| ²é¿´: 237 | »Ø¸´: 2 | ||||
[ÇóÖú]
Çó΢Æ×!
|
| 16.7,29.7,36.0,40.8,53.7,55.2,55.9,62.9,63.4,77.2,80.0,112.7,113.7,118.0,123.8,128.6,132.6,134.6,144.4,146.2,152.4,195.6 |
» ²ÂÄãϲ»¶
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ39È˻ظ´
353Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸211µç×ÓÐÅÏ¢347Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
323Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
22408 266Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
313Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
305Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ11È˻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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
º£ÀËÖðÃÎ: ½ð±Ò+4, ¡ïÓаïÖú 2013-07-03 10:48:02
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
º£ÀËÖðÃÎ: ½ð±Ò+4, ¡ïÓаïÖú 2013-07-03 10:48:02
|
°´´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 16.7,29.7,36.0,40.8,53.7,55.2,55.9,62.9,63.4,77.2,80.0,112.7,113.7,118.0,123.8,128.6,132.6,134.6,144.4,146.2,152.4,195.6 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½149¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 3-[2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxylmethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate C22H26O7 ÏàËÆ¶È:59.0% Natural Product Communications 2010 5 1627 - 1630 Two Pairs of Enantiomeric Neolignans fromLobelia chinensis Jian-Xin Chen, Shen-Hui Huang, Lei Wanga, Wei-Li Han, Ying Wang, Dong-Mei Zhangand Wen-Cai Ye Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . dihydrodehydrodiconiferyl alcohol ÏàËÆ¶È:54.5% Phytochemistry 2000 55 597-601 nor-Lignans from the leaves of Styrax ferrugineus (Styracaceae) with antibacterial and antifungal activity Patricia Mendonça Pauletti, Angela Regina Ara¨²joa, Maria Claudia Marx Young, Astr¨¦a M. Giesbrecht, Vanderlan da Silva Bolzani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . dihydrodehydrodiconiferyl alcohol C20H24O6 ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 1996 44 1418-1420 Two New Benzofuran-Type Lignans from the Wood of Viburnum awabuki Yoshiyasu FUKUYAMA,Mai NAKAHARA,Hiroyuki MINAMI and Mitsuaki KODAMA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . balanophonin ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 1982 30 1525-1527 BALANOPHONIN, A NEW NEO-LIGNAN FROM BALANOPHORA JAPONICA MAKINO Mitsumasa Haruna,Tomoko Koube,Kazuo Ito and Hiroyuki Murata Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . dihydrodiconiferyl C20H24O6 ÏàËÆ¶È:54.5% Chemistry of Natural Compounds 1993 29 545-546 TWO PHENOLIC COMPOUNDS FROM Aconitum baicalense Ts. Zhapova N. N. Pogodaeva, A. G. Gorshkov,and A. A. Semenov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . melianoninol C20H20O6 ÏàËÆ¶È:54.5% Journal of Chinese Pharmaceutical Sciences 1992 1 7-11 Studies on the Chemical Constituents of Melia azedarach Ren-Sheng Xu; Wen-Han Lin; Jiu Han; Wen-Lu Wang; Shan-Huan Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . melianoninol C20H20O6 ÏàËÆ¶È:54.5% Acta Pharmaceutica Sinica 1991 26 426-429 STUDIES ON THE CHEMICAL CONSTITUENTS OF MELIA AZEDARACH L. J Han; WH Lin; RS Xu; WL Wang and SH Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . dihydrodehydrodiconifenyl alcohol ÏàËÆ¶È:54.5% Journal of Asian Natural Products Research 2008 10 499-502 One new dihydrobenzofuran lignan from Vitex trifolia Qiong Gu, Xue-Mei Zhang, Jun Zhou, Sheng-Xiang Qiu and Ji-Jun Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . balanophonin C20H20O6 ÏàËÆ¶È:54.5% Phytochemistry 1999 50 781-785 Coniferaldehyde derivatives from tissue culture of Artemisia annua and Tanacetum parthenium Lai-King Sy, Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . compound 4 ÏàËÆ¶È:54.5% Phytochemistry 1998 48 719-723 Neolignan glucosides from Jasminum urophyllum Ya-Ching Shen, Pei-Wen Hsieh, Yao-Haur Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (-)-balanophonin C20H20O6 ÏàËÆ¶È:54.5% Korean Journal of Pharmacognosy 2001 32(4) 302-306 Chemical Components from the Stem Barks of Kalopanax septemlobus Hong, Sung-Su; Han, Doo-Il; Hwang, Bang-Yeon; Choi, Woo-Hoi; Kang, Ho-Sang; Lee, Myung-Koo; Lee, Don-Koo; Lee, Kyong-Soon; Ro, Jai-Seup Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . lennoxamine analogue C21H23NO5 ÏàËÆ¶È:54.5% Tetrahedron Letters 2000 41 8007-8010 A novel synthesis of isoindolobenzazepine alkaloids: application to the synthesis of lennoxamine Somsak Ruchirawat, Poolsak Sahakitpichan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (7S,8R)-4,9-Dihydroxy-3,3',5-trimethoxy-4',7-epoxy-8,5'-neolignan-9'-oic Acid Methyl Ester C22H26O8 ÏàËÆ¶È:54.5% Helvetica Chimica Acta 2010 93 2467-2477 Neolignans and Caffeoyl Derivatives from Selaginella moellendorffii Yue-Hu Wang, Qian-Yun Sun, Fu-Mei Yang, Chun-Lin Long, Fu-Wei Zhao, Gui-Hua Tang, Hong-Mei Niu, Huan Wang, Qiao-Qin Huang, Jin-Jin Xu and Li-Juan Ma Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . Diethyl 1-[N-(2-fluorophenyl)amino]-3-phenyl-2-propenylphosphonate C19H23FNO3P ÏàËÆ¶È:54.5% Molecules 2010 15 5782-5796 Asymmetric Synthesis of ¦Á-Aminophosphonates Using the Inexpensive Chiral Catalyst 1,1¡¯-Binaphthol Phosphate Weiming Xu, Sha Zhang, Song Yang, Lin-Hong Jin, Pinaki S. Bhadury, De-Yu Hu and Yuping Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . compound 6 ÏàËÆ¶È:54.5% Chinese Pharmaceutical Journal 2002 37 14-17 Study on chemical constituents isolated from Glycosmis citrifolia SHEN Xiao-Ling, ZENG Hui-Fang, CHEN Zhen, ZHONG Guang-Hua Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 4,9-dihydroxy-3,5'-dimethoxy-4',7-epoxy-8,5'-neolignane-9'-y lacetate ÏàËÆ¶È:54.5% Natural Product Research and Development 2010 22 945-948 Lignans from the Stem of Schima superba XU Wen; ZHOU Guang-xiong; YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . dihydrodehydrodiconifery alcohol ÏàËÆ¶È:54.5% Natural Product Research and Development 2010 22 945-948 Lignans from the Stem of Schima superba XU Wen; ZHOU Guang-xiong; YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . ((8R,8'S)-7-(4-hydroxy-3-methoxyphenyl)-8'-methylbutan-8-yl)-3'-methoxybenzene-4',5'-diol C19H24O5 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry Letters 2011 21 6884-6887 Inhibitory effect on NO production of phenolic compounds from Myristica fragrans To Dao Cuong, Tran Manh Hung, MinKyun Na, Do Thi Ha, Jin Cheol Kim, Dongho Lee, SungWoo Ryoo, Jeong Hyung Lee, Jae Sue Choi, Byung Sun Min Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (E)-3-[(2S,3R)-2,3-dihydro-2-(4'-hydroxy-3'-methoxyphenyl)-3-hydroxymethyl-7-methoxy-1-benzofuran-5-yl]-2-propenal C20H20O6 ÏàËÆ¶È:54.5% Tetrahedron 1998 54 12429-12444 On the absolute structure of optically active neolignans containing a dihydrobenzofuran skeleton Mabel S.M. Yuen, Feng Xue, Thomas C.W. Mak, Henry N.C. Wong Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-07-03 08:30:56
nkx1979
ľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 151 (¸ßÖÐÉú)
- ½ð±Ò: 2074
- É¢½ð: 20
- ºì»¨: 3
- Ìû×Ó: 953
- ÔÚÏß: 64.3Сʱ
- ³æºÅ: 2111800
- ×¢²á: 2012-11-07
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
º£ÀËÖðÃÎ: ½ð±Ò+1, ¡ïÓаïÖú 2013-07-03 10:48:10
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
º£ÀËÖðÃÎ: ½ð±Ò+1, ¡ïÓаïÖú 2013-07-03 10:48:10
|
1 . 3-[2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxylmethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate C22H26O7 ÏàËÆ¶È:59.0% Natural Product Communications 2010 5 1627 - 1630 Two Pairs of Enantiomeric Neolignans fromLobelia chinensis Jian-Xin Chen, Shen-Hui Huang, Lei Wanga, Wei-Li Han, Ying Wang, Dong-Mei Zhangand Wen-Cai Ye Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . dihydrodehydrodiconiferyl alcohol ÏàËÆ¶È:54.5% Phytochemistry 2000 55 597-601 nor-Lignans from the leaves of Styrax ferrugineus (Styracaceae) with antibacterial and antifungal activity Patricia Mendonça Pauletti, Angela Regina Ara¨²joa, Maria Claudia Marx Young, Astr¨¦a M. Giesbrecht, Vanderlan da Silva Bolzani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . dihydrodehydrodiconiferyl alcohol C20H24O6 ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 1996 44 1418-1420 Two New Benzofuran-Type Lignans from the Wood of Viburnum awabuki Yoshiyasu FUKUYAMA,Mai NAKAHARA,Hiroyuki MINAMI and Mitsuaki KODAMA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- |

3Â¥2013-07-03 09:56:00















»Ø¸´´ËÂ¥