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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´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 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½451¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 4',6,7-trihydroxy-isoflavone ÏàËÆ¶È:100% Canadian Journal of Chemistry 1980 58 1211-1219 Carbon-13 chemical shift assignments of chromones and isoflavones Hem Chandra Jha, Fritz Zilliken, Eberhard Breitmaier Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 4',6,7-trihydroxy-isoflavone ÏàËÆ¶È:100% Magnetic Resonance in Chemistry 1986 24 225-230 Carbon-13 nuclear magnetic resonance spectra of isoflavones M. Sree Rama Murthy, E. Venkata Rao and R. S. Ward Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 4',6-dihydroxy-7-methoxy-isoflavone ÏàËÆ¶È:87.5% Canadian Journal of Chemistry 1980 58 1211-1219 Carbon-13 chemical shift assignments of chromones and isoflavones Hem Chandra Jha, Fritz Zilliken, Eberhard Breitmaier Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 6,4'-dihydroxy-7-methoxy-isoflavone ÏàËÆ¶È:87.5% Magnetic Resonance in Chemistry 1986 24 225-230 Carbon-13 nuclear magnetic resonance spectra of isoflavones M. Sree Rama Murthy, E. Venkata Rao and R. S. Ward Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 6,7,4,-trihydroxyisoflavone ÏàËÆ¶È:86.6% Bioorganic & Medicinal Chemistry Letters 2008 18 5006-5009 ortho-Dihydroxyisoflavone derivatives from aged Doenjang (Korean fermented soypaste) and its radical scavenging activity Jun-Seong Park, Hye Yoon Park, Dong Hyun Kim, Duck Hee Kim, Han Kon Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 6,7,4'-trihydroxyisoflavone ÏàËÆ¶È:86.6% Bioorganic & Medicinal Chemistry Letters 2010 20 1162-1164 Natural ortho-dihydroxyisoflavone derivatives from aged Korean fermented soybean paste as potent tyrosinase and melanin formation inhibitors Jun-Seong Park, Dong Hyun Kim, Jae Kyoung Lee, Jin Young Lee, Duck Hee Kim, Han Kon Kim, Hak-Ju Lee, Ho Cheol Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 6,7-dihydroxy-4'-isopropyloxy-isoflavone ÏàËÆ¶È:82.3% Canadian Journal of Chemistry 1980 58 1211-1219 Carbon-13 chemical shift assignments of chromones and isoflavones Hem Chandra Jha, Fritz Zilliken, Eberhard Breitmaier Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . glycitrin ÏàËÆ¶È:81.2% China Journal of Chinese Materia Medica 2003 28 43-47 Isolation and Elucidation of Chemical Constituents with Antiviral Action from Yinqiaosan on Influenza Virus SHI Yue, SHI Renbing, LIU Bin, LU Yunru, DU Lijun Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 4',7-dihydroxy-6-methoxy-isoflavone ÏàËÆ¶È:81.2% Canadian Journal of Chemistry 1980 58 1211-1219 Carbon-13 chemical shift assignments of chromones and isoflavones Hem Chandra Jha, Fritz Zilliken, Eberhard Breitmaier Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 6-methoxy-7,4'-dihydroxy-isoflavone ÏàËÆ¶È:81.2% Magnetic Resonance in Chemistry 1986 24 225-230 Carbon-13 nuclear magnetic resonance spectra of isoflavones M. Sree Rama Murthy, E. Venkata Rao and R. S. Ward Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 4',6-dihydroxy-7-methoxyisoflavone C16H12O5 ÏàËÆ¶È:80% Chemical & Pharmaceutical Bulletin 2009 57 346-360 Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities Hideyuki Goto, Yoshiyasu Terao and Shuji Akai Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-07-08 10:36:24
wangkaibo123
