| ²é¿´: 273 | »Ø¸´: 1 | |||
liangtingmei½ð³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú,лл ÒÑÓÐ1È˲ÎÓë
|
|
ÈܼÁ CD3COCD3 55.22,59.74,103.34,114.36,115.09,115.84,118.18,120.38,122.70,125.70,130.32,132.61,143.73,144.02,144.51,144.69,153.56 |
» ²ÂÄãϲ»¶
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð»~~
ÒѾÓÐ3È˻ظ´
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
Çó΢Æ×°ïæ,лл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý4¸ö
ÒѾÓÐ6È˻ظ´
΢Æ×ÇóÖú3¸ö»¯ºÏÎï
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾ÝÇóÖúлл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
·çÐÐÕß007
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1309 (½²Ê¦)
- ½ð±Ò: 12672.8
- ºì»¨: 15
- Ìû×Ó: 1490
- ÔÚÏß: 299.5Сʱ
- ³æºÅ: 2542465
- ×¢²á: 2013-07-12
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
liangtingmei: ½ð±Ò+10 2015-06-01 18:53:20
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
liangtingmei: ½ð±Ò+10 2015-06-01 18:53:20
|
²éѯ½á¹û£º¹²²éµ½39¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Neotaiwanensol B C18H18O4 ÏàËÆ¶È:61.1% Phytochemistry 2013 93 203-209 Neolignans and phenylpropanoids from the roots of Piper taiwanense and their antiplatelet and antitubercular activities Si Chen, Hung-Yi Huang, Ming-Jen Cheng, Chin-Chung Wu, Tsutomu Ishikawa, Chien-Fang Peng, Hsun-Shou Chang, Chyi-Jia Wang, Su-Ling Wong, Ih-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 6-(2,3-dibromo-4,5-dihydroxybenzyl)-2,3-dibromo-4,5-dihydroxy benzyl methyl ether C15H14Br2O6 ÏàËÆ¶È:58.8% Journal of Natural Products 2004 67 1661-1666 Dibenzyl Bromophenols with Diverse Dimerization Patterns from the Brown Alga Leathesia nana Xiuli Xu, Fuhang Song, Sujuan Wang, Shuai Li, Fan Xiao, Jielu Zhao, Yongchun Yang, Suqing Shang, L Yang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . rooperol ÏàËÆ¶È:58.8% Phytochemistry 1989 28 153-156 Structure determination of a phenolic pent-1-en-4-yne derivative from Hypoxis rooperi Siegfried E. Drewes,Ursula J. Scogings,George L. Wenteler Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . isomelacacidin ÏàËÆ¶È:58.8% Phytochemistry 1986 25 1961-1965 Diastereoisomeric leucoanthocyanidins from the heartwood of acacia melanoxylon Lai Yeap Foo, Herbert Wong Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 5 C17H14O4 ÏàËÆ¶È:58.8% Tetrahedron 1982 38 1683-1687 Research on African medicinal plants¡ªII: Hypoxoside, a new glycoside of uncommon structure from hypoxis obtusa busch G.B.Marini Bettolo, M. Patamia, M. Nicoletti, C. Galeffi, I. Messana Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . variegatic acid C18H12O9 ÏàËÆ¶È:55.5% Bioscience, Biotechnology, and Biochemistry 2009 73 855-860 In Vitro Inhibitory Effects of Pulvinic Acid Derivatives Isolated from Chinese Edible Mushrooms, Boletus calopus and Suillus bovinus, on Cytochrome P450 Activity Yu-Ting HUANG, Jun-ichi ONOSE, Naoki ABE and Kunie YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . xerocomic acid C18H12O8 ÏàËÆ¶È:55.5% Bioscience, Biotechnology, and Biochemistry 2009 73 855-860 In Vitro Inhibitory Effects of Pulvinic Acid Derivatives Isolated from Chinese Edible Mushrooms, Boletus calopus and Suillus bovinus, on Cytochrome P450 Activity Yu-Ting HUANG, Jun-ichi ONOSE, Naoki ABE and Kunie YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . terphenyllin ÏàËÆ¶È:55% Natural Product Communications 2012 7 1057-1062 Two New p-Terphenyl Derivatives from the Marine Fungal Strain Aspergillus sp. AF119 Shao-Song Liu, Bao-Bing Zhao, Chun-Hua Lu, Jing-Jing Huang and Yue-Mao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 2-(3-bromo-5-hydroxy-4-methoxyphenyl)-3-(2,3-dibromo-4,5-dihydroxyphenyl)propionic acid methyl ester ÏàËÆ¶È:52.9% Journal of Natural Products 2004 67 1032-1035 Bromophenol Derivatives from the Red Alga Rhodomela confervoides Jielu Zhao, Xiao Fan, Sujuan Wang, Shuai Li, Suqin Shang, Yongchun Yang, Nianjun Xu, Yang L, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 