| ²é¿´: 351 | »Ø¸´: 1 | ||
zyh256389½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú2 ÒÑÓÐ1È˲ÎÓë
|
| ÈܼÁÊÇDMSO 25.2,55.9,63.2,73.2,74.9,99.7,107.9,109.7,147.8,164.2,166.0,202.2 |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸»ªÄÏʦ·¶´óѧ0702ÎïÀíѧ305µ÷¼Á
ÒѾÓÐ5È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ30È˻ظ´
266Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
297Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ4È˻ظ´
288Çóµ÷¼Á£¬Ò»Ö¾Ô¸»ªÄÏÀí¹¤´óѧ071005
ÒѾÓÐ3È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
µ÷¼Á
ÒѾÓÐ18È˻ظ´
293µ÷¼Á
ÒѾÓÐ4È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´

mrdone.0907
½ð³æ (ÕýʽдÊÖ)
- PhEPI: 1
- Ó¦Öú: 21 (СѧÉú)
- ½ð±Ò: 817.5
- É¢½ð: 104
- ºì»¨: 16
- Ìû×Ó: 556
- ÔÚÏß: 161.4Сʱ
- ³æºÅ: 868670
- ×¢²á: 2009-10-11
- ÐÔ±ð: GG
- רҵ: º£ÑóÒ©Îï
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zyh256389(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+10 2015-05-21 15:16:46
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zyh256389(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+10 2015-05-21 15:16:46
|
1 . 3,4-Dihydro-3-(2(¦Î)-hydroxypropyl)-3(¦Î),6,8-trihydroxy-1(2H)-naphthalenone C13H16O5 ÏàËÆ¶È:69.2% Phytochemistry Letters 2009 2 207-210 Dihydronaphthalenones from the endophytic fungus Botryosphaeria sp. BCC 8200 Masahiko Isaka, Arunrat Yangchum, Pranee Rachtawee, Punsa Khoyaiklang, Nattawut Boonyuen, Saisamorn Lumyong Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3,4-Dihydro-3-(2(¦Î)-hydroxypropyl)-3(¦Î),6,8-trihydroxy-1(2H)-naphthalenone C13H16O5 ÏàËÆ¶È:69.2% Phytochemistry Letters 2009 2 207-210 Dihydronaphthalenones from the endophytic fungus Botryosphaeria sp. BCC 8200 Masahiko Isaka, Arunrat Yangchum, Pranee Rachtawee, Punsa Khoyaiklang, Nattawut Boonyuen, Saisamorn Lumyong Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (3S,4S)-3,4,8-trihydroxy-6-methoxy-3,4-dihydro-1(2H)-naphthalenone C11H12O5 ÏàËÆ¶È:58.3% Planta Medica 2008 74 281-286 Antimycobacterial Substances from Phaeosphaeria sp BCC8292 Pattama Pittayakhajonwut, Pairoh Sohsomboon, Aibrohim Dramae, Rapheephat Suvannakad, Sanisa Lapanun, Morakot Tantichareon Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . balticol C C12H14O6 ÏàËÆ¶È:58.3% Chemistry & Biodiversity 2009 6 127-137 Balticols A¨CF, New Naphthalenone Derivatives with Antiviral Activity, from an Ascomycetous Fungus Muftah A. M. Shushni, Renate Mentel, Ulrike Lindequist, and Rolf Jansen Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Paeonol ÏàËÆ¶È:58.3% Archives of Pharmacal Research 2005 28 775-783 Antioxidative constituents from Paeonia lactiflora Seung Chul Lee, Yong Soo Kwon, Kyung Hun Son, Hyun Pyo Kim and Moon Young Heo Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . µ¤Æ¤·Ó ÏàËÆ¶È:58.3% Journal of Shenyang Pharmaceutical University 2009 26 191-194 Antibacterial constituents of extracts of the aerial parts of D iscocleidion rufescens TIAN Ye, TANG Hai-feng, QIU Feng, WANG Xiao-juan, XUE Gai-jin, LI Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 8 ÏàËÆ¶È:58.3% Bulletin of the Chemical Society of Japan 1983 56 542-544 Chemical Studies on the Mistletoe. V. The Structure of Taxillusin, a New Flavonoid Glycoside Isolated from Taxillus kaempferi Atsushi Sakurai, Yasuaki Okumura Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . paeonol ÏàËÆ¶È:58.3% Journal of Integrative Plant Biology 2005 47 892-896 Components of Stem Barks of Winchia calophylla A. DC. and Their Bronchodilator Activities Wei-Ming ZHU, Hong-Ping HE, Li-Ming FAN, Yue-Mao SHEN, Jun ZHOU and Xiao-Jiang HAO* Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . paeonol ÏàËÆ¶È:58.3% Journal of Chinese Medicinal Materials 2013 36 567-569 Study on the Chemical Constituent from the Dichloromethane Extract of the Pine Needle of Cedrus deodara( ¢ò) BAI Chao-hui, SHI Xiao-feng, LIU Dong-yan, LI Shuang Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3,4-dihydro-4,8-dihydroxy-7-(2-hydroxy-ethyl)-6-methoxy-1(2H)-naphthalen-1-one C13H16O5 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry Letters 2010 20 3326-3328 The metabolites of mangrove endophytic fungus Zh6-B1 from the South China Sea Kai-Kai Li, Yong-Jun Lu, Xiao-Hong Song, Zhi-Gang She, Xi-Wei Wu, Lin-Kun An, Chuang-Xing Ye, Yong-Cheng Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3a,9a-deoxy-3a-hydroxy-1-dehydroxyarthrinone C13H14O6 ÏàËÆ¶È:53.8% Canadian Journal of Chemistry 1997 75 768-772 New antifungal metabolites from the coprophilous fungus Cercophorasordarioides Authrine C. Whyte, Katherine B. Gloer, James B. Gloer, Brenda Koster, David Malloch Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . paeonol ÏàËÆ¶È:50% Journal of Natural Products 1999 62 1142-1144 Metabolism of Paeonol in Rats Takaaki Yasuda, Rinko Kon, Takahiro Nakazawa, and Keisuke Ohsawa Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . balticol E C14H18O6 ÏàËÆ¶È:50% Chemistry & Biodiversity 2009 6 127-137 Balticols A¨CF, New Naphthalenone Derivatives with Antiviral Activity, from an Ascomycetous Fungus Muftah A. M. Shushni, Renate Mentel, Ulrike Lindequist, and Rolf Jansen Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . paeonol C9H10O3 ÏàËÆ¶È:50% Acta Botanica Sinica 2003 45 1003-1007 Two New Triterpenes from Neonauclea sessilifolia KANG Wen-Yi, LI Guo-Hong, HAO Xiao-Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . epi-radicinol epoxide C12H14O6 ÏàËÆ¶È:50% Phytochemistry 1997 45 41-45 Phytotoxins and related metabolites produced by Bipolaris coicis, the pathogen of job's tears Hiromitsu Nakajima, Tatsuaki Ishida, Yuzuru Otsuka, Takashi Hamasaki, Masakatsu Ichinoe |

2Â¥2015-05-21 10:53:08














»Ø¸´´ËÂ¥