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´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 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½459¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . glycitein 7-O-¦Â-(6''-O-succinyl)-D-glucoside C26H26O13 ÏàËÆ¶È:83.3% Biological and Pharmaceutical Bulletin 1999 22 1193-1201 New 6-O-Acyl Isoflavone Glycosides from Soybeans Fermented with Bacillus subtilis (natto). I. 6-O-Succinylated Isoflavone Glycosides and Their Preventive Effects on Bone Loss in Ovariectomized Rats Fed a Calcium-Deficient Diet Toshiya TODA, Takehiko UESUGI, Kuniaki HIRAI, Haruo NUKAYA, Kuniro TSUJI, Hitoshi ISHIDA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 4',6,7-trihydroxyisoflavone-6-methylether-7-O-¦Â-D-xylopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside ÏàËÆ¶È:76% Phytochemistry 1999 51 147-151 Isoflavone glycosides from the flowers of Pueraria thunbergiana Hee-Juhn Park, Jong-Hee Park, Jeon-Ok Moon, Kyung-Tae Lee, Won-Tae Jung, Sei-Ryang Ohe, Hyeong-Kyu Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 6''-O-malonyldaidzin C24H22O12 ÏàËÆ¶È:75% Phytochemistry 1997 46 921-928 Phenolic glucosides from the root of Pueraria lobata Kazuhiro Hirakura, Makoto Morita, Kaoru Nakajima, Koh Sugama, Koji Takagi, Kazuaki Niitsu, Yukinobu Ikeya, Masao Maruno, Minoru Okada Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 6''-O-acetylononin ÏàËÆ¶È:75% Phytochemistry 1989 28 161-164 Resorcinol derivatives and other components of Ononis speciosa Alejandro F. Barrero,Juan F. Sanchez,Antonio Barr¨®n,Fernando Corrales,Ignacio Rodriguez Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 6''-O-acetylononin ÏàËÆ¶È:75% Natural Product Research and Development 2002 14(6) 14-17 CHEMICAL CONSTITUENTS OF HUANGQI INJECTION DOU Hui; FU Tie-jun; ZHANG Fan; LIU Zhong-rong; DING Li-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . glycitin C42H22O10 ÏàËÆ¶È:75% European Journal of Organic Chemistry 2008 2008 5622-5629 An Efficient Method for the Glycosylation of Isoflavones Nawaf Al-Maharik and Nigel P. Botting Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . glycitein 7-O-glucuronide ÏàËÆ¶È:75% Natural Medicines 2004 58 71-75 Soy Isoflavone Metabolites Isolated from Human Urine TSUCHIHASHI Ryota,OKAWA Masafumi, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 6''-O-ÒÒõ£»ùâ±ú»¨ÜÕ ÏàËÆ¶È:75% China Journal of Chinese Materia Medica 2012 37 3243-3248 Isoflavonoids from roots of Astragalus membranaceus var. mongholicus ZHANG Ya-zhou; XU Feng; LIANG Jing; TANG Jing-shu; SHANG Ming-ying; WANG Xuan; CAI Shao-qing Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Glycitin ÏàËÆ¶È:75% Chemistry of Natural Compounds 2013 48 966-969 A new isoflavone derivative from Streptomyces sp. YIM GS3536 Rong Huang, Zhang-Gui Ding, Yun-Feng Long Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 6''-O-acetyl daidzin C23H22O10 ÏàËÆ¶È:75% Journal of Chinese Medicinal Materials 2008 31 1172-1174 µ¶¹ôùÖеĻ¯Ñ§³É·Ö ԬɺÇÙ, ÓÚÄܽ, ÕÔÒãÃñ, Ðì±ó Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 6''-O-acetylononin C24H24O10 ÏàËÆ¶È:70.8% Chemistry of Natural Compounds 2008 44 31-34 LOW-MOLECULAR-WEIGHT PHENOLIC COMPOUNDS FROM Hedysarum theinum ROOTS I. V. Nechepurenko, M. P. Polovinka, N. I. Komarova, D. V. Korchagina, N. F. Salakhutdinov,and S. B. Nechepurenko Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 4',6-Dimethoxyisoflavone-7-O-¦Â-D-glucopyranoside ÏàËÆ¶È:70.8% Chemistry of Natural Compounds 2006 42 415-418 ISOFLAVONE GLYCOSIDES FROM THE BARK OF Amorpha fruticosa Hyun-Jung Lee, Oh-Kyu Lee, Yeong-Han Kwon,Don-Ha Choi, Ha-Young Kang, Hyeon-Yong Lee,Ki-Hyon Paik,and Hak-Ju Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 7-hydroxy-4',6-dimethoxyisoflavone-7-O- ¦Â-D-apiofuranosyl-(1¡ú6)-¦Â-D-glucopyranoside ÏàËÆ¶È:70.8% Acta Pharmaceutica Sinica 2009 Vol 44 63-68 Isoflavone glycosides from the bark of Maackia amurensis LI Xiong; LI Jian-fang; WANG Dong; WANG Wei-ning; CUI Zheng Structure 13C NMR ̼Æ×Ä£Äâͼ |

4Â¥2014-07-08 13:06:15














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