4'-methoxy-2'',3',3''-tribromo-4'',5',5''-trihydroxydiphenylacetic acid C15H11O6Br3 ÏàËÆ¶È:52.9% Journal of Natural Products 2004 67 1032-1035 Bromophenol Derivatives from the Red Alga Rhodomela confervoides Jielu Zhao, Xiao Fan, Sujuan Wang, Shuai Li, Suqin Shang, Yongchun Yang, Nianjun Xu, Yang L, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 6-(2,3,6-tribromo-4,5-dihydroxybenzyl)-2,5-dibromo-3,4-dihydroxybenzyl methyl ether C15H11Br5O5 ÏàËÆ¶È:52.9% Journal of Natural Products 2007 70 1210-1213 Highly Brominated Mono- and Bis-phenols from the Marine Red Alga Symphyocladia latiuscula with Radical-Scavenging Activity Xiao-Juan Duan,Xiao-Ming Li,and Bin-Gui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3,6-dihydroxy-5-methoxy-7-phenyl-3H-benzo[de]isochromene-1-one C19H12O5 ÏàËÆ¶È:52.9% Journal of Natural Products 2002 65 1122-1130 Phenylphenalenone-Related Compounds: Chemotaxonomic Markers of the Haemodoraceae from Xiphidium caeruleum Stefan Opitz, Dirk Hölscher, Neil J. Oldham, Stefan Bartram, and Bernd Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 4-methoxy-9,10-dihydrophenanthrene-2,3,6,7-tetrol C15H14O5 ÏàËÆ¶È:52.9% Phytochemistry 1999 50 1237-1241 Phenanthrene and other aromatic constituents of Bulbophyllum vaginatum Yuan-Wah Leong¦Á,Leslie J. Harrison¦Á, Andrew D. Powell Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 2,2',3-tribromo-3',4,4',5-tetrahydroxy-6'-hydroxymethyldiphenylmethane ÏàËÆ¶È:52.9% Chinese Journal of Marine Drugs 2003 22(2) 1-4,10 Studies on the chemical constituents of the marine alga Rhodomela confervoides XU Nian-jun, FAN Xiao, SHI Jian-gong Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 7,3',4'-Trihydroxy-3-benzyl-2H-chromene C16H14O4 ÏàËÆ¶È:52.9% Journal of Natural Medicines 2008 62 325-327 A new homoisoflavan from Caesalpinia sappan Huanxin Zhao, Hong Bai, Yuanshu Wang, Wei Li and Kazuo Koike Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 2,3,3'-tribromo-4,4',5,5'-tetrahydroxyl-1'-ethyloxymethyldiphenyl methane ÏàËÆ¶È:52.9% Chinese Traditional and Herbal Drugs 2007 38 652-655 Cytotoxic constituents from red alga Gymnogongrus flabelliformis YUAN Zhao-hui; HAN Li-jun; FAN Xiao; LI Shuai; SHI Da-yong; SUN Jie; YANG Yong-chun; SHI Jian-gong Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 3-bromo-4-(2,3-dibromo-4,5-dihydroxybenzyl)-5-methoxymethylpyrocatechol ÏàËÆ¶È:52.9% Chinese Traditional and Herbal Drugs 2006 37 1462-1465 Chemical constituents from Polysiphonia urceolata LIU Quan-wen; LI Gui-hua; LIU Ke; ZHANG Ting; FAN Xiao; GUO Hong-yan Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . rosmarinic acid ÏàËÆ¶È:52.9% Chinese Journal of Natural Medicines 2007 5 27-30 Water-Soluble Constituents of Clerodendranthus spicatus WANG Min; LIANG Jing-Yu; CHEN Xue-Ying Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 3,4,3',4'-tetrahydroxy-chalcone ÏàËÆ¶È:52.9% Food Chemistry 2011 126 241-248 Hydroxychalcones as potent antioxidants: Structure¨Cactivity relationship analysis and mechanism considerations Yi-Ping Qian, Ya-Jing Shang, Qing-Feng Teng, Jin Chang, Gui-Juan Fan, Xia Wei, Ran-Ran Li, Hong-Ping Li, Xiao-Jun Yao, Fang Dai, Bo Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . hypoxoside ÏàËÆ¶È:52.9% Food Chemistry 2007 101 1425-1437 Isolation, characterization and antioxidant capacity assessment of the bioactive compounds derived from Hypoxis rooperi corm extract (African potato) Olga Laporta, Laura P¨¦rez-Fons, Ricardo Mallavia, Nuria Caturla, Vicente Micol Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 3-amino-N'-[1-(2,5-dimethoxyphenyl)ethylidene)-5,6-dihydro-4H-cyclopenta-thiophene-2-carbohydrazide C18H21N3O3S ÏàËÆ¶È:52.9% Archives of Pharmacal Research 2012 35 965-973 Antitumor activity of novel pyridine, thiophene and thiazole derivatives Mostafa M. Ghorab and Mansour S. Al-Said Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-05-29 16:25:01













»Ø¸´´ËÂ¥
100