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103.20,108.54,115.35,115.36,117.04,123.17,123.38,130.52,130.53,145.09,151.30,152.69,152.83,157.49,174.86

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21.06,56.30,63.79,70.20,73.41,74.27,76.99,99.82,103.97,105.26,115.44,115.45,118.37,123.02,123.62,130.52,130.53,147.86,151.59,151.69,153.55,157.65,170.69,174.85
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wangkaibo123

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zky_panmeng: ½ð±Ò+10 2014-07-08 11:24:21
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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
2Â¥2014-07-08 10:36:24
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

zky_panmeng

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2Â¥: Originally posted by wangkaibo123 at 2014-07-08 10:36:24
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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

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21.06,56.30,63.79,70.20,73.41,74.27,76.99,99.82,103.97,105.26,115.44,115.45,118.37,123.02,123.62,130.52,130.53,147.86,151.59,151.69,153.55,157.65,170.69,174.85
3Â¥2014-07-08 11:24:15
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

wangkaibo123

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kerry

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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
4Â¥2014-07-08 13:06:15
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