-oxopentyl)cyclohexanone C13H22O2 ÏàËÆ¶È:57.1% The Journal of Organic Chemistry 1998 63 306-313 Total Synthesis of Allocyathin B2, a Metabolite of Bird's Nest Fungi Motoo Tori, Naoko Toyoda, and Masakazu Sono Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-10-15 08:12:25














»Ø¸´´ËÂ¥
10