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[ÇóÖú] ΢Æ×ÇóÖú 30-H-8-F9 ÒÑÓÐ1È˲ÎÓë

in DMSO£º
16.07,28.58,42.54,59.88,61.04,61.17,61.31,61.38,65.08,67.61,69.96,70.18,70.21,70.27,71.83,73.49,73.68,75.46,76.45,76.53,76.78,77.09,77.12,77.53,77.56,78.83,79.57,82.93,86.97,95.96,97.05,100.07,100.73,101.68,103.74,104.84,107.75,116.7,128.67,132.14,148.74,158.09,163.09,163.41,165.81,197.5
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thanwen: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-19 14:37:37
²éѯ½á¹û£º¹²²éµ½146¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     Kaempferol-3-O-(2-O-sinapoyl)-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside-7-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:60.8%
Archives of Pharmacal Research          2009          32          1379-1384
Kaempferol glycosides with antioxidant activity from Brassica juncea
Hyun Ah Jung, Ju Jung Woo, Mee Jung Jung, Geum-Sook Hwang and Jae Sue Choi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     saxatilisin A
C46H62O30     ÏàËÆ¶È:60.8%
Phytochemistry          2013          88          85-91
Highly glycosylated flavonols with an O-linked branched pentasaccharide from Iberis saxatilis (Brassicaceae)
Thomas A.K. Prescott, Geoffrey C. Kite, Elaine A. Porter, Nigel C. Veitch
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     oligosaccharide 2
    ÏàËÆ¶È:59.5%
Carbohydrate Research          1995          266          103-113
Structure of simusan, a new acidic exopolysaccharide from Arthrobacter sp.
Soph'ya N. Senchenkova, Yuriy A. Knirel, Leonid M. Likhosherstov, Aleksander S. Shashkov, Vladimir N. Shibaev, Lyubov' A. Starukhina, Vladimir V. Deryabin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     Quercetin 3-O-[2G-(E)-Coumaroyl-3G-O-¦Â-D-glucosyl-3R-O-¦Â-D-glucosylrutinoside]
C48H56O28     ÏàËÆ¶È:58.6%
Chemical & Pharmaceutical Bulletin          2008          56          851-853
Structural Determination and DPPH Radical-Scavenging Activity of Two Acylated Flavonoid Tetraglycosides in Oolong Tea (Camellia sinensis)
Viola Szu-Yuan Lee, Chiy-Rong Chen, Yun-Wen Liao, Jason Tze-Cheng Tzen, Chi-I Chang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     peonidin 3-O-[6-O-(4-O-(4-O-trans-(¦Â-D-glucopyranosyl)-p-coumaroyl)-¦Á-L-rhamnopyranosyl)-¦Â-D-glucopyranoside]-5-O-[¦Â-D-glucopyranoside]
C49H59O27     ÏàËÆ¶È:57.4%
Heterocycles          2004          63          509-517
Acylated Peonidin 3-Rutinoside-5-glucosides from Commercial Petunia Cultivars with Pink Flowers
Fumi Tatsuzawa, Yukiko Toya, Hitoshi Watanabe, Yuji Hirayama, Koichi Shinoda, Ritsuko Hara, Hiroko Seki, and Toshio Ando*
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     28-(O-¦Â-D-galactopyranosyl-(1¡ú4)-O-[¦Â-D-glucopyranosyl-(1¡ú3)]-O-¦Â-D-xylopyranosyl-(1¡ú4)-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-{4-O-[(Z)-4-methoxycinnamoyl]}-¦Â-D-fucopyranosyl) ester
C75H112O36     ÏàËÆ¶È:56.5%
Helvetica Chimica Acta          2003          Vol. 86          2404
New Acylated Triterpene Saponins from Polygala arenaria
Anne-Claire Mitaine-Offer, Tomofumi Miyamoto, V¨¦ronique Laurens, Cl¨¦ment Delaude, and Marie-Aleth Lacaille-Dubois
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     3-O-(¦Â-D-glucopyranosyl)presenegenin 28-(O-¦Â-D-galactopyranosyl-(1¡ú4)-O-[¦Â-D-glucopyranosyl-(1 3)]-O-¦Â-D-xylopyranosyl-(1¡ú4)-O-¦Á-L-rhamnopyranosyl-(1 2)-{4-O-[(Z)-3,4-dimethoxycinnamoyl]}-¦Â-D-fucopyranosyl) ester
C76H114O37     ÏàËÆ¶È:56.5%
Helvetica Chimica Acta          2003          Vol. 86          2404
New Acylated Triterpene Saponins from Polygala arenaria
Anne-Claire Mitaine-Offer, Tomofumi Miyamoto, V¨¦ronique Laurens, Cl¨¦ment Delaude, and Marie-Aleth Lacaille-Dubois
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     (-)-(2R,3S)-1-{4-[¦Â-D-glucopyranosyl-(1¡ú3)-¦Â-D-glucopyranosyloxy]benzyl}-2-O-¦Â-D-glucopyranosyl-4-(4-¦Â-D-glucopyranosyloxybenzyl)- 2-isobutyltartrate
C46H66O28     ÏàËÆ¶È:56.5%
Journal of Natural Products          2008          71(5)          799-805
Glycosidic Constituents of the Tubers of Gymnadenia conopsea
Jiachen Zi, Shuai Li, Mingtao Liu, Maoluo Gan, Sheng Lin, Weixia Song, Yanling Zhang, Xiaona Fan, Yongchun Yang, Jianjun Zhang, Jiangong Shi, and Duolong Di
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     compound 1b
    ÏàËÆ¶È:56.5%
Chemical & Pharmaceutical Bulletin          1998          46          1891-1900
Studies on the Constituents of Clematis Species. VII. Triterpenoid Saponins from the Roots of Clematis terniflora DC. var. robusta TAMURA
Yukio KAWATA,Haruhisa KIZU and Tsuyoshi TOMIMORI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     compound 9a
    ÏàËÆ¶È:56.5%
Chemical & Pharmaceutical Bulletin          1998          46          1891-1900
Studies on the Constituents of Clematis Species. VII. Triterpenoid Saponins from the Roots of Clematis terniflora DC. var. robusta TAMURA
Yukio KAWATA,Haruhisa KIZU and Tsuyoshi TOMIMORI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     3¦Â-O-[¦Â-D-glucopyranosyl-(1¡ú3)-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Á-L-arabinopyranosyl]olean-12-ene-28-O-[¦Â-D-glucopyranosyl-(1¡ú3)-¦Á-L-rhamnopyranosyl (1¡ú4)-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranosyl]ester
C71H116O35     ÏàËÆ¶È:56.5%
Journal of Natural Products          2000          63          308-314
Antiproliferative Triterpene Saponins from Trevesia palmata
Nunziatina De Tommasi, Giuseppina Autore, Aurora Bellino, Aldo Pinto, Cosimo Pizza,Raffaella Sorrentino, and Pietro Venturella
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     kaempferol 3-O-[¦Â-D-glucopyranosyl-(1¡ú2)-{¦Â-D-glucopyranosyl-(1¡ú3)}-{¦Â-D-glucopyranosyl-(1¡ú4)}-¦Á-L-rhamnopyranoside]-7-O-[¦Á-L-rhamnopyranoside]
C45H60O29     ÏàËÆ¶È:56.5%
Chemical & Pharmaceutical Bulletin          2009          57          276-279
Two New Flavonol Glycosides from Otostegia limbata BENTH.
Afsar Khan, Viqar Uddin Ahmad, Umar Farooq, Sadia Bader and Saima Arshad
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     descaffeoylmontbretin A
    ÏàËÆ¶È:56.5%
Phytochemistry          1988          27          1497-1501
Acylated flavonols from Crocosmia crocosmiiflora
Yoshihisa Asada,Yutaka Hirayama,Tsutomu Furuya
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     4''-O-alpha-D-maltosyl stevioside
C50H80O28     ÏàËÆ¶È:56.5%
Biotechnology Letters          2009          31          1415-1420
Simple and efficient enzymatic transglycosylation of stevioside by ¦Â-cyclodextrin glucanotransferase from Bacillus firmus
V. Jaitak, V. Kumar Kaul, Bandna, N. Kumar, B. Singh, L. S. Savergave, V. V. Jogdand, S. Nene
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     I-(2,3)-dihydro-I-7,II-7-di-O-¦Â-D-glucopyranosyl-amentoflavone
C42H40O20     ÏàËÆ¶È:56.5%
Natural Product Research          2014          28          41-47
Two new dihydroamentoflavone glycosides from Cycas revoluta
Abeer Moawad, Mona Hetta, Jordan K. Zjawiony, Daneel Ferreira & Mohamed Hifnawy
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     6''-O-(3R-1-N-¦Â-D-glucopyranosyl-2-oxo-3-hydroxy-indole-3-acetyl)spinosin
C44H49NO23     ÏàËÆ¶È:56.5%
Fitoterapia          2014          99          48-55
Indoleacetic acid derivatives from the seeds of Ziziphus jujuba var. spinosa
Min Li, Yu Wang, Bun Tsoi, Xiao-jie Jin, Rong-Rong He, Xiao-jun Yao, Yi Dai, Hiroshi Kurihara, Xin-Sheng Yao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     Kaempferol 3-O-[2G-(E)-Coumaroyl-3G-O-¦Â-D-glucosyl-3R-O-¦Â-D-glucosylrutinoside]
C48H56O27     ÏàËÆ¶È:56.5%
Chemical & Pharmaceutical Bulletin          2008          56          851-853
Structural Determination and DPPH Radical-Scavenging Activity of Two Acylated Flavonoid Tetraglycosides in Oolong Tea (Camellia sinensis)
Viola Szu-Yuan Lee, Chiy-Rong Chen, Yun-Wen Liao, Jason Tze-Cheng Tzen, Chi-I Chang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-[(¦Á-l-rhamnopyranosyl)oxy]-4H-chromen-3-yl b-d-glucopyranosyl-(1¡ú2)-[¦Â-D-glucopyranosyl-(1¡ú4)]-[6-O-[(2E)-3- (4-hydroxyphenyl)prop-2-enoyl]-¦Â-D-glucopyranosyl-(1¡ú3)]-¦Á-L-rhamnopyranoside
C54H66O31     ÏàËÆ¶È:56%
Helvetica Chimica Acta          2009          92          731-739
Two New Acylated Flavonol Glycosides from the Roots of Otostegia limbata
Afsar Khan, Viqar U. Ahmad, Umar Farooq
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-03-19 12:35:01
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