| ²é¿´: 531 | »Ø¸´: 3 | |||||
| µ±Ç°Ö»ÏÔʾÂú×ãÖ¸¶¨Ìõ¼þµÄ»ØÌû£¬µã»÷ÕâÀï²é¿´±¾»°ÌâµÄËùÓлØÌû | |||||
baojie668гæ (³õÈëÎÄ̳)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý²éѯ
|
||||
|
L-12 19.0£¬21.5£¬23.8£¬30.8£¬32.1£¬33.7£¬37.8£¬38.7£¬56.6£¬68.3£¬103.8£¬103.9£¬108.7£¬111.1£¬122.3£¬154.4£¬158.3£¬164.4£¬168.0£¬170.9£¬173.4 |
» ²ÂÄãϲ»¶
¸´ÊÔµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ11È˻ظ´
Ò»Ö¾Ô¸±±¾©2£¬²ÄÁÏÓ뻯¹¤308Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
0817»¯Ñ§¹¤³ÌÓë¼¼ÊõÇóµ÷¼Á£¬Ò»Ö¾Ô¸Öк£Ñó319
ÒѾÓÐ9È˻ظ´
Ò»Ö¾Ô¸µç×ӿƼ¼´óѧ085600²ÄÁÏÓ뻯¹¤ 329·ÖÇóµ÷¼Á
ÒѾÓÐ6È˻ظ´
304Çóµ÷¼Á£¨085602£¬¹ýËļ¶£¬Ò»Ö¾Ô¸985£©
ÒѾÓÐ7È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤´óѧ£¬³õÊԳɼ¨350Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
323·Ö£¨¼ÆËã»úÊÓ¾õºÍ´óÄ£ÐÍÏîÄ¿£©ÄÜÖ±½ÓÉÏÊÖ
ÒѾÓÐ3È˻ظ´
311·Ö 22408 Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻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
|
°´´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£º¹²²éµ½30¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 14-acetyl-12-methoxypodocarpa-8,11,13-triene-7-one C20H26O3 ÏàËÆ¶È:57.1% Australian Journal of Chemistry 1993 46 1825-1843 Investigation of the Structures of Some Natural Products From the Neem Tree JG Bendall, RC Cambie, PS Rutledge and PD Woodgate Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . isodonhenrin B C23H32O7 ÏàËÆ¶È:56.5% Chemical & Pharmaceutical Bulletin 2011 59 1562-1566 Cytotoxic ent-Kaurane Diterpenoids from Isodon henryi Zhuo Hu, Rui Zhan, Xue Du, Jia Su, Xiao-Nian Li, Jian-Hong Yang, Hai-Bo Zhang, Yan Li, Han-Dong Sun, Gan-Peng Li and Jian-Xin Pu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 18-hydroxy-3-deoxyhugorosenone C20H30O2 ÏàËÆ¶È:52.3% Phytochemistry 2008 69 200-205 Antifungal rosane diterpenes and other constituents of Hugonia castaneifolia Lilechi D. Baraza, Cosam C. Joseph, Joan J.E. Munissi, Mayunga H.H. Nkunya,Norbert Arnold, Andrea Porzel, Ludger Wessjohann Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . cinnamadin C17H24O5 ÏàËÆ¶È:52.3% Journal of Natural Products 2008 71(1) 123-126 Secondary Metabolites of Cinnamosma madagascariensis and Their #-Glucosidase Inhibitory Properties Liva Harinantenaina, Katsuyoshi Matsunami, Hideaki Otsuka,Masatoshi Kawahata, Kentaro Yamaguchi, and Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . cinnamodial 11¦Á,12¦Â-dimethyl¦Âacetal C19H30O6 ÏàËÆ¶È:52.3% Journal of Natural Products 2008 71(1) 123-126 Secondary Metabolites of Cinnamosma madagascariensis and Their #-Glucosidase Inhibitory Properties Liva Harinantenaina, Katsuyoshi Matsunami, Hideaki Otsuka,Masatoshi Kawahata, Kentaro Yamaguchi, and Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . deoxycorticosterone ÏàËÆ¶È:52.3% Phytochemistry 1998 49 2359-2362 The microbiological hydroxylation of some steroids with a cortical side chain by Cephalosporium aphidicola James R. Hanson, A. Christy Hunter Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 10 ÏàËÆ¶È:52.3% Phytochemistry 1989 28 3377-3381 Drimane-type sesquiterpenoids from the liverwort Makinoa crispata Toshihiro Hashimoto,Motoo Tori,Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 1-adamantyl-3-chloro-4-(2-(2,4-dihydroxyphenyl)-5-methoxy-1H-indol-3-yl)azetidin-2-one C28H29ClN2O4 ÏàËÆ¶È:52.3% Indian Journal of Chemistry 2010 49B 1398-1405 Synthesis and antiparkinsonian activity of some new adamantyl thiazolidinonyl/azeti-dinonyl in-dole derivatives Sunil Kumar,Hemlata Kaur,K K Saxena,Monica Sharma,Pinki Vishwakarma & Ashok Kumar* Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (R)-N-benzyloxycarbonyl-S-4-methoxybenzyl-2-methylcysteine-L-threonine methyl ester C25H32N2O7S ÏàËÆ¶È:52.3% Heterocycles 2002 58 601-634 Thiazoline Ring Formation from 2-Methylcysteines and 2-Halomethylalanines Brant L. Kedrowski and Clayton H. Heathcock* Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . cochliodone A C34H38O12 ÏàËÆ¶È:52.3% Tetrahedron 2008 64 9636-9645 Bis-spiro-azaphilones and azaphilones from the fungi Chaetomium cochliodes VTh01 and C. cochliodes CTh05 Nutchanat Phonkerd, Somdej Kanokmedhakul, Kwanjai Kanokmedhakul, Kasem Soytong, Samran Prabpai, Palangpon Kongsearee Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (5aR,6aS,10aS,10cR)-7,7,10a,10c-tetra-methyl-2,5a,6,6a,7,8,9,10,10a,10c-decahydro-4H-5-oxa-acephenanthrylene-3-carboxylic acid methyl ester C21H30O3 ÏàËÆ¶È:52.3% Tetrahedron 2003 59 9523-9536 Synthetic studies on the preparation of oxygenated spongiane diterpenes from carvone Antonio Abad, Consuelo Agull¨®, Ana C Cuñat, Ana Bel¨¦n Garcı́a, Carlos Gim¨¦nez-Saiz Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 7¦Á-hydroxy-11-oxo-spongia-13-en-16-one C20H28O4 ÏàËÆ¶È:52.3% Tetrahedron 2005 61 1961-1970 Syntheses of oxygenated spongiane diterpenes from carvone. Synthesis of dorisenone C Antonio Abad, Consuelo Agull¨®, Ana C. Cuñat, Ana Bel¨¦n Garc¨ªa Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 11¦Â,17¦Á-dihydroxypregna-4-ene-3,20-dione ÏàËÆ¶È:52.3% Organic Magnetic Resonance 1984 22 586-591 A carbon-13 nuclear magnetic resonance study of the 1,4-diene analogues of steroid hormones and related steroids Mario D. Gonzalez and Gerardo Burton Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 21-Hydroxypregn-4-ene-3,20-dione deoxycorticosterone C21H30O3 ÏàËÆ¶È:52.3% Organic Magnetic Resonance 1977 9 439-464 13C N.m.r. Spectra of steroids¡ªA Survey and Commentary J.W.Blunt and J.B.Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ |

4Â¥2013-07-24 10:35:29
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

2Â¥2013-07-24 08:45:01
baojie668
гæ (³õÈëÎÄ̳)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 124.5
- Ìû×Ó: 13
- ÔÚÏß: 9.8Сʱ
- ³æºÅ: 829878
- ×¢²á: 2009-08-18
- רҵ: Ò©Îﻯѧ
3Â¥2013-07-24 09:19:14














»Ø¸´´ËÂ¥