| ²é¿´: 231 | »Ø¸´: 1 | ||
yangliguo007ľ³æ (ÖøÃûдÊÖ)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð»¡£ ÒÑÓÐ1È˲ÎÓë
|
| 28.1,34.1,45.2,56.9,57.0,74.2,102.6,103.4,109.5,120.7,133.4,133.7,134.7,135.6,139.7,148.7,148.9,178.4 |
» ²ÂÄãϲ»¶
294Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
324Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
Ò»Ö¾Ô¸ÉϺ£´óѧÉúÎïѧ346
ÒѾÓÐ3È˻ظ´
322Çóµ÷¼Á£ºÒ»Ö¾Ô¸ºþÄÏ´óѧ ²ÄÁÏÓ뻯¹¤£¨085600£©£¬ÒѹýÁù¼¶¡£
ÒѾÓÐ16È˻ظ´
µ÷¼Á
ÒѾÓÐ10È˻ظ´
283Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
0703µ÷¼Á
ÒѾÓÐ6È˻ظ´
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ6È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬ÀàËÆéÎÆ¤ËصĶà¶à¸ø
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý4¸ö
ÒѾÓÐ6È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
Çó´óϺ²é΢Æ×£¬Íò·Ö¸Ðл°¡£¡£¡£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻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 ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yangliguo007: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ллÄú£¬ÐÁ¿àÁË¡£ 2014-12-22 11:11:13
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yangliguo007: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ллÄú£¬ÐÁ¿àÁË¡£ 2014-12-22 11:11:13
|
²éѯ½á¹û£º¹²²éµ½42¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Aurein B C22H26O6 ÏàËÆ¶È:57.8% Phytochemistry 1992 31 360-361 Neolignans from Licaria aurea Marcia Ortiz M. Marques, Massayoshi Yoshida, Otto R. Gottlieb, Jose¡äG.S. Maia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 3-Methoxy-6-(1-(3,4,5-trimethoxyphenyl)-1H-1,2,3-triazol-5-yl)benzene-1,2-diamine C18H21N5O4 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2012 20 234-242 Synthesis, biological evaluation and molecular modeling of 1,2,3-triazole analogs of combretastatin A-1 Øyvind W. Akselsen, Kristin Odlo, Jing-Jy Cheng, Giorgio Maccari, Maurizio Botta,Trond Vidar Hansen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . justiciresinol C21H26O7 ÏàËÆ¶È:55.5% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 61-63 Chemical Constituents of Ethyl Acetate Extract Part of Stelmatocrypton khasianum MO Xiao-yu, MAI Jing-biao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 4',5'-¶þÈ¥¼×»ù¹í¾Ê¶¾ËØ£¨4',5'-didemethylpodophyllotoxin) C20H18O8 ÏàËÆ¶È:55% Chinese Traditional and Herbal Drugs 2011 42(4) 634-639 Chemical constituents from Dysosma versipellis JIANG Fei, TIAN Hai-yan, ZHANG Jian-long, YE Qing-mei, JIANG Ren-wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 6,7-dimethoxy-2-(3-(3,4,5-trimethoxyphenyl)-2-propenylidene)-1-tetralone C24H26O6 ÏàËÆ¶È:52.6% Bioorganic & Medicinal Chemistry 2014 22 2311-2319 Synthesis, biological evaluation and 3D-QSAR studies of new chalcone derivatives as inhibitors of human P-glycoprotein Zahida Parveen, Gerda Brunhofer, Ishrat Jabeen, Thomas Erker, Peter Chiba, Gerhard F. Ecker Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . kurryam C20H21NO4 ÏàËÆ¶È:52.6% Natural Product Communications 2008 3 1679-1682 A New Carbazole Alkaloid from Murraya koenigii Spreng(Rutaceae) Suvra Mandal, Anupam Nayak,Samir K. Banerjee, Julie Banerji and Avijit Banerji Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 1-(4'-hydroxy-3'-methoxyphenyl)-2-[4''-(3-hydroxypropyl)-2'',6''-dimethoxyphenoxy] propane-1,3-diol ÏàËÆ¶È:52.6% Chinese Traditional and Herbal Drugs 2012 43 1057-1060 Chemical constituents of Acanthopanax senticosus and their free radical scavenging activities ZHANG Tao; PIAO Jun-hong; YUAN Lei; LI Xi-feng; Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-peltatin C22H22O8 ÏàËÆ¶È:52.3% Acta Botanica Yunnanica 1989 11 479-481 CHEMICAL COMPONENTS OF DYSOSMA VEITCHII Jiang Zihua, Chen Siying Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . burseneolignan C22H30O9 ÏàËÆ¶È:50% Phytochemistry 2005 66 2745-2751 Bioactive constituents from roots of Bursera tonkinensis Aranya Jutiviboonsuk, Hongjie Zhang, Ghee Teng Tan, Cuiying Ma,Nguyen Van Hung, Nguyen Manh Cuong, Nuntavan Bunyapraphatsara,D. Doel Soejarto, Harry H.S. Fong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 6-epi-gomisin C22H24O7 ÏàËÆ¶È:50% Journal of Natural Products 2006 69 963-966 C 18 Dibenzocyclooctadiene Lignans from Kadsura philippinensis Ya-Ching Shen, Chia-Ching Liaw, Yuan-Bin Cheng, Atallah F. Ahmed, Mei-Chou Lai, Shorong-Shii Liou, Tian-Shung Wu, Yao-Haur Kuo, and Yu-Chi Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 5-allohydroxymatairesinol dimethyl ether ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1980 28 850-860 Introduction of an Alcoholic Hydroxyl Group into 2, 3-Dibenzylbutyrolactone Lignans with Oxidizing Agents and Carbon-13 Nuclear Magnetic Resonance Spectra of the Oxidation Products SANSEI NISHIBE,MARIKO CHIBA,AKIYO SAKUSHIMA,SUEO HISADA,SAKAE YAMANOUCHI,MICHIO TAKIDO,USHIO SANKAWA and AKIRA SAKAKIBARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (Z)-3(4-Bromobenzyl)-5-(3-nitrobenzylidene)furan-2(5H)-one C18H12BrNO4 ÏàËÆ¶È:50% Molecules 2007 12 1101-1116 Synthesis and Cytotoxic Activity of Some 3-Benzyl-5-Arylidenefuran-2(5H)-ones R¨®bson R. Teixeira, Luiz C. Barbosa, C¨¦lia R. Maltha, Marcelo E. Rocha, Daniel P. Bezerra, Let¨ªcia V. Costa-Lotuf, Cl¨¢udia Pessoa and Manoel O. Moraes Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 3-(3,4-dimethoxy-benzyl)-4-(7-methoxy-benzo[1,3]dioxol-5-ylmethyl)-dihydrofuran-2-one C22H24O7 ÏàËÆ¶È:50% Journal of Asian Natural Products Research 2009 11 562-568 Two new lignans from Phyllanthus amarus Manju Singh, Neerja Tiwari, Karuna Shanker, Ram Kishore Verma, Anil Kumar Gupta and Madan Mohan Gupta Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . (16R)-16,17-dihydrouleine ÏàËÆ¶È:50% Journal of Natural Products 1983 Vol 46 206-210 Studies on the Uleine Alkaloids. II. Some Chemical Transformations of Uleine Robert P. Borris, David C. Lankin, Geoffrey A. Cordell Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 3-Methoxy-6-(1-(3,4,5-trimethoxyphenyl)-1H-1,2,3-triazol-4-yl)benzene-1,2-diamine C18H21N5O4 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2012 20 234-242 Synthesis, biological evaluation and molecular modeling of 1,2,3-triazole analogs of combretastatin A-1 Øyvind W. Akselsen, Kristin Odlo, Jing-Jy Cheng, Giorgio Maccari, Maurizio Botta,Trond Vidar Hansen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 3-Methoxy-6-(1-(3,4,5-trimethoxyphenyl)-1H-1,2,3-triazol-5-yl)benzene-1,2-diol C18H19N3O6 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2012 20 234-242 Synthesis, biological evaluation and molecular modeling of 1,2,3-triazole analogs of combretastatin A-1 Øyvind W. Akselsen, Kristin Odlo, Jing-Jy Cheng, Giorgio Maccari, Maurizio Botta,Trond Vidar Hansen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . pachycanthine C20H19NO4 ÏàËÆ¶È:50% Indian Journal of Chemistry Section B 2008 47B 945-951 Pachycanthine: A new isoquinoline alkaloid and its antihepatotoxic activity from Berberis pachycantha Koehne Ahmed,Bahar; Masoodi,Mubashir H; Khan,Shamshir Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 4-Phenyl-5-[2-(3,4-methylenedioxyphenyl)-ethyl]-1,3,4-thiadiazolium-2-phenylamine chloride C23H20N3SO2Cl ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2008 16 2984-2991 Novel 1,3,4-thiadiazolium-2-phenylamine chlorides derived from natural piperine as trypanocidal agents: Chemical and biological studies Welisson da Silva Ferreira, Leonardo Freire-de-Lima, V¨ªctor Barbosa Saraiva, Frederico Alisson-Silva, Lucia Mendonça-Previato, Jos¨¦ Osvaldo Previato, Aurea Echevarria, Marco Edilson Freire de Lima Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-12-22 10:50:30














»Ø¸´´ËÂ¥