| ²é¿´: 195 | »Ø¸´: 1 | ||
swaucq½ð³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹
|
| 6.53,8.37,11.75,17.20,23.53,78.05,102.15,108.93,110.85,115.48,116.00,120.07,137.01,140.05,150.64,158.02,160.96,163.74,169.99 |
» 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×ÇóÖú3¸ö»¯ºÏÎï
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇëÎÊÈçºÎ¸ù¾ÝÇâÆ×̼Æ×Êý¾ÝÍÆ²â»¯ºÏÎï½á¹¹
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÍÆ¼ö¹ØÓÚ»¯ºÏÎï½á¹¹Óë»îÐÔ¹ØÏµµÄÆÚ¿¯
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
¼±Çó΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
¡¾·ÖÏí¡¿Ãâ·ÑµÄ20¸öÆ×ͼÊý¾Ý¿â
ÒѾÓÐ13È˻ظ´

yangliguo007
ľ³æ (ÖøÃûдÊÖ)
- PhEPI: 1
- Ó¦Öú: 184 (¸ßÖÐÉú)
- ½ð±Ò: 4828
- É¢½ð: 36
- ºì»¨: 12
- Ìû×Ó: 1328
- ÔÚÏß: 741.5Сʱ
- ³æºÅ: 874624
- ×¢²á: 2009-10-16
- ÐÔ±ð: GG
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
²éѯ½á¹û£º¹²²éµ½10¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . Hypotrachynic acid C18H16O7 ÏàËÆ¶È:52.6% Molecules 2007 12 997-1005 ¦Â-Orcinol Metabolites from the Lichen Hypotrachyna revoluta Panagiota Papadopoulou, Olga Tzakou, Constantinos Vagias, Panagiotis Kefalas and Vassilios Roussis Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 3-formyl-2,4-dihydroxy-6-methylbenzoic acid 3-hydroxy-4-(methoxycarbonyl)-2,5-di-methylphenyl ether ÏàËÆ¶È:52.6% Fitoterapia 2001 72 565-567 Antifungal constituent from Gordonia dassanayakei P.S. Athukoralage, H.M.T.B. Herath,S.A. Deraniyagala, R.L.C ijesundera,P.A. Weerasinghe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . cladonioidesin ÏàËÆ¶È:52.6% Fitoterapia 2001 72 832-833 Constituents from Lethariella cladonioides Bei Jiang, Qin-Shi Zhao, Hui Yang, Ai-Jun Hou,Zhong-Wen Lin, Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 3-hydroxy-2,4,5-trimethylphenyl 2,4-dihydroxy-3,6-dimethylbenzoate C18H20O5 ÏàËÆ¶È:52.6% Helvetica Chimica Acta 2011 94 1077-1084 Antimicrobial Depsides Produced by Cladosporium uredinicola, an Endophytic Fungus Isolated from Psidium guajava Fruits L¨ªvia Soman de Medeiros, Michael Murgu, Antônia Q. L. de Souza, and Edson Rodrigues-Fo. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . atranorin ÏàËÆ¶È:52.6% Phytochemical Analysis 1999 10 279-284 1H and 13C-NMR and biological activity investigations of four lichen-derived compounds Gabriele M. König and Anthony D. Wright Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . atranorin ÏàËÆ¶È:52.6% Chemical & Pharmaceutical Bulletin 2013 69 176-183 Cytotoxic Evaluation of Phenolic Compounds from Lichens against Melanoma Cells Luiz Fabr¨ªcio Gardini Brandão, Glaucia Braz Alcantara, Maria de F¨¢tima Cepa Matos, Danielle Bogo, Deisy dos Santos Freitas, Nath¨¢lia Mitsuko Oyama, Neli Kika Honda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . atranorin ÏàËÆ¶È:52.6% Journal of Chemical Ecology 2003 29 2049-2071 Identification and Quantitation of Allelochemicals from the Lichen Lethariella canariensis: Phytotoxicity and Antioxidative Activity F. J. Toledo Marante, A. Garc¨ªa Castellano, F. Est¨¦vez Rosas, J. Quintana Aguiar, J. Bermejo Barrera Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . pseudocalanolide C C22H26O5 ÏàËÆ¶È:50% Journal of Natural Products 1995 Vol 58 916-920 The Pseudocalanolides: Structure Revision of Calanolides C and D Tawnya C. McKee, John H. Cardellina II, Geoffrey B. Dreyer, Michael R. Boyd Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 3-[2'-(5'-hydroxymethyl)furyl]-1(2H)-isoquinolinone-7-O-¦Â-D-glucosdie C20H21NO9 ÏàËÆ¶È:50% Acta Pharmaceutica Sinica 2006 Vol 41 1193-1196 Chemical constituents from water extract of Radix isatidis HE Li-wei; LI Xiang; CHEN Jian-wei; SUN Dong-dong; J¦a Wen-zheng; WANG Kang-cai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . calanolide C C22H26O5 ÏàËÆ¶È:50% Journal of Medicinal Chemistry 1992 35 2735-2743 HIV inhibitory natural products. Part 7. The calanolides, a novel HIV-inhibitory class of coumarin derivatives from the tropical rainforest tree, Calophyllum lanigerum Yoel Kashman, Kirk R. Gustafson, Richard W. Fuller, John H. Cardellina II, James B. McMahon, Michael J. Currens, Robert W. Buckheit Jr., Stephen H. Hughes, Gordon M. Cragg, Michael R. Boyd Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-09-21 16:01:24














»Ø¸´´ËÂ